Model NO.: 864070-44-0
Description: White or White Alike Crystalline Powder
Synonyms: 3-Hydroxy-5-Androstan-17-One;5-Androstan-3-Ol-17-O
Einecs: 206-253-5
Loss on Drying: 0.5% Max
Melting Pointt: 176-180ºC
Shelf Life: 2 Years
Residual Solvents: Meets The Requirements
Delivery Ways: EMS, DHL, TNT, FedEx, UPS, Toll E
MW: C19h24o2
Mf: 410.55
Trademark: JZY
Transport Package: Discreet Package
Specification: White Powder
Origin: China
HS Code: 3001909099
Model NO.: 864070-44-0
Description: White or White Alike Crystalline Powder
Synonyms: 3-Hydroxy-5-Androstan-17-One;5-Androstan-3-Ol-17-O
Einecs: 206-253-5
Loss on Drying: 0.5% Max
Melting Pointt: 176-180ºC
Shelf Life: 2 Years
Residual Solvents: Meets The Requirements
Delivery Ways: EMS, DHL, TNT, FedEx, UPS, Toll E
MW: C19h24o2
Mf: 410.55
Trademark: JZY
Transport Package: Discreet Package
Specification: White Powder
Origin: China
HS Code: 3001909099
Product Description
EMpagliflozinAnother Name: 1-Pyrrolidineacetamide,N-[2-(Diisopropylamino)ethyl]-2-(2-oxopyrrolidin-1-yl)acetamide
CASÂ Number:Â 68497-62-1
Molecular Weight: 450.90928
Molecular Formula: C23H27ClO7
Density:Â 1.036Â g/cm3
Boiling Point: 665ºC
Flash Point: 1.398
Appearance:Â white powder
Usage:
Empagliflozin is a novel, potent and selective SGLT-2 inhibitor, improves glycaemic control and features of metabolic syndrome in diabetic rats.
What's :Empagliflozin?
Empagliflozin is a selective inhibitor of SGLT-2 with IC50 value of 3.1 nM .
Sodium glucose cotransporter-2 (SGLT-2) is a member of sodium glucose co-transporter family and plays a pivotal role in glucose reabsorption in the kidney .
Empagliflozin is a potent SGLT-2 inhibitor and has a high degree of selectivity over SGLT-1, 4, 5 and 6 than other reported SGLT-2 inhibitors. When tested with a panel of human cell lines over-expressed SGLT-1, 2, 4, 5 and 6,
Empagliflozin treatment competitively bind to SGLT-2 over glucose at low dose . In human proximal tublular cell (PTC) cell line HK2 cells, Empagliflozin treatment for 72 h inhibits the expression of SGLT-2 which in turn reversed high glucose induced TLR4 expression, NF-κB binding, IL-6 secretion, AP-1 binding and CIV expression .
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SARMS Raw Powder
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| CAS:159752-10-0 | MK-677(Ibutamoren) |
| CAS:1165910-22-4 | LGD-4033 (Ligandrol) |
| CAS:317318-70-0 | GW-501516 |
| CAS:1202044-20-9/841205-47-8 | MK-2866(Ostarine ) |
| CAS:1182367-47-0 | RAD-140 |
| CAS:401900-40-1 | Andarine (S4) |
| CAS:431579-34-9 | YK-11 |
| CAS:1379686-30-2 | SR9009 |
| CAS:314728-85-3 | Sunifiram(DM-235) |
Product Description
EMpagliflozinAnother Name: 1-Pyrrolidineacetamide,N-[2-(Diisopropylamino)ethyl]-2-(2-oxopyrrolidin-1-yl)acetamide
CASÂ Number:Â 68497-62-1
Molecular Weight: 450.90928
Molecular Formula: C23H27ClO7
Density:Â 1.036Â g/cm3
Boiling Point: 665ºC
Flash Point: 1.398
Appearance:Â white powder
Usage:
Empagliflozin is a novel, potent and selective SGLT-2 inhibitor, improves glycaemic control and features of metabolic syndrome in diabetic rats.
What's :Empagliflozin?
Empagliflozin is a selective inhibitor of SGLT-2 with IC50 value of 3.1 nM .
Sodium glucose cotransporter-2 (SGLT-2) is a member of sodium glucose co-transporter family and plays a pivotal role in glucose reabsorption in the kidney .
Empagliflozin is a potent SGLT-2 inhibitor and has a high degree of selectivity over SGLT-1, 4, 5 and 6 than other reported SGLT-2 inhibitors. When tested with a panel of human cell lines over-expressed SGLT-1, 2, 4, 5 and 6,
Empagliflozin treatment competitively bind to SGLT-2 over glucose at low dose . In human proximal tublular cell (PTC) cell line HK2 cells, Empagliflozin treatment for 72 h inhibits the expression of SGLT-2 which in turn reversed high glucose induced TLR4 expression, NF-κB binding, IL-6 secretion, AP-1 binding and CIV expression .
Â
SARMS Raw Powder
Â
| CAS:159752-10-0 | MK-677(Ibutamoren) |
| CAS:1165910-22-4 | LGD-4033 (Ligandrol) |
| CAS:317318-70-0 | GW-501516 |
| CAS:1202044-20-9/841205-47-8 | MK-2866(Ostarine ) |
| CAS:1182367-47-0 | RAD-140 |
| CAS:401900-40-1 | Andarine (S4) |
| CAS:431579-34-9 | YK-11 |
| CAS:1379686-30-2 | SR9009 |
| CAS:314728-85-3 | Sunifiram(DM-235) |
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