U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C29H46Cl2N2O6
Molecular Weight 589.591
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORAMPHENICOL STEARATE

SMILES

CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)C1=CC=C(C=C1)[N+]([O-])=O

InChI

InChIKey=IDWDXHQLOMJDRU-XNMGPUDCSA-N
InChI=1S/C29H46Cl2N2O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-26(34)39-22-25(32-29(36)28(30)31)27(35)23-18-20-24(21-19-23)33(37)38/h18-21,25,27-28,35H,2-17,22H2,1H3,(H,32,36)/t25-,27-/m1/s1

HIDE SMILES / InChI

Molecular Formula C29H46Cl2N2O6
Molecular Weight 589.591
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
[Pseudomorphism of chloramphenicol stearate and palmitate in relationship availability].
1983 Apr
Surface area and crystallinity of Form A of chloramphenicol palmitic and stearic esters: which one is the limiting factor in the enzymatic hydrolysis?
1987 Dec
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:35:38 GMT 2023
Edited
by admin
on Sat Dec 16 01:35:38 GMT 2023
Record UNII
DL2A9M9D6X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORAMPHENICOL STEARATE
WHO-DD  
Common Name English
MADOMICETINA
Common Name English
CHLORAMPHENICOL STEARIC ACID ESTER
Common Name English
EUSYNTHOMYCIN
Common Name English
OCTADECANOIC ACID, (2R,3R)-2-((2,2-DICHLOROACETYL)AMINO)-3-HYDROXY-3-(4-NITROPHENYL)PROPYL ESTER
Common Name English
LEVOMYCETIN STEARATE
Common Name English
(-)-CHLORAMPHENICOL STEARATE
Common Name English
Chloramphenicol stearate [WHO-DD]
Common Name English
Code System Code Type Description
PUBCHEM
83945
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY
MESH
C032008
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY
FDA UNII
DL2A9M9D6X
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY
EVMPD
SUB26903
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY
SMS_ID
100000090227
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY
RXCUI
20768
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
240-363-4
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID20167407
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY
CAS
16255-48-4
Created by admin on Sat Dec 16 01:35:38 GMT 2023 , Edited by admin on Sat Dec 16 01:35:38 GMT 2023
PRIMARY