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• 1099644-42-4 | ITD-1 (Catalog# : 101902)ITD-1 is a selective inhibitor of TGF- signaling, displays little or no inhibition of
• 1454700-89-0 | IN00076730 (Catalog# : 91816)Coming soon!
• 1643-29-4 | 3-(4-Iodophenyl)propionic acid (Catalog# : 90711)Coming soon!
• 1100318-96-4 | 4-iodo-7H-pyrrolo[2,3-d]pyrimidine (Catalog# : 81005)Coming soon!
• 1110709-70-0 | 3-Iodo-4-(trifluoromethoxy)benzoic acid (Catalog# : 80316)Coming soon!
• 1204669-37-3 | IDO inhibitor 1 (Catalog# : 72806)IDO is an enzyme that catalyzes the degradation of the essential amino acid L-tryptop
• 1029712-80-8 | INCB28060 (Catalog# : 52609)INCB28060 is a novel orally active inhibitor (IC50=0.13 nM) of c-MET kinase.
• 159752-10-0 | Ibutamoren Mesylate (Catalog# : 51804)Ibutamoren mesylate (MK-0677) is an orally active nonpeptide growth hormone (GH) secr
• 1191252-49-9 | IOWH032 (Catalog# : 52203)IOWH032 is a syntheticCFTRinhibitor withIC50of 1.01 M in CHO-CFTR cell based assays.
• 1998725-11-3 | JHU-083 (Catalog# : 24108)JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性，并防止慢
• 1404380-58-0 | JTE-151 (Catalog# : 20594)
• 1627902-21-9 | JNJ-54175446 (Catalog# : 20534)JNJ-54175446 is a potent and selective P2X7 Receptor Antagonist. JNJ-54175446 is pote
• 1638611-48-9 | JC124 (Catalog# : 20495)JC124 is a NLRP3 Inflammasome Inhibitor.
• 188791-09-5 | JTE-607 HCl (Catalog# : 20479)JTE-607, also known as TO-207, is a cytokine production inhibitor potentially for the
• 1309784-09-5 | JTE-051 (Catalog# : 20458)JTE-051 is a novel inhibitor of interleukin-2-inducible T cell kinase (ITK), suppress
• 1380392-05-1 | JMS-17-2 (Catalog# : 2071624)JMS-17-2 is a potent and selective antagonist of CX3CR1.
• 1443235-95-7 | JAK3-IN-2 (Catalog# : 2071551)JAK3-IN-2 is a potent and highly selective JAK3 inhibitor.
• 1572510-42-9 | JNJ-632 (Catalog# : 2071507)JNJ-632 is a potent HVV capsid assembly modulator and HBV replication inhibitor with
• 1408064-71-0 | JNK-IN-7 (Catalog# : 2061305)JNK-IN-7 is a relatively selective JNKs inhibitor(IC50= 1.54/1.99/0.75 for JNK1/2/3);
• 1408064-71-0 | JNK-IN-7 (Catalog# : 2061305)
• 1597402-27-1 | JPH203 HCl ( Nanvuranlat ) (Catalog# : 18381)JPH203,也称为KYT- 0353,是一个强有力的和选择性(l型氨基酸转运蛋白
• 1142363-52-7 | JNJ-40346527 (Catalog# : 1711221)JNJ-40346527是一种小分子和口服抑制剂，可用于促结肠菌素- 1受体(
• 1254977-87-1 | JNJ-42153605 (Catalog# : 1791311)JNJ-42153605是一种强效的选择性mGlu2受体PAM可接受的药代动力学在啮
• 1346528-51-5 | JNJ-42165279(2HCl salt) (Catalog# : 1783012)JNJ-42165279具有良好的ADME和药效学特性，可以证明其在大鼠的大脑
• 1346528-52-6 | JNJ-42165279(mono HCl salt) (Catalog# : 1783011)JNJ-42165279(mono HCl salt)是一种强力的选择性脂肪酸酰胺水解酶(FAAH)抑
• 1913252-04-6 | JQ-EZ-05 (Catalog# : 2017871)JQ-EZ-05也称为JQEZ5, 是一种生物活性化学药品。 
• 1410880-22-6 | JNK-IN-8 (Catalog# : 16123027)JNK-IN-8, also known as JNK Inhibitor XVI, is a selective JNK inhibitor that inhibits
• 1802326-66-4 | JNJ 63533054 (Catalog# : 16123026)JNJ 63533054 is a potent and selective GPR139 agonist (EC50 = 16 nM) that is brain an
• 1346528-50-4 | JNJ-42165279 (Catalog# : 16123025)JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. J
• 1037592-40-7 | JPH203(KYT-0353) (Catalog# : 6112701)JPH203(also known as KYT-0353) is a potent and selective LAT1 selective ( L-type amin