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T124154Mussaenosidic acid；化合物 Mussaenosidic acidMussaenosidic acid
Mussaenosidic acid is a useful organic compound for research related to life sciences. The catalog number is T124154 and the CAS number is 82451-22-7.
价 格：￥电议型 号：T124154产 地：中国大陆
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T12154LN-Desethyl amodiaquine dihydrochloride；去乙基阿莫地喹盐酸盐N-Desethyl amodiaquine dihydrochloride
N-Desethyl amodiaquine dihydrochloride is an antiparasitic agent and the major biologically active amodiaquine metabolite. Its IC50 values against strains V1/S and 3D7 were 97 nM and 25 nM, respectively.
价 格：￥电议型 号：T12154L产 地：中国大陆
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T12154N-Desethyl amodiaquine；去乙基阿莫地喹N-Desethyl amodiaquine
N-Desethyl amodiaquine is an antiparasitic agent and the major bioactive amodiaquine metabolite. Its IC50 values against strains V1/S and 3D7 were 97 nM and 25 nM, respectively.
价 格：￥电议型 号：T12154产 地：中国大陆
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T11912LY3154207；化合物 T11912LY3154207
LY3154207 is a subtype selective, potent, and orally available human dopamine D1 receptor positive allosteric modulator (PAM) with minimal allosteric agonist activity (EC50=3 nM).
价 格：￥电议型 号：T11912产 地：中国大陆
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T11657INH154；化合物INH154INH154
INH154 is a potent Nek2 and Hec1 binding (INH) inhibitor with IC50s of 120 nM in MB468 cells and 200 nM in Hela cells for INH.
价 格：￥电议型 号：T11657产 地：中国大陆
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T11549Helioxanthin 8-1；化合物 T11549Helioxanthin analogue 8-1；Helioxanthin analogue 8-1
Helioxanthin 8-1, an analogue of helioxanthin, exhibits significant in vitro anti-HBV/HCV/HSV-1/HIV activity with EC50 of >5/10/1.4/15 μM.
价 格：￥电议型 号：T11549产 地：中国大陆
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T11548LHCV-IN-7 hydrochloride；化合物 T11548LHCV-IN-7 hydrochloride
HCV-IN-7 hydrochloride is an orally active and potent pan-genotypic HCV NS5A inhibitor (IC50s: 3-47 pM). It shows a superior pan-genotypic profile and a good pharmacokinetic profile coupled with a favorable liver uptake.
价 格：￥电议型 号：T11548L产 地：中国大陆
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T11548HCV-IN-7；化合物 T11548HCV-IN-7
HCV-IN-7 is an orally active and potent pan-genotypic HCV NS5A inhibitor (IC50s: 3-47 pM). It shows a superior pan-genotypic profile and a good pharmacokinetic profile coupled with a favorable liver uptake.
价 格：￥电议型 号：T11548产 地：中国大陆
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T11547hDHODH-IN-2；化合物 T11547hDHODH-IN-2
hDHODH-IN-2 is an analogue of the active metabolite of Leflunomide. hDHODH-IN-2 is a human dihydroorotate dehydrogenase (hDHODH) inhibitor with anti-inflammatory activity.
价 格：￥电议型 号：T11547产 地：中国大陆
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T11546hDHODH-IN-1；化合物hDHODH-IN-1hDHODH-IN-1
hDHODH-IN-1 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH) with an anti-inflammatory effect.
价 格：￥电议型 号：T11546产 地：中国大陆
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T11545LhDDAH-1-IN-2 sulfate (2408834-77-3 free base)；化合物 T11545LhDDAH-1-IN-2 sulfate；hDDAH-1-IN-2 sulfate
hDDAH-1-IN-2 sulfate is an orally active human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) inhibitor.
价 格：￥电议型 号：T11545L产 地：中国大陆
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T11545hDDAH-1-IN-2；化合物 T11545hDDAH-1-IN-2
hDDAH-1-IN-2 is an orally active human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) inhibitor.
价 格：￥电议型 号：T11545产 地：中国大陆
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T11544HDACs/mTOR Inhibitor 1；化合物 T11544HDACs/mTOR Inhibitor 1
HDACs/mTOR Inhibitor 1 is a dual HDACs and mammalian target of Rapamycin (mTOR) target inhibitor for treating hematologic malignancies (IC50s: 0.19 nM, 1.8 nM, 1.2 nM, and >500 nM for HDAC1, HDAC6, mTOR and PI3Kα).
价 格：￥电议型 号：T11544产 地：中国大陆
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T11543HDAC-IN-5；化合物 T11543HDAC-IN-5
HDAC-IN-5 is a histone deacetylase (HDAC) inhibitor.
价 格：￥电议型 号：T11543产 地：中国大陆
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T11542HDAC-IN-4；化合物 T11542HDAC-IN-4
HDAC-IN-4 is a selective HDAC6 and HDAC10 inhibitor (pIC50s: 7.2 and 6.8 in BRET assay) with antitumoral activity.
价 格：￥电议型 号：T11542产 地：中国大陆
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T11541HCV-IN-30；化合物HCV-IN-30u00A0HCV-IN-30
HCV-IN-30 is an HCV NS5A replication complex inhibitor (IC50s: 901 and 102 nM for genotypes 1a and 1b replicons).
价 格：￥电议型 号：T11541产 地：中国大陆
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T11540HCV-IN-3；化合物 T11540HCV-IN-3
HCV-IN-3 is a hepatitis C virus (HCV) NS3/4a protein inhibitor (IC50: 20 μM; Kd: 29 μM).
价 格：￥电议型 号：T11540产 地：中国大陆
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T11154LEG01377 2HCl；EG01377二盐酸盐EG01377 2HCl(2227996-00-9 Free base)；EG01377 2HCl(2227996-00-9 Free base)
EG01377 2HCl is a potent, bioavailable and selective inhibitor of neuropilin-1 (NRP1) with a Kd value of 1.32 μM and an IC50 value of 609 nM for both EG01377 2HCl against NRP1-a1 and NRP1-b1.EG01377 exhibits anti-angiogenic, antimigratory and antitumor activities.
价 格：￥电议型 号：T11154L产 地：中国大陆
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T11154EG01377；化合物 T11154EG01377
EG01377 has antiangiogenic, antimigratory, and antitumor effects.EG01377 is a neuropilin-1 (NRP1) antagonist, with a Kd of 1.32 μM for NRP1-b1, and IC50s of both 609 nM for NRP1-a1 and NRP1-b1, but shows no effect on NRP2.
价 格：￥电议型 号：T11154产 地：中国大陆
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T10783CGS 15435；化合物CGS 15435CGS 15435
CGS 15435 is a potent thromboxen (TxA2) synthetase inhibitor (IC50: 1 nM). CGS 15435 acts on PGI2 synthase, cyclooxygenase and liposynthase with much less selectivity than on thromboxin synthase.
价 格：￥电议型 号：T10783产 地：中国大陆
