LX2761
LX2761 is an orally active, dual SGLT1/SGLT2 inhibitor with IC50 values of 2.2 nM and 2.7 nM against human SGLT1 and SGLT2, respectively. LX2761 locks human SGLT1 in an outward-open conformation and blocks its putative water permeation pathway. After oral administration, LX2761 is confined exclusively to the intestinal lumen, delays intestinal glucose absorption, regulates intestinal glucose metabolism, increases cecal glucose levels, reduces cecal pH, improves glycemic control and elevates plasma total GLP-1 levels. However, LX2761 induces diarrhea in a dose-dependent manner. LX2761 can be used in diabetes-related research.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 1610954-97-6
- 分子式: C32H47N3O6S
- 分子量:601.80
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
生物活性
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hSGLT1 2.2 nM (IC50) |
hSGLT2 2.7 nM (IC50) |
mSGLT1 3.7 nM (IC50) |
rSGLT1 5.7 nM (IC50) |
mSGLT2 1.0 nM (IC50) |
rSGLT2 1.1 nM (IC50) |
SGLT1 5.1 nM (IC50, dog) |
SGLT1 1.4 nM (IC50, monkey) |
SGLT2 1.8 nM (IC50, dog) |
SGLT2 1.1 nM (IC50, monkey) |
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HEK293 | IC50 |
2.2 nM
Compound: 21
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Inhibition of human HA-tagged SGLT1 expressed in HEK293 cells assessed as decrease in [14C]-AMG uptake measured after 1 to 2 hrs by scintillation counting method
Inhibition of human HA-tagged SGLT1 expressed in HEK293 cells assessed as decrease in [14C]-AMG uptake measured after 1 to 2 hrs by scintillation counting method
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[PMID: 28045524] |
| HEK293 | IC50 |
2.7 nM
Compound: 21
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Inhibition of human HA-tagged SGLT2 expressed in HEK293 cells assessed as decrease in [14C]-AMG uptake measured after 1 to 2 hrs by scintillation counting method
Inhibition of human HA-tagged SGLT2 expressed in HEK293 cells assessed as decrease in [14C]-AMG uptake measured after 1 to 2 hrs by scintillation counting method
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[PMID: 28045524] |
LX2761 (1.0-5.7 nM) potently inhibits SGLT1 and SGLT2 across multiple mammalian species, with IC50 values ranging from 1.0 nM to 5.7 nM in HEK293 cells expressing the respective transporters[2].
LX2761 (1-400 μM; 1 h) binds with high affinity to the hSGLT1-MAP17 complex, locking it in an outward-open conformation and blocking the transporter's water permeation pathway[3].
LX2761 (0.01-1000 nM; 1 h) potently inhibits 1-NBD-glucose uptake by non-tagged wild-type hSGLT1 in AD293 cells with an IC50 of 2.03 nM[3].
LX2761 (0.01-1000 nM; 1 h) potently inhibits 1-NBD-glucose uptake by the hSGLT1_GFP-MAP17_nb complex in AD293 cells with an IC50 of 2.30 nM[3].
LX2761 (0.01-1000 nM; 1 h) has reduced potency for inhibition of 1-NBD-glucose uptake in AD293 cells due to the L274A mutation in hSGLT1[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
LX2761 (0.0225-0.25 mg/kg; p.o.; once daily; for 5 consecutive days) dose-dependently reduces postprandial blood glucose fluctuations and increases tGLP-1 levels in healthy rats fed a high-fat and high-glucose (HGD) diet; the 0.0625 mg/kg dose produces a significant hypoglycemic effect without inducing diarrhea[2].
LX2761 (3 mg/kg; p.o.; once daily; for 49 consecutive days) improves glycemic control, significantly increases the survival rate of mice with advanced Streptozotocin (HY-13753)-induced diabetes, while reducing fasting blood glucose, improving A1C and decreasing postprandial blood glucose fluctuations[2].
A stepwise oral dose escalation regimen of LX2761 (0.5-0.7 mg/kg; p.o.; daily; for 7 consecutive days, with dose escalation gradually implemented between days 45 and 59) significantly reduces the incidence of diarrhea in mice fed a HGD diet, compared to acute administration at the same final dose[2].
Diarrhea induced by LX2761 (0.2-1.5 mg/kg; p.o.; daily; for 4 consecutive days) in HGD mice is antagonized by resistant starch, without impairing the glucose-lowering efficacy of LX2761[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:C57BL/6-Tyrc-Brd (male, adult, streptozotocin-induced early-onset diabetes)[2]
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Dosage:1.5 mg/kg; 3 mg/kg
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Administration:p.o.; daily; 39 days
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Result:Significantly and dose-dependently decreased OGTT glucose excursions on days 21 and 39.
Significantly decreased fasting blood glucose levels after 32 days of treatment.
Slowed the rise in A1C levels relative to vehicle after 32 days of treatment.
Significantly increased cecal glucose levels and decreased cecal pH at necropsy.
Did not alter plasma tGLP-1 levels post-glucose challenge.
Did not significantly affect food consumption and body weight.
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Animal Model:C57BL/6-Tyrc-Brd (male, adult, streptozotocin-induced advanced-onset diabetes)[2]
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Dosage:1.5 mg/kg; 3 mg/kg
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Administration:p.o.; daily; 49 days
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Result:Significantly improved mouse survival relative to vehicle at 3 mg/kg.
Significantly decreased baseline blood glucose and OGTT glucose excursions on day 20 at both doses.
Significantly improved A1C values on day 30 at 3 mg/kg.
Significantly decreased fasting blood glucose and OGTT glucose excursions on day 49 at both doses.
Significantly increased plasma tGLP-1 levels, cecal glucose levels, and decreased cecal pH relative to vehicle at 3 mg/kg on day 49.
Caused rarely observed diarrhea limited to the first few days of treatment.
化学情報
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CAS 番号 1610954-97-6
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分子量 601.80
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分子式 C32H47N3O6S
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SMILES
CC1=CC=C([C@H]2[C@H](O)[C@@H](O)[C@H](O)[C@@H](SC)O2)C=C1CC3=CC=C(CCCC(NC(C(NCCN(C)C)=O)(C)C)=O)C=C3
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
[1]. Spatola L, et al. SGLT1 and SGLT1 Inhibitors: A Role to Be Assessed in the Current Clinical Practice. Diabetes Ther. 2018;9(1):427-430. [Content Brief]
[2]. Powell DR, et al. LX2761, a Sodium/Glucose Cotransporter 1 Inhibitor Restricted to the Intestine, Improves Glycemic Control in Mice. J Pharmacol Exp Ther. 2017;362(1):85-97. [Content Brief]
[3]. Niu Y, et al. Structural mechanism of SGLT1 inhibitors. Nat Commun. 2022;13(1):6440. Published 2022 Oct 28. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
LX2761 関連分類
HY-101122 関連分類
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