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T1190Cefmenoxime hydrochloride；盐酸头孢甲肟Cefmenoxime hemihydrochloride|||SCE-1365 hemihydrochloride；Cefmenoxi
Cefmenoxime hydrochloride (Cefmenoxime hemihydrochloride) is a cephalosporin antibiotic that is administered intravenously or intramuscularly. It is active against most common gram-positive and gram-negative microorganisms, is a potent inhibitor of Enterobacteriaceae, and is highly resistant to hydrolysis by beta-lactamases. The drug has a high rate of efficacy in many types of infection and to date, no severe side effects have been noted.
价 格：￥电议型 号：T1190产 地：中国大陆
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T11836Lefamulin acetate；醋酸来法莫林BC-3781 acetate；BC-3781 acetate|||醋酸来法莫林
Lefamulin acetate (BC-3781 acetate) (formally BC-3781 acetate) is a novel pleuromutilin antibiotic and is the first to be used for the systemic treatment of bacterial infections in humans. Lefamulin acetate (BC-3781 acetate) inhibits protein synthesis by binding to the peptidyl transferase center of the 50S bacterial ribosome, preventing the binding of transfer RNA for peptide transfer.?Lefamulin acetate (BC-3781 acetate) is an orally active antibiotic for community-acquired bacterial pneumonia
价 格：￥电议型 号：T11836产 地：中国大陆
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T11794L-368,899 hydrochloride；化合物 T11794L-368,899 hydrochloride
L-368,899 hydrochloride, used as a tocolytic agent, is a potent, selective, orally bioavailable, non-peptide oxytocin receptor antagonist, with IC50s of 8.9 nM and 26 nM for rat uterus and human uterus oxytocin receptor, respectively.
价 格：￥电议型 号：T11794产 地：中国大陆
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T1178Temozolomide；替莫唑胺NSC 362856|||TZM|||CCRG 81045|||TMZ；NSC 362856|||替莫唑胺|||TZM|||CCRG 81045|||TMZ
Temozolomide (TMZ) is a DNA alkylating agent with blood-brain barrier permeability and oral activity. Temozolomide has antitumor activity and antiangiogenic activity, and also induces apoptosis and autophagy. Temozolomide is stable under acidic conditions and hydrolyzes under neutral or slightly alkaline conditions.
价 格：￥电议型 号：T1178产 地：中国大陆
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T11736K-Ras G12C-IN-2；化合物 T11736K-Ras G12C-IN-2
K-Ras G12C-IN-2 is a covalent kras g12c inhibitor.
价 格：￥电议型 号：T11736产 地：中国大陆
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T11675Irbesartan-d4；厄贝沙坦 D4SR-47436 D4|||BMS-186295 D4；厄贝沙坦 D4|||SR-47436 D4|||BMS-186295 D4
Irbesartan D4, a deuterium-labeled variant of Irbesartan, is a highly potent and specific antagonist of the angiotensin II type 1 (AT1) receptor.
价 格：￥电议型 号：T11675产 地：中国大陆
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T11636IL-17A antagonist 3；化合物 T11636IL-17A antagonist 3
IL-17A antagonist 3 is an IL-17A antagonist.
价 格：￥电议型 号：T11636产 地：中国大陆
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T11616IDO-IN-13；化合物IDO-IN-13GS-4361；GS-4361
IDO-IN-13 (GS-4361) is a potent indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor (EC50: 17 nM).
价 格：￥电议型 号：T11616产 地：中国大陆
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T11500LGSK3368715 dihydrochlorideGSK3368715盐酸盐EPZ019997 dihydrochloride|||GSK3368715 2HCl|||EPZ019997 2HCl
GSK3368715 dihydrochloride (EPZ019997 dihydrochloride) is an orally active and potent inhibitor of type I protein arginine methyltransferases (PRMTs) with anticancer and antitumor activity, inhibiting PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8, and can be used to study advanced solid tumors.
价 格：￥电议型 号：T11500L产 地：中国大陆
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T11500GSK3368715；化合物 T11500EPZ019997；EPZ019997
GSK3368715 is an orally active, reversible, and S-adenosyl-L-methionine (SAM) uncompetitive type I protein arginine methyltransferases (PRMTs) inhibitor (IC50s: 3.1 nM (PRMT1), 48 nM (PRMT3), 1148 nM (PRMT4), 5.7 nM (PRMT6), 1.7 nM (PRMT8)). It has strong anti-cancer activity.
价 格：￥电议型 号：T11500产 地：中国大陆
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T11497Ganfeborole HCl；Ganfeborole 盐酸盐GSK3036656 HCl|||GSK656 HCl；GSK3036656 HCl|||GSK656 HCl
Ganfeborole HCl (GSK3036656 HCl) is a small molecule compound with anti-tuberculosis activity and is an inhibitor of Mycobacterium tuberculosis (Mtb) leucyl-tRNA synthetase (LeuRS; IC50: 0.2 μM).
价 格：￥电议型 号：T11497产 地：中国大陆
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T11470GSK 366；化合物 T11470GSK 366
GSK 366 is a potent kynurenine-3-monooxygenase (KMO) inhibitor (IC50s: 0.7 nM and 2.3 nM for P. fluorescens-KMO and human KMO).
价 格：￥电议型 号：T11470产 地：中国大陆
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T11466GSK-2793660；化合物 T11466GSK-2793660
GSK-2793660 is an orally active and irreversible inhibitor of Cathepsin C (CTSC). GSK-2793660 is a bioactive dipeptide that can be used for the research of bronchiectasis [1] [2].
价 格：￥电议型 号：T11466产 地：中国大陆
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T11463GR 103691；化合物GR 103691GR 103691
GR 103691 is a potent, selective dopamine D3 receptor antagonist (Ki: 0.4 nM). It shows more than 100-fold selectivity for human dopamine human (h)D3 over hD4 and hD1 sites.
价 格：￥电议型 号：T11463产 地：中国大陆
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T11446GNF362；化合物 T11446GNF362
GNF362 is a selective and orally bioavailable inhibitor of inositol trisphosphate 3’ kinase B (Itpkb; IC50: 9 nM). GNF362 also inhibits Itpka and Itpkc (IC50s: 20 nM and 19 nM).
价 格：￥电议型 号：T11446产 地：中国大陆
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T11436GNA002；化合物 T11436GNA002
GNA002 is a highly potent, specific, and covalent EZH2 (Enhancer of zeste homolog 2) inhibitor (IC50: 1.1 μM).
价 格：￥电议型 号：T11436产 地：中国大陆
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T11400Gisadenafil besylate；化合物 T11400UK 369003-26；UK 369003-26
Gisadenafil besylate (UK 369003-26) is a specific, orally active phosphodiesterase 5 (PDE5) inhibitor ,prevents degradation of cyclic guanosine monophosphate (cGMP), with an IC50 of 3.6 nM .
价 格：￥电议型 号：T11400产 地：中国大陆
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T11383GDP366；化合物GDP366GDP366
GDP366, induces cell growth inhibition, cellular senescence and mitotic catastrophe in human cancer cells. a dual inhibitor of survivin and Op18.
价 格：￥电议型 号：T11383产 地：中国大陆
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T11369LGB-110 hydrochloride (1252806-70-4 free base)；化合物 T11369LGB-110 hydrochloride；GB-110 hydrochloride
GB-110 hydrochloride selectively induces PAR2-mediated intracellular Ca2+ release in HT29 cells with an EC50 of 0.28 μM. GB-110 hydrochloride is a potent, orally active, and nonpeptidic protease activated receptor 2 (PAR2) agonist.
价 格：￥电议型 号：T11369L产 地：中国大陆
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T11369GB-110；化合物 T11369GB-110
GB-110 selectively induces PAR2-mediated intracellular Ca2+ release in HT29 cells with an EC50 of 0.28 μM. GB-110 is a potent, orally active, and nonpeptidic protease activated receptor 2 (PAR2) agonist.
价 格：￥电议型 号：T11369产 地：中国大陆
