Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C37H42N2O7 |
| Molecular Weight | 626.7386 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@]2(O)C(=O)COC(=O)COC5=NN(CC6=CC=CC=C6)C7=C5C=CC=C7
InChI
InChIKey=DYVIEGCPUPGXOH-HGGPGNIHSA-N
InChI=1S/C37H42N2O7/c1-35-16-14-25(40)18-24(35)12-13-26-28-15-17-37(44,36(28,2)19-30(41)33(26)35)31(42)21-45-32(43)22-46-34-27-10-6-7-11-29(27)39(38-34)20-23-8-4-3-5-9-23/h3-11,18,26,28,30,33,41,44H,12-17,19-22H2,1-2H3/t26-,28-,30-,33+,35-,36-,37-/m0/s1
| Molecular Formula | C37H42N2O7 |
| Molecular Weight | 626.7386 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Bendacort is an ester of glucocorticosteroid hydrocortisone and non-steroidal anti-inflammatory drug bendazac. In vivo studies demonstrated that bendacort has a wider spectrum of anti-inflammatory effects than bendazac or hydrocortisone alone: bendacort acts on responses with a necrotic evolution where tissue damage predominates, and in cases where the reaction of tissue defense predominates, as for example in the healing of wounds. Bendacort was marketed in Italy under tradename Versacort for the treatment of sensitive steroid dermatoses, contact eczema, dyshidrosis, insect bites.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:52:43 GMT 2025
by
admin
on
Mon Mar 31 19:52:43 GMT 2025
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| Record UNII |
EF5DH3EFH5
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| Record Status |
Validated (UNII)
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| Record Version |
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53716-43-1
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DTXSID00968474
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EF5DH3EFH5
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258-710-3
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admin on Mon Mar 31 19:52:43 GMT 2025 , Edited by admin on Mon Mar 31 19:52:43 GMT 2025
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