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T16545Pivanex；化合物PivanexPivalyloxymethyl butyrate|||AN-9；Pivalyloxymethyl butyrate|||AN-9
Pivanex (Pivalyloxymethyl butyrate) is an orally active HDAC inhibitor and an antimetastatic and antiangiogenic agent. Pivanex downregulates the Bcr-Abl protein and enhances apoptosis.
价 格：￥电议型 号：T16545产 地：中国大陆
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T1437D-Panthenol；D-泛醇D-Pantothenyl alcohol|||Ilopan|||Dexpanthenol|||Pantothenol；D-泛醇|||D-Pantothenyl alc
D-Panthenol (D-Pantothenyl alcohol) is an alcoholic analogue of D-pantothenic acid and cholinergic agent. D-Panthenol acts as a precursor of coenzyme A necessary for acetylation reactions and is involved in the synthesis of acetylcholine. Although the exact mechanism of the actions of D-Panthenol is unclear, it may enhance the effect of acetylcholine. D-Panthenol acts on the gastrointestinal tract and increases lower intestinal motility. It is also applied topically to the skin to relieve itchin
价 格：￥电议型 号：T1437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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T11011Dexpramipexole dihydrochloride；右旋普拉克索二盐酸盐KNS-760704 dihydrochloride|||R-(+)-Pramipexole dihydrochlor
Dexpramipexole dihydrochloride (KNS-760704 dihydrochloride) ((R)-Pramipexole dihydrochloride) is a neuroprotective agent and is a weak non-ergoline dopamine agonist.
价 格：￥电议型 号：T11011产 地：中国大陆
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T10612Brexpiprazole S-oxide；化合物 T10612DM-3411；DM-3411
Brexpiprazole S-oxide (DM-3411) is a main metabolite of Brexpiprazole. Brexpiprazole is a partial agonist of human 5-HT1A and dopamine receptors (Kis: 0.12 nM and 0.3 nM).
价 格：￥电议型 号：T10612产 地：中国大陆
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T10610Brexpiprazole-d8；化合物 T10610OPC-34712 D8；OPC-34712 D8
Brexpiprazole D8 (OPC-34712 D8) is a deuterium-labeled Brexpiprazole. Brexpiprazole is a partial agonist of human 5-HT1A and dopamine receptors (Ki: 0.12 nM and 0.3 nM).
价 格：￥电议型 号：T10610产 地：中国大陆
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T0030LBupivacaine；布比卡因AH 250|||AH-250|||AH250|||Bupivacaina|||Exparel|||Anekain；AH 250|||AH-250|||AH250|||
Bupivacaine (AH-250) is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain.
价 格：￥电议型 号：T0030L产 地：中国大陆
