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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H30N8O8
Molecular Weight 498.4903
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Mildiomycin D

SMILES

N[C@@H](CO)C(=O)N[C@H]1C=C[C@@H](O[C@@H]1[C@](O)(CCCNC(N)=N)C(O)=O)N2C=C(CO)C(N)=NC2=O

InChI

InChIKey=GVLLATLXQPLOAJ-LGSFDMRSSA-N
InChI=1S/C19H30N8O8/c20-10(8-29)15(30)25-11-2-3-12(27-6-9(7-28)14(21)26-18(27)33)35-13(11)19(34,16(31)32)4-1-5-24-17(22)23/h2-3,6,10-13,28-29,34H,1,4-5,7-8,20H2,(H,25,30)(H,31,32)(H2,21,26,33)(H4,22,23,24)/t10-,11-,12+,13-,19+/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H30N8O8
Molecular Weight 498.4903
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:05:20 GMT 2025
Edited
by admin
on Mon Mar 31 23:05:20 GMT 2025
Record UNII
5RLP33N8Z6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Mildiomycin D
Common Name English
2H-Pyran-2-acetic acid, 6-[4-amino-5-(hydroxymethyl)-2-oxo-1(2H)-pyrimidinyl]-3-[(2-amino-3-hydroxy-1-oxopropyl)amino]-?-[3-[(aminoiminomethyl)amino]propyl]-3,6-dihydro-?-hydroxy-, [2S-[2?(S*),3?(R*),6?]]-
Preferred Name English
L-arabino-Hept-6-enonic acid, 7-C-[4-amino-5-(hydroxymethyl)-2-oxo-1(2H)-pyrimidinyl]-4-[[(2S)-2-amino-3-hydroxy-1-oxopropyl]amino]-2-C-[3-[(aminoiminomethyl)amino]propyl]-3,7-anhydro-4,5,6-trideoxy-, (7R)-
Systematic Name English
Code System Code Type Description
CAS
86432-24-8
Created by admin on Mon Mar 31 23:05:20 GMT 2025 , Edited by admin on Mon Mar 31 23:05:20 GMT 2025
PRIMARY
PUBCHEM
3070418
Created by admin on Mon Mar 31 23:05:20 GMT 2025 , Edited by admin on Mon Mar 31 23:05:20 GMT 2025
PRIMARY
FDA UNII
5RLP33N8Z6
Created by admin on Mon Mar 31 23:05:20 GMT 2025 , Edited by admin on Mon Mar 31 23:05:20 GMT 2025
PRIMARY
EPA CompTox
DTXSID60235538
Created by admin on Mon Mar 31 23:05:20 GMT 2025 , Edited by admin on Mon Mar 31 23:05:20 GMT 2025
PRIMARY