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T24214Phenamacril；苯那普利JS39919|||JS399 19；JS39919|||苯那普利|||JS399 19
Phenamacril (JS39919) is acyanoacrylate fungicide, has powerful inhibition against Fusarium species, especially to Fusarium graminearum. Phenamacril is a specific Fusarium myosin I inhibitor.
价 格：￥电议型 号：T24214产 地：中国大陆
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T24170Iodoantipyrine；碘安替比林Jodantipyrine|||EINECS 204-966-6|||Arthripur|||Iodophenazone；碘安替比林|||Jodantipyri
Iodoantipyrine (Arthripur) is a commonly-used indicator and is used to evaluate in rats by measuring torcular venous efflux after systemic injection of the indicator under conditions of normal and high CBF.
价 格：￥电议型 号：T24170产 地：中国大陆
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T24137HENA；化合物 T24137HENA
HENA is a novel activator of large conductance, voltage- and Ca2+-gated K+ (BK) channels.
价 格：￥电议型 号：T24137产 地：中国大陆
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T2409Tenofovir alafenamide；替诺福韦艾拉酚胺GS-7340；替诺福韦艾拉酚胺|||替诺福韦|||GS-7340
Tenofovir alafenamide (GS-7340) is a nucleotide reverse transcriptase inhibitor (NRTI) and a novel ester prodrug of the antiretroviral tenofovir.
价 格：￥电议型 号：T2409产 地：中国大陆
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T2403Bromfenac sodium hydrate；溴芬酸钠Bromfenac sodium|||Bromfenac monosodium salt sesquihydrate；Bromfenac so
Bromfenac sodium hydrate (Bromfenac monosodium salt sesquihydrate) is the sodium salt form of bromfenac, a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and anti-inflammatory activities. Upon ophthalmic administration, bromfenac binds to and inhibits the activity of cyclooxygenase II (COX II), an enzyme which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins (PG). By inhibiting PG formation, bromfenac is able to inhibit PG-induced inflammation, thereby
价 格：￥电议型 号：T2403产 地：中国大陆
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T23780Benalaxyl, (+)-；化合物 T23780Benalaxyl, (+)-
Benalaxyl, (+)- is a fungicide agent.
价 格：￥电议型 号：T23780产 地：中国大陆
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T2373Vipadenant；化合物VipadenantCEB-4520|||BIIB-014；CEB-4520|||BIIB-014
Vipadenant (CEB-4520)(BIIB-014) is an adenosine A2a antagonist with Ki of 1.3 nM; less potent for A1(Ki=69 nM).
价 格：￥电议型 号：T2373产 地：中国大陆
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T23635Adenallene；化合物 T23635Adenallene
Adenallene inhibits replication and cytopathic effects of HIV in vitro.
价 格：￥电议型 号：T23635产 地：中国大陆
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T2346LEnasidenib mesylate；恩西地平甲磺酸盐AG221 mesylate|||AG 221 mesylate|||AG-221 mesylate；AG221 mesylate|||AG 2
Enasidenib mesylate (AG-221 mesylate) is a potent and selective IDH2 mutase inhibitor that promotes differentiation of leukemia myeloid cells for the treatment of acute myeloid leukemia.
价 格：￥电议型 号：T2346L产 地：中国大陆
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T2346Enasidenib；恩西地平AG-221；恩西地平|||AG-221
Enasidenib (AG-221) is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity.
价 格：￥电议型 号：T2346产 地：中国大陆
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T23379Solifenacin hydrochloride；化合物 T23379Solifenacin hydrochloride
Solifenacin Hcl is a muscarinic receptor antagonist.
价 格：￥电议型 号：T23379产 地：中国大陆
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T2336Vitamin K2；四烯甲萘醌Menatetrenone；Menatetrenone|||四烯甲萘醌
Vitamin K2 (Menatetrenone) is a menaquinone compound and form of vitamin K2 with potential antineoplastic activity. Menatetrenone may act by modulating the signaling of certain tyrosine kinases, thereby affecting several transcription factors including c-myc and c-fos. This agent inhibits tumor cell growth by inducing apoptosis and cell cycle arrest.
价 格：￥电议型 号：T2336产 地：中国大陆
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T22922Lenalidomide hemihydrate；来那度胺半水合物Lenalidomide hemihydrate
Lenalidomide hemihydrate is a TNF-α secretion inhibitor (IC50 = 13 nM). Lenalidomide hemihydrate could bound endogenous CRBN and recombinant CRBN-DNA damage binding protein-1 (DDB1) complexes.
价 格：￥电议型 号：T22922产 地：中国大陆
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T22589Asenapine hydrochloride；阿塞那平盐酸盐Asenapine hydrochloride
Asenapine is a new atypical antipsychotic developed for the treatment of schizophrenia and acute mania associated with bipolar disorder.
价 格：￥电议型 号：T22589产 地：中国大陆
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T225379-Phenanthrol；9-羟基菲9-Phenanthrol
9-Phenanthrol is inhibitor of the transient receptor potential melastatin 4 (TRPM) channel, a Ca2+ -activated non-selective cation channel.
价 格：￥电议型 号：T22537产 地：中国大陆
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T22452Valbenazine tosylate；結苯那嗪NBI-98854；結苯那嗪|||NBI-98854
Valbenazine tosylate, the tosylate salt of valbenazine, is a vesicular monoamine transporter 2 (VMAT2) inhibitor with a Ki value of 150 nM while displaying no significant binding to VAMT1(Ki<10 μM).
价 格：￥电议型 号：T22452产 地：中国大陆
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T22450Tyrphostin B44, (+) enantiomer酪氨酸磷酸化抑制剂AG 835酪氨酸磷酸化抑制剂AG 835
Tyrphostin B44, (+) enantiomer is an inhibitor of epidermal growth factor receptor (EGFR) kinase with IC50 of 0.86 μM and has less active than the (-) enantiomer.
价 格：￥电议型 号：T22450产 地：中国大陆
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T22401PNU-282987 S enantiomer hydrochloride；化合物PNU-282987 S enantiomer hydrochloride(S)-PNU-282987 HCl；(S)
(S)-PNU-282987 is the absolute stereochemistry form of PNU-282987. PNU 282987, a potent agonist of α7-containing neuronal nicotinic acetylcholine receptors (nAChRs) with Ki of 26 nM for the rat receptor, has negligible activity against α1β1γδ and α3β4 nAChRs as well as a panel of monoamine, glutamate, muscarinic,and GABA receptors, except 5-HT3 with Ki of 930 nM.
价 格：￥电议型 号：T22401产 地：中国大陆
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T22330Fenamic acid；N-苯基邻氨基苯甲酸2-Anilinobenzoic acid|||Diphenylamine-2-carboxylic acid|||2-(Phenylamino)benz
Fenamic acid (N-Phenylanthranilic acid) is a chloride channel blocker that causes renal papillary necrosis in rats. Fenamic acid serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including flufenamic acid, tolfenamic acid, mefenamic acid, and meclofenamic acid.
价 格：￥电议型 号：T22330产 地：中国大陆
