Search By Initial

Cas Index 1

• 112275-50-0 | 1-Boc-hexahydro-1,4-diazepine (Catalog# : 81024)Coming soon!
• 13343-63-0 | Benzyl-2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside (Catalog# : 80301)Coming Soon
• 1009817-63-3 | b-AP15 (Catalog# : 73106)b-AP15 is a specific inhibitor of the deubiquitinating enzymes Uch37 and Usp14 of the
• 188011-69-0 | Bikinin (Catalog# : 61002)Bikinin(Abrasin) is a potent inhibitor of plant GSK-3/Shaggy-like kinase; activates B
• 1538604-68-0 | BLU9931 (Catalog# : 60303)BLU9931 is a potent and irreversible small-molecule inhibitor of FGFR4, as a targeted
• 1092443-52-1 | BS-181 (Catalog# : 52755)BS-181 is a highly selective CDK7 inhibitor with IC50 of 21 nM. ; >40-fold selecti
• 19542-67-7 | BAY 11-7082 (Catalog# : 52713)BAY 11-7082 is aNF-Binhibitor, inhibits TNF-inducedIBphosphorylation withIC50of 10 M
• 196309-76-9 | Bay 11-7085 (Catalog# : 52712)BAY 11-7085 is an irreversible inhibitor of TNF-inducedIBphosphorylation withIC50of 1
• 153559-49-0 | Bexarotene (Catalog# : 52601)Bexarotene (Targretin) is a selective RXR agonist approved for the treatment of CTCL.
• 1397219-81-6 | BS-181 HCl (Catalog# : 52578)BS-181 HCl is a highly selectiveCDK7inhibitor withIC50of 21 nM. It is more than 40-fo
• 1174046-72-0 | BMS-794833 (Catalog# : 52205)BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2 with IC50 of 1.7/15 nM
• 1187594-09-7 | Baricitinib (Catalog# : 51908)Baricitinib (also known as LY3009104 or INCB028050) is a novel and potent small molec
• 1403859-14-2 | CC90001 free base (Catalog# : 24095)CC-90001 is a potent and selective JNK inhibitor, which is 12.9-fold more potent for
• 1261451-92-6 | 5-chloro-2-methoxypyridine-3-sulfonyl chloride (Catalog# : 24022)5-chloro-2-methoxypyridine-3-sulfonyl chloride, CAS 1261451-92-6.
• 1370032-20-4 | CUR5g (Catalog# : 20678)CUR5g is a potent autophagy inhibitor.
• 1112968-42-9 | Contezolid free base (Catalog# : 20653)Contezolid (Youxitai ®), an orally administered oxazolidinone antibacterial agent, i
• 1610759-22-2 | CFI-402257 free base (Catalog# : 20626)CFI-402257 was discontinued for commercial reason.
• 1345858-76-5 | CYM-50308 (Catalog# : 20488)CYM 50308 is a novel agonist of SIP4 (EC50 = 56 nM) that displays 37-fold selectivity
• 1623747-97-6 | CRANAD-28 (Catalog# : 20478)CRANAD-28 is a blood brain barrier (BBB) penetrable two-photon imaging probe. It acts
• 1621164-74-6 | Camlipixant ( BLU-5937 ) (Catalog# : 20455)Camlipixant is an investigational, twice-daily oral P2X3 receptor antagonist for the
• 127094-58-0 | 6-Chloro-4-hydroxy-[1,5]naphthyridine-3-carboxylic acid ethyl ester (Catalog# : 20423)
• 1446321-95-4 | 3-(chloromethyl)-2-(1-isopropyl-1H-pyrazol-5-yl)pyridine hydrochloride (Catalog# : 20408)
• 1786438-30-9 | CR8 hydrochloride (Catalog# : L20350)CR8 is a potent and selective inhibitor of CDK. CR8 is a more potent pyridyl analogue
• 1618658-88-0 | CC-671 (Catalog# : L20343)CC-671 is a potent and selective dual inhibitor of TTK (Mps1) and CLK2.
• 1258296-60-4 | CS-2667 (Catalog# : L20340)RO495 (CS-2667) is a potent inhibitor of Non-receptor tyrosine-protein kinase 2 (TYK2
• 1038984-34-7 | 3-cyclopropyl-7-methyl-6-nitro-2H-benzo[e][1,3]oxazin-4(3H)-one (Catalog# : 20328)
• 1262414-04-9 | Cenerimod ( ACT-334441 ) (Catalog# : 20313)Cenerimod is a potent and orally active immunomodulator, exhibited EC50 value of 2.7
• 16499-64-2 | 4-chloro-6-(trifluoromethyl)quinazoline (Catalog# : 20310)
• 1979939-16-6 | CRT0273750 (Catalog# : 20258)CRT0273750 modulates LPA levels in plasma and is suitable for in vivo studies.
• 1628265-17-7 | 2-chloro-4-(4-fluorophenyl)thiazole-5-carbonitrile (Catalog# : 2091202)