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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
2051507IUN767501690176-75-098% Min.
IUN76750 is a PAR-2 signaling pathway inhibitor. IUN76750 has CAS#1690176-75-0, has n
204306ICEC0942 mesylate98% Min.
ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
204305ICEC0942 HCl1805789-54-1 (HCl)98% Min.
ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
204304ICEC0942 free base1805833-75-3 (free base)98% Min.
ICEC0942, also known as PPDA-001 and CT7001, is a potent, orally active and selective
54192ITI-2141160521-50-5>98%
ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic
512193ITI-214(phosphate)1642303-38-598% Min.
ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic
19319IDH8891429179-07-6>98%
IDH889 is a potent and selective inhibitors of IDH1. IDH899 shows IDH (R132H) IC50 =
191143INCB3284 mesylate887401-93-6>98%
INCB3284 is a potent, selective, and orally bioavailable hCCR2 Antagonist.
1812131Indeglitazar835619-41-5>98%
Indeglitazar, also known as PPM-204 and PLX-204, is an orally available peroxisome pr
181025IU1-47670270-31-2>98%
IU1-47 is a potent and selective inhibitor of USP14.
186277Inarigivir soproxil942123-43-5>98%
Inarigivir soproxil, also known as SB 9200, is an antiviral agent.
186276IT-9011584121-99-2>98%
IT-901 is a c-Rel Inhibitor That Mediates Anticancer Properties in Hematologic Malign
186253INX 08189 1234490-83-5>98%
INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor potentially for the trea
186222IWP-O12074607-48-8>98%
IWP-O1 is highly potent Porcn inhibitor, is essential for the secretion of Wnt protei
185232INCB0576431820889-23-3>98%
INCB057643 is a BET inhibitor. INCB054329 reduces homologous recombination efficiency
185216Iberdomide1323403-33-3>98%
Iberdomide, also known as CC-220, is potentially for the treatment of systemic lupus
185215INCB33441262238-11-8>98%
INCB3344 is a potent and selective antagonist of CCR2 receptor with IC(50) values of
18492iCRT3901751-47-1>98%
iCRT3 is an inhibitor of the Wnt/wingless signaling pathway. iCRT3 efficiently block
184317IDO-IN-21668565-74-9>98%
IDO inhibitor 1 is a potent inhibitor of IDO (indoleamine-(2,3)-dioxygenase) with IC5
18433IPI-3063 1425043-73-7>98%
IPI-3063 is a Selective Phosphoinoside-3-Kinase p110δ Inhibitor. IPI-3063 Potently S
17122925-Iodo-1-methyl-1H-imidazole71759-88-1>98%
5-iodo-1-methylimidazole is a building blocks.
17101236-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amine1448427-99-3>98%
6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amine
179134IDRA-2122503-72-698.0%
IDRA-21 is a positive AMPA receptor modulator. IDRA-21 inhibits synaptic and extrasyn
1791118ISCK03945526-43-298.0%
ISCK03 is a potent c-kit inhibitor. ISCK03 inhibits SCF/c-kit signaling in 501mel hum
1783019IACS-95711800477-30-898.0%
IACS-9571 is a potent and selective inhibitor TRIM24 and BRPF1. The bromodomain conta
178017Isosulfan blue68238-36-8≧98.0%
Isosulfan blue is a synthetic visual lymphatic imaging agent. Injected into the perip
17031013Importazole662163-81-798% 
Importazole is a small molecule inhibitor of the transport receptor importin- speci
17030309IDE11160927-48-998% 
IDE1 is a potent cell-permeable definitive endoderm formation inducer (EC50 = 125 nM,
17022713ISX-9832115-62-598% 
ISX-9 is a neurogenic agent. Isx-9 promotes neurogenesis in vivo, enhancing the proli
16123024Ixazomib (MLN-2238)1072833-77-298%
Ixazomib, also known as MLN-2238, is a potent proteasome inhibitor (PI) with potentia