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T11092DPBQ；化合物DPBQZINC1620467|||2,3-Diphenylbenzo[g]quinoxaline-5,10-dione；ZINC1620467|||2,3-Diphenylbenzo
DPBQ (ZINC1620467) is a p53 activator. DPBQ could activate p53 and trigger apoptosis in a polyploid-specific manner, without inhibition of topoisomerase or bind DNA.
价 格：￥电议型 号：T11092产 地：中国大陆
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T1107Sarafloxacin hydrochloride；盐酸沙拉沙星Sarafloxacin HCl|||A-56620 (hydrochloride)|||A-56620 HCl；Sarafloxac
Sarafloxacin hydrochloride (A-56620 (hydrochloride)), a quinolone antibiotic drug, is a hydrochloride salt form of sarafloxacin.
价 格：￥电议型 号：T1107产 地：中国大陆
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T11062dmDNA31；化合物 T11062dmDNA31
dmDNA31 is a rifamycin antibiotic that can inhibit the DNA-dependent RNA polymerase of bacteria and has strong bactericidal activity against Staphylococcus aureus.
价 格：￥电议型 号：T11062产 地：中国大陆
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T11017DGN462；化合物 T11017DGN462
DGN462 is an effective DNA alkylating agent with anti-tumor activity, as in acute myeloid leukemia (AML). DGN462 can be used as a cytotoxic component of antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T11017产 地：中国大陆
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T10946D4-abiraterone；化合物 T10946Abiraterone D4A metabolite|||CB-7627|||Δ4-Abiraterone；Abiraterone D4A metab
D4-Abiraterone is an inhibitor of CYP17A1, 3b-hydroxysteroid dehydrogenase (3βHSD) and steroid 5a-reductase (SRD5A), the main metabolite of abiraterone. D4-Abiraterone is also an antagonist of androgen receptor.
价 格：￥电议型 号：T10946产 地：中国大陆
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T1088Repaglinide；瑞格列奈AG-EE 388 ZW|||AG-EE 623ZW；AG-EE 388 ZW|||AG-EE 623ZW|||瑞格列奈
Repaglinide (AG-EE 623ZW) is a benzoic acid derivative that stimulates insulin secretion from the pancreas and is used in the therapy of type 2 diabetes. Repaglinide has been linked to rare instances of clinically apparent acute liver injury.
价 格：￥电议型 号：T1088产 地：中国大陆
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T10862Collagen proline hydroxylase inhibitor；胶原蛋白脯氨酸羟化酶抑制剂Collagen proline hydroxylase inhibitor
Collagen proline hydroxylase inhibitor is an inhibitor collagen proline hydroxylase and useful for antifibrotic proliferative agents.
价 格：￥电议型 号：T10862产 地：中国大陆
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T10830CL 316243；化合物CL 316243CL 316243
CL316243 is a highly potent selective agonist of β3-adrenoceptor, with a EC50 of 3 nM. CL316243 is an effective stimulant of adipocyte lipolysis and increases brown adipose tissue thermogenesis and metabolic rate. CL316243 has the potential for the treatment obesity, diabetes and urge urinary incontinence.
价 格：￥电议型 号：T10830产 地：中国大陆
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T10762Ceranib1；化合物Ceranib1Ceranib1
Ceranib1 is an inhibitor of ceramidase. It inhibits the proliferation of ovarian cancer cells. Ceranib1 inhibits ceramidase activity toward an exogenous ceramide analog, induces the accumulation of multiple ceramide species, decreases levels of S1P and sphingosine.
价 格：￥电议型 号：T10762产 地：中国大陆
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T10719CCT365623 hydrochloride；化合物 T10719CCT365623 hydrochloride
CCT365623 hydrochloride is an orally active inhibitor of lysyl oxidase (LOX) (IC50: 0.89 μM). It suppresses EGFR (pY1068) and AKT phosphorylation driven by EGF.
价 格：￥电议型 号：T10719产 地：中国大陆
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T10662LCalcimycin；离子载体(钙镁盐混合物)Antibiotic A-23187|||A-23187；Antibiotic A-23187|||离子载体(钙镁盐混合物)|||A-23187
Calcimycin (A-23187) is an ionophorous, polyether carboxylic antibiotic from Streptomyces chartreusensis. It binds and transports calcium and other divalent cations across membranes and uncouples oxidative phosphorylation while inhibiting ATPase of rat liver mitochondria. The substance is used mostly as a biochemical tool to study the role of divalent cations in various biological systems.
价 格：￥电议型 号：T10662L产 地：中国大陆
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T10662Calcimycin hemicalcium salt；化合物 T10662Antibiotic A-23187 hemicalcium salt|||A-23187 hemicalcium salt
Calcimycin (A-23187) hemicalcium salt is an antibiotic and a unique divalent cation ionophore (like calcium and magnesium). It induces Ca2+-dependent cell death by increasing intracellular calcium concentration.
价 格：￥电议型 号：T10662产 地：中国大陆
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T10658CA inhibitor 1；化合物 T10658GS-6207 analog；GS-6207 analog
CA inhibitor 1 (GS-6207 analog) is a potent inhibitor of the HIV capsid.
价 格：￥电议型 号：T10658产 地：中国大陆
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T10629Btk inhibitor 2；化合物Btk inhibitor 2BGB-3111 analog；BGB-3111 analog
Btk inhibitor 2 (BGB-3111 analog) is a BTK inhibitor.
价 格：￥电议型 号：T10629产 地：中国大陆
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T10628BTK inhibitor 13；化合物 T10628BTK inhibitor 13
BTK inhibitor 13 (compound 8) is an effective and selective BTK inhibitor(IC50: 1.2 nM).
价 格：￥电议型 号：T10628产 地：中国大陆
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T10627BTK inhibitor 10；化合物 T10627BTK inhibitor 10
BTK inhibitor 10 is a potent and orally active BTK inhibitor. It has the potential for rheumatoid arthritis treatment.
价 格：￥电议型 号：T10627产 地：中国大陆
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T10626(Rac)-IBT6A；化合物(Rac)-IBT6A(Rac)-IBT6A
(Rac)-IBT6A is a racemate of IBT6A. IBT6A is an impurity of Ibrutinib and can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct.
价 格：￥电议型 号：T10626产 地：中国大陆
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T10625L2IBT6A hydrochloride；化合物 T10625L2IBT6A hydrochloride
IBT6A hydrochloride is an impurity of Ibrutinib. Ibrutinib is a Btk inhibitor (IC50: 0.5 nM). IBT6A can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct.
价 格：￥电议型 号：T10625L2产 地：中国大陆
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T10625L(Rac)-IBT6A hydrochloride (1412418-47-3 free base)；化合物 T10625L(Rac)-IBT6A hydrochloride；(Rac)-IBT6A
(Rac)-IBT6A hydrochloride is a racemate of IBT6A. IBT6A is an impurity of Ibrutinib. IBT6A can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a Btk inhibitor (IC50: 0.5 nM).
价 格：￥电议型 号：T10625L产 地：中国大陆
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T10625IBT6A依鲁替尼中间体依鲁替尼中间体
IBT6A is an impurity of Ibrutinib. Ibrutinib is a Btk inhibitor (IC50: 0.5 nM). IBT6A can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct.
价 格：￥电议型 号：T10625产 地：中国大陆
