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T11650INCB3344 R-isomer；化合物 T11650INCB3344 R-isomer
INCB3344 is a potent CCR2 antagonist. INCB3344 R-isomer is the R-isomer of INCB3344.
价 格：￥电议型 号：T11650产 地：中国大陆
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T1165Ethionamide乙硫异烟胺Bayer 5312|||乙硫异烟胺|||2-ethylthioisonicotinamide|||Ethinamide
Ethionamide (2-ethylthioisonicotinamide) is a nicotinamide derivative, with antibacterial activity, used to treat tuberculosis. Although the exact mechanism of action of ethionamide is unknown, it may inhibit the synthesis of mycolic acid, a saturated fatty acid found in the bacterial cell wall, thereby inhibiting bacterial cell wall synthesis. This eventually leads to bacterial cell wall disruption and cell lysis. Ethionamide may be bacteriostatic or bactericidal in action, depending on the con
价 格：￥电议型 号：T1165产 地：中国大陆
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T11649INCB054329 Racemate；化合物 T11649INCB054329 Racemate
INCB054329 Racemate is an inhibitor of BET protein.
价 格：￥电议型 号：T11649产 地：中国大陆
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T11648INCB 3284；化合物 T11648INCB 3284
INCB 3284, a potent and selective human CCR2 antagonist with an oral bioavailability, is utilized in the study of acute liver failure. It effectively inhibits the binding of monocyte chemoattractant protein-1 (MCP-1) to hCCR2, demonstrating an IC50 of 3.7 nM.
价 格：￥电议型 号：T11648产 地：中国大陆
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T11647INCB 3284 dimesylate；化合物 T11647INCB 3284 dimesylate
INCB 3284 dimesylate is a selective and orally bioavailable human CCR2 antagonist, inhibiting monocyte chemoattractant protein-1 binding to hCCR2 (IC50: 3.7 nM). It can be used in the research of acute liver failure.
价 格：￥电议型 号：T11647产 地：中国大陆
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T11646Impurity F of Calcipotriol；化合物 T11646Impurity F of Calcipotriol
Impurity F of Calcipotriol is a impurity of Calcipotriol. Calcipotriol (MC 903; Calcipotriene) is a ligand of VDR-like receptors.
价 格：￥电议型 号：T11646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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T11644Impurity C of Alfacalcidol；阿法骨化醇杂质 CImpurity C of Alfacalcidol
Impurity of Alfacalcidol is an impurity of Alfacalcidol. Alfacalcidol is a non-selective VDR activator medication.
价 格：￥电议型 号：T11644产 地：中国大陆
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T11643Impurity B of Calcitriol；化合物 T116431β,25-Dihydroxyvitamin-D3|||1-Epicalcitriol；1β,25-Dihydroxyvitami
Impurity B of Calcitriol is an impurity of Calcitriol. Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
价 格：￥电议型 号：T11643产 地：中国大陆
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T11641N-Desmethyl imatinibN-去甲基伊马替尼Imatinib metabolite N-Desmethyl imatinib|||Norimatinib|||N-去甲基伊马替尼
N-Desmethyl imatinib (Imatinib metabolite N-Desmethyl imatinib) is a metabolite of Imatinib, which is a multi-target inhibitor of c-Kit, v-Abl, and PDGFR.
价 格：￥电议型 号：T11641产 地：中国大陆
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T11640Imatinib-d8；化合物 T11640CGP-57148B D8|||STI571 D8；CGP-57148B D8|||STI571 D8
Imatinib D8 is a deuterium-labeled Imatinib. Imatinib is an orally bioavailable tyrosine kinases inhibitor that inhibits BCR/ABL, PDGFR, v-Abl, and c-kit kinase activity.
价 格：￥电议型 号：T11640产 地：中国大陆
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T11638Ilorasertib hydrochloride；化合物 T11638ABT-348 hydrochloride；ABT-348 hydrochloride
Ilorasertib hydrochloride (ABT-348 hydrochloride) is an ATP-competitive multitargeted kinase inhibitor, which inhibits Aurora C, Aurora B, and Aurora A (IC50s: 1 nM, 7 nM, 120 nM). It also suppresses RET tyrosine kinase, PDGFRβ, and Flt1 (IC50s: 7 nM, 3 nM, and 32 nM).
价 格：￥电议型 号：T11638产 地：中国大陆
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T11637Iloperidone metabolite Hydroxy Iloperidone；伊潘立酮代谢物P88|||Hydroxy Iloperidone；P88|||伊潘立酮代谢物|||Hydroxy
Iloperidone metabolite Hydroxy Iloperidone is an atypical antipsychotic. It is a metabolite of Iloperidone.
价 格：￥电议型 号：T11637产 地：中国大陆
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T11636IL-17A antagonist 3；化合物 T11636IL-17A antagonist 3
IL-17A antagonist 3 is an IL-17A antagonist.
价 格：￥电议型 号：T11636产 地：中国大陆
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T11635IL-17A antagonist 1；IL-17A 拮抗剂1IL-17A antagonist 1
IL-17A antagonist 1 is an IL-17A antagonist for the study of interleukin-related inflammatory and immune diseases.
价 格：￥电议型 号：T11635产 地：中国大陆
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T11634IL-15-IN-1；化合物IL-15-IN-1IL-15-IN-1
IL-15-IN-1 is a selective and potent Interleukin 15 (IL-15) inhibitor, inhibiting the proliferation of IL-15-dependent cells (IC50: 0.8 μM).
价 格：￥电议型 号：T11634产 地：中国大陆
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T11632IIIM-290；化合物 T11632IIIM-290
IIIM-290 is an oral CDK inhibitor (IC50s: 90 and 94 nM for CDK2/A and CDK9/T1).
价 格：￥电议型 号：T11632产 地：中国大陆
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T11630LIFN alpha-IFNAR-IN-1；化合物 T11630LIFN alpha-IFNAR-IN-1
IFN alpha-IFNAR-IN-1 is a nonpeptidic, low-molecular-weight inhibitor of the interaction between IFN-α and IFNAR. It inhibits MVA-induced IFN-α responses by BM-pDCs (IC50: 2-8 μM).
价 格：￥电议型 号：T11630L产 地：中国大陆
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T11630IFN alpha-IFNAR-IN-1 hydrochloride；化合物IFN alpha-IFNAR-IN-1 hydrochlorideIFN alpha-IFNAR-IN-1 hydroch
IFN alpha-IFNAR-IN-1 hydrochloride is an inhibitor of the interaction between IFN-α and IFNAR. IFN alpha-IFNAR-IN-1 hydrochloride inhibits MVA-induced IFN-α responses by BM-pDCs with IC50 of 2-8 μM.
价 格：￥电议型 号：T11630产 地：中国大陆
