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T12221Nicardipine-d3 hydrochloride；盐酸尼卡地平 D3YC-93 D3；盐酸尼卡地平 D3|||YC-93 D3
Nicardipine D3 hydrochloride is the deuterium labeled Nicardipine hydrochloride.
价 格：￥电议型 号：T12221产 地：中国大陆
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T12185Naveglitazar racemate；化合物 T12185Naveglitazar racemate
Naveglitazar racemate is the racemate of Naveglitazar.
价 格：￥电议型 号：T12185产 地：中国大陆
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T12176Naratriptan D3 Hydrochloride；化合物 T12176GR-85548A D3；GR-85548A D3
Naratriptan D3 Hydrochloride is the deuterium labeled Naratriptan, is a selective agonist of 5-HT1 receptor subtype.
价 格：￥电议型 号：T12176产 地：中国大陆
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T12164N6-(4-Hydroxybenzyl)adenosine；N6-羟苄腺苷Para-topolin riboside；Para-topolin riboside|||N6-羟苄腺苷
N6-(4-Hydroxybenzyl)adenosine (Para-topolin riboside) is a platelet aggregation inhibitor.
价 格：￥电议型 号：T12164产 地：中国大陆
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T1215Nicardipine hydrochloride；盐酸尼卡地平RS-69216|||Nicardipine HCl|||YC-93 Hydrochloride；盐酸尼卡地平|||RS-69216||
Nicardipine hydrochloride (YC-93 Hydrochloride) is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium channel blocker, Nicardipine (Nifedipine Family) blocks calcium ions from certain cell walls and inhibits contraction of coronary and peripheral arteries, resulting in lowered oxygen requirements for heart muscle and decreased arterial contraction and spasm. It is used clinically as a cerebral and coronary vasodilator.
价 格：￥电议型 号：T1215产 地：中国大陆
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T1212Ketorolac tromethamine salt酮咯酸氨丁三醇酮咯酸氨丁三醇|||Acular LS|||Toradol|||Ketorolac tris salt|||Acular
Ketorolac tromethamine salt (Ketorolac tris salt) non-selective inhibits the enzymes cyclooxygenase 1 (COX-1) and COX-2with anti-inflammatory, analgesic, and antipyretic activities.
价 格：￥电议型 号：T1212产 地：中国大陆
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T12095Monomethyl fumarate；富马酸单甲酯Monomethyl fumarate
Monomethyl fumarate is a potent agonist of GPR109A .
价 格：￥电议型 号：T12095产 地：中国大陆
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T12064Niraparib (R-enantiomer)；化合物Niraparib R-enantiomerMK 4827 (R-enantiomer)|||Niraparib R-enantiomer；MK
Niraparib R-enantiomer (MK 4827 R-enantiomer) is an inhibitor of PARP1(IC50 of 2.4 nM).
价 格：￥电议型 号：T12064产 地：中国大陆
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T12045(-)-Hydroxycitric acid lactone；藤黄内酯Garcinia lactone；藤黄内酯|||Garcinia lactone
(-)-Hydroxycitric acid lactone (Garcinia lactone) is an anti-obesity agent.(-)-Hydroxycitric acid lactone was a potent inhibitor of ATP citrate lyase, which catalyzes the extramitochondrial cleavage of citrate to oxaloacetate and acetyl-CoA.
价 格：￥电议型 号：T12045产 地：中国大陆
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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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T12014Methyl carnosate；化合物 Methyl carnosateMethyl carnosate
Methyl carnosate is a diterpene compound with antioxidant and antimicrobial activity isolated from sage or rosemary.
价 格：￥电议型 号：T12014产 地：中国大陆
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T12006Metarrestin；化合物MetarrestinML246；ML246
Metarrestin (ML246) is a first-in-class perinucleolar compartment inhibitor with a favorable PK profile, which effectively suppresses metastasis. Metarrestin disrupts the nucleolar structure and inhibits RNA polymerase (Pol) I transcription, at least in part by interacting with the translation elongation factor eEF1A2.
价 格：￥电议型 号：T12006产 地：中国大陆
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T12003Mensacarcin；化合物 T12003Mensacarcin
Mensacarcin, a highly complex polyketide compound, exhibits multifaceted effects on cellular processes. Specifically, it targets mitochondria, perturbs energy metabolism within these organelles, and activates caspase-dependent apoptotic pathways. Functionally, Mensacarcin can serve as a cytotoxic constituent in antibody-drug conjugates (ADCs). Furthermore, this antibiotic compound displays broad-spectrum inhibition of cell growth across various cancer cell lines and demonstrates potent induction
价 格：￥电议型 号：T12003产 地：中国大陆
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T11999Meluadrine tartrate；化合物 T11999Meluadrine tartrate
Meluadrine tartrate is an endogenous metabolite.
价 格：￥电议型 号：T11999产 地：中国大陆
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T11991Mefentrifluconazole氯氟醚菌唑CYPs|||aromatase|||Inhibitor
Mefentrifluconazole is a potent, selective and orally active fungal CYP51 (Kd= 0.5 nM) inhibitor, but shows less inhibitory activity on human aromatase (IC50=0.92 μM). Mefentrifluconazole is a novel azole derivative and used as an agrochemical broad-spectrum antifungal agent.
价 格：￥电议型 号：T11991产 地：中国大陆
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T11947MARK4 inhibitor 1；化合物MARK4 inhibitor 1MARK4 inhibitor 1
MARK4 inhibitor 1 inhibits cancer cell proliferation, metastasis and induces apoptosis. MARK4 inhibitor 1 is a potent microtubule affinity-regulating kinase 4 (MARK4) inhibitor, with an IC50 of 1.54 μM.
价 格：￥电议型 号：T11947产 地：中国大陆
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T11946MARK-IN-2；化合物 T11946MARK-IN-2
MARK-IN-2 is a potent microtubule affinity regulating kinase (MARK) inhibitor,(IC50:5 nM).
价 格：￥电议型 号：T11946产 地：中国大陆
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T11945MARK-IN-1；化合物 T11945MARK-IN-1
MARK-IN-1 is a potent microtubule affinity regulating kinase (MARK) inhibitor, (IC50<0.25 nM).
价 格：￥电议型 号：T11945产 地：中国大陆
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T11944Maritoclax；化合物MaritoclaxMarinopyrrole A；Marinopyrrole A
Maritoclax (Marinopyrrole A) (Marinopyrrole A) is a novel and specific Mcl-1 inhibitor, shows >8 fold selectivity than BCL-xl (IC50 > 80 μM),with an IC50 value of 10.1 μM.
价 格：￥电议型 号：T11944产 地：中国大陆
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T11919LysRs-IN-1；化合物LysRs-IN-19-carboxymethylguanine；9-carboxymethylguanine
LysRs-IN-1 is an inhibitor of Lysyl-tRNA synthetase (LysRs).
价 格：￥电议型 号：T11919产 地：中国大陆
