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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H19N3O7S2
Molecular Weight 429.468
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SUNCILLIN

SMILES

CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](NS(O)(=O)=O)C3=CC=CC=C3)C(=O)N2[C@H]1C(O)=O

InChI

InChIKey=OIECDSKSPRTZHG-NJBDSQKTSA-N
InChI=1S/C16H19N3O7S2/c1-16(2)11(15(22)23)19-13(21)10(14(19)27-16)17-12(20)9(18-28(24,25)26)8-6-4-3-5-7-8/h3-7,9-11,14,18H,1-2H3,(H,17,20)(H,22,23)(H,24,25,26)/t9-,10-,11+,14-/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H19N3O7S2
Molecular Weight 429.468
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Suncillin is an antibacteria and antifungal agent produced in Phytera's laboratory from a cell culture of a plant. Suncillin was patented by Bristol-Myers Co. In 1968 for the Pseudomonas bacteria treatment but was never marketed.

Approval Year

PubMed

PubMed

TitleDatePubMed
In vitro bacteriological study of a new antibiotic substance: sisomicin.
1975-01
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Sources: Current Therapeutic Research (1970), 12, (6), 363-8.
18-​30 g​/day
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:40:54 GMT 2025
Edited
by admin
on Mon Mar 31 19:40:54 GMT 2025
Record UNII
D6XHM6R84S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SUNCILLIN
INN  
INN  
Official Name English
3,3-DIMETHYL-7-OXO-6-(2-PHENYL-D-2-(SULFOAMINO)ACETAMIDO)-4-THIA-1-AZABICYCLO-(3.2.0)HEPTANE-2-CARBOXYLIC ACID
Preferred Name English
suncillin [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1500
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
Code System Code Type Description
PUBCHEM
3034014
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
EVMPD
SUB10773MIG
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
CAS
22164-94-9
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
SMS_ID
100000082963
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
MESH
C003818
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID801043223
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
INN
2977
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
ChEMBL
CHEMBL2111139
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
NCI_THESAURUS
C152471
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
FDA UNII
D6XHM6R84S
Created by admin on Mon Mar 31 19:40:54 GMT 2025 , Edited by admin on Mon Mar 31 19:40:54 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY