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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H30O13
Molecular Weight 574.53
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Steffimycin

SMILES

CO[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@H]2[C@H](OC)[C@](C)(O)C(=O)C3=CC4=C(C(=O)C5=C(O)C=C(OC)C=C5C4=O)C(O)=C23

InChI

InChIKey=HWMJTJZEJBSVCG-GPDBLRFJSA-N
InChI=1S/C28H30O13/c1-9-18(30)22(34)24(38-4)27(40-9)41-23-17-13(25(35)28(2,36)26(23)39-5)8-12-16(21(17)33)20(32)15-11(19(12)31)6-10(37-3)7-14(15)29/h6-9,18,22-24,26-27,29-30,33-34,36H,1-5H3/t9-,18-,22+,23+,24+,26-,27-,28+/m0/s1

HIDE SMILES / InChI
Steffimycin is a potent inhibitor of DNA dependent-RNA synthesis patented by Upjohn Co. as an antibiotic. Steffimycin interferes with amino acid incorporation mediated by synthetic polyribonucleotides in cell-free bacterial systems. This inhibition is a secondary activity of the antibiotic, which acts primarily as a suppressor of RNA synthesis in bacteria and bacterial cell-free systems. Inhibition of peptide biosynthesis is apparent only at a drug concentration higher than that necessary for inhibition of RNA synthesis in cell-free systems. In addition to antibiotic activity vs certain gram-positive organisms, Steffimycin inhibits the growth of KB cells and several fungi and shows antiviral activity against herpes simplex in mice

Approval Year

PubMed

PubMed

TitleDatePubMed
One-Pot Enzymatic Total Synthesis of Presteffimycinone, an Early Intermediate of the Anthracycline Antibiotic Steffimycin Biosynthesis.
2017-02-03
Patents

Patents

Name Type Language
NSC-93419
Preferred Name English
Steffimycin
INN   USAN  
USAN   INN  
Official Name English
U-20661
Code English
STEFFIMYCIN [USAN]
Common Name English
steffimycin [INN]
Common Name English
U-20,661
Code English
Classification Tree Code System Code
NCI_THESAURUS C1594
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
Code System Code Type Description
FDA UNII
48V353KY77
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
NCI_THESAURUS
C152426
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
PUBCHEM
70683013
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
SMS_ID
300000034443
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
CAS
11033-34-4
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
INN
2529
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
NSC
93419
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
MESH
C009944
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105537
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID20891356
Created by admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
PRIMARY