Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H24ClFO7 |
| Molecular Weight | 454.873 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC1=CC=C(CC2=CC(=CC=C2Cl)[C@@]34OC[C@@](CO)(O3)[C@@H](O)[C@H](O)[C@H]4O)C=C1F
InChI
InChIKey=HYTPDMFFHVZBOR-VNXMGFANSA-N
InChI=1S/C22H24ClFO7/c1-2-29-17-6-3-12(8-16(17)24)7-13-9-14(4-5-15(13)23)22-20(28)18(26)19(27)21(10-25,31-22)11-30-22/h3-6,8-9,18-20,25-28H,2,7,10-11H2,1H3/t18-,19-,20+,21+,22+/m0/s1
| Molecular Formula | C22H24ClFO7 |
| Molecular Weight | 454.873 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Henagliflozin (also known as SHR3824) was developed by Jiangsu HengRui Medicine as a sodium glucose cotransporter 2 (SGLT2) inhibitor for the treatment of type 2 diabetes mellitus. This drug successfully passed phase I clinical trials, however, information about further development is not available.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| SHR3824, a novel selective inhibitor of renal sodium glucose cotransporter 2, exhibits antidiabetic efficacy in rodent models. | 2014 May |
|
| Pharmacokinetics and Pharmacodynamics of Henagliflozin, a Sodium Glucose Co-Transporter 2 Inhibitor, in Chinese Patients with Type 2 Diabetes Mellitus. | 2016 Mar |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:57:18 GMT 2023
by
admin
on
Fri Dec 15 16:57:18 GMT 2023
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| Record UNII |
21P2M98388
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| Record Status |
Validated (UNII)
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| Record Version |
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21P2M98388
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56832738
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DB11939
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1623804-44-3
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admin on Fri Dec 15 16:57:18 GMT 2023 , Edited by admin on Fri Dec 15 16:57:18 GMT 2023
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| Related Record | Type | Details | ||
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TARGET -> INHIBITOR | |||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
