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T15257Etripamil；化合物EtripamilMSP-2017|||(-)-MSP-2017；MSP-2017|||(-)-MSP-2017
Etripamil (MSP-2017) displays atrioventricular nodal conduction and prolongs atrioventricular nodal refractory periods by inhibiting calcium ion influx through the calcium slow channels in the atrioventricular node cells. Etripamil is an antagonist of short-acting L-type calcium-channel. It has a rapid onset of action designed for intranasal administration. It is also used to treat Paroxysmal Supraventricular Tachycardia.
价 格：￥电议型 号：T15257产 地：中国大陆
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T15250ETC-206；化合物ETC-206ETC-206
ETC-206 is a selective inhibitor of MNK1 and MNK2 (IC50s: 64 nM and 86 nM).
价 格：￥电议型 号：T15250产 地：中国大陆
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T15220Enbucrilate恩布酯恩布酯|||Butyl cyanoacrylate
Enbucrilate (Butyl cyanoacrylate) is a cyanoacrylate ester that has been used as surgical tissue adhesive. Enbucrilate is a tissue adhesive, forming polymer films at oil-water interfaces and revealing films of diverse morphology.
价 格：￥电议型 号：T15220产 地：中国大陆
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T15209Elobixibat；依洛西巴特AZD 7806|||A 3309；AZD 7806|||A 3309
Elobixibat (A 3309) is an inhibitor of the ileal bile acid transporter (IC50: 0.13 nM, 0.53 nM, and 5.8 nM for mouse, human, and canine IBAT). Elobixibat can be used in studies about chronic idiopathic constipation.
价 格：￥电议型 号：T15209产 地：中国大陆
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T15208Elisartan；化合物 T15208HN 65021；HN 65021
Elisartan is a non-peptide pro-drug of angiotensin II AT1 receptor antagonist HN-12206. It also shows anti-hypertension activities.
价 格：￥电议型 号：T15208产 地：中国大陆
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T15207Eleclazine hydrochloride；化合物Eleclazine hydrochlorideGS 6615 hydrochloride；GS 6615 hydrochloride
Eleclazine hydrochloride (GS 6615 hydrochloride) is a novel inhibitor of late Na+ current (IC50: 0.7 uM).
价 格：￥电议型 号：T15207产 地：中国大陆
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T15206Eldecalcitol；艾地骨化醇ED-71|||2-(3-hydroxypropoxy)-1,25-dihydroxyvitamin D3；艾地骨化醇|||ED-71|||2-(3-hydroxy
Eldecalcitol possesses a potent inhibitory effect on bone resorption and induces a significant increase in bone mineral density. Eldecalcitol is an orally active analogue of active vitamin D. It also is used in the treatment of osteoporosis .
价 格：￥电议型 号：T15206产 地：中国大陆
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T15205EL-102；化合物 EL-102EL102；EL102
EL-102 is a HIF1α inhibitor with anticancer activity that inhibits microtubule protein polymerization and can be used to study prostate cancer.
价 格：￥电议型 号：T15205产 地：中国大陆
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T15204EHT 1610；化合物EHT 1610EHT 5372；EHT 5372
EHT 1610 (EHT 5372) is a potent inhibitor of DYRK, with an IC50 of 0.36 nM and 0.59 nM for DYRK1A and DYRK1B, respectively. EHT 1610 has an inhibitory effect on leukemia, regulating cell cycle and inducing cell apoptosis.
价 格：￥电议型 号：T15204产 地：中国大陆
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T15203EGNHS；化合物EGNHSEGS crosslinker；EGS crosslinker
EGNHS (EGS crosslinker) is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格：￥电议型 号：T15203产 地：中国大陆
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T15202EF-5；化合物EF-52-Nitroimidazole|||EF5；2-Nitroimidazole|||EF5
EF-5 (2-Nitroimidazole) is a agent of hypoxia labeling. It is used to identify hypoxia in cells.
价 格：￥电议型 号：T15202产 地：中国大陆
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T15201MAK683；化合物MAK683MAK683
MAK683 is an inhibitor of embryonic ectoderm development (EED) (IC50s: 59, 89, 26 nM in EED Alphascreen binding, LC-MS and ELISA assay).
价 格：￥电议型 号：T15201产 地：中国大陆
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T15200Edotecarin；化合物 T15200PF 804950|||J 107088；PF 804950|||J 107088
Edotecarin is a potent topoisomerase I inhibitor. It can decrease single-strand DNA cleavage (IC50: 50 nM).
价 格：￥电议型 号：T15200产 地：中国大陆
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T1520Aliskiren hemifumarate阿利克仑半富马酸盐阿利克仑半富马酸盐|||CGP 60536|||SPP 100|||CGP60536B
Aliskiren hemifumarate (CGP60536B) is an orally active nonpeptide renin inhibitor with antihypertensive activity.
价 格：￥电议型 号：T1520产 地：中国大陆
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T15196EC23；化合物EC23BASF-46928|||AGN 190205；BASF-46928|||AGN 190205
EC23 (AGN 190205) is a stable synthetic retinoid analogue. It is also induces neuronal differentiation.
价 格：￥电议型 号：T15196产 地：中国大陆
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T15184E 2012化合物E 2012(E)-1-[(1S)-1-(4-氟苯基)乙基]-3-[3-甲氧基-4-(4-甲基-1H-咪唑-1-YL)亚苄基]哌啶-2-酮
E2012 is a γ-secretase modulator (GSM). E2012 inhibits 3β-hydroxysterol Δ24-reductase (DHCR24) at the final step in the cholesterol biosynthesis. E 2012 aims at Alzheimer´s disease by reduction of amyloid β-42, and induces cataract following repeated doses in the rat.
价 格：￥电议型 号：T15184产 地：中国大陆
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T15170DS28120313；化合物 T15170DS28120313
DS28120313 is an oral inhibitor of hepcidin production (IC50: 0.093 μM).
价 格：￥电议型 号：T15170产 地：中国大陆
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T15020CU-CPT22；化合物CU-CPT22CU-CPT22
CU-CPT22 is the first probe for the complex between toll-like receptors TLR1 and TLR2. CU-CPT22 binds at the interface of TLR1 and TLR2 (IC50 = 0.58 μM). It competes with the synthetic triacylated lipoprotein (Pam3CSK4) binding to TLR1/2 (Ki: 0.41 μM).
价 格：￥电议型 号：T15020产 地：中国大陆
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T15003CP-20961；化合物 T15003CP-20961
CP-20961 is a synthetic non-immunogenic adjuvant. It induces arthritis.
价 格：￥电议型 号：T15003产 地：中国大陆
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T14936Ivaltinostat；化合物 T14936CG-200745；CG-200745
CG-200745 is a potent inhibitor of HDAC. CG200745 induces apoptosis and also inhibits the deacetylation of histone H3 and tubulin.
价 格：￥电议型 号：T14936产 地：中国大陆
