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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T15364 | G-1 | Estrogen Receptor/ERR , GPR | |
G-1 is a nonsteroidal, high-affinity and selective GPR30 agonist (Ki: 11 nM). | |||
T67755 | Protein kinase G inhibitor-1 | PKA | |
Protein kinase G inhibitor-1 is a potent Protein kinase G inhibitor, IC50= 0.9 uM. | |||
T27066 | Prostaglandin G/H synthase 1 inhibitor | CP74006,CP 74006,2-Amino-N-(4-chlorophenyl)benzamide | Others |
Prostaglandin G/H synthase 1 inhibitor (CP 74006) is a selective D5D inhibitor with an IC(50) value of 20 nM. | |||
T8640 | G6PDi-1 | Dehydrogenase | |
G6PDi-1 is an effective G6PD inhibitor. It depletes NADPH and decreases inflammatory cytokine production. | |||
T4661 | PKG drug G1 | PKA | |
PKG drug G1 targets PKG Iα C42. PKG drug G1 can couple to vasodilation and blood pressure lowering by a C42 PKG Iα-independent mechanism. | |||
T8328 | STING agonist-1 | G10 | Virus Protease , STING |
STING agonist-1 (G10) is a human-specific STING agonist,elicits antiviral activity against emerging Alphaviruses. | |||
T67900 | PKM2 inhibitor G | PKM | |
PKM2 inhibitor G is a inhibitor of pyruvate kinase. | |||
T6843 | GDC-0623 | G-868,GDC0623,RG 7421,MEK inhibitor 1 | Apoptosis , MEK |
GDC-0623 (RG 7421) is a potent and ATP-uncompetitive MEK1 inhibitor with Ki of 0.13 nM. Phase 1. | |||
TN1555 | Platycoside G1 | Deapi-platycoside E | Others |
Platycoside G1 (Deapi-platycoside E) may have anti-inflammatory effects. | |||
T8818 | TC-G 1005 | GPCR19 | |
TC-G 1005 is a potent and selective GPBA agonist (EC50 :0.72 nM; hTGR5). Selective for TGR5 over FXR (farnesoid X receptor). Increases plasma GLP-1 levels and reduces blood glucose in mice. Orally available. | |||
T7428 | SBI-115 | GPCR19 | |
SBI-115 is an antagonist of TGR5. SBI-115 decreases hepatic cystogenesis with polycystic liver diseases via inhibiting TGR5 | |||
TN6985 | Anhydronotoptol | 4-{[(2E,5E)-3,7-dimethylocta-2,5,7-trien-1-yl]oxy}-7H-furo[3,2-g]chromen-7-one | NO Synthase |
Anhydronotoptol (4-{[(2E,5E)-3,7-dimethylocta-2,5,7-trien-1-yl]oxy}-7H-furo[3,2-g]chromen-7-one), a natural compound extracted from the umbelliferae plant Qiangwu, is a potent inhibitor of nitric oxide production, inhibi... | |||
T18883 | 2-Di-1-ASP | Others | |
2-Di-1-ASP is a mono-stryryl dye and widely used as mitochondrial stain and groove-binding fluorescent probes for double-stranded DNA. It has selective for G-quadruplex (G4) and double-stranded DNA. | |||
T4083 | BAR501 | BAR 501 | GPCR19 |
BAR501 is an effective and specific GPBAR1 agonist (EC50: 1 μM). | |||
TQ0252 | BAR502 | FXR , GPCR19 , Autophagy | |
BAR502 is a dual GPBAR1 and FXR agonist (IC50s: 0.4 μM and 2 μM). | |||
T4352 | SB756050 | SB-756050,SB 756050 | GPCR19 |
SB756050 is a specific TGR5 agonist. | |||
T4288 | HVEGF-IN-1 | VEGFR | |
hVEGF-IN-1 inhibits human VEGF-A translation and has antitumor activity. | |||
TP1543L | G280-9 acetate(156761-76-1 free base) | Others | |
G280-9 acetate is a common melanoma gp100 epitope restricted by MHC-associated HLA-A2. The G280-9 sequence is unique because it could be recognized by cytotoxic T lymphocytes at very low concentrations, however it shows ... | |||
T5077 | Deoxycholic acid sodium salt | Sodium deoxycholate,Sodium Desoxycholate | Endogenous Metabolite , GPCR19 |
Deoxycholic acid sodium salt (Sodium deoxycholate) can activate the G protein-coupled bile acid receptor TGR5 that stimulates brown adipose tissue (BAT) thermogenic activity. | |||
T25199 | Cafaminol | Cafaminolum,G1,G-1,G 1 | |
Cafaminol (methylcoffanolamine) is a vasoconstrictor and anticatarrhal of the methylxanthine family related to caffeine which is used as a nasal decongestant. |