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ZT-12-037-01
Catalog No. A18395 ATP-competitive STK19 inhibitorZT-12-037-01 is a potent, selective, ATP-competitive STK19 inhibitor. ZT-12-037-01 effectively blocks oncogenic NRAS-driven melanocyte malignant transformation and melanoma growth in vitro and in vivo. 了解更多 -
Collagen proline hydroxylase inhibitor-1
Catalog No. A11370 Collagen proline hydroxylase inhibitor-1 is an antifibroproliferative agents. 了解更多 -
Pancopride
Catalog No. A12967 5-HT3 receptor antagonistPancopride is a new potent and selective 5-HT3 receptor antagonist. 了解更多 -
Carbetocin
Catalog No. A18080 peripheral oxytocin receptors agonistCarbetocin (Lonactene; Duratocin) is an obstetric drug used to control postpartum hemorrhage and bleeding after giving birth; an agonist at peripheral oxytocin receptors. 了解更多 -
Solenopsin
Catalog No. A21087 ATP-competitive AKT inhibitorSolenopsin is an ATP-competitive AKT inhibitor with IC50 value of 10 μM . 了解更多 -
Arhalofenate
Catalog No. A21135 PPARγ agonistArhalofenate (MBX 102) is a selective partial agonist of peroxisome proliferator-activated receptor (PPAR)-γ, used for the treatment of type 2 diabetes. 了解更多 -
5-Hydroxy Propafenone D5 Hydrochloride
Catalog No. A21604 5-Hydroxy Propafenone D5 Hcl is the deuterium labeled 5-Hydroxy Propafenone. 了解更多 -
Ensartinib hydrochloride
Catalog No. A21719 ALK/MET inhibitorEnsartinib hydrochloride (X-396 hydrochloride) is a potent and dual ALK/MET inhibitor with IC50s of <0.4 nM and 0.74 nM, respectively. 了解更多 -
Liarozole dihydrochloride
Catalog No. A21853 CYP450 dependent inhibitorLiarozole dihydrochloride (R75251; R85246) is a cytochrome P450 (CYP450) dependent inhibitor, orally active, it also a potent inhibitor of estrogen (via inhibition of aromatase) and testicular androgen synthesis (inhibition of 17 ,20-lyase). 了解更多 -
MSI-1436 lactate
Catalog No. A21929 PTB1B inhibitorMSI-1436 lactate is a selective, non-competitive inhibitor of the enzyme protein-tyrosine phosphatase 1B (PTB1B), with an IC50 of 1 μM, 200-fold preference over TCPTP (IC50 of 224 μM). 了解更多 -
Fexinidazole
Catalog No. A21274 Fexinidazole is a 5-nitroimidazole drug currently in clinical development for the treatment of human sleeping sickness (human African trypanosomiasis [HAT]), caused by infection with species of the protozoan parasite Trypanosoma brucei. 了解更多 -
Ionomycin calcium
Catalog No. A21370 Ionomycin calcium (SQ23377 calcium) is a potent, selective calcium ionophore and an antibiotic produced by Streptomyces conglobatus. 了解更多 -
BB-Cl-Amidine
Catalog No. A19265 -
Acetylazide
Catalog No. A19370 Acetylazide is a synthetic broad-spectrum bacteriostatic antibiotic. 了解更多 -
GlyRS-IN-1
Catalog No. A19543 GlyRS inhibitorGlyRS-IN-1 is a glycyl-tRNA synthase (GlyRS) inhibitor extracted from patent WO 2017066459 A1. GlyRS-IN-1 can also inhibit the growth of bacteria. 了解更多 -
Ensartinib
Catalog No. A19720 ALK/MET inhibitorEnsartinib (X-396) is a potent and dual ALK/MET inhibitor with IC50s of <0.4 nM and 0.74 nM, respectively. 了解更多 -
Diethyl-pythiDC
Catalog No. A19766 CP4Hs inhibitorDiethyl-pythiDC is an inhibitor of collagen prolyl 4-hydroxylases (CP4Hs). 了解更多 -
PF 03709270
Catalog No. A19948 PF 03709270 is an orally available ester prodrug form of sulopenem, with broad-spectrum antibacterial activity against most gram-positive and gram-negative bacteria. 了解更多 -
Tubulin inhibitor 1
Catalog No. A19998 tubulin inhibitorTubulin inhibitor 1 is a tubulin inhibitor, inhibits tubulin polymerization. 了解更多 -
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide
Catalog No. A20334 2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound that inhibits stress-induced ulcer and low toxicity, and can maintain the content of phospholipase A2 and prostaglandin E2 in ulcerated rats induced by water immersed restrained stress. 了解更多 -
Gambogenic acid
Catalog No. A22383 EZH2 inhibitorGambogenic acid is an active ingredient in gamboge, with anticancer activity. Gambogenic acid acts as an effective inhibitor of EZH2, specifically and covalently binds to Cys668 within the EZH2-SET domain, and induces EZH2 ubiquitination. 了解更多 -
PF-562271 hydrochloride
Catalog No. A22370 FAK and Pyk2 kinase inhibitorPF-562271 hydrochloride is a potent, ATP-competitive and reversible FAK and Pyk2 kinase inhibitor with IC50s of 1.5 nM and 13 nM, respectively. 了解更多 -
TSPC (HUN86320)
Catalog No. A22250 inhibitor for GA perceptionTSPC is an inhibitor for GA perception by in vitro and in planta evaluations. 了解更多 -
Molnupiravir
Catalog No. A22165 broad-spectrum antiviral activityMolnupiravir (EIDD-2801, MK-4482) is an orally bioavailable prodrug of the ribonucleoside analog β-d-N4-hydroxycytidine (NHC; EIDD-1931) with broad-spectrum antiviral activity against SARS-CoV-2, MERS-CoV, SARS-CoV, and the causative agent of COVID-19. 了解更多 -
(Z)-JIB-04
Catalog No. A22137 Jumonji histone demethylase inihibitorZ-JIB-04 (NSC 693627, JIB-04 Z-isomer) is an isomer of JIB-04. JIB-04 is a pan-selective Jumonji histone demethylase inihibitor with IC50 of 230 nM, 340 nM, 855 nM, 445 nM, 435 nM, 1100 nM and 290 nM for JARID1A, JMJD2E, JMJD3, JMJD2A, JMJD2B, JMJD2C, and JMJD2D, respectively. 了解更多
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