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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H31NO9
Molecular Weight 513.5363
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Feudomycin A

SMILES

[H][C@@]1(C[C@H](N)[C@H](O)[C@H](C)O1)O[C@H]2C[C@](O)(CC)CC3=C2C(O)=C4C(=O)C5=C(OC)C=CC=C5C(=O)C4=C3O

InChI

InChIKey=XAMIMZAWZUSOPA-JIGXQNLBSA-N
InChI=1S/C27H31NO9/c1-4-27(34)9-13-19(16(10-27)37-17-8-14(28)22(29)11(2)36-17)26(33)21-20(24(13)31)23(30)12-6-5-7-15(35-3)18(12)25(21)32/h5-7,11,14,16-17,22,29,31,33-34H,4,8-10,28H2,1-3H3/t11-,14-,16-,17-,22+,27-/m0/s1

HIDE SMILES / InChI

Molecular Formula C27H31NO9
Molecular Weight 513.5363
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 19:50:52 GMT 2023
Edited
by admin
on Sat Dec 16 19:50:52 GMT 2023
Record UNII
CMR78YDZ6K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Feudomycin A
Common Name English
(7S,9S)-7-[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy-9-ethyl-6,9,11-trihydroxy-4-methoxy-8,10-dihydro-7H-tetracene-5,12-dione
Systematic Name English
Daunorubicin Hydrochloride Impurity G [Ep Impurity]
Common Name English
13-Deoxydaunomycin
Common Name English
5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-8-ethyl-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-, (8S-cis)
Common Name English
(8S,10S)-10-[(3-Amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-8-ethyl-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-naphthacenedione
Systematic Name English
5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-8-ethyl-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-, (8S,10S)-
Common Name English
Code System Code Type Description
PUBCHEM
157384
Created by admin on Sat Dec 16 19:50:52 GMT 2023 , Edited by admin on Sat Dec 16 19:50:52 GMT 2023
PRIMARY
FDA UNII
CMR78YDZ6K
Created by admin on Sat Dec 16 19:50:52 GMT 2023 , Edited by admin on Sat Dec 16 19:50:52 GMT 2023
PRIMARY
CAS
79466-09-4
Created by admin on Sat Dec 16 19:50:52 GMT 2023 , Edited by admin on Sat Dec 16 19:50:52 GMT 2023
PRIMARY
EPA CompTox
DTXSID80229696
Created by admin on Sat Dec 16 19:50:52 GMT 2023 , Edited by admin on Sat Dec 16 19:50:52 GMT 2023
PRIMARY
Related Record Type Details
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