Known Bioactive Library: Selleck Bioactive 10mM, 3.33mM, 1.11mM ICCB-L Plate (10mM / 3.33mM / ICCB-L Max Solubility Vendor ID Compound Name Pathway Targets Information CAS Number Form URL 1.11mM) Well in DMSO (mM) Afatinib (BIBW2992) irreversibly inhibits EGFR/HER2 including EGFR(wt), http://www.selleckchem.c Protein Tyrosine EGFR(L858R), EGFR(L858R/T790M) and HER2 with IC50 of 0.5 nM, 0.4 3651 / 3658 / 3665 A03 S1011 Afatinib (BIBW2992) 199 EGFR,HER2 439081-18-2 free base om/products/BIBW2992. Kinase nM, 10 nM and 14 nM, respectively; 100-fold more active against Gefitinib- html resistant L858R-T790M EGFR mutant. Phase 3. http://www.selleckchem.c Deflazacort(Calcort) is a glucocorticoid used as an anti-inflammatory and 3651 / 3658 / 3665 A04 S1888 Deflazacort 199 Others Others 14484-47-0 free base om/products/Deflazacor. immunosuppressant. html http://www.selleckchem.c Irinotecan is a topoisomerase I inhibitor for LoVo cells and HT-29 cells with 3651 / 3658 / 3665 A05 S1198 Irinotecan 17 DNA Damage Topoisomerase 97682-44-5 free base om/products/Irinotecan.ht IC50 of 15.8 μM and 5.17 μM, respectively. ml Enalapril Maleate, the active metabolite of enalapril, competes with http://www.selleckchem.c Endocrinology & 3651 / 3658 / 3665 A06 S1941 Enalapril Maleate 201 RAAS angiotensin I for binding at the angiotensin-converting enzyme, blocking the 76095-16-4 maleate om/products/Enalapril- Hormones conversion of angiotensin I to angiotensin II. maleate(Vasotec).html BX795 is a potent and specific PDK1 inhibitor with IC50 of 6 nM, 140- and 1600-fold more selective for PDK1 than PKA and PKC, respectively. http://www.selleckchem.c 3651 / 3658 / 3665 A07 S1274 BX-795 169 PI3K/Akt/mTOR IκB/IKK,PDK-1 702675-74-9 free base Meanwhile, in comparison to GSK3β more than 100-fold selectivity om/products/bx-795.html observed for PDK1. http://www.selleckchem.c PF-573228 is an ATP-competitive inhibitor of FAK with IC50 of 4 nM, ~50- 3651 / 3658 / 3665 A08 S2013 PF-573228 52 Angiogenesis FAK 869288-64-2 free base om/products/pf- to 250-fold selective for FAK than Pyk2, CDK1/7 and GSK-3β. 573228.html http://www.selleckchem.c 3651 / 3658 / 3665 A09 S1343 Ginkgolide B 200 Others PAFR Ginkgolide B is a PAFR antagonist with IC50 of 3.6 μM. 15291-77-7 free base om/products/Ginkgolide- B.html http://www.selleckchem.c Neuronal Orphenadrine citrate is a skeletal muscle relaxant, it acts in the central 3651 / 3658 / 3665 A10 S2054 Orphenadrine Citrate 199 AChR 4682-36-4 citrate om/products/orphenadrin Signaling nervous system to produce its muscle relaxant effects. e-citrate-norflex.html http://www.selleckchem.c Transmembrane Autophagy,Proto Omeprazole(Prilosec) is a proton pump inhibitor used in the treatment of 3651 / 3658 / 3665 A11 S1389 Omeprazole 199 73590-58-6 free base om/products/Omeprazole Transporters n Pump dyspepsia. .html http://www.selleckchem.c Neuronal Almotriptan Malate is a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) 3651 / 3658 / 3665 A12 S2096 Almotriptan Malate 200 5-HT Receptor 181183-52-8 malate om/products/almotriptan- Signaling receptor agonist, used for the treatment of Migraine attacks in adults. malate-axert.html http://www.selleckchem.c GPCR & G Cannabinoid AM-1241 is a selective cannabinoid CB2 receptor agonist with Ki of 3.4 nM, 3651 / 3658 / 3665 A13 S1544 AM1241 200 444912-48-5 free base om/products/AM- Protein Receptor exhibits 82-fold selectivity over CB1 receptor. 1241.html http://www.selleckchem.c 5-alpha CGS 21680 HCl is an adenosine A2 receptor agonist with IC50 of 22 nM, 3651 / 3658 / 3665 A14 S2153 CGS 21680 HCl 199 Angiogenesis 124431-80-7 hydrochloride om/products/CGS-21680- Reductase exhibits 140-fold over A1 receptor. hydrochloride.html http://www.selleckchem.c Neuronal Ibuprofen (Dolgesic) is an anti-inflammatory inhibitor targeting COX-1 and 3651 / 3658 / 3665 A15 S1638 Ibuprofen 198 COX 15687-27-1 free base om/products/Ibuprofen(A Signaling COX-2 with IC50 of 13 μM and 370 μM, respectively. dvil).html http://www.selleckchem.c om/products/Irinotecan- 3651 / 3658 / 3665 A16 S2217 Irinotecan HCl Trihydrate 199 DNA Damage Topoisomerase Irinotecan prevents DNA from unwinding by inhibition of topoisomerase 1. 136572-09-3 hydrate Hcl-Trihydrate- Campto.html http://www.selleckchem.c Hydrocortisone is a steroid hormone or glucocorticoid produced by the 3651 / 3658 / 3665 A17 S1696 Hydrocortisone 201 Others Others 50-23-7 free base om/products/Hydrocortis adrenal gland. one.html http://www.selleckchem.c DL-Carnitine hydrochloride is a quaternary ammonium compound om/products/DL- 3651 / 3658 / 3665 A18 S2293 DL-Carnitine HCl 202 Others Others 461-05-2 hydrochloride biosynthesized from the amino acids lysine and methionine. Carnitine- hydrochloride.html Quetiapine fumarate(Seroquel) is an atypical antipsychotic used in the http://www.selleckchem.c Neuronal Dopamine 3651 / 3658 / 3665 A19 S1763 Quetiapine Fumarate 40 treatment of schizophrenia, bipolar I mania, bipolar II depression, bipolar I 111974-72-2 fumarate om/products/Quetiapine- Signaling Receptor depression. fumarate(Seroquel).html http://www.selleckchem.c Myricitrin, a flavonoid compound isolated from the root bark of Myrica 3651 / 3658 / 3665 A20 S2327 Myricitrin 200 Others Others 17912-87-7 free base om/products/Myricitrin(M cerifera, which exerts antinociceptive effects. yricitrine).html http://www.selleckchem.c 3651 / 3658 / 3665 A21 S1829 Pranlukast 22 Others Others Pranlukast is a selective cysteinyl leukotriene receptor antagonist. 103177-37-3 free base om/products/pranlukast.h tml Selleck Bioactive Page 1 of 89 Created 9/2015 ICCB-L Plate (10mM / 3.33mM / ICCB-L Max Solubility Vendor ID Compound Name Pathway Targets Information CAS Number Form URL 1.11mM) Well in DMSO (mM) Tangeretin, a natural polymethoxylated flavone concentrated in the peel of http://www.selleckchem.c 3651 / 3658 / 3665 A22 S2363 Tangeretin 21 Others Others citrus fruits, is known to have antiproliferative, antiinvasive, antimetastatic 481-53-8 free base om/products/Tangeretin( and antioxidant activities. Tangeritin).html http://www.selleckchem.c 3651 / 3658 / 3665 B03 S2393 Sorbitol 197 Others Others Sorbitol is a sugar alcohol and a sugar substitute. 50-70-4 free base om/products/Sorbitol(Glu citol).html GW5074 is a potent and selective c-Raf inhibitor with IC50 of 9 nM, no http://www.selleckchem.c 3651 / 3658 / 3665 B04 S2872 GW5074 199 MAPK Raf effect on the activities of JNK1/2/3, MEK1, MKK6/7, CDK1/2, c-Src, p38 220904-83-6 free base om/products/gw5074.htm MAP, VEGFR2 or c-Fms is noted. l Equol ,a metabolite of soybeans, is an important isoflavone in Endocrinology & Estrogen/progest http://www.selleckchem.c 3651 / 3658 / 3665 B05 S2450 Equol 198 humans，specifically binds to 5α-DHT, has a modest affinity for 531-95-3 free base Hormones ogen Receptor om/products/equol.html recombinant estrogen receptor ERβ. Phase 2. PJ-34 is a PARP inhibitor with EC50 of 20 nM and is equally potent to http://www.selleckchem.c 3651 / 3658 / 3665 B06 S2886 PJ34 94 DNA Damage PARP 344458-19-1 hydrochloride PARP1/2. om/products/pj34.html http://www.selleckchem.c Ascorbyl palmitate is an ester formed from ascorbic acid and palmitic acid 3651 / 3658 / 3665 B07 S2532 L-Ascorbyl 6-palmitate 200 Others Others 137-66-6 free base om/products/L-Ascorbyl- creating a fat-soluble form of vitamin C. 6-palmitate.html http://www.selleckchem.c P450 (e.g. Cobicistat (GS-9350) is a potent and selective inhibitor of CYP3A with IC50 3651 / 3658 / 3665 B08 S2900 Cobicistat (GS-9350) 10 Metabolism 1004316-88-4 free base om/products/cobicistat- CYP17) of 30-285 nM. gs-9350.html http://www.selleckchem.c Brompheniramine hydrogen Neuronal Histamine 3651 / 3658 / 3665 B09 S2585 10 Brompheniramine hydrogen maleate is a histamine H1 receptors antagonist.980-71-2 maleate om/products/bromphenir maleate Signaling Receptor amine.html http://www.selleckchem.c TEMPOL is a superoxide scavenger that displays neuroprotective, anti- 3651 / 3658 / 3665 B10 S2910 Tempol 197 Others Others 2226-96-2 free base om/products/tempol-4- inflammatory and analgesic effects. hydroxy-tempo.html BMY 7378 is a multi-targeted inhibitor of α2C-adrenoceptor and α1D- http://www.selleckchem.c Neuronal 3651 / 3658 / 3665 B11 S2691 BMY 7378 200 5-HT Receptor adrenoceptor with pKi of 6.54 and 8.2, respectively, and acts as a mixed 21102-95-4 dihydrochloride om/products/bmy- Signaling agonist and antagonist for 5-HT1A receptor with pKi of 8.3. 7378.html IOX2 is a potent inhibitor of HIF-1α prolyl hydroxylase-2 (PHD2) with IC50 of http://www.selleckchem.c 3651 / 3658 / 3665 B12 S2919 IOX2 19 Angiogenesis HIF 21 nM, >100-fold selectivity over JMJD2A, JMJD2C, JMJD2E, JMJD3, or 931398-72-0 free base om/products/iox2.html the 2OG oxygenase FIH. Sirtinol is a specific SIRT1 and SIRT2 inhibitor with IC50 of 131 μM and 38 http://www.selleckchem.c 3651 / 3658 / 3665 B13 S2804 Sirtinol 58 Epigenetics Sirtuin 410536-97-9 free base μM, respectively. om/products/sirtinol.html http://www.selleckchem.c Pifithrin-μ is a specific p53 inhibitor by reducing its affinity to Bcl-xL and Bcl- 3651 / 3658 / 3665 B14 S2930 Pifithrin-μ 198 Apoptosis p53 64984-31-2 free base om/products/pifithrin- 2, and also inhibits HSP70 function and autophagy. u.html AM251 block the inhibitory effects of endocannabinoids and synthetic GPCR & G Cannabinoid http://www.selleckchem.c 3651 / 3658 / 3665 B15 S2819 AM251 72 cannabinoid agonists on transmitter release through an action at 183232-66-8 free base Protein Receptor om/products/am251.html presynaptic cannabinoid 1 receptors in brain. http://www.selleckchem.c Fosaprepitant is a water-soluble phosphoryl prodrug for Aprepitant which is 3651 / 3658 / 3665 B16 S3038 Fosaprepitant dimeglumine salt 200 Others Others 265121-04-8 meglumine om/products/fosaprepitan a NK1 antagonist.