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T8425Linoleoyl Ethanolamidefood,intake,Cannabinoid Receptor,feeding,Linoleic acid monoethanolamide,ananda
Linoleoyl Ethanolamide is an endocannabinoid agent. It acts by binding to TRPV1 increasing ERK phosphorylation and AP-1 dependent transcription in CB-receptor in an independent manner.
价 格：￥电议型 号：T8425产 地：中国大陆
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T8428Subasumstatinhibit,Ubiquitin ligase,E1/E2/E3 Enzyme,Subasumstat,TAK 981,E1 activating enzyme,Ubiquit
TAK-981 is a selective the SUMOylation enzymatic cascade inhibitor, has potential immune-activating and antineoplastic activities.
价 格：￥电议型 号：T8428产 地：中国大陆
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T2709TAK-901TAK 901,Inhibitor,TAK-901,Aurora Kinase,inhibit
TAK-901 has been used in trials studying the treatment of Lymphoma, Myelofibrosis, Multiple Myeloma, Myeloid Metaplasia, and Advanced Solid Tumors, among others.
价 格：￥电议型 号：T2709产 地：中国大陆
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T7387Ceftaroline fosamilN-phosphono,PPI 0903,inhibit,TAK599,MRSA,TAK 599,PPI-0903,T-91825,Bacterial,Inhib
Ceftaroline fosamil is a cephalosporin, with activity against Gram-positive pathogens.
价 格：￥电议型 号：T7387产 地：中国大陆
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T6895TAK-580BIIB024,TAK-580,Raf kinases,inhibit,MLN-2480,TAK580,BIIB 024,TAK 580,Raf,Inhibitor,MLN 2480
MLN2480 is an oral, selective pan-Raf kinase inhibitor in Clinicalal trials.
价 格：￥电议型 号：T6895产 地：中国大陆
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T8128Mosapride5-hydroxytryptamine Receptor,inhibit,Inhibitor,TAK 370,Mosapride,TAK370,5-HT Receptor,Serot
Mosapride is a selective 5HT4 agonist
价 格：￥电议型 号：T8128产 地：中国大陆
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T6219Azilsartan Medoxomil阿齐沙坦酯；TAK-491
Azilsartan medoxomil(TAK 491) is an orally administered angiotensin II receptor type 1 antagonist with IC50 of 0.62 nM, which used in the treatment of adults with essential hypertension.
价 格：￥电议型 号：T6219产 地：中国大陆
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T6124Mubritinib木利替尼；TAK-165
Mubritinib (TAK-165) is a potent inhibitor of HER2/ErbB2 with IC50 of 6 nM.
价 格：￥电议型 号：T6124产 地：中国大陆
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T6050TAK-700(S/R)-Orteronel；Orteronel
TAK-700 (Orteronel) is a potent and highly selective human 17, 20-lyase inhibitor with IC50 of 38 nM, exhibits >1000-fold selectivity over other CYPs (e.g. 11-hydroxylase and CYP3A4). Phase 3.
价 格：￥电议型 号：T6050产 地：中国大陆
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T4264TakinibEDHS-206
Takinib is a specific and effective TAK1 inhibitor(IC50= 9.5 nM).
价 格：￥电议型 号：T4264产 地：中国大陆
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T4209TAK-659 hydrochlorideTAK-659
TAK-659 is a potent and selective inhibitor of spleen tyrosine kinase (SYK) with an IC50 value of 3.2 nM. It is selective against most other kinases, but potent toward both SYK and FLT3.
价 格：￥电议型 号：T4209产 地：中国大陆
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T3630RelugolixRVT-601；TAK-385；瑞卢戈利
Relugolix is an orally available, non-peptide gonadotropin-releasing hormone (GnRH or luteinizing hormone-releasing hormone (LHRH)) antagonist, with potential antineoplastic activity. Relugolix competitively binds to and blocks the GnRH receptor in the an
价 格：￥电议型 号：T3630产 地：中国大陆
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T3538SufugolixTAK-013
TAK-013 is a potent and orally available luteinizing hormone-releasing hormone LHRH receptor.
价 格：￥电议型 号：T3538产 地：中国大陆
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T3153SerabelisibINK1117；MLN1117；TAK-117
MLN1117 (INK1117) is a p110α/β/γ/δ inhibitor (IC50: 15/4.5/1.9/13.39 μM).
价 格：￥电议型 号：T3153产 地：中国大陆
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T27624Iptakalim Hydrochloride
Iptakalim, a lipophilic para-amino compound, is a novel ATP-sensitive potassium channel (KATP) opener, as well as an α4β2-containing nicotinic acetylcholine receptor (nAChR) antagonist. Iptakalim is also a K(ir) 6.1/SUR2B activator that can attenuate hypo
价 格：￥电议型 号：T27624产 地：中国大陆
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T2684JNJ-1661010JNJ 1661010；Takeda-25；JNJ1661010
JNJ-1661010 is an effective and specific FAAH inhibitor (IC50: 10/ 12 nM for rat/human), shows >100-fold selectivity for FAAH-1 than FAAH-2.
价 格：￥电议型 号：T2684产 地：中国大陆
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T2571Benactyzine hydrochlorideAmitakon；Tranquilline；Neuroleptone；胃复康；盐酸贝那替嗪
Benactyzine hydrochloride is a centrally acting muscarinic antagonist. Benactyzine has been used in the treatment of depression and is used in research to investigate the role of cholinergic systems on behavior.
价 格：￥电议型 号：T2571产 地：中国大陆
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T24850Takeda103ACMPD103A；Takeda-103A；CMPD-103A；Takeda 103 A；Takeda-103-A
Takeda103A is the GRK2-dependent bovine tubulin oxidation effective inhibitor.
价 格：￥电议型 号：T24850产 地：中国大陆
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T2404Vonoprazan fumarate富马酸沃诺拉赞；TAK-438
Vonoprazan Fumarate (TAK-438) is a novel P-CAB (potassium-competitive acid blocker) that reversibly inhibits H+/K+, ATPase.
价 格：￥电议型 号：T2404产 地：中国大陆
