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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H24NO4
Molecular Weight 342.4089
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of CYCLANOLINE

SMILES

COC1=CC=C2C[C@H]3C4=CC(O)=C(OC)C=C4CC[N@@+]3(C)CC2=C1O

InChI

InChIKey=LKLWVKCEYSPQHL-KKSFZXQISA-O
InChI=1S/C20H23NO4/c1-21-7-6-13-9-19(25-3)17(22)10-14(13)16(21)8-12-4-5-18(24-2)20(23)15(12)11-21/h4-5,9-10,16H,6-8,11H2,1-3H3,(H-,22,23)/p+1/t16-,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H23NO4
Molecular Weight 341.4009
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 1 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:46:25 GMT 2025
Edited
by admin
on Mon Mar 31 21:46:25 GMT 2025
Record UNII
77QC59KBD2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(-)-Cissamine
Preferred Name English
CYCLANOLINE
Common Name English
(7S,13aS)-5,8,13,13a-Tetrahydro-2,9-dihydroxy-3,10-dimethoxy-7-methyl-6H-dibenzo[a,g]quinolizinium
Systematic Name English
6H-Dibenzo[a,g]quinolizinium, 5,8,13,13a-tetrahydro-2,9-dihydroxy-3,10-dimethoxy-7-methyl-, (7S,13aS)-
Systematic Name English
?-Cyclanoline
Common Name English
(-)-Cyclanoline
Common Name English
6H-Dibenzo[a,g]quinolizinium, 5,8,13,13a-tetrahydro-2,9-dihydroxy-3,10-dimethoxy-7-methyl-, (7S-cis)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID00171789
Created by admin on Mon Mar 31 21:46:25 GMT 2025 , Edited by admin on Mon Mar 31 21:46:25 GMT 2025
PRIMARY
PUBCHEM
3082134
Created by admin on Mon Mar 31 21:46:25 GMT 2025 , Edited by admin on Mon Mar 31 21:46:25 GMT 2025
PRIMARY
WIKIPEDIA
Cyclanoline
Created by admin on Mon Mar 31 21:46:25 GMT 2025 , Edited by admin on Mon Mar 31 21:46:25 GMT 2025
PRIMARY
CAS
18556-27-9
Created by admin on Mon Mar 31 21:46:25 GMT 2025 , Edited by admin on Mon Mar 31 21:46:25 GMT 2025
PRIMARY
FDA UNII
77QC59KBD2
Created by admin on Mon Mar 31 21:46:25 GMT 2025 , Edited by admin on Mon Mar 31 21:46:25 GMT 2025
PRIMARY