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T10395LATM-3507化合物 ATM-3507ATM3507|||ATM 3507
ATM-3507 is a protomyosin inhibitor with anticancer activity that inhibits human melanoma and can be used to study ovarian cancer.
价 格：￥电议型 号：T10395L产 地：中国大陆
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T10395ATM-3507 trihydrochloride (1861449-70-8 free base)；化合物 T10395ATM-3507 trihydrochloride；ATM-3507 trih
ATM-3507 trihydrochloride is a potent tropomyosin inhibitor (IC50s: 3.83-6.84 μM in human melanoma cell lines).
价 格：￥电议型 号：T10395产 地：中国大陆
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T10394LATB107 hydrochloride；化合物ATB107盐酸盐ATB107 hydrochloride(455325-51-6 Free base)；ATB107 hydrochloride(45
ATB107 hydrochloride is a novel and potent inhibitor of indole-3-glycerol phosphate synthase (IGPS) with a KD of 3 μM.
价 格：￥电议型 号：T10394L产 地：中国大陆
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T10394ATB107；化合物 T10394ATB107
ATB107 is a potent and novel inhibitor of indole-3-glycerol phosphate synthase (IGPS, KD: 3 μM).
价 格：￥电议型 号：T10394产 地：中国大陆
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T10393AT-007；化合物AT-007AT-007
AT-007 is an orally active CNS penetrant Aldose Reductase inhibitor for the treatment of Galactosemia (IC50: 100 pM). It reduces toxic galactitol levels and prevents disease complications in GALT deficiency rats.
价 格：￥电议型 号：T10393产 地：中国大陆
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T10387ASP1126；化合物 T10387ASP1126
ASP1126 is a selective and orally active sphingosine-1-phosphate (S1P) agonist (EC50s: 7.12 nM, 517 nM for hS1P1 and hS1P3).
价 格：￥电议型 号：T10387产 地：中国大陆
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T10381AS2717638；化合物AS2717638AS2717638
AS2717638 is an orally active and selective lysophosphatidic acid receptor 5 (LPA5) antagonist (IC50: 38 nM for hLPA5). It also significantly improves PGF2α-, PGE2-, and AMPA-induced allodynia.
价 格：￥电议型 号：T10381产 地：中国大陆
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T10379Arzoxifene hydrochloride；化合物 T10379SERM 3|||LY 353381 HCl；SERM 3|||LY 353381 HCl
Arzoxifene hydrochloride is a selective estrogen receptor modulator that is a potent estrogen antagonist in mammary and uterine tissue.
价 格：￥电议型 号：T10379产 地：中国大陆
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T10378Artelinic acid；化合物 Artelinic acidArtelinic acid
Artelinic acid is a water-soluble artemisinin analog with antimalarial activity and is used for the treatment of multi-drug resistant strains of Plasmodium falciparum.
价 格：￥电议型 号：T10378产 地：中国大陆
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T10377Artefenomel；化合物 T10377OZ439；OZ439
Artefenomel (OZ439) is a synthetic antimalarial agent with the artemisinin pharmacophore.
价 格：￥电议型 号：T10377产 地：中国大陆
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T10376ARS-1630；化合物ARS-1630ARS-1630
ARS-1630 is a mutant K-ras G12C inhibitor. It is a less active enantiomer of ARS-1620.
价 格：￥电议型 号：T10376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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T10373(R)-Filanesib；化合物 T10373(R)-ARRY-520；(R)-ARRY-520
(R)-Filanesib is the R-enantiomer of ARRY-520. (R)-Filanesib is a synthetic kinesin spindle protein (KSP) inhibitor (IC50: 6 nM).
价 格：￥电议型 号：T10373产 地：中国大陆
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T10372ARQ 069；化合物 T10372ARQ 069
ARQ 069 (3.8-60 μM; for 2 hours) reduces the degree of phosphorylation of FGFR (predominantly FGFR2) in a concentration-dependent manner, without decreasing β-actin. ARQ 069 shows an affinity for FGFR2 of 5.2 μM. ARQ 069 inhibits FGFR phosphorylation in Kato III cells (IC50: 9.7 μM). ARQ 069 targets the inactive forms of FGFR1 and FGFR2 kinases and inhibits their enzymatic activity. When ARQ 069 is preincubated with either phosphorylated FGFR1 or FGFR2, the potency of ARQ 069 in inhibiting Pyk2
价 格：￥电议型 号：T10372产 地：中国大陆
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T10371Arotinolol；阿罗洛尔Arotinolol
Arotinolol is a nonselective α/β-adrenergic receptor blocker and a vasodilating β-blocker. Arotinolol also shows potency for inhibiting the binding of the radioligand 125I-ICYP to 5HT1B-serotonergic receptor sites. It is an antihypertensive agent.
价 格：￥电议型 号：T10371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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T1037Doripenem monohydrate；多尼培南(一水合物)S 4661 monohydrate|||Doripenem Hydrate|||S-4661；多尼培南(一水合物)|||S 4661
Doripenem monohydrate (S 4661 monohydrate) is a broad-spectrum injectable antibiotic, used for Gram-positive, Gram-negative and anaerobic pathogens.
价 格：￥电议型 号：T1037产 地：中国大陆
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T10368Aripiprazole (D8)；化合物 T10368OPC-14597u00A0D8；OPC-14597u00A0D8
Aripiprazole D8 (OPC-14597 D8) is the deuterium-labeled Aripiprazole. Aripiprazole is a human 5-HT1A receptor partial agonist (Ki: 4.2 nM).
价 格：￥电议型 号：T10368产 地：中国大陆
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T10367Arginase inhibitor 1；化合物 T10367Arginase inhibitor 1
Arginase inhibitor 1 is a potent inhibitor of human arginases I and II (IC50s: 223 and 509 nM).
价 格：￥电议型 号：T10367产 地：中国大陆
