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LM10 98%

(E)-3-(2-(1H-TETRAZOL-5-YL)VINYL)-6-FLUORO-1H-INDOLE

源葉(MedMol)
S81285
1316695-35-8
C11H8FN5
229.2131232
品牌 貨號 產品規格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數量
源葉(MedMol) S81285-5mg 98% ¥110.00元 8 - - -
源葉(MedMol) S81285-25mg 98% ¥430.00元 9 - - -
源葉(MedMol) S81285-100mg 98% ¥1300.00元 7 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

LM10 is a potent inhibitor of tryptophan 2,3-dioxygenase (TDO). Tryptophan 2,3-dioxygenase (TDO) is an unrelated hepatic enzyme that also degrades tryptophan along the kynurenine pathway. LM10 has the potential for the research of cancer diseases
產品描述: LM10 is a potent inhibitor of tryptophan 2,3-dioxygenase (TDO). Tryptophan 2,3-dioxygenase (TDO) is an unrelated hepatic enzyme that also degrades tryptophan along the kynurenine pathway. LM10 has the potential for the research of cancer diseases
靶點: TDO;Others
體內研究:
LM10 (160 mg/kg; p.o.) prevents the growth of TDO-expressing P815 tumor cells and promotes better rejection of control clone P815B cl1, which does not express TDO. LM10 displays a good TDO inhibition (Ki = 5.6 μM) with a competitive inhibition profile. LM10 does not inhibit IDO and has a high solubility and bioavailability without obvious signs of toxicity. The plasma concentration of LM10 after oral administration of 160 mg/kg/day is between 20 and 40 μg/mL (87-175 μM), a concentration about 40 times above the IC50 measured in the cellular assay performed with the physiological concentration of plasma tryptophan.
參考文獻:
1. Pilotte L, et al. Reversal of tumoral immune resistance by inhibition of tryptophan 2,3-dioxygenase. Proc Natl Acad Sci U S A. 2012;109(7):2497-2502.
溶解性: DMSO  :  50  mg/mL  (218.14  mM;  Need  ultrasonic)
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 4.363 ml 21.814 ml 43.628 ml
5 mM 0.873 ml 4.363 ml 8.726 ml
10 mM 0.436 ml 2.181 ml 4.363 ml
50 mM 0.087 ml 0.436 ml 0.873 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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批號:C10000001 貨號:A800001-25g
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摩爾濃度計算器

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