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Details

Stereochemistry UNKNOWN
Molecular Formula C37H56N2O3.2ClH
Molecular Weight 649.774
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MENABITAN HYDROCHLORIDE

SMILES

Cl.Cl.CCCCCC(C)C(C)C1=CC(OC(=O)C(C)CCN2CCCCC2C)=C3C(OC(C)(C)C4=C3CN(CC#C)CC4)=C1

InChI

InChIKey=VYBDZIGAEAYRMM-UHFFFAOYSA-N
InChI=1S/C37H56N2O3.2ClH/c1-9-11-12-15-26(3)29(6)30-23-33(41-36(40)27(4)17-22-39-20-14-13-16-28(39)5)35-31-25-38(19-10-2)21-18-32(31)37(7,8)42-34(35)24-30;;/h2,23-24,26-29H,9,11-22,25H2,1,3-8H3;2*1H

HIDE SMILES / InChI

Molecular Formula C37H56N2O3
Molecular Weight 576.8521
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Originator

Curator's Comment: reference retrieved from https://link.springer.com/book/10.1007/978-1-4757-2085-3#about

Approval Year

PubMed

PubMed

TitleDatePubMed
Drugs derived from cannabinoids. 2. Basic esters of nitrogen and carbocyclic analogs.
1976-04
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:35:55 GMT 2025
Edited
by admin
on Mon Mar 31 18:35:55 GMT 2025
Record UNII
ZEI0YBM796
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MENABITAN HYDROCHLORIDE
USAN  
USAN  
Official Name English
SP-204
Preferred Name English
1-PIPERIDINEBUTANOIC ACID, .ALPHA.,2-DIMETHYL-, 8-(1,2-DIMETHYLHEPTYL)-1,3,4,5-TETRAHYDRO-5,5-DIMETHYL-2-(2-PROPYNYL)-2H-(1)BENZOPYRANO(4,3-C)PYRIDIN-10-YL ESTER, DIHYDROCHLORIDE, (±)-
Common Name English
(±)-8-(1,2-DIMETHYLHEPTYL)-1,3,4,5-TETRAHYDRO-5,5-DIMETHYL-2-(2-PROPYNYL)-2H-(1)BENZOPYRANO(4,3-C)PYRIDIN-10-YL .ALPHA.,2-DIMETHYL-1-PIPERIDINEBUTYRATE, DIHYDROCHLORIDE
Common Name English
MENABITAN HCL
Common Name English
MENABITAN HYDROCHLORIDE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C241
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID40973603
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
PRIMARY
ChEMBL
CHEMBL2110875
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
PRIMARY
USAN
T-93
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
PRIMARY
FDA UNII
ZEI0YBM796
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
PRIMARY
CAS
58019-50-4
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
PRIMARY
NCI_THESAURUS
C87591
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
PRIMARY
SMS_ID
300000055258
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
PRIMARY
PUBCHEM
189876
Created by admin on Mon Mar 31 18:35:55 GMT 2025 , Edited by admin on Mon Mar 31 18:35:55 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY