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T12352Oxidopamine hydrochloride；6-羟基多巴胺盐酸盐6-Hydroxydopamine hydrochloride|||6-OHDA hydrochloride；6-Hydroxy
Oxidopamine hydrochloride (6-Hydroxydopamine hydrochloride) is an neurotransmitter dopamine antagonist.
价 格：￥电议型 号：T12352产 地：中国大陆
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T12351p53 and MDM2 proteins-interaction-inhibitor (racemic)；化合物 T12351p53-and-mdm2-proteins-interaction-in
p53 and MDM2 proteins-interaction-inhibitor (racemic) is an inhibitor of the interaction between p53 and MDM2 proteins.
价 格：￥电议型 号：T12351产 地：中国大陆
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T12350p53 and MDM2 proteins-interaction-inhibitor dihydrochloride；化合物 T12350p53 and MDM2 proteins-interact
p53 and MDM2 proteins-interaction-inhibitor dihydrochloride is a interaction inhibitor between p53 and MDM2 proteins.
价 格：￥电议型 号：T12350产 地：中国大陆
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T1235Lincomycin hydrochloride monohydrate林可霉素洁霉素盐酸盐|||林可霉素|||Lincomycin hydrochloride hydrate
Lincomycin hydrochloride monohydrate (Lincomycin hydrochloride hydrate) is an antibiotic produced by Streptomyces lincolnensis var. lincolnensis. It has been used in the treatment of staphylococcal, streptococcal, and Bacteroides fragilis infections.
价 格：￥电议型 号：T1235产 地：中国大陆
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T12235NMDI14；化合物NMDI14NMDI14
NMDI14 is an inhibitor of nonsense mediated RNA decay (NMD).
价 格：￥电议型 号：T12235产 地：中国大陆
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T11826LCH-7749944；化合物LCH-7749944GNF-PF-2356；GNF-PF-2356
LCH-7749944 (GNF-PF-2356) effectively suppresses the proliferation of human gastric cancer cells through downregulation of PAK4/c-Src/EGFR/cyclin D1 pathway and induces apoptosis. LCH-7749944 is a potent PAK4 inhibitor with an IC50 of 14.93 μM.
价 格：￥电议型 号：T11826产 地：中国大陆
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T11701J22352；化合物 T11701J22352
J22352, a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC50 value of 4.7 nM, enhances anticancer effects in glioblastoma by promoting HDAC6 degradation. It does so by inhibiting autophagy and stimulating the antitumor immune response, further restoring host antitumor activity through the reduction of PD-L1´s immunosuppressive activity.
价 格：￥电议型 号：T11701产 地：中国大陆
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T11250Ezetimibe-d4；化合物 T11250SCH 58235 D4；SCH 58235 D4
Ezetimibe D4, a deuterium-labeled variant of Ezetimibe, functions as an inhibitor of Niemann-Pick C1-like1 (NPC1L1) and is recognized for its potent activation of Nrf2.
价 格：￥电议型 号：T11250产 地：中国大陆
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T11235Estradiol 3-sulfamate；雌二醇 3-氨基磺酸E2MATE|||BLE 00084|||ES-J 995；E2MATE|||BLE 00084|||ES-J 995
Estradiol 3-sulfamate (BLE 00084) is an orally active and highly potent steroidal estrone sulfatase (ES) inhibitor.Estradiol 3-sulfamate has a K(i) value of 73 nM for ES in human placental microsomes and can be used in the study of breast cancer.
价 格：￥电议型 号：T11235产 地：中国大陆
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T11205ent-Ezetimibe；ENT-依折麦布ent-SCH 58235；ent-SCH 58235|||ENT-依折麦布
Ezetimibe is a Niemann-Pick C1-like1 (NPC1L1) inhibitor, and is a potent Nrf2 activator.ent-Ezetimibe (ent-SCH 58235) (ent-SCH 58235) is the RRS-enantiomer of Ezetimibe. Ezetimibe is a potent cholesterol absorption inhibitor.?
价 格：￥电议型 号：T11205产 地：中国大陆
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T10720CD235；化合物 T10720CD235
CD235 is a structurally similar analog of CD161. CD161 is an orally bioavailable inhibitor of BET bromodomain.
价 格：￥电议型 号：T10720产 地：中国大陆
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T10411AU1235；化合物AU1235AU1235
AU1235 is a Mycobacterium tuberculosis inhibitor.
价 格：￥电议型 号：T10411产 地：中国大陆
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T10235Acetyllovastatin；化合物 T10235Acetyllovastatin
Acetyllovastatin (acetate of Lovastatin) presents a moderate inhibitory effect against the acetylcholinesterase (IC50: 79 μg/mL). Lovastatin displays antifungal activity and suppresses the proliferation of a number of transformed cell lines.
价 格：￥电议型 号：T10235产 地：中国大陆
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T0711Niclosamide；氯硝柳胺BAY2353|||Niclocide；BAY2353|||Niclocide|||氯硝柳胺
Niclosamide (Niclocide)(BAY2353) is used to treat most tapeworm infections by inhibiting DNA replication.
价 格：￥电议型 号：T0711产 地：中国大陆
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T0235Modaline sulfate；硫酸莫达林Modaline sulfate
Modaline was a 2-methyl-3-piperidinopyrazine derivative found to inhibit monoamine oxidase (MAO) and showed a curative effect for the anti-depressant. Similar to other MAO inhibitors, it enhanced convulsions induced by tryptamine and hyperthermia induced by dopa.
价 格：￥电议型 号：T0235产 地：中国大陆
