Products

Catalog No	Chemical Name	CAS Number	Purity
17011709	SMER28	307538-42-7	98%
SMER28 is a small molecule modulator of autophagy, inducing autophagy independently o
17011707	SKF-38393 hydrochloride	62717-42-4	98%
SKF-38393, aslo known as (+/-)-SKF-38393, is a synthetic compound of the benzazepine
17011706	Sitafloxacin anhydrous	127254-12-0	98%
Sitafloxacin is a new-generation, broad-spectrum oral fluoroquinolone that is very ac
17011704	SHP099 HCl	1801747-11-4	98%
SHP099 is a potent, selective, orally bioavailable, and efficacious SHP2 inhibitor wi
17011703	Shogaol (6-Shogaol)	555-66-8	98%
Shogaol, also known as (6)-shogaol, is a pungent constituent of ginger similar in che
17011702	SGC707	1687736-54-4	98%
SGC707 is a potent, selective and cell-active allosteric inhibitor of protein arginin
17011701	SC66	871361-88-5	98%
SC66 is a novel and potent AKT inhibitor, which reduced cell viability in a dose- and
71161	SBI0206965	1884220-36-3	98%
SBI0206965 is a potent and selective autophagy Kinase ULK1 Inhibitor. Many tumors bec
17011609	SB-743921 HCl	940929-33-9	98%
SB-743921 is a synthetic small molecule with potential antineoplastic properties. SB-
17011607	Sardomozide	149400-88-4	98%
Sardomozide , also known as SAM486A or CGP48664, is a second-generation polyamine syn
17011606	SAR407899 HCl	923262-96-8	98%
SAR407899 is a potent and selective Rho kinase inhibitor with promising antihypertens
17011605	SAR131675	1092539-44-0	98%
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
161227110	4SC-202	910462-43-0	98%
4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone de
16122784	SKL2001	909089-13-0	98%
SKL2001 is a novel agonist of the Wnt/-catenin pathway that disrupts the Axin/-cateni
16122766	Salicylanilide	87-17-2	98%
Salicylanilides are a group of compounds with a wide range of biological activities i
16122760	Sivelestat (ONO-5046)	127373-66-4	98%
Sivelestat is a potent and selective inhibitor of neutrophil elastase with IC50 of 44
16122758	Sivelestat sodium	201677-61-4	98%
Sivelestat sodium is a competitive inhibitor of human neutrophil elastase, also inhib
16122748	SC75741	913822-46-5	98%
SC75741 is a potent NF-B inhibitor with EC50 of 200 nM.SC75741 shows immunosuppressiv
16122726	SQ22536	17318-31-9	98%
SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 M. It can inhibit PGE
16122721	SIS3	521984-48-5	98%
SIS3, a novel specific inhibitor of Smad3, inhibits TGF- and activin signaling by sup
16122716	Saccharin 1-methylimidazole (SMI)	482333-74-4	98%
SMI is considered a general-purpose activator for DNA and RNA synthesis.
16122706	STA-21	111540-00-2	98%
STA-21 is a selective STAT3 inhibitor.In cells, STA-21 inhibits Stat3 DNA binding act
6111526	SKI II	312636-16-1	98%
SKI-II is a synthetic inhibitor of sphingosine kinase (SK) activity with IC50 of 78 M
6111522	SR1001	1335106-03-0	98%
SR1001 is a selective ROR and ROR inverse agonist; suppresses TH17 cell differentiati
61119	S1P1 Agonist III	1324003-64-6	98%
S1P1 Agonist III is a potent and orally active S1P1 agonist with EC50 of 18 nM; no ac
161113	SCH 546738	906805-42-3	98%
SCH 546738 is a novel, potent and non-competitive small molecule CXCR3 antagonist wit
611937	4SC-202	1186222-89-8	98%
4SC-202 is an orally available potent HDACi specific for class I HDAC isoenzymes(NO H
611930	SJB3-019A	2070015-29-9	98%
SJB3-019A is a potent and novel usp1 inhibitor. SJB3-019A (IC50 = 0.0781 uM) was 5 ti
611915	SR-3029	1454585-06-8	98%
SR 3029 is a potent and highly specific CK1/CK1 inhibitor with the IC50 of 97 nM.SR-3
161009026	SB-216763	280744-09-4	98% by HPLC
SB-216763 is a glycogen synthase kinase-3 (GSK3) inhibitor, which can maintain mouse