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T12016Methyl L-pyroglutamate；L-焦谷氨酸甲酯L-Pyroglutamic acid methyl ester|||(S)-Methyl 5-oxopyrrolidine-2-carb
Methyl L-pyroglutamate (L-Pyroglutamic acid methyl ester) shows anti-inflammatory activity. Methyl L-pyroglutamate is isolated from Portulaca?oleracea?L..
价 格：￥电议型 号：T12016产 地：中国大陆
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T12009Telomerase-IN-1；端粒酶-IN-1Telomerase-IN-1
Telomerase-IN-1 is a telomerase inhibitor (IC50: 0.19 μM). telomerase-IN-1 activates hTERT expression through the endoplasmic reticulum stress (ERS) of the ER overreaction (EOR), which then induces ERS, leading to apoptosis. telomerase-IN-1 leads to inhibition of cell proliferation through the expression of downstream signaling molecules including Telomease-IN-1 has high inhibitory activity against telomerase, high anti-proliferative capacity against SMMC-7721 cells, and no significant toxic eff
价 格：￥电议型 号：T12009产 地：中国大陆
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T12001Menaquinone-7维生素 K2(35)Vitamin MK-7|||维生素 K2(35)|||Vitamin K2-7|||Vitamin K2(35)
Menaquinone-7 (Vitamin K2(35)) is a vitamin K2 analog, is originally discovered as the anti-hemorrhagic factors. Menaquinone-7 (Vitamin K2(35)) is identified as the most bioactive cofactor for the carboxylation reaction of Gla-proteins.
价 格：￥电议型 号：T12001产 地：中国大陆
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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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T11891Lumefantrine-d18；苯芴醇 D18Benflumetol D18|||Lumefantrine D18；Benflumetol D18|||苯芴醇 D18|||Lumefantrine
Lumefantrine D18 is an antimalarial drug, and is the deuterium labeled Lumefantrine.
价 格：￥电议型 号：T11891产 地：中国大陆
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T11869Losartan (D4 Carboxylic Acid)；氯沙坦羧酸 D4E-3174 D4|||EXP-3174 D4；E-3174 D4|||氯沙坦羧酸 D4|||EXP-3174 D4
Losartan D4 Carboxylic Acid is the deuterium labeled Losartan, which is an angiotensin II receptor antagonist.
价 格：￥电议型 号：T11869产 地：中国大陆
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T11867Loperamide-d6 hydrochloride；化合物 T11867R-18553 D6 hydrochloride；R-18553 D6 hydrochloride
Loperamide D6 hydrochloride, a deuterium-labeled variant of Loperamide hydrochloride, acts as an opioid receptor agonist utilized for diarrhea treatment.
价 格：￥电议型 号：T11867产 地：中国大陆
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T11866LolCDE-IN-2；化合物 T11866LolCDE-IN-2
LolCDE-IN-2 is a potent Lol protein (LolCDE) inhibitor. LolCDE-IN-2 shows antibacterial activity with a MIC of 2 μg/ml against E. coli MG1655 [1].
价 格：￥电议型 号：T11866产 地：中国大陆
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T11816Lansoprazole-d4；化合物 T11816AG-1749 D4|||Lansoprazole D4；AG-1749 D4|||Lansoprazole D4
Lansoprazole D4 (AG-1749 D4) is a deuterium labeled Lansoprazole. Lansoprazole is an inhibitor of proton pump which prevents the stomach from producing acid.
价 格：￥电议型 号：T11816产 地：中国大陆
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T11729JTE-952；化合物 T11729JTE-952
JTE-952 is a oral, potent active and selective Type II inhibitor of colony stimulating factor-1 receptor (CSF-1R or cFMS, type III receptor tyrosine kinase), with IC50 values of 13 nM and 261 nM for CSF1R and TrkA , respectively. Effective against a mouse collagen-induced model of arthritis.
价 格：￥电议型 号：T11729产 地：中国大陆
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T11696Ivachtin；化合物IVACHTINCaspase-3 Inhibitor VII；Caspase-3 Inhibitor VII
Ivachtin (Caspase-3 Inhibitor VII) is a nonpeptide, noncompetitive and reversibl caspase-3 inhibitor(IC50 = 23 nM) and is a modest inhibitor of the remaining caspases.
价 格：￥电议型 号：T11696产 地：中国大陆
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T11694Ivabradine-d6 hydrochloride；盐酸伊伐布雷定 D6Ivabradine D6 hydrochloride；盐酸伊伐布雷定 D6|||Ivabradine D6 hydroch
Ivabradine hydrochloride is a new If inhibitor with IC50 of 2.9 μM, and used as a pure heart rate lowering agent. Ivabradine D6 hydrochloride is the deuterium labeled Ivabradine hydrochloride.
价 格：￥电议型 号：T11694产 地：中国大陆
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T11692Ivabradine-d3 hydrochloride；盐酸伊伐布雷定 D3Ivabradine D3 Hydrochloride；盐酸伊伐布雷定 D3|||Ivabradine D3 Hydroch
Ivabradine hydrochloride is a new If inhibitor with IC50 of 2.9 μM, and used as a pure heart rate lowering agent. Ivabradine D3 Hydrochloride is the deuterium labeled Ivabradine hydrochloride.
价 格：￥电议型 号：T11692产 地：中国大陆
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T11645Impurity C of Calcitriol；PRE-骨化三醇PTAD加合物Impurity C of Calcitriol
Impurity C of Calcitriol is an impurity of Calcitriol.Impurity C of Calcitriol is used in the synthesis of vitamin D3.
价 格：￥电议型 号：T11645产 地：中国大陆
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T11593I-OMe-Tyrphostin AG 538；化合物T11593I-OMe-AG 538；I-OMe-AG 538
I-OMe-Tyrphostin AG 538 is a specific IGF-1R inhibitor and ATP-competitive inhibitor of PI5P4Kα (IC50: 1 ?M).I-OMe-Tyrphostin AG 538 inhibits IGF-1R-mediated signaling and exhibits preferential cytotoxicity to nutrient-deficient PANC1 cells.
价 格：￥电议型 号：T11593产 地：中国大陆
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T11580LHeme Oxygenase-1-IN-1 hydrochloride；化合物 T11580LHO-1-IN-1 hydrochloride；HO-1-IN-1 hydrochloride
HO-1-IN-1 hydrochloride is a heme oxygenase 1 (HO-1) inhibitor (IC50: 250 nM).
价 格：￥电议型 号：T11580L产 地：中国大陆
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T11580Heme Oxygenase-1-IN-1；化合物Heme Oxygenase-1-IN-1HO-1-IN-1；HO-1-IN-1
Heme Oxygenase-1-IN-1 (HO-1-IN-1) is a heme oxygenase 1 (HO-1) inhibitor (IC50: 250 nM).
价 格：￥电议型 号：T11580产 地：中国大陆
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T11441GNE-987；化合物 T11441GNE-987
GNE-987 is a highly active chimeric BET degrader. GNE-987 binds equipotently to the BD1 and BD2 bromodomains of BRD4 with low nanomolar affinities (IC50: 4.7 and 4.4 nM, respectively). GNE-987 exhibits picomolar cell BRD4 degradation activity (DC50: 0.03 nM for EOL-1 AML cell line).
价 格：￥电议型 号：T11441产 地：中国大陆
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T11440GNE-8505；化合物 T11440GNE-8505
GNE-8505 is an orally available inhibitor of Dual leucine zipper kinase (DLK).
价 格：￥电议型 号：T11440产 地：中国大陆
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T11439GNE-616；化合物 T11439GNE-616
GNE-616 is a highly potent, metabolically stable, orally bioavailable, and subtype-selective Nav1.7 inhibitor (Ki: 0.79 nM, Kd: 0.38 nM for hNav1.7) for the treatment of chronic pain.
价 格：￥电议型 号：T11439产 地：中国大陆
