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Cas Index 1

• 143851-98-3 | Elacridar HCl (Catalog# : 19121)Elacridar, also known as GF120918A, is a P-glycoprotein (P-gp) inhibitor, and has bee
• 1181770-72-8 | EMD638683 (Catalog# : 1810253)EMD638683 is a potent inhibitor of SGK1 with an IC50 value of 3 μM.
• 189453-10-9 | Epothilone D (Catalog# : 186292)Epothilone D is a natural polyketide compound isolated from the myxobacterium Sorangi
• 1628830-21-6 | EZM2302 (Catalog# : 186272)EZM2302 is a potent, selective, and orally available arginine methyltransferase CARM1
• 169869-90-3 | Exatecan mesylate (Catalog# : 186271)Exatecan, also known as DX 8951, is semisynthetic, water-soluble camptothecin derivat
• 164650-44-6 | Efinaconazole (Catalog# : 186213)Efinaconazole is a triazole antifungal. It is approved for use in Canada and the USA
• 1197194-61-8 | Endoxifen E-isomer HCl (Catalog# : 184124)Endoxifen E-isomer is a tamoxifen metabolite and potent Selective Estrogen Response M
• 1370651-20-9 | Ensartinib ( X396 ) (Catalog# : 184321)Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
• 1914078-41-3 | eCF506 ( NXP 900 ) (Catalog# : 18382)eCF506 targets a molecule called Src tyrosine kinase that is required for breast canc
• 1632006-28-0 | Esaxerenone (Catalog# : 1710121)Esaxerenone (INN) (developmental code names CS-3150, XL-550) is a nonsteroidal antimi
• 1616391-65-1 | EPZ015666 (Catalog# : 011309)EPZ015666 is a potent, selective and orally bioavailable PRMT5 inhibitor with Ki of 5
• 1346242-81-6 | Erdafitinib(JNJ-42756493) (Catalog# : 651701)Erdafitinib(JNJ-42756493)is a potent and selective orally bioavailable, pan fibroblas
• 13275-31-5 | Ethyl 2-cyclohexyl-2-oxoacetate (Catalog# : 178157)Ethyl 2-cyclohexyl-2-oxoacetate
• 1140964-99-3 | E7449 (Catalog# : 178903)E7449 is an orally available small molecule inhibitor of the nuclear enzymes poly (AD
• 1388651-30-6 | Elenbecestat ( E2609 ) (Catalog# : 2017878)Elenbecestat (E2609) is a potent, orally bioavailable and CNS-penetrant BACE-1 inhibi
• 117091-64-2 | Etoposide Phosphate (Catalog# : 20178213)Etoposide phosphate is a phosphate salt of a semisynthetic derivative of podophylloto
• 1206123-37-6 | Etrasimod (Catalog# : 17031018)Etrasimod ( APD334 ) is a potent, once-daily, oral, highly selective sphingosine 1-ph
• 1849590-01-7 | eFT-508 (Catalog# : 17031010)eFT-508 (eFT508) is a potent and selective MNK1/2 inhibitor, potentially resulting
• 1234563-16-6 | Epetraborole hydrochloride (Catalog# : 17022806)Epetraborole hydrochloride is a novel leucyl-tRNA synthetase (LeuRS) inhibitor.
• 1693758-51-8 | Eganelisib ( IPI-549 ) (Catalog# : 711401)Eganelisib (IPI-549) is a first-in-class, orally administered, highly selective PI3Kγ
• 124750-92-1 | EXP-3174 (Catalog# : 16122943)EXP-3174, also known as Losartan Carboxylic Acid, is a physiologically active metabol
• 179756-85-5 | Eptapirone (Catalog# : 16122941)Eptapirone, also known as F11440, is a potent, selective, high efficacy 5-HT1A recept
• 1349723-93-8 | Elacestrant dihydrochloride (Catalog# : 16122810)Elacestrant dihydrochloride, also known as RAD1901, is an orally available, selective
• 154598-52-4 | Efavirenz (Catalog# : 16122763)Efavirenz is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with ant
• 134381-21-8 | Epoxomicin (Catalog# : 16122762)Epoxomicin is a selective proteasome inhibitor with anti-inflammatory activity, inhib
• 1942114-09-1 | EAI045 (Catalog# : 16122734)EAI045 is an allosteric inhibitor that targets selected drug-resistant EGFR mutants b
• 1234479-76-5 | ERK5-IN-1 (Catalog# : 6111502)ERK5-IN-1 exhibits potent inhibition of ERK5 with cellular EC50 values of 0.19 M and
• 1352608-82-2 | EW-7197 (Catalog# : 6111007)EW-7197 is a highly potent, selective, and orally bioavailable TGF- receptor ALK4/ALK
• 1252594-99-2 | ETP-46321 (Catalog# : 611825)ETP-46321 is a potent and orally bioavailable PI3K / inhibitor with IC50 of 2.3/14.2
• 1345675-02-6 | ETP-46464 (Catalog# : 161009015)ATR,Bioactive Small Molecule Alphabetical Index,Bioactive Small Molecules,Cell Biolog