46 Results for "

cotransporter 2

" in MedChemExpress (MCE) Product Catalog:
Products (46)

46 Results for "cotransporter 2" in MCE Product Catalog:

97
97 Publications Verification
Cat. No.: HY-15409
CAS No.: 864070-44-0
Purity:  99.90%
Synonyms: BI 10773
Target:  

SGLT

Research Areas:  

Infection Metabolic Disease Cancer

Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2 .
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72
72 Cited Publications
Cat. No.: HY-10450
CAS No.: 461432-26-8
Purity:  99.97%
Synonyms: BMS-512148
Target:  

SGLT

Research Areas:  

Metabolic Disease Cancer

Dapagliflozin (BMS-512148), a new type of agent used to treat diabetes mellitus (DM), is a competitive sodium/glucose cotransporter 2 (SGLT2) inhibitor, which results in excretion of glucose into the urine . Dapagliflozin induces HIF1 expression and attenuates renal IR injury .
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72
72 Cited Publications
Cat. No.: HY-10450A
CAS No.: 960404-48-2
Purity:  99.97%
Synonyms: BMS-512148 (2S)-1,2-propanediol, hydrate
Target:  

SGLT

Research Areas:  

Metabolic Disease Cancer

Dapagliflozin ((2S)-1,2-propanediol, hydrate) is the S-enantiomer of Dapagliflozin 1,2-propanediol, hydrate. Dapagliflozin ((2S)-1,2-propanediol, hydrate), a new type of agent used to treat diabetes mellitus (DM), is a competitive sodium/glucose cotransporter 2 (SGLT2) inhibitor, which results in excretion of glucose into the urine . Dapagliflozin ((2S)-1,2-propanediol, hydrate) induces HIF1 expression and attenuates renal IR injury .
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5
5 Cited Publications
Cat. No.: HY-15461
CAS No.: 1210344-57-2
Purity:  99.92%
Synonyms: PF-04971729
Target:  

SGLT

Research Areas:  

Metabolic Disease

Ertugliflozin (PF-04971729) is a potent, selective and orally active inhibitor of the sodium-dependent glucose cotransporter 2 (SGLT2), with an IC50 of 0.877 nM for h-SGLT2 . Has the potential for the treatment of type 2 diabetes mellitus .
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5
5 Cited Publications
Cat. No.: HY-15461A
CAS No.: 1210344-83-4
Purity:  99.84%
Synonyms: PF-04971729 L-pyroglutamic acid
Target:  

SGLT

Research Areas:  

Metabolic Disease

Ertugliflozin L-pyroglutamic acid (PF-04971729 L-pyroglutamic acid) is a potent, selective and orally active inhibitor of the sodium-dependent glucose cotransporter 2 (SGLT2), with an IC50 of 0.877 nM for h-SGLT2 . Has the potential for the treatment of type 2 diabetes mellitus .
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4
4 Cited Publications
Cat. No.: HY-13413
CAS No.: 1201913-82-7
Purity:  98.48%
Synonyms: CSG-452 hydrate
Research Areas:  

Metabolic Disease

Tofogliflozin hydrate (CSG-452 hydrate) is a potent and highly specific sodium/glucose cotransporter 2 (SGLT2) inhibitor with an IC50 of 2.9 nM and Ki values of 2.9 nM, 14.9 nM, and 6.4 nM for human, rat, and mouse SGLT2 . Tofogliflozin partially inhibits high glucose-induced reactive oxyen species (ROS) generation in tubular cells .
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4
4 Cited Publications
Cat. No.: HY-14902
CAS No.: 903565-83-3
Synonyms: CSG452
Target:  

SGLT

Research Areas:  

Metabolic Disease

Tofogliflozin(CSG-452) is a potent and highly specific sodium/glucose cotransporter 2(SGLT2) inhibitor with Ki values of 2.9, 14.9, and 6.4 nM for human, rat, and mouse SGLT2.
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1
1 Cited Publications
Cat. No.: HY-109018
CAS No.: 946525-65-1
Purity:  99.76%
Target:  

SGLT

Research Areas:  

Metabolic Disease

Velagliflozin is an orally available sodium-glucose cotransporter 2 (SGLT2) inhibitor, with anti-diabetic activity.
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1
1 Cited Publications
Cat. No.: HY-109018B
CAS No.: 1661838-94-3
Purity:  99.43%
Target:  

SGLT

Research Areas:  

Metabolic Disease

Velagliflozin proline hydrate is the clinical form of Velagliflozin (HY-109018). Velagliflozin is an oral sodium-glucose cotransporter 2 (SGLT2) inhibitor with antidiabetic activity. Velagliflozin reduces renal glucose reabsorption and stimulates glycosuria, which lowers blood sugar and insulin concentrations .
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1
1 Cited Publications
Cat. No.: HY-109018A
CAS No.: 1539295-26-5
Purity:  99.43%
Target:  

SGLT

Research Areas:  

Metabolic Disease

Velagliflozin proline is an oral sodium-glucose cotransporter 2 (SGLT2) inhibitor with antidiabetic activity. Velagliflozin proline reduces renal glucose reabsorption and stimulates glycosuria, which lowers blood sugar and insulin concentrations .
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Cat. No.: HY-109144
CAS No.: 1415472-28-4
Purity:  98.43%
Synonyms: DWP-16001
Target:  

SGLT

Research Areas:  

Metabolic Disease

Enavogliflozin (DWP-16001), an antidiabetic agent, is an orally active, best-in-class and selective sodium-glucose cotransporter-2 (SGLT-2) inhibitor .
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Cat. No.: HY-15409R
CAS No.: 864070-44-0
Synonyms: BI 10773 (Standard)
Research Areas:  

Metabolic Disease

Empagliflozin (Standard) is the analytical standard of Empagliflozin. This product is intended for research and analytical applications. Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2 .
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Cat. No.: HY-15409S
CAS No.: 2749293-95-4
Purity:  97.64%
Synonyms: BI 10773-d4
Empagliflozin-d4 is deuterium labeled Empagliflozin. Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2 .
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Cat. No.: HY-10450R
CAS No.: 461432-26-8
Synonyms: BMS-512148 (Standard)
Research Areas:  

Metabolic Disease Cancer

Dapagliflozin (Standard) is the analytical standard of Dapagliflozin. This product is intended for research and analytical applications. Dapagliflozin (BMS-512148), a new type of agent used to treat diabetes mellitus (DM), is a competitive sodium/glucose cotransporter 2 (SGLT2) inhibitor, which results in excretion of glucose into the urine . Dapagliflozin induces HIF1 expression and attenuates renal IR injury .
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Cat. No.: HY-15461R
CAS No.: 1210344-57-2
Synonyms: PF-04971729 (Standard)
Research Areas:  

Metabolic Disease

Ertugliflozin (Standard) is the analytical standard of Ertugliflozin. This product is intended for research and analytical applications. Ertugliflozin (PF-04971729) is a potent, selective and orally active inhibitor of the sodium-dependent glucose cotransporter 2 (SGLT2), with an IC50 of 0.877 nM for h-SGLT2 . Has the potential for the treatment of type 2 diabetes mellitus .
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Cat. No.: HY-13414
CAS No.: 329045-45-6
Synonyms: Remogliflozin A
Target:  

SGLT

Research Areas:  

Metabolic Disease

Remogliflozin (Remogliflozin A) is an orally active, highly selective sodium-glucose cotransporter 2 (SGLT2) inhibitor, with a Ki of 12.4 nM for human SGLT2 and 26.0 nM for rat SGLT2. Remogliflozin increases urinary glucose excretion by inhibiting renal glucose reabsorption. Without insulin stimulation, remogliflozin suppresses the elevation of plasma glucose, reduces fasting blood glucose and glycated hemoglobin, and improves glycosuria, hyperglycemia, hyperinsulinemia, hypertriglyceridemia and insulin resistance in diabetic rodents. Remogliflozin can be used in research related to type 2 diabetes .
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Cat. No.: HY-153113
CAS No.: 2648020-91-9
Synonyms: DJT1116PG
Target:  

SGLT

Research Areas:  

Endocrinology

Rongliflozin (DJT1116PG) is a selective and orally active inhibitor of sodium-glucose co-transporter-2 (SGLT-2). Rongliflozin can be used for the research of type 2 diabetes mellitus (T2DM) .
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Cat. No.: HY-116223
CAS No.: 1461750-27-5
Purity:  99.96%
Target:  

SGLT

Research Areas:  

Metabolic Disease

Tianagliflozin is a sodium/glucose cotransporter 2 (SGLT-2) inhibitor with potential for investigation in type 2 diabetes .
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Cat. No.: HY-15409S1
Synonyms: BI 10773-13C6
Empagliflozin- 13C6 (BI 10773- 13C6) is 13C labeled Empagliflozin. Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2 .
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Cat. No.: HY-15409S2
Synonyms: BI 10773-d6
Empagliflozin-d6 (BI 10773-d6) is deuterium labeled Empagliflozin. Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2 .
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