Chemsrc provides Others's classification. They are divided into Androgen Receptor, Aromatase, Estrogen Receptor/ERR, Progesterone Receptor, Thyroid Hormone Receptor, Others according to their Biological activity.


Anti-infection >
Arenavirus Bacterial CMV Enterovirus Filovirus Fungal HBV HCV HIV HSV Influenza Virus Parasite Reverse Transcriptase RSV SARS-CoV
Antibody-drug Conjugate >
ADC Cytotoxin ADC Linker Drug-Linker Conjugates for ADC PROTAC-linker Conjugate for PAC
Apoptosis >
Apoptosis Bcl-2 Family c-Myc Caspase DAPK Ferroptosis IAP MDM-2/p53 PKD RIP kinase Survivin Thymidylate Synthase TNF Receptor
Autophagy >
Autophagy LRRK2 ULK Mitophagy
Cell Cycle/DNA Damage >
Antifolate APC ATM/ATR Aurora Kinase Casein Kinase CDK Checkpoint Kinase (Chk) CRISPR/Cas9 Deubiquitinase DNA Alkylator/Crosslinker DNA-PK DNA/RNA Synthesis Eukaryotic Initiation Factor (eIF) G-quadruplex Haspin Kinase HDAC HSP IRE1 Kinesin LIM Kinase (LIMK) Microtubule/Tubulin Mps1 Nucleoside Antimetabolite/Analog p97 PAK PARP PERK Polo-like Kinase (PLK) PPAR RAD51 ROCK Sirtuin SRPK Telomerase TOPK Topoisomerase Wee1
Cytoskeleton >
Arp2/3 Complex Dynamin Gap Junction Protein Integrin Kinesin Microtubule/Tubulin Mps1 Myosin PAK
Epigenetics >
AMPK Aurora Kinase DNA Methyltransferase Epigenetic Reader Domain HDAC Histone Acetyltransferase Histone Demethylase Histone Methyltransferase JAK MicroRNA PARP PKC Sirtuin Protein Arginine Deiminase
GPCR/G Protein >
5-HT Receptor Adenosine Receptor Adenylate Cyclase Adiponectin Receptor Adrenergic Receptor Angiotensin Receptor Bombesin Receptor Bradykinin Receptor Cannabinoid Receptor CaSR CCR CGRP Receptor Cholecystokinin Receptor CRFR CXCR Dopamine Receptor EBI2/GPR183 Endothelin Receptor GHSR Glucagon Receptor Glucocorticoid Receptor GNRH Receptor GPCR19 GPR109A GPR119 GPR120 GPR139 GPR40 GPR55 GPR84 Guanylate Cyclase Histamine Receptor Imidazoline Receptor Leukotriene Receptor LPL Receptor mAChR MCHR1 (GPR24) Melatonin Receptor mGluR Motilin Receptor Neurokinin Receptor Neuropeptide Y Receptor Neurotensin Receptor Opioid Receptor Orexin Receptor (OX Receptor) Oxytocin Receptor P2Y Receptor Prostaglandin Receptor Protease-Activated Receptor (PAR) Ras RGS Protein Sigma Receptor Somatostatin Receptor TSH Receptor Urotensin Receptor Vasopressin Receptor Melanocortin Receptor
Immunology/Inflammation >
Aryl Hydrocarbon Receptor CCR Complement System COX CXCR FLAP Histamine Receptor IFNAR Interleukin Related IRAK MyD88 NO Synthase NOD-like Receptor (NLR) PD-1/PD-L1 PGE synthase Salt-inducible Kinase (SIK) SPHK STING Thrombopoietin Receptor Toll-like Receptor (TLR) Arginase
JAK/STAT Signaling >
EGFR JAK Pim STAT
MAPK/ERK Pathway >
ERK JNK KLF MAP3K MAP4K MAPKAPK2 (MK2) MEK Mixed Lineage Kinase MNK p38 MAPK Raf Ribosomal S6 Kinase (RSK)
Membrane Transporter/Ion Channel >
ATP Synthase BCRP Calcium Channel CFTR Chloride Channel CRAC Channel CRM1 EAAT2 GABA Receptor GlyT HCN Channel iGluR Monoamine Transporter Monocarboxylate Transporter Na+/Ca2+ Exchanger Na+/HCO3- Cotransporter Na+/K+ ATPase nAChR NKCC P-glycoprotein P2X Receptor Potassium Channel Proton Pump SGLT Sodium Channel TRP Channel URAT1
Metabolic Enzyme/Protease >
15-PGDH 5 alpha Reductase 5-Lipoxygenase Acetyl-CoA Carboxylase Acyltransferase Adenosine Deaminase Adenosine Kinase Aldehyde Dehydrogenase (ALDH) Aldose Reductase Aminopeptidase Angiotensin-converting Enzyme (ACE) ATGL ATP Citrate Lyase Carbonic Anhydrase Carboxypeptidase Cathepsin CETP COMT Cytochrome P450 Dipeptidyl Peptidase Dopamine β-hydroxylase E1/E2/E3 Enzyme Elastase Enolase FAAH FABP Factor Xa Farnesyl Transferase Fatty Acid Synthase (FAS) FXR Glucokinase GSNOR Gutathione S-transferase HCV Protease Hexokinase HIF/HIF Prolyl-Hydroxylase HIV Integrase HIV Protease HMG-CoA Reductase (HMGCR) HSP Indoleamine 2,3-Dioxygenase (IDO) Isocitrate Dehydrogenase (IDH) Lactate Dehydrogenase LXR MAGL Mineralocorticoid Receptor Mitochondrial Metabolism MMP Nampt NEDD8-activating Enzyme Neprilysin PAI-1 PDHK PGC-1α Phosphatase Phosphodiesterase (PDE) Phospholipase Procollagen C Proteinase Proteasome Pyruvate Kinase RAR/RXR Renin ROR Ser/Thr Protease SGK Stearoyl-CoA Desaturase (SCD) Thrombin Tryptophan Hydroxylase Tyrosinase Xanthine Oxidase
Neuronal Signaling >
5-HT Receptor AChE Adenosine Kinase Amyloid-β Beta-secretase CaMK CGRP Receptor COMT Dopamine Receptor Dopamine Transporter FAAH GABA Receptor GlyT iGluR Imidazoline Receptor mAChR Melatonin Receptor Monoamine Oxidase nAChR Neurokinin Receptor Opioid Receptor Serotonin Transporter γ-secretase
NF-κB >
NF-κB IKK Keap1-Nrf2 MALT1
PI3K/Akt/mTOR >
Akt AMPK ATM/ATR DNA-PK GSK-3 MELK mTOR PDK-1 PI3K PI4K PIKfyve PTEN
PROTAC >
PROTAC E3 Ligase Ligand-Linker Conjugate Ligand for E3 Ligase PROTAC Linker PROTAC-linker Conjugate for PAC
Protein Tyrosine Kinase/RTK >
Ack1 ALK Bcr-Abl BMX Kinase Btk c-Fms c-Kit c-Met/HGFR Discoidin Domain Receptor DYRK EGFR Ephrin Receptor FAK FGFR FLT3 IGF-1R Insulin Receptor IRAK Itk PDGFR PKA Pyk2 ROS Src Syk TAM Receptor Trk Receptor VEGFR
Stem Cell/Wnt >
Casein Kinase ERK Gli GSK-3 Hedgehog Hippo (MST) JAK Notch Oct3/4 PKA Porcupine ROCK sFRP-1 Smo STAT TGF-beta/Smad Wnt YAP β-catenin γ-secretase
TGF-beta/Smad >
TGF-beta/Smad PKC ROCK TGF-β Receptor
Vitamin D Related >
VD/VDR
Others >
Androgen Receptor Aromatase Estrogen Receptor/ERR Progesterone Receptor Thyroid Hormone Receptor Others

Modotuximab

Modotuximab (Anti-Human EGFR Recombinant Antibody) is an IgG1κ-type chimeric antibody targeting human EGFR protein. Modotuximab contains a portion of Futuximab that binds to two independent, non-overlapping epitopes on EGFR. Modotuximab promotes cross-linking of EGFR on the cell surface and promotes EGFR cellular internalization and degradation. Modotuximab has antitumor activity in vivo[1].

  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Mifepristone

Mifepristone is a progesterone receptor (PR) and glucocorticoid receptor (GR) antagonist with IC50s of 0.2 nM and 2.6 nM in in vitro assay.

  • CAS Number: 84371-65-3
  • MF: C29H35NO2
  • MW: 429.594
  • Catalog: Autophagy
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 628.6±55.0 °C at 760 mmHg
  • Melting Point: 195-198°C
  • Flash Point: 334.0±31.5 °C

Presenilin 1 (349-361)

Presenilin 1 (349-361) is an active petide, and synthetic peptides representing amino acids 349–361 can be phosphorylated by glycogen synthase kinase-3β(GSK3β) in vitro. Presenilin 1 (349-361) can be used for the research of various diseases[1].

  • CAS Number: 956004-39-0
  • MF: C56H93N21O19
  • MW: 1364.47
  • Catalog: Cancer
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Catechin 7-O-beta-D-glucopyranoside

Catechin 7-O-beta-D-glucopyranoside is an orally active natural product found in Ulmus davidiana and Paeonia obovata. Catechin 7-O-β-D-glucopyranoside shows antioxidant and anti-inflammatory activities, and attenuates mitochondrial dysfunction. Catechin 7-O-beta-D-glucopyranoside can be used in intestinal inflammatory disease research[1][2][3].

  • CAS Number: 65597-47-9
  • MF: C10H9N3O2
  • MW: 203.19700
  • Catalog: Inflammation/Immunology
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Isoescin Ie

Isoescin Ie is a derivative of Aescine in Aesculi Semen extract[1].

  • CAS Number: 1613506-28-7
  • MF: C49H76O19
  • MW: 969.12
  • Catalog: Others
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

5-PT

5-PT is a serotonin derivative that can be functionalized with various reporter groups via click chemistry to investigate protein serotonylation. 5-PT can be used in vivo to observe endogenous protein serotonylation[1].

  • CAS Number: 92085-05-7
  • MF: C13H14N2O
  • MW: 214.26
  • Catalog: Others
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Etamivan

Etamivan is a respiratory stimulant drug, mainly used in the treatment of barbiturate overdose and chronic obstructive pulmonary disease.

  • CAS Number: 304-84-7
  • MF: C12H17NO3
  • MW: 223.26800
  • Catalog: Neurological Disease
  • Density: 1.115g/cm3
  • Boiling Point: 401.4ºC at 760mmHg
  • Melting Point: 96-97ºC
  • Flash Point: 196.6ºC

Isoamylase

Isoamylase (Glycogen α-1,6-glucanohydrolase) catalyzes the hydrolysis of α-1,6-glycosidic linkages in glycogen, amylopectin and α/β-limit dextrins[1].

  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Cis-Emodin bianthrone

Cis-Emodin bianthrone (compound 4) is a highly condensed oxygen of emodin anthrone. Cis-Emodin bianthrone stable in acetone solution in air[1].

  • CAS Number: 61281-19-4
  • MF: C30H22O8
  • MW: 510.49
  • Catalog: Others
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

(+)-syringaresinol

(+)-Syringaresinol, a lignan, is a NFAT transcription factor inhibitor, with an IC50 of 329.4 μM. (+)-Syringaresinol also can be used for the research of lymphocytic leukemia[1][2].

  • CAS Number: 21453-69-0
  • MF: C22H26O8
  • MW: 418.437
  • Catalog: Cancer
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 594.7±50.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 313.5±30.1 °C

POLY(ACRYLIC ACID)

Carbomer copolymer can be used as an excipient, such as Bioadhesives, emulsifiers, release modifiers, suspending agents, tablet binders, viscosity enhancers, etc. Pharmaceutical excipients, or pharmaceutical auxiliaries, refer to other chemical substances used in the pharmaceutical process other than pharmaceutical ingredients. Pharmaceutical excipients generally refer to inactive ingredients in pharmaceutical preparations, which can improve the stability, solubility and processability of pharmaceutical preparations. Pharmaceutical excipients also affect the absorption, distribution, metabolism, and elimination (ADME) processes of co-administered drugs[1].

  • CAS Number: 9007-20-9
  • MF: C3H4O2
  • MW: 280.747
  • Catalog: Others
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 502.0±45.0 °C at 760 mmHg
  • Melting Point: 12.5ºC
  • Flash Point: 257.4±28.7 °C

Wighteone

Wighteone is a compound isolated from the aerial parts of Genista ephedroides[1].

  • CAS Number: 51225-30-0
  • MF: C20H18O5
  • MW: 338.354
  • Catalog: Others
  • Density: 1.4±0.1 g/cm3
  • Boiling Point: 586.1±50.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 212.8±23.6 °C

H-Leu-OBzl.TosOH

L-Leucine benzyl ester p-toluenesulfonate is a leucine derivative[1].

  • CAS Number: 1738-77-8
  • MF: C20H27NO5S
  • MW: 393.497
  • Catalog: Others
  • Density: N/A
  • Boiling Point: 302.5ºC at 760 mmHg
  • Melting Point: 153-160 °C
  • Flash Point: 157.6ºC

N-Acetylglycyl-D-glutamic acid

N-Acetylglycyl-D-glutamic acid is a peptide with excitatory effect. N-Acetylglycyl-D-glutamic acid induces seizures in mice[1].

  • CAS Number: 135701-69-8
  • MF: C9H14N2O6
  • MW: 246.21700
  • Catalog: Neurological Disease
  • Density: 1.378g/cm3
  • Boiling Point: 666.4ºC at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 356.8ºC

Butyrospermol

Butyrospermol is a natural product[1].

  • CAS Number: 472-28-6
  • MF: C30H50O
  • MW: 426.71700
  • Catalog: Others
  • Density: 0.986g/cm3
  • Boiling Point: 498.303°C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 220.984°C

(1-OH)-Exatecan

(1-OH)-Exatecan is a quinoline ring compound. (1-OH)-Exatecan has substantial antiproliferative effects. (1-OH)-Exatecan can be used for cancer diseases research[1].

  • CAS Number: 2894780-53-9
  • MF: C24H21FN2O5
  • MW: 436.43
  • Catalog: Cancer
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Estrogen receptor antagonist 1

Estrogen receptor antagonist 1 is a selective estrogen receptor antagonist. Estrogen (E2) and estrogen alpha receptor (ERα) are important drivers of breast cancer development. Estrogen receptor antagonist 1 has the potential for the research of breast cancer diseases (extracted from patent WO2021249533A1, compound 4)[1].

  • CAS Number: 2751609-45-5
  • MF: C28H33F4N5
  • MW: 515.59
  • Catalog: Cancer
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

3-Azidopropanoic acid-PFP ester

3-Azidopropanoic acid-PFP ester is an azidopropanoic acid linker that contains an activated PFP ester. The azide group can undergo copper-catalyzed Click Chemistry reactions with alkynes, DBCO and BCN to form triazole linkages. The activated PFP ester can react with amine groups to form stable amide bonds[1].

  • CAS Number: 1240801-10-8
  • MF: C9H4F5N3O2
  • MW: 281.14
  • Catalog: Others
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

2",4"-Di-O-(Z-p-coumaroyl)afzelin

2'',4''-Di-O-(Z-p-Coumaroyl)afzelin (compound 9) is a compound isolated from the leaf extract of Machilusphilippinense Merr.[1].

  • CAS Number: 205534-17-4
  • MF: C39H32O14
  • MW: 724.66
  • Catalog: Others
  • Density: 1.6±0.1 g/cm3
  • Boiling Point: 966.9±65.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 302.1±27.8 °C

Shanzhiside

Shanziside is a iridoid glucoside isolated from Phlomis tuberosa L[1].

  • CAS Number: 29836-27-9
  • MF: C16H24O11
  • MW: 392.355
  • Catalog: Others
  • Density: 1.7±0.1 g/cm3
  • Boiling Point: 692.3±55.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 251.6±25.0 °C

Span 80

Sorbitan monooleate is a renewable polyol with unique molecular structures for the development and design of bio-based waterborne polyurethane (WPU) with versatility and excellent mechanical properties. Sorbitan monooleate can be used as an excipient, such as nonionic surfactants, emulsifiers. Pharmaceutical excipients, or pharmaceutical auxiliaries, refer to other chemical substances used in the pharmaceutical process other than pharmaceutical ingredients. Pharmaceutical excipients generally refer to inactive ingredients in pharmaceutical preparations, which can improve the stability, solubility and processability of pharmaceutical preparations. Pharmaceutical excipients also affect the absorption, distribution, metabolism, and elimination (ADME) processes of co-administered drugs[1][2].

  • CAS Number: 1338-43-8
  • MF: C24H44O6
  • MW: 428.603
  • Catalog: Others
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 579.3±50.0 °C at 760 mmHg
  • Melting Point: 0.986ºC
  • Flash Point: 186.2±23.6 °C

Boc-3-(2-quinolyl)-DL-Ala-OH

Boc-3-(2-quinolyl)-DL-Ala-OH is an alanine derivative[1].

  • CAS Number: 401813-49-8
  • MF: C17H20N2O4
  • MW: 316.352
  • Catalog: Others
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 505.6±45.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 259.6±28.7 °C

3-epi-Isocucurbitacin B

3-epi-Isocucurbitacin B (Compound 5) is a cucurbitane triterpene derived from Trichosanthes kirilowii. 3-epi-Isocucurbitacin B shows significant cytotoxicity to human tumor cells A-549, SK-OV-3, SK-MEL-2, XF-498 and HCT15[1].

  • CAS Number: 89647-62-1
  • MF: C32H46O8
  • MW: 558.70
  • Catalog: Cancer
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 702.4±60.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 219.9±26.4 °C

HER2-IN-6

HER2-IN-6 is a potent inhibitor of HER2. HER2-IN-6 has the potential for the research of wild and/or mutant EGFR and/or HER2 kinase mediated tumor (extracted from patent WO2021164697A1, compound 11)[1].

  • CAS Number: 2691891-38-8
  • MF: C26H32N8O3
  • MW: 504.58
  • Catalog: Cancer
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

bromfenac sodium salt sesquihydrate

Bromfenac (sodium hydrate) is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity(1) Bromfenac (sodium hydrate) (1 mg/kg, i.v.) is metabolited into an unusual conjugate, bromfenac N-glucoside, in rats bile(2) Bromfenac (sodium hydrate) permeation was found to be 1.62-fold higher through ChS-CS-NPs

  • CAS Number: 120638-55-3
  • MF: C15H12BrNO3.3/2H2O.Na
  • MW: 383.17
  • Catalog: Inflammation/Immunology
  • Density: 1.6±0.1 g/cm3
  • Boiling Point: 562.2±50.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 293.8±30.1 °C

dl-valine ethyl ester hydrochloride

H-DL-Val-OEt.HCl is a valine derivative[1].

  • CAS Number: 23358-42-1
  • MF: C7H16ClNO2
  • MW: 181.660
  • Catalog: Others
  • Density: N/A
  • Boiling Point: 169.2ºC at 760mmHg
  • Melting Point: 94ºC
  • Flash Point: 42.7ºC

4-(((2S,4S)-1-([1,1'-Biphenyl]-4-yl)-5-ethoxy-4-methyl-5-oxopentan-2-yl)amino)-4-oxobutanoic acid

2S,4S-Sacubitril is the impurity of Sacubitril. Sacubitril is approved by the Food and Drug Administration for use in combination with valsartan for the treatment of patients with heart failure.

  • CAS Number: 149709-63-7
  • MF: C24H29NO5
  • MW: 411.491
  • Catalog: Cardiovascular Disease
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 656.9±55.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 351.1±31.5 °C

2-C-Methyl-D-erythrono-1,4-lactone

(–)-Erythro-saccharinic acid lactone (compound2) can be isolated from the leaves of Talauma arcabucoana[1].

  • CAS Number: 18465-71-9
  • MF: C5H8O4
  • MW: 132.115
  • Catalog: Others
  • Density: 1.5±0.1 g/cm3
  • Boiling Point: 254.0±7.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 111.9±11.7 °C

MeIQ

Me-IQ (Methyl-IQ), an orally active heterocyclic amine, is carcinogenic and mutagenic. Me-IQ is several hundred-fold more mutagenic in liver than in lung microsomal preparations from uninduced mice and rabbits[1][2].

  • CAS Number: 77094-11-2
  • MF: C12H12N4
  • MW: 212.25000
  • Catalog: Cancer
  • Density: 1.36g/cm3
  • Boiling Point: 465.7ºC at 760 mmHg
  • Melting Point: 291-293ºC
  • Flash Point: 235.4ºC

Gadodiamide

Gadodiamide is a gadolinium-based contrast agent used in MR imaging procedures to assist in the visualization of blood vessels. Target: OthersGadodiamide(Omniscan) is a gadolinium-based contrast agent used in MR imaging procedures to assist in the visualization of blood vessels. Gadodiamide is a contrast medium for cranial and spinal magnetic resonance imaging (MRI) and for general MRI of the body after intravenous administration. The product provides contrast enhancement and facilitates visualisation of abnormal structures or lesions in various parts of the body including the central nervous system (CNS). A recent review takes the question of toxicity caused by loss of gadolinium from the complex. "The challenge for nephrologists includes (a) evidence of transmetallation, such as gadolinium deposits in bone, increased urinary zinc excretion, iron-transferrin dissociation or 'spurious hypocalcemia' in exposed people" [1].

  • CAS Number: 122795-43-1
  • MF: C16H28GdN5O9
  • MW: 591.67200
  • Catalog: Others
  • Density: N/A
  • Boiling Point: 769.1ºC at 760mmHg
  • Melting Point: N/A
  • Flash Point: 419ºC