Chemsrc provides Signaling Pathways's classification. They are divided into Anti-infection, Antibody-drug Conjugate, Apoptosis, Autophagy, Cell Cycle/DNA Damage, Cytoskeleton, Epigenetics, GPCR/G Protein, Immunology/Inflammation, JAK/STAT Signaling, MAPK/ERK Pathway, Membrane Transporter/Ion Channel, Metabolic Enzyme/Protease, Neuronal Signaling, NF-κB, PI3K/Akt/mTOR, PROTAC, Protein Tyrosine Kinase/RTK, Stem Cell/Wnt, TGF-beta/Smad, Vitamin D Related, 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

Sirexatamab

Sirexatamab is an active peptide. Sirexatamab can be used for various biochemical studies.

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

9-Aminoacridine

9-Aminoacridine is a highly fluorescent dye used clinically as a topical antiseptic and experimentally as a mutagen, an intracellular pH indicator.

  • CAS Number: 90-45-9
  • MF: C13H10N2
  • MW: 194.23200
  • Catalog: Dye Reagents
  • Density: 1.268g/cm3
  • Boiling Point: 413.5ºC at 760 mmHg
  • Melting Point: 241ºC
  • Flash Point: 233.2ºC

Tiopronin 13C D3

Tiopronin 13C D3 is deuterium labeled Tiopronin.

  • CAS Number: 1189695-13-3
  • MF: C413CH4D3NO3S
  • MW: 165.19
  • Catalog: Metabolic Disease
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Starch

Starch from corn is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

  • CAS Number: 9005-25-8
  • MF: (C6H10O5)n
  • MW:
  • Catalog: Others
  • Density: 1.5
  • Boiling Point: 1.5 g/mL at 25ºC(lit.)
  • Melting Point: 256-258ºC
  • Flash Point: 357.8ºC

2-Pentyloxycarbanilic acid 1-methoxymethyl-2-(1-perhydroazepinyl)ethyl ester hydrochloride

Antiarrhythmic agent-2 is a nonspecific Ca2+ inward current blocker that inhibits ionic currents in sensory neuron membranes. Antiarrhythmic agent-2 can be used in the study of cardiovascular diseases, such as arrhythmias[1].

  • CAS Number: 105919-73-1
  • MF: C22H36N2O4
  • MW: 392.53200
  • Catalog: Calcium Channel
  • Density: 1.071g/cm3
  • Boiling Point: 485.9ºC at 760mmHg
  • Melting Point: N/A
  • Flash Point: 247.7ºC

Boc-D-Ala-OH

N-tert-Butoxycarbonyl-D-alanine is an alanine derivative[1].

  • CAS Number: 7764-95-6
  • MF: C8H15NO4
  • MW: 189.209
  • Catalog: Others
  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 320.9±25.0 °C at 760 mmHg
  • Melting Point: 81-83ºC
  • Flash Point: 147.9±23.2 °C

ProtopluMericin A

Protoplumericin A is a bioactive ingredient of Plumeria obtusa L. attenuates. Protoplumericin A mitigated lipopolysaccharide (LPS) -induced acute lung injury in mice. Protoplumericin A can be used to study the LPS-induced anti-inflammatory effect [1].

  • CAS Number: 80396-57-2
  • MF: C36H42O19
  • MW: 778.707
  • Catalog: Inflammation/Immunology
  • Density: 1.6±0.1 g/cm3
  • Boiling Point: 1040.3±65.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 322.5±27.8 °C

BOC-D-4-Nitrophe

(R)-2-((tert-Butoxycarbonyl)amino)-3-(4-nitrophenyl)propanoic acid is a phenylalanine derivative[1].

  • CAS Number: 61280-75-9
  • MF: C14H18N2O6
  • MW: 310.302
  • Catalog: Others
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 509.3±45.0 °C at 760 mmHg
  • Melting Point: 120ºC
  • Flash Point: 261.8±28.7 °C

d-serine benzyl ester benzenesulfonate

D-Serine benzyl ester benzenesulfonate is a serine derivative[1].

  • CAS Number: 141527-77-7
  • MF: C16H19NO6S
  • MW: 353.39000
  • Catalog: Others
  • Density: N/A
  • Boiling Point: 599ºC at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 316.1ºC

Quercitrin

Quercitrin is a natural compound found in Tartary buckwheat with a potential anti-inflammation effect that is used to treat heart and vascular conditions.IC50 value:Target:In vitro: There were significant increases in caspase-3 activity, loss of MMP, and increases in the apoptotic cell population in response to quercitrin in DLD-1 colon cancer cells in a time- and dose-dependent manner. [1] In vivo: ICR mice received CCl4 intraperitoneally with or without quercitrin co-administration for 4 weeks. Data showed that quercitrin significantly suppressed the elevation of reactive oxygen species (ROS) production and malondialdehyde (MDA) content, reduced tissue plasminogen activator (t-PA) activity, enhanced the antioxidant enzyme activities and abrogated cytochrome P450 2E1 (CYP2E1) induction in mouse brains. [2]

  • CAS Number: 522-12-3
  • MF: C21H20O11
  • MW: 448.377
  • Catalog: Autophagy
  • Density: 1.8±0.1 g/cm3
  • Boiling Point: 814.0±65.0 °C at 760 mmHg
  • Melting Point: 174-183ºC
  • Flash Point: 288.3±27.8 °C

Ertiprotafib

Ertiprotafib is an inhibitor of PTP1B, IkB kinase β (IKK-β), and a dual PPARα and PPARβ agonist, with an IC50 of 1.6 μM for PTP1B, 400 nM for IKK-β, an EC50 of ~1 μM for PPARα/PPARβ.

  • CAS Number: 251303-04-5
  • MF: C31H27BrO3S
  • MW: 559.513
  • Catalog: Phosphatase
  • Density: 1.4±0.1 g/cm3
  • Boiling Point: 690.7±55.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 371.5±31.5 °C

STING agonist-10

STING agonist-10 (Compound 91) is a potent small molecule cyclic urea activator of STING with the EC50 of 2600 nM. Activation of STING is a highly promising approach in immunotherapy[1].

  • CAS Number: 2259308-69-3
  • MF: C25H20ClF4N3O2
  • MW: 505.89
  • Catalog: STING
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Vindoline

Vindoline, a vinca alkaloid extracted from the leaves of Catharanthus roseus, weakly inhibits tubulin self-assembly[1].

  • CAS Number: 2182-14-1
  • MF: C25H32N2O6
  • MW: 456.531
  • Catalog: Microtubule/Tubulin
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 569.8±50.0 °C at 760 mmHg
  • Melting Point: 163-165ºC
  • Flash Point: 298.4±30.1 °C

Benzyl-PEG9-alcohol

Benzyl-PEG9-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

  • CAS Number: 868594-48-3
  • MF: C25H44O10
  • MW: 504.61100
  • Catalog: PROTAC Linker
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

5-Iodotubercidin

5-Iodotubercidin is a potent adenosine kinase inhibitor with IC50 of 26 nM.

  • CAS Number: 24386-93-4
  • MF: C11H13IN4O4
  • MW: 392.150
  • Catalog: Adenosine Kinase
  • Density: 2.5±0.1 g/cm3
  • Boiling Point: 701.5±60.0 °C at 760 mmHg
  • Melting Point: 216-217ºC dec.
  • Flash Point: 378.0±32.9 °C

Anticancer agent 60

Anticancer agent 60 (compound 3h) has antiproliferative activity against human HepG2 cells (IC50 = 4.13 μM) and presents antitumor efficacy in a human HepG2 xenograft mouse model[1].

  • CAS Number: 2162169-14-2
  • MF: C27H33N5O4S
  • MW: 523.65
  • Catalog: Microtubule/Tubulin
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Glycyrrhizic acid

Glycyrrhizic acid is a triterpenoid saponinl, acting as a direct HMGB1 antagonist, with anti-tumor, anti-diabetic activities.

  • CAS Number: 1405-86-3
  • MF: C42H62O16
  • MW: 822.932
  • Catalog: Cancer
  • Density: 1.4±0.1 g/cm3
  • Boiling Point: 971.4±65.0 °C at 760 mmHg
  • Melting Point: 220ºC decomposes
  • Flash Point: 288.1±27.8 °C

Glyburide (potassium salt)

Glibenclamide (Glyburide) potassium is a potassium salt of Glibenclamide (HY-15206). Glibenclamid potassium exists in anhydrous and hydrate forms, with higher solubility compared to pure Glibenclamide[1].

  • CAS Number: 52169-36-5
  • MF: C23H28ClKN3O5S+
  • MW: 533.10200
  • Catalog: CFTR
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

WKYMVM TFA

WKYMVM (TFA) is a potent N-formyl peptide receptor (FPR1) and FPRL1/2 agonist, also activates several leukocyte effector functions such as chemotaxis, mobilization of complement receptor-3, and activation of the NADPH oxidase[1][2].

  • CAS Number: 1313730-09-4
  • MF: C43H62F3N9O9S2
  • MW: 970.13
  • Catalog: Inflammation/Immunology
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Succinobucol

Succinobucol is a phenolic antioxidant with anti-inflammatory and antiplatelet effects.

  • CAS Number: 216167-82-7
  • MF: C35H52O5S2
  • MW: 616.91400
  • Catalog: Cardiovascular Disease
  • Density: 1.13g/cm3
  • Boiling Point: 659.5ºC at 760mmHg
  • Melting Point: N/A
  • Flash Point: 352.7ºC

MPI-5a

MPI_5a is a potent and selective HDAC6 inhibitor (IC50=36 nM). MPI_5a weakly inhibits other HDAC isoforms. MPI_5a inhibits acyl-tubulin accumulation in cells with an IC50 value of 210 nM[1].

  • CAS Number: 1259296-46-2
  • MF: C16H17N3O3
  • MW: 299.324
  • Catalog: HDAC
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

PLX-4720

PLX-4720 is a potent and selective inhibitor of B-RafV600E with IC50 of 13 nM in a cell-free assay, equally potent to c-Raf-1(Y340D and Y341D mutations), and 10-fold selectivity for B-RafV600E than wild-type B-Raf.

  • CAS Number: 918505-84-7
  • MF: C17H14ClF2N3O3S
  • MW: 413.826
  • Catalog: Raf
  • Density: 1.5±0.1 g/cm3
  • Boiling Point: 621.4±65.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 329.6±34.3 °C

2-Acetamido-2-cyclohexylacetic acid

2-Acetamido-2-cyclohexylacetic acid is a Glycine (HY-Y0966) derivative[1].

  • CAS Number: 107020-80-4
  • MF: C10H17NO3
  • MW: 199.24700
  • Catalog: Others
  • Density: 1.134 g/cm3
  • Boiling Point: 428.641ºC at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 213.035°C

(-)-bornyl ferulate

(-)-Bornyl ferulate is a 5-lipoxygenase and COX inhibitor with IC50s of 10.4 μM and 12.0 μM, respectively[1].

  • CAS Number: 55511-07-4
  • MF: C20H26O4
  • MW: 330.41800
  • Catalog: COX
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

2,6-Dimethyl-L-tyrosine

2,6-Dimethyl-L-tyrosine (Dmt) is a tyrosine derivative that enhances receptor affinity, functional bioactivity and in vivo analgesia of opioid peptides[1].

  • CAS Number: 123715-02-6
  • MF: C11H15NO3
  • MW: 209.242
  • Catalog: Opioid Receptor
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 412.8±45.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 203.4±28.7 °C

Biotin-PEG12-acid

Biotin-PEG12-acid is a biotin-labeled, PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

  • CAS Number: 1621423-14-0
  • MF: C37H69N3O16S
  • MW: 844.019
  • Catalog: PROTAC Linker
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 932.7±65.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 517.9±34.3 °C

BES sodium salt

BES sodium is a secondary standard biochemical buffer with effective pH range of 6.4 to 7.8 (pKa: 7.15 at 20 ℃). BES sodium is used in the diagnostic testing area.

  • CAS Number: 66992-27-6
  • MF: C6H14NNaO5S
  • MW: 235.234
  • Catalog: Others
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

Sodium L-lactate-(C)3

L-Lactic acid-13C3 ((S)-2-hydroxypropanoic-13-C3) sodium is the 13C labeled L-Lactic acid. L-Lactic acid-13C3 sodium can be used for lactate metabolism research[1].

  • CAS Number: 201595-71-3
  • MF: C3H5NaO3
  • MW: 115.03800
  • Catalog: Metabolic Disease
  • Density: N/A
  • Boiling Point: N/A
  • Melting Point: 163-165 ℃(lit.)
  • Flash Point: N/A

GS-443902

GS-443902 (Remdesivir metabolite) is a potent viral RNA-dependent RNA-polymerases (RdRp) inhibitor with IC50s of 5.6 µM, 1.1 µM, 5 µM for TP RdRp, RSV RdRp and HCV RdRp, respectively. GS-443902 is the active triphosphate metabolite of Remdesivir[1][2].

  • CAS Number: 1355149-45-9
  • MF: C12H16N5O13P3
  • MW: 531.202
  • Catalog: HCV
  • Density: 2.4±0.1 g/cm3
  • Boiling Point: N/A
  • Melting Point: N/A
  • Flash Point: N/A

phenyl propanol

1-Phenyl-1-propanol is used as a chiral building block and synthetic intermediate in the pharmaceutical industries. 1-Phenyl-1-propanol is an intermediate of anti-depressant drug Fluoxetine[1][2].

  • CAS Number: 93-54-9
  • MF: C9H12O
  • MW: 136.191
  • Catalog: Others
  • Density: 1.0±0.1 g/cm3
  • Boiling Point: 219.0±8.0 °C at 760 mmHg
  • Melting Point: N/A
  • Flash Point: 90.6±0.0 °C