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T10495LBefiradol化合物 T10495LNLX-112|||F13640
Befiradol (NLX-112) is an agonist of 5-HT1A receptor.
价 格：￥电议型 号：T10495L产 地：中国大陆
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T10493Beclabuvir；贝拉布韦BMS-791325；BMS-791325
Beclabuvir (BMS-791325) is a potent NS5A replication complex inhibitor that inhibits the activity of the NS5B protein expressed by HCV genotypes 1, 2, 4, and 5 and is used in the study of HCV infection.
价 格：￥电议型 号：T10493产 地：中国大陆
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T10460Batabulin；巴他布林T138067；巴他布林|||T138067
Batabulin (T138067) is an antitumor compound, which binds covalently and selectively to a subset of the β-tubulin isotypes, thereby disrupting microtubule polymerization. Batabulin affects cell morphology and leads to cell-cycle arrest ultimately induce apoptotic cell death.
价 格：￥电议型 号：T10460产 地：中国大陆
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T10413Autogramin-1；化合物Autogramin-1Autogramin-1
Autogramin-1 potently inhibits starvation-induced autophagy with IC50 of 0.17 μM. Autogramin-1 also inhibits Rapamycin (mTORC1)-induced autophagy with IC50 of 0.44 μM.
价 格：￥电议型 号：T10413产 地：中国大陆
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T10375ARS-1323；化合物ARS-1323ARS-1323
ARS-1323 is the racemate of ARS-1620 and a mutant K-ras G12C inhibitor.
价 格：￥电议型 号：T10375产 地：中国大陆
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T10374ARS-1323-alkyne；化合物ARS-1323-alkyneARS-1323-alkyne
ARS-1323-alkyne is a switch-II pocket (S-IIP) inhibitor and a conformational specific chemical reporter of KRASG12C nucleotide state in living cells.
价 格：￥电议型 号：T10374产 地：中国大陆
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T10370ARN 077化合物 T10370URB913
ARN 077 is a selective N-acylethanolamine acid amidase (NAAA) inhibitor (IC50: 7 nM for human NAAA). ARN 077 significantly increases palmitoyl ethanolamine (PEA) levels within the CNS.
价 格：￥电议型 号：T10370产 地：中国大陆
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T10364Arbutamine；阿布他明GP 21213；GP 21213
Arbutamine (GP 21213) is a novel potent non-selective beta-adrenoceptor agonist with alpha-1-sympathomimetic activity.Arbutamine promotes cardiac stress and increases heart rate, cardiac contractility.Arbutamine can be used to study cardiac stress and coronary artery disease
价 格：￥电议型 号：T10364产 地：中国大陆
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T10358L2Netarsudil mesylate；化合物 T10358L2AR-13324 (mesylate)；AR-13324 (mesylate)
Netarsudil mesylate is an inhibitor of Rho-associated protein kinase (ROCK) and norepinephrine transporter (NET) with effective in intraocular pressure (IOP) reduction.
价 格：￥电议型 号：T10358L2产 地：中国大陆
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T10358LAR-13324 M1 metabolite；化合物 T10358LAR-13324 M1 metabolite
AR-13324 M1 metabolite is a hydrolysis metabolite of AR-13324 mesylate.
价 格：￥电议型 号：T10358L产 地：中国大陆
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T10358Netarsudil Dihydrochloride；化合物Netarsudil DihydrochlorideAR-13324 Dihydrochloride；AR-13324 Dihydrochl
Netarsudil Dihydrochloride (AR-13324 Dihydrochloride) is an inhibitor of Rho-associated protein kinase (ROCK) and norepinephrine transporter (NET) with effective in intraocular pressure (IOP) reduction.
价 格：￥电议型 号：T10358产 地：中国大陆
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T10357AR-13324 analog mesylate；化合物 T10357AR-13324 analog mesylate
AR-13324 analog mesylate is an inhibitor of Rho-kinase and a norepinephrine transporter and reduces intraocular pressure in normotensive monkey eyes.
价 格：￥电议型 号：T10357产 地：中国大陆
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T10356AQ-13 dihydrochloride；化合物AQ-13 dihydrochlorideAQ-13 dihydrochloride
AQ-13 dihydrochloride is an antimalarial drug. It is effective against drug-resistant strains of Plasmodium falciparum.
价 格：￥电议型 号：T10356产 地：中国大陆
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T10351Aprocitentan D4；化合物 T10351ACT-132577 D4；ACT-132577 D4
Aprocitentan D4 (ACT-132577 D4) is a deuterium-labeled Aprocitentan. Aprocitentan is a major and pharmacologically active metabolite of Macitentan. Aprocitentan is a dual ETA/ETB antagonist (IC50s: 3.4 nM and 987 nM; pA2s: 6.7 and 5.5).
价 格：￥电议型 号：T10351产 地：中国大陆
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T10313AMXT-1501 tetrahydrochloride；化合物 T10313AMXT-1501 tetrahydrochloride
AMXT-1501 tetrahydrochloride is an inhibitor of polyamine transport. It blocks tumor growth in immunocompetent mice but not in athymic nude mice lacking T cells.
价 格：￥电议型 号：T10313产 地：中国大陆
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T10305Amiselimod hydrochloride；化合物Amiselimod hydrochlorideMT-1303 hydrochloride；MT-1303 hydrochloride
Amiselimod hydrochloride (MT-1303 hydrochloride) is a sphingosine 1-phosphate receptor-1 (S1P1) modulator.
价 格：￥电议型 号：T10305产 地：中国大陆
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T10288Alogliptin (13CD3)；化合物 T10288SYR-322 (13CD3)；SYR-322 (13CD3)
Alogliptin (SYR-322) 13CD3 is the deuterium-labeled Alogliptin. Alogliptin is a selective inhibitor of DPP-4.
价 格：￥电议型 号：T10288产 地：中国大陆
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T10255AES-135；化合物AES-135AES-135
AES-135 is a potent HDAC inhibitor, inhibits HDAC3, HDAC6, HDAC11 (IC50s: 654, 190, and 636 nM) with anti-tumor activity.
价 格：￥电议型 号：T10255产 地：中国大陆
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T10249Adoprazine；阿哆嗪SLV313；SLV313
Adoprazine (SLV313) is a potential atypical antipsychotic bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties.
价 格：￥电议型 号：T10249产 地：中国大陆
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T10214A7132；化合物A7132A7132
A7132 is an antibacterial agent and possesses broad and potent antibacterial activity.
价 格：￥电议型 号：T10214产 地：中国大陆
