Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C27H31NO11 |
| Molecular Weight | 545.5351 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]1(C[C@H](N)[C@H](O)[C@H](C)O1)O[C@H]2C[C@@](O)(CC3=C(O)C4=C(C(=O)C5=C(OC)C=CC=C5C4=O)C(O)=C23)[C@@H](O)CO
InChI
InChIKey=NKZRZOVSJNSBFR-FEMMEMONSA-N
InChI=1S/C27H31NO11/c1-10-22(31)13(28)6-17(38-10)39-15-8-27(36,16(30)9-29)7-12-19(15)26(35)21-20(24(12)33)23(32)11-4-3-5-14(37-2)18(11)25(21)34/h3-5,10,13,15-17,22,29-31,33,35-36H,6-9,28H2,1-2H3/t10-,13-,15-,16-,17-,22+,27-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The role of biotransformation in anthracycline-induced cardiotoxicity in mice. | 1993 Sep |
|
| Doxorubicin irreversibly inactivates iron regulatory proteins 1 and 2 in cardiomyocytes: evidence for distinct metabolic pathways and implications for iron-mediated cardiotoxicity of antitumor therapy. | 2001 Dec 1 |
|
| Identification of carbonyl reductase 1 as a resveratrol-binding protein by affinity chromatography using 4'-amino-3,5-dihydroxy-trans-stilbene. | 2013 |
|
| Metabolism of doxorubicin to the cardiotoxic metabolite doxorubicinol is increased in a mouse model of chronic glutathione deficiency: A potential role for carbonyl reductase 3. | 2015 Jun 5 |
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HUH05KI4CF
Created by
admin on Sat Dec 16 08:37:32 GMT 2023 , Edited by admin on Sat Dec 16 08:37:32 GMT 2023
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133817
Created by
admin on Sat Dec 16 08:37:32 GMT 2023 , Edited by admin on Sat Dec 16 08:37:32 GMT 2023
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54193-28-1
Created by
admin on Sat Dec 16 08:37:32 GMT 2023 , Edited by admin on Sat Dec 16 08:37:32 GMT 2023
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83970
Created by
admin on Sat Dec 16 08:37:32 GMT 2023 , Edited by admin on Sat Dec 16 08:37:32 GMT 2023
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PRIMARY |
PARENT (METABOLITE)
SUBSTANCE RECORD
