前往化源商城

4497-40-9 靶点实验数据

HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:NON-PROTEIN TARGET
External ID: CHEMBL3370107
Protocol: N/A
Comment: Journal: Bioorg. Med. Chem. Lett.
Year: 2014
Volume: 24
Issue: 16
First Page: 3797
Last Page: 3801
DOI: 10.1016/j.bmcl.2014.06.067

Target ChEMBL ID: CHEMBL3879801
ChEMBL Target Name: NON-PROTEIN TARGET
ChEMBL Target Type: NON-MOLECULAR - Target has not been defined at a molecular level, only the non-molecular entity which is affected (e.g., organism, cell line etc)
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
Standard TypeStandard UnitsActivity Comment
Inhibition%Not Active
Inhibition%Not Active
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:K562
External ID: CHEMBL3370108
Protocol: N/A
Comment: Journal: Bioorg. Med. Chem. Lett.
Year: 2014
Volume: 24
Issue: 16
First Page: 3797
Last Page: 3801
DOI: 10.1016/j.bmcl.2014.06.067

Target ChEMBL ID: CHEMBL385
ChEMBL Target Name: K562
ChEMBL Target Type: CELL-LINE - Target is a specific cell-line
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
Standard TypeActivity Comment
ActivityNot Active
ActivityNot Active
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Histone deacetylase 5
External ID: CHEMBL3370105
Protocol: N/A
Comment: Journal: Bioorg. Med. Chem. Lett.
Year: 2014
Volume: 24
Issue: 16
First Page: 3797
Last Page: 3801
DOI: 10.1016/j.bmcl.2014.06.067

Target ChEMBL ID: CHEMBL2093865
ChEMBL Target Name: Histone deacetylase
ChEMBL Target Type: PROTEIN FAMILY - Target is a group of closely related proteins
Relationship Type: D - Direct protein target assigned
Confidence: Multiple direct protein targets may be assigned
Standard TypeStandard RelationStandard ValueStandard Units
Activity=80%
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:NON-PROTEIN TARGET
External ID: CHEMBL3370106
Protocol: N/A
Comment: Journal: Bioorg. Med. Chem. Lett.
Year: 2014
Volume: 24
Issue: 16
First Page: 3797
Last Page: 3801
DOI: 10.1016/j.bmcl.2014.06.067

Target ChEMBL ID: CHEMBL3879801
ChEMBL Target Name: NON-PROTEIN TARGET
ChEMBL Target Type: NON-MOLECULAR - Target has not been defined at a molecular level, only the non-molecular entity which is affected (e.g., organism, cell line etc)
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
Standard TypeStandard UnitsActivity Comment
Inhibition%Active
Inhibition%Active
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Trichophyton rubrum
External ID: CHEMBL3075363
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL612649
ChEMBL Target Name: Trichophyton rubrum
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity Comment
600MIC=600000nM
3720MIC=3720000nM
920MIC=920000nM
6160MIC=6160000nM
830MIC=830000nM
770MIC=770000nM
MICNot Active
3080MIC=3080000nM
2600MIC=2600000nM
160MIC=160000nM
730MIC=730000nM
8990MIC=8990000nM
MICNot Active
990MIC=990000nM
350MIC=350000nM
MICNot Active
MICNot Active
810MIC=810000nM
1700MIC=1700000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Aspergillus parasiticus
External ID: CHEMBL3074439
Protocol: N/A
Comment: Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL613814
ChEMBL Target Name: Aspergillus parasiticus
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
1200MIC=1200000nM
14900MIC=14900000nMOutside typical range
1830MIC=1830000nM
MICNot Active
3330MIC=3330000nM
3080MIC=3080000nM
MICNot Active
MICNot Active
2600MIC=2600000nM
2550MIC=2550000nM
MICNot Active
MICNot Active
MICNot Active
1990MIC=1990000nM
710MIC=710000nM
MICNot Active
MICNot Active
MICNot Active
1700MIC=1700000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Aspergillus sydowii
External ID: CHEMBL3074438
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL2367171
ChEMBL Target Name: Aspergillus sydowii
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity Comment
2400MIC=2400000nM
3720MIC=3720000nM
1830MIC=1830000nM
MICNot Active
3330MIC=3330000nM
3080MIC=3080000nM
MICNot Active
MICNot Active
5200MIC=5200000nM
5100MIC=5100000nM
MICNot Active
4500MIC=4500000nM
MICNot Active
1990MIC=1990000nM
350MIC=350000nM
MICNot Active
MICNot Active
MICNot Active
850MIC=850000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Pichia kudriavzevii
External ID: CHEMBL3074441
Protocol: N/A
Comment: Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL612841
ChEMBL Target Name: Pichia kudriavzevii
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity Comment
1200MIC=1200000nM
3720MIC=3720000nM
3670MIC=3670000nM
6160MIC=6160000nM
830MIC=830000nM
770MIC=770000nM
6740MIC=6740000nM
MICNot Active
2600MIC=2600000nM
2550MIC=2550000nM
730MIC=730000nM
8990MIC=8990000nM
MICNot Active
490MIC=490000nM
350MIC=350000nM
MICNot Active
MICNot Active
1620MIC=1620000nM
1700MIC=1700000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Human immunodeficiency virus 1
External ID: CHEMBL949642
Protocol: N/A
Comment: Journal: J. Nat. Prod.
Year: 2001
Volume: 64
Issue: 10
First Page: 1278
Last Page: 1281
DOI: 10.1021/np010211x

Target ChEMBL ID: CHEMBL378
ChEMBL Target Name: Human immunodeficiency virus 1
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
Standard TypeStandard RelationStandard ValueStandard UnitsActivity Comment
EC50Not Active
EC50=0.00289ug.mL-1
EC50=0.22ug.mL-1
EC50Not Active
EC50Not Active
EC50Not Active
EC50=2.19ug.mL-1
EC50=2.7ug.mL-1
EC50<0.1ug.mL-1
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Aspergillus niger
External ID: CHEMBL3074440
Protocol: N/A
Comment: Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL358
ChEMBL Target Name: Aspergillus niger
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity Comment
4800MIC=4800000nM
7450MIC=7450000nM
7340MIC=7340000nM
MICNot Active
3330MIC=3330000nM
3080MIC=3080000nM
MICNot Active
MICNot Active
5200MIC=5200000nM
5100MIC=5100000nM
MICNot Active
MICNot Active
MICNot Active
990MIC=990000nM
1420MIC=1420000nM
MICNot Active
MICNot Active
MICNot Active
1700MIC=1700000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:H9
External ID: CHEMBL949641
Protocol: N/A
Comment: Journal: J. Nat. Prod.
Year: 2001
Volume: 64
Issue: 10
First Page: 1278
Last Page: 1281
DOI: 10.1021/np010211x

Target ChEMBL ID: CHEMBL614806
ChEMBL Target Name: H9
ChEMBL Target Type: CELL-LINE - Target is a specific cell-line
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
Standard TypeStandard RelationStandard ValueStandard UnitsData Validity Comment
IC50>100ug.mL-1Outside typical range
IC50=500ug.mL-1Outside typical range
IC50=1.8ug.mL-1
IC50=0.205ug.mL-1
IC50=2.14ug.mL-1
IC50=18.8ug.mL-1
IC50=18.9ug.mL-1
IC50=22.1ug.mL-1
IC50=18.6ug.mL-1
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:NIAID 靶标:N/A
External ID: HIV Cellular Data
Protocol: N/A
Comment: N/A
SpeciesStrainIsPseudotypeVirusAssayMethCellTypeCellType2TargetMutationsEC50ModEC50EC50UnitECOtherPctECOtherPctUnitECOtherConcECOtherConcUnitToxAssayMethToxCellTypeCC50ModCC50CC50UnitTIModTIRelResFoldChgCommentsReferenceCitationOther Information
HIV-1LAIRTHuT TK+HuT 78Reverse transcriptase<1uM100%1uMMTT>10uM>10HuT TK+=HuT 78 CELLS EXPRESSING HSV-1 THYMIDINE KINASE; MEASUREMENT WAS MADE ON DAY10 POSTINFECTION AT 10 TCID509281520USE OF HERPES SIMPLEX VIRUS THYMIDINE KINASE TO IMPROVE THE ANTIVIRAL ACTIVITY OF ZIDOVUDINE. Virology 1997, 235, 398-405.
HIV-1MNRTHuT TK+HuT 78Reverse transcriptase<0.3uM76.74%0.3uMMTT>10uM>33.3HuT TK+=HuT 78 CELLS EXPRESSING HSV-1 THYMIDINE KINASE; MEASUREMENT WAS MADE ON DAY14 POSTINFECTION AT 10 TCID509281520USE OF HERPES SIMPLEX VIRUS THYMIDINE KINASE TO IMPROVE THE ANTIVIRAL ACTIVITY OF ZIDOVUDINE. Virology 1997, 235, 398-405.
HIV-1MNRTHuT TK+HuT 78Reverse transcriptase<0.3uM69%0.3uMMTT>10uM>33.3HuT TK+=HuT 78 CELLS EXPRESSING HSV-1 THYMIDINE KINASE; MEASUREMENT WAS MADE ON DAY14 POSTINFECTION AT 100 TCID509281520USE OF HERPES SIMPLEX VIRUS THYMIDINE KINASE TO IMPROVE THE ANTIVIRAL ACTIVITY OF ZIDOVUDINE. Virology 1997, 235, 398-405.
R5; CLINICAL ISOLATE1(JSL)P24PBMCReverse transcriptaseMDR0.07uM90%1uMMTT>100uM>1428HIV-1(JSL) WAS ISOLATED FROM PATIENTS WHO RECEIVED ANTIRETROVIRAL THERAPY FOR A LONG PERIOD AND WHOSE VIRUS ACQUIRED A NUMBER OF MUTATIONS IN THE RT- AND PR-ENCODING GENES; DETAILS OF MUTATIONS NOT GIVEN15280474SPIRODIKETOPIPERAZINE-BASED CCR5 INHIBITOR WHICH PRESERVES CC-CHEMOKINE/CCR5 INTERACTIONS AND EXERTS POTENT ACTIVITY AGAINST R5 HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 IN VITRO. Journal of Virology 2004, 78(16), 8654-8662.ECOtherConcMod:>
HIV-1NL4-3LUCIFERASE1G5 TReverse transcriptase<1uM99%1uMTRYPAN BLUE>1uM>1ASSAY WAS CONDUCTED ON DAY 3 POST-INFECTION16725040INHIBITION OF HIGHLY PRODUCTIVE HIV-1 INFECTION IN T CELLS, PRIMARY HUMAN MACROPHAGES, MICROGLIA, AND ASTROCYTES BY SARGASSUM FUSIFORME. AIDS Research and Therapy 2006, 3(1), 15 PP.CCOtherPct:6 | CCOtherPctUnit:% | CCOtherConc:1 | CCOtherConcUnit:uM
HIV-1NL4-3LUCIFERASE1G5 TReverse transcriptase<1uM99%1uMTRYPAN BLUE>1uM>1ASSAY WAS CONDUCTED ON DAY 5 POST-INFECTION16725040INHIBITION OF HIGHLY PRODUCTIVE HIV-1 INFECTION IN T CELLS, PRIMARY HUMAN MACROPHAGES, MICROGLIA, AND ASTROCYTES BY SARGASSUM FUSIFORME. AIDS Research and Therapy 2006, 3(1), 15 PP.CCOtherPct:7 | CCOtherPctUnit:% | CCOtherConc:1 | CCOtherConcUnit:uM
HIV-1NL4-3LUCIFERASE1G5 TReverse transcriptase<1uM99%1uMTRYPAN BLUE>1uM>1ASSAY WAS CONDUCTED ON DAY 7 POST-INFECTION16725040INHIBITION OF HIGHLY PRODUCTIVE HIV-1 INFECTION IN T CELLS, PRIMARY HUMAN MACROPHAGES, MICROGLIA, AND ASTROCYTES BY SARGASSUM FUSIFORME. AIDS Research and Therapy 2006, 3(1), 15 PP.CCOtherPct:3 | CCOtherPctUnit:% | CCOtherConc:1 | CCOtherConcUnit:uM
HIV-1LAVRTU1(THF-.alpha. STIM)U1Tumor necrosis factor alpha~30ug/mL70%50ug/mL>50ug/mL>1.66CHRONICALLY HIV-1 INFECTED PROMONOCYTE CELL LINE8327469THALIDOMIDE INHIBITS THE REPLICATION OF HUMAN IMMUNODEFICIENCY VIRUS TYPE 1. Proceedings of the National Academy of Sciences of the United States of America 1993, 90, 5974-5978.CCOtherPct:0 | CCOtherPctUnit:% | CCOtherConc:50 | CCOtherConcUnit:ug/mL
HIV-1BaLP24 (DAY 18)MACROPHAGES(GM-CSF)MacrophageRibonucleotide reductase<10uM75%10uM>1000uM>10MAXIMAL P24 EXPRESSION AT DAY 187973634HYDROXYUREA AS AN INHIBITOR OF HUMAN IMMUNODEFICIENCY VIRUS-TYPE 1 REPLICATION. Science 1994, 266(5186), 801-805.CCOtherPct:0 | CCOtherPctUnit:% | CCOtherConc:1000 | CCOtherConcUnit:uM
HIV-1BaLP24 (DAY 18)MACROPHAGES(GM-CSF)MacrophageRibonucleotide reductase<10uM38%2uM>1000uM>10MAXIMAL P24 EXPRESSION AT DAY 187973634HYDROXYUREA AS AN INHIBITOR OF HUMAN IMMUNODEFICIENCY VIRUS-TYPE 1 REPLICATION. Science 1994, 266(5186), 801-805.CCOtherPct:0 | CCOtherPctUnit:% | CCOtherConc:1000 | CCOtherConcUnit:uM
HIV-1BaLP24 (DAY 18)MACROPHAGES(GM-CSF)MacrophageRibonucleotide reductase<10uM99%50uM>1000uM>10MAXIMAL P24 EXPRESSION AT DAY 187973634HYDROXYUREA AS AN INHIBITOR OF HUMAN IMMUNODEFICIENCY VIRUS-TYPE 1 REPLICATION. Science 1994, 266(5186), 801-805.ECOtherPctMod:> | CCOtherPct:0 | CCOtherPctUnit:% | CCOtherConc:1000 | CCOtherConcUnit:uM
HIV-1IIIBRTHT4(R116; AZT RESISTANT CELLS)HT4Reverse transcriptase~0.01uM70%0.01uM~`1uM~100FLOXURIDINE APPEARS TO POTENTIATE AZT ACTIVITY AND ALSO HAVE SOME ANTI-HIV ACTIVITY IN AZT RESISTANT CELL LINES8827211USE OF FLOXURIDINE TO MODULATE THE ANTIVIRAL ACTIVITY OF ZIDOVUDINE. AIDS Research and Human Retroviruses 1996, 12(11), 965-968.ECOtherPctMod:~ | CCOtherPct:35 | CCOtherPctUnit:% | CCOtherConc:.1 | CCOtherConcUnit:uM
HIV-11.beta.GAL AS A MEASURE OF TAT-MEDIATED TRANSACTIVATIONHeLa H12(HIV-1 LTR-Laz, TAT)HeLaTat:TAR/LTR<0.1uM52%0.1uMTRYPAN BLUE>100uM>1000DRUG AND RECOMBINANT TAT WERE INTRODUCED INTO CELLS THROUGH ELECTROPORATION9561563CURCUMIN AND CURCUMIN DERIVATIVES INHIBIT TAT-MEDIATED TRANSACTIVATION OF TYPE 1 HUMAN IMMUNODEFICIENCY VIRUS LONG TERMINAL REPEAT. Research in Virology 1998, 149(1), 43-52.
HIV-11.beta.GAL AS A MEASURE OF TAT-MEDIATED TRANSACTIVATIONHeLa H12(HIV-1 LTR-Laz, TAT)HeLaTat:TAR/LTR<0.01uM78%0.01uMTRYPAN BLUE>100uM>10000DRUG AND RECOMBINANT TAT WERE INTRODUCED INTO CELLS THROUGH ELECTROPORATION9561563CURCUMIN AND CURCUMIN DERIVATIVES INHIBIT TAT-MEDIATED TRANSACTIVATION OF TYPE 1 HUMAN IMMUNODEFICIENCY VIRUS LONG TERMINAL REPEAT. Research in Virology 1998, 149(1), 43-52.
HIV-1IIIBSYNCYT FORMMOLT-4/H9(HIV-1(IIIB))MOLT-4gp120<1uM95%10uM-10010uM>10CHRONICALLY INFECTED H9 CELLS9343823TRIAZINE DYES INHIBIT HIV-1 ENTRY BY BINDING TO ENVELOPE GLYCOPROTEINS. Microbiology and Immunology 1997, 41(9), 717-724.CCOtherPct:30 | CCOtherPctUnit:% | CCOtherConc:10 | CCOtherConcUnit:uM
HIV-11.beta.GAL AS A MEASURE OF TAT-MEDIATED TRANSACTIVATIONHeLa H12(HIV-1 LTR-Laz, TAT)HeLaTat:TAR/LTR<0.01uM75%0.01uMTRYPAN BLUE>100uM>10000DRUG AND RECOMBINANT TAT WERE INTRODUCED INTO CELLS THROUGH ELECTROPORATION9561563CURCUMIN AND CURCUMIN DERIVATIVES INHIBIT TAT-MEDIATED TRANSACTIVATION OF TYPE 1 HUMAN IMMUNODEFICIENCY VIRUS LONG TERMINAL REPEAT. Research in Virology 1998, 149(1), 43-52.
HIV-11P24MT-4Integrase<0.25uM95%0.25uMMICROSCOPIC EXAMINATION>20uM>80IN THE PRESENCE OF 50% NHS16554152A SERIES OF 5-AMINOSUBSTITUTED 4-FLUOROBENZYL-8-HYDROXY-[1,6]NAPHTHYRIDINE-7-CARBOXAMIDE HIV-1 INTEGRASE INHIBITORS. Bioorganic & Medical Chemistry Letters 2006, 16(11), 2900-2904.ECOtherPctMod:>
HIV-11P24MT-4Integrase<0.103uM95%0.103uMMICROSCOPIC EXAMINATION>20uM>194IN THE PRESENCE OF 10% FBS16554152A SERIES OF 5-AMINOSUBSTITUTED 4-FLUOROBENZYL-8-HYDROXY-[1,6]NAPHTHYRIDINE-7-CARBOXAMIDE HIV-1 INTEGRASE INHIBITORS. Bioorganic & Medical Chemistry Letters 2006, 16(11), 2900-2904.ECOtherPctMod:>
HIV-1NL4-3RTMT-4Reverse transcriptase<1uM100%1uMWST-8>1uM>1MEASUREMENTS WERE MADE ON DAY 4, 6 AND 8 POST INFECTION15371436POLYARGININE INHIBITS GP160 PROCESSING BY FURIN AND SUPPRESSES PRODUCTIVE HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 INFECTION. The Journal of Biological Chemistry 2004, 279(47), 49055-49063.
HIV-1LAIRTHuT 78Reverse transcriptase<1uM57.14%1uMMTT>10uM>10MEASUREMENT WAS MADE ON DAY10 POSTINFECTION AT 10 TCID509281520USE OF HERPES SIMPLEX VIRUS THYMIDINE KINASE TO IMPROVE THE ANTIVIRAL ACTIVITY OF ZIDOVUDINE. Virology 1997, 235, 398-405.
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Enterobacter cloacae
External ID: CHEMBL3074443
Protocol: N/A
Comment: Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL349
ChEMBL Target Name: Enterobacter cloacae
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
9600MIC=9600000nM
7450MIC=7450000nM
14690MIC=14690000nMOutside typical range
5700MIC=5700000nM
MICNot Active
3330MIC=3330000nM
3080MIC=3080000nM
MICNot Active
MICNot Active
10400MIC=10400000nMOutside typical range
10190MIC=10190000nMOutside typical range
MICNot Active
MICNot Active
11410MIC=11410000nMOutside typical range
990MIC=990000nM
1420MIC=1420000nM
MICNot Active
10460MIC=10460000nMOutside typical range
810MIC=810000nM
MICNot Active
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Candida albicans
External ID: CHEMBL3074442
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL366
ChEMBL Target Name: Candida albicans
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity Comment
600MIC=600000nM
3720MIC=3720000nM
3670MIC=3670000nM
6160MIC=6160000nM
830MIC=830000nM
770MIC=770000nM
6740MIC=6740000nM
MICNot Active
2600MIC=2600000nM
2550MIC=2550000nM
730MIC=730000nM
8990MIC=8990000nM
MICNot Active
990MIC=990000nM
350MIC=350000nM
MICNot Active
MICNot Active
810MIC=810000nM
1700MIC=1700000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:N/A
External ID: CHEMBL949643
Protocol: N/A
Comment: Journal: J. Nat. Prod.
Year: 2001
Volume: 64
Issue: 10
First Page: 1278
Last Page: 1281
DOI: 10.1021/np010211x
Standard TypeStandard RelationStandard ValueActivity Comment
Ratio IC50/EC50Not Active
Ratio IC50/EC50=173000
Ratio IC50/EC50=8
Ratio IC50/EC50Not Active
Ratio IC50/EC50Not Active
Ratio IC50/EC50Not Active
Ratio IC50/EC50=8.62
Ratio IC50/EC50=8.17
Ratio IC50/EC50>186
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:N/A
External ID: CHEMBL965954
Protocol: N/A
Comment: Journal: J. Nat. Prod.
Year: 2002
Volume: 65
Issue: 9
First Page: 1278
Last Page: 1282
DOI: 10.1021/np0202475
Standard TypeStandard RelationStandard ValueStandard Units
IC50=2.3ug.mL-1
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Quinone oxidoreductase
External ID: CHEMBL961907
Protocol: N/A
Comment: Journal: J. Nat. Prod.
Year: 2002
Volume: 65
Issue: 9
First Page: 1278
Last Page: 1282
DOI: 10.1021/np0202475

Target ChEMBL ID: CHEMBL4332
ChEMBL Target Name: Quinone oxidoreductase
ChEMBL Target Type: SINGLE PROTEIN - Target is a single protein chain
Relationship Type: D - Direct protein target assigned
Confidence: Direct single protein target assigned
Standard TypeStandard RelationStandard ValueStandard Units
CD=9.5ug ml-1
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:PBMC
External ID: CHEMBL3370104
Protocol: N/A
Comment: Journal: Bioorg. Med. Chem. Lett.
Year: 2014
Volume: 24
Issue: 16
First Page: 3797
Last Page: 3801
DOI: 10.1016/j.bmcl.2014.06.067

Target ChEMBL ID: CHEMBL613107
ChEMBL Target Name: PBMC
ChEMBL Target Type: CELL-LINE - Target is a specific cell-line
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
Standard TypeActivity Comment
ActivityNon-toxic
ActivityNon-toxic
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:K562
External ID: CHEMBL3370101
Protocol: N/A
Comment: Journal: Bioorg. Med. Chem. Lett.
Year: 2014
Volume: 24
Issue: 16
First Page: 3797
Last Page: 3801
DOI: 10.1016/j.bmcl.2014.06.067

Target ChEMBL ID: CHEMBL385
ChEMBL Target Name: K562
ChEMBL Target Type: CELL-LINE - Target is a specific cell-line
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
Standard TypeStandard UnitsActivity Comment
Inhibition%Not Active
Inhibition%Not Active
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Klebsiella pneumoniae
External ID: CHEMBL3074445
Protocol: N/A
Comment: Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL350
ChEMBL Target Name: Klebsiella pneumoniae
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
MICNot Active
7450MIC=7450000nM
14690MIC=14690000nMOutside typical range
5700MIC=5700000nM
MICNot Active
3330MIC=3330000nM
3080MIC=3080000nM
MICNot Active
MICNot Active
10400MIC=10400000nMOutside typical range
10190MIC=10190000nMOutside typical range
MICNot Active
MICNot Active
MICNot Active
990MIC=990000nM
1420MIC=1420000nM
MICNot Active
10460MIC=10460000nMOutside typical range
810MIC=810000nM
MICNot Active
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Pseudomonas aeruginosa
External ID: CHEMBL3074444
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL348
ChEMBL Target Name: Pseudomonas aeruginosa
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
MICNot Active
7450MIC=7450000nM
MICNot Active
2800MIC=2800000nM
MICNot Active
830MIC=830000nM
770MIC=770000nM
MICNot Active
MICNot Active
2600MIC=2600000nM
2550MIC=2550000nM
MICNot Active
MICNot Active
MICNot Active
250MIC=250000nM
350MIC=350000nM
MICNot Active
2610MIC=2610000nM
810MIC=810000nM
MICNot Active
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Burkholderia cepacia
External ID: CHEMBL3074447
Protocol: N/A
Comment: Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL612499
ChEMBL Target Name: Burkholderia cepacia
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
MICNot Active
14900MIC=14900000nMOutside typical range
14690MIC=14690000nMOutside typical range
5700MIC=5700000nM
MICNot Active
MICNot Active
MICNot Active
MICNot Active
MICNot Active
5200MIC=5200000nM
5100MIC=5100000nM
730MIC=730000nM
MICNot Active
MICNot Active
490MIC=490000nM
710MIC=710000nM
MICNot Active
2610MIC=2610000nM
810MIC=810000nM
1700MIC=1700000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Escherichia coli
External ID: CHEMBL3074446
Protocol: N/A
Comment: Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL354
ChEMBL Target Name: Escherichia coli
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
MICNot Active
7450MIC=7450000nM
14690MIC=14690000nMOutside typical range
80MIC=80000nM
MICNot Active
3330MIC=3330000nM
3080MIC=3080000nM
MICNot Active
MICNot Active
10400MIC=10400000nMOutside typical range
10190MIC=10190000nMOutside typical range
MICNot Active
MICNot Active
MICNot Active
1990MIC=1990000nM
2840MIC=2840000nM
MICNot Active
2610MIC=2610000nM
810MIC=810000nM
MICNot Active
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Bacillus subtilis
External ID: CHEMBL3074449
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL359
ChEMBL Target Name: Bacillus subtilis
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
MICNot Active
7450MIC=7450000nM
14690MIC=14690000nMOutside typical range
10MIC=10000nM
MICNot Active
6660MIC=6660000nM
6160MIC=6160000nM
MICNot Active
MICNot Active
5200MIC=5200000nM
5100MIC=5100000nM
730MIC=730000nM
MICNot Active
MICNot Active
1990MIC=1990000nM
2840MIC=2840000nM
MICNot Active
2610MIC=2610000nM
400MIC=400000nM
850MIC=850000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Micrococcus luteus
External ID: CHEMBL3074448
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL614421
ChEMBL Target Name: Micrococcus luteus
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
MICNot Active
7450MIC=7450000nM
MICNot Active
10MIC=10000nM
MICNot Active
3330MIC=3330000nM
3080MIC=3080000nM
MICNot Active
MICNot Active
2600MIC=2600000nM
2550MIC=2550000nM
730MIC=730000nM
2250MIC=2250000nM
11410MIC=11410000nMOutside typical range
990MIC=990000nM
2840MIC=2840000nM
MICNot Active
2610MIC=2610000nM
200MIC=200000nM
850MIC=850000nM
HepG2 Cytotoxicity Assay Measured in Cell-Based System Using Plate Reader - 7071-02_Inhibitor_Dose_DryPowder_Activity_Set16
来源:ChEMBL 靶标:Staphylococcus aureus
External ID: CHEMBL3074450
Protocol: N/A
Comment: Compounds with activity <= 10uM or explicitly reported as active by ChEMBL are flagged as active in this PubChem assay presentation.

Journal: Med Chem Res
Year: 2013
Volume: 22
Issue: 11
First Page: 5129
Last Page: 5140
DOI: 10.1007/s00044-013-0484-9

Target ChEMBL ID: CHEMBL352
ChEMBL Target Name: Staphylococcus aureus
ChEMBL Target Type: ORGANISM - Target is a complete organism
Relationship Type: N - Non-molecular target assigned
Confidence: Target assigned is non-molecular
PubChem Standard ValueStandard TypeStandard RelationStandard ValueStandard UnitsActivity CommentData Validity Comment
MICNot Active
14900MIC=14900000nMOutside typical range
1830MIC=1830000nM
10MIC=10000nM
MICNot Active
3330MIC=3330000nM
3080MIC=3080000nM
MICNot Active
MICNot Active
5200MIC=5200000nM
5100MIC=5100000nM
730MIC=730000nM
MICNot Active
MICNot Active
1990MIC=1990000nM
2840MIC=2840000nM
MICNot Active
10460MIC=10460000nMOutside typical range
200MIC=200000nM
850MIC=850000nM