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Details

Stereochemistry UNKNOWN
Molecular Formula C23H35NO9
Molecular Weight 469.5253
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SPIRANINE

SMILES

CCC(C)[C@@]1(O)[C@@H](O)C(=O)O[C@H](C)[C@@](O)(C(C)C)C(=O)OCC2=CCN3CC[C@@H](OC1=O)[C@@H]23

InChI

InChIKey=LYCHAEUHBIADIF-CRUIESPDSA-N
InChI=1S/C23H35NO9/c1-6-13(4)23(30)18(25)19(26)32-14(5)22(29,12(2)3)20(27)31-11-15-7-9-24-10-8-16(17(15)24)33-21(23)28/h7,12-14,16-18,25,29-30H,6,8-11H2,1-5H3/t13?,14-,16-,17-,18+,22+,23-/m1/s1

HIDE SMILES / InChI

Molecular Formula C23H35NO9
Molecular Weight 469.5253
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 6 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:20:21 GMT 2025
Edited
by admin
on Mon Mar 31 23:20:21 GMT 2025
Record UNII
4758ROY4TY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SPIRANINE
Common Name English
25-NORPARSONSINE, 24-ETHYL-16-HYDROXY-, (12.XI.,13.XI.,17.XI.)-
Preferred Name English
7H-(1,5,10)TRIOXACYCLOTETRADECINO(7,8,9-GH)PYRROLIZINE-2,5,9(8H)-TRIONE, 3,4,11,13,15,16,16A,16B-OCTAHYDRO-3,4,8-TRIHYDROXY-7-METHYL-8-(1-METHYLETHYL)-3-(1-METHYLPROPYL)-, (16AR,16BR)-(PARTIAL)-
Systematic Name English
7H-(1,5,10)TRIOXACYCLOTETRADECINO(7,8,9-GH)PYRROLIZINE-2,5,9(8H)-TRIONE, 3,4,11,13,15,16,16A,16B-OCTAHYDRO-3,4,8-TRIHYDROXY-7-METHYL-8-(1-METHYLETHYL)-3-(1-METHYLPROPYL)-, (16AR,16BR)-
Systematic Name English
Code System Code Type Description
PUBCHEM
14845643
Created by admin on Mon Mar 31 23:20:21 GMT 2025 , Edited by admin on Mon Mar 31 23:20:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID40998412
Created by admin on Mon Mar 31 23:20:21 GMT 2025 , Edited by admin on Mon Mar 31 23:20:21 GMT 2025
PRIMARY
FDA UNII
4758ROY4TY
Created by admin on Mon Mar 31 23:20:21 GMT 2025 , Edited by admin on Mon Mar 31 23:20:21 GMT 2025
PRIMARY
CAS
77156-23-1
Created by admin on Mon Mar 31 23:20:21 GMT 2025 , Edited by admin on Mon Mar 31 23:20:21 GMT 2025
PRIMARY