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T68298Oteracil；化合物 OteracilOteracil
Oteracil is an antagonist of urate oxidase.
价 格：￥电议型 号：T68298产 地：中国大陆
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T68063Elopiprazole；依吡哌唑DU 29840；DU 29840
Elopiprazole(DU 29840) is an anti-neurological compound that can be used to study neurological disorders.
价 格：￥电议型 号：T68063产 地：中国大陆
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T67905GS-829845；化合物GS-829845GS-829845
GS-829845 is a JAK1 inhibitor, the main component of the active metabolite of Filgotinib, which is approximately 10-fold less potent and has a longer half-life than the parent.
价 格：￥电议型 号：T67905产 地：中国大陆
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T672982-Amino-3-methoxybenzoic acid；化合物 2-Amino-3-methoxybenzoic acid2-Amino-3-methoxybenzoic acid
2-Amino-3-methoxybenzoic acid is a useful organic compound for research related to life sciences. The catalog number is T67298 and the CAS number is 3177-80-8.
价 格：￥电议型 号：T67298产 地：中国大陆
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T66298(8S,9S,10R,14S)-13-Ethyl-11-methylene-2,3,7,8,9,10,11,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phe
(8S,9S,10R,14S)-13-Ethyl-11-methylene-2,3,7,8,9,10,11,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(6H)-one is a useful organic compound for research related to life sciences. The catalog number is T66298 and the CAS number is 54024-21-4.
价 格：￥电议型 号：T66298产 地：中国大陆
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T65298(4aR,4bS,6aS,7S,9aS,9bS,11aR)-Methyl 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetra
(4aR,4bS,6aS,7S,9aS,9bS,11aR)-Methyl 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylate is a useful organic compound for research related to life sciences and the catalog number is T65298.
价 格：￥电议型 号：T65298产 地：中国大陆
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T64298Turoctocog alfa；化合物 Turoctocog alfaTuroctocog alfa
Turoctocog alfa is a recombinant coagulation factor VIII (FVIII) derived from Chinese hamster ovary (CHO) cells. turoctocog alfa can be used in the study of haemophilia A.
价 格：￥电议型 号：T64298产 地：中国大陆
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T63298B10-S；化合物 B10-SB10-S
B10-S is a potent anti-allergenic agent that inhibits LAD2 degranulation induced by P substances.
价 格：￥电议型 号：T63298产 地：中国大陆
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T62989IRAK4-IN-12；化合物 IRAK4-IN-12IRAK4-IN-12
IRAK4-IN-12 (compound 37) is a potent inhibitor of IRAK4 (IC50: 0.015 μM) with cellular pIRAK4 potency (IC50: 0.5 μM).
价 格：￥电议型 号：T62989产 地：中国大陆
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T62988Mufemilast；化合物 MufemilastMufemilast
Mufemilast is an inhibitor of phosphodiesterase 4 (PDE4).
价 格：￥电议型 号：T62988产 地：中国大陆
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T62987iNOs-IN-1；化合物 iNOs-IN-1iNOs-IN-1
iNOs-IN-1 (YPW) is a potent inhibitor of inducible nitric oxide synthase (iNOS) with anti-inflammatory effects. iNOs-IN-1 significantly inhibits IL-6 and iNOS expression in a dose-dependent manner in murine macrophages, and also inhibits LPS-induced NO generation.
价 格：￥电议型 号：T62987产 地：中国大陆
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T62986CCG-271423；化合物 CCG-271423CCG-271423
CCG-271423 is a potent and selective inhibitor of GRK5, acting on both GRK5 (IC50: 0.0021 μM) and GRK2 (IC50: 44 μM). CCG-271423 reduces Ca2+ transients and inhibits cardiomyocyte contractility.
价 格：￥电议型 号：T62986产 地：中国大陆
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T62985Cofrogliptin；化合物 CofrogliptinCofrogliptin
Cofrogliptin (HSK7653) (compound 2) is a tetrahydropyran derivative that is an orally active DPP-4 inhibitor with long-lasting hypoglycaemic effects.Cofrogliptin (compound 2) has potential for studies in type 2 diabetes mellitus (T2DM).
价 格：￥电议型 号：T62985产 地：中国大陆
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T62984MAT2A-IN-2；化合物 MAT2A-IN-2MAT2A-IN-2
MAT2A-IN-2 is a potent inhibitor of MAT2A. MAT2A-IN-2 has potential for cancer disease research.
价 格：￥电议型 号：T62984产 地：中国大陆
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T62983Raltegravir sodium；化合物 Raltegravir sodiumRaltegravir sodium
Raltegravir (MK 0518) sodium is a potent, orally active HIV integrase (IN) inhibitor.
价 格：￥电议型 号：T62983产 地：中国大陆
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T62982Aripiprazole monohydrate；化合物 Aripiprazole monohydrateAripiprazole monohydrate
Aripiprazole (OPC-14597) monohydrate is an atypical antipsychotic that is a potent, high-affinity partial agonist of the dopamine D2 receptor.Aripiprazole monohydrate is an inverse agonist of the 5-HT2B and 5-HT2A receptors, and is active on 5-HT1A, 5-HT2C, D3 and D4. Aripiprazole monohydrate can be used to study schizophrenia and COVID19.
价 格：￥电议型 号：T62982产 地：中国大陆
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T62981KRAS inhibitor-17；化合物 KRAS inhibitor-17KRAS inhibitor-17
KRAS inhibitor-17 (compound 3-9) is a potent inhibitor of KRAS G12C (IC50: 3.37 μM). KRAS inhibitor-17 exhibits p-ERK inhibition with IC50 = 9.25 μM in MIA PaCA-2 cells and >33.3 μM in A549 cells. KRAS inhibitor-17 has the potential to be studied in pancreatic, colorectal and lung cancers.
价 格：￥电议型 号：T62981产 地：中国大陆
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T62980GGTI-286 hydrochloride；化合物 GGTI-286 hydrochlorideGGTI-286 hydrochloride
GGTI-286 hydrochloride is a potent inhibitor of GGTase I (IC50: 2 μM) and is also effective in inhibiting K-Ras4B (IC50: 1 μM). farnesylation (IC50=2 and >30 μM).
价 格：￥电议型 号：T62980产 地：中国大陆
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T62298PHD2/HDACs-IN-1；化合物 PHD2/HDACs-IN-1PHD2/HDACs-IN-1
PHD2/HDACs-IN-1 is a potent mixed inhibitor of PHD2/HDACs, acting on PHD2 (IC50: 1.15 μM), HDAC1 (IC50: 19.75 μM), HDAC2 (IC50: 26.60 μM), HDAC16 (IC50: 15.98 μM). HDACs-IN-1 is a low toxicity nephroprotective agent that can be used in studies of cisplatin-induced acute kidney injury (AKI).
价 格：￥电议型 号：T62298产 地：中国大陆
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T61383Diaziquone；地吖醌NSC 182986；NSC 182986
Diaziquone (NSC-182986) is a water-soluble synthetic azacyclic benzoquinone that enhances penetration of the blood-brain barrier, has antitumor activity, and is used in the treatment of extreme renal failure.
价 格：￥电议型 号：T61383产 地：中国大陆
