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Details

Stereochemistry MIXED
Molecular Formula C35H52N2O3.ClH
Molecular Weight 585.26
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NABITAN HYDROCHLORIDE

SMILES

Cl.CCCCCC(C)C(C)C1=CC(OC(=O)CCCN2CCCCC2)=C3C(OC(C)(C)C4=C3CN(CC#C)CC4)=C1

InChI

InChIKey=KWXQFOPVLBPXHY-UHFFFAOYSA-N
InChI=1S/C35H52N2O3.ClH/c1-7-9-11-15-26(3)27(4)28-23-31(39-33(38)16-14-21-36-19-12-10-13-20-36)34-29-25-37(18-8-2)22-17-30(29)35(5,6)40-32(34)24-28;/h2,23-24,26-27H,7,9-22,25H2,1,3-6H3;1H

HIDE SMILES / InChI
Nabitan is a synthetic cannabinoid analog of dronabinol with antiemetic and analgesic effects. Nabitan is not currently used in medicine as dronabinol or nabilone are felt to be more useful for most conditions, however, it is sometimes used in research into the potential therapeutic applications of cannabinoids.

Originator

Sources: US730351; U. S. Pat. Appl. 19 pp. Avail. NTIS. Patent 1976

Approval Year

Patents

Patents

Name Type Language
NABITAN HYDROCHLORIDE
USAN  
USAN  
Official Name English
NIB
Preferred 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 1-piperidinebutyrate monohydrochloride
Systematic Name English
NABITAN HYDROCHLORIDE [USAN]
Common Name English
SP-106
Code English
NABUTAN HYDROCHLORIDE
Common Name English
1-PIPERIDINEBUTANOIC ACID, 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 MONOHYDROCHLORIDE-
Common Name English
Code System Code Type Description
FDA UNII
2F3L1A6VXE
Created by admin on Mon Mar 31 18:56:41 GMT 2025 , Edited by admin on Mon Mar 31 18:56:41 GMT 2025
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SMS_ID
300000055513
Created by admin on Mon Mar 31 18:56:41 GMT 2025 , Edited by admin on Mon Mar 31 18:56:41 GMT 2025
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ChEMBL
CHEMBL2110593
Created by admin on Mon Mar 31 18:56:41 GMT 2025 , Edited by admin on Mon Mar 31 18:56:41 GMT 2025
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NCI_THESAURUS
C166569
Created by admin on Mon Mar 31 18:56:41 GMT 2025 , Edited by admin on Mon Mar 31 18:56:41 GMT 2025
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PUBCHEM
39502
Created by admin on Mon Mar 31 18:56:41 GMT 2025 , Edited by admin on Mon Mar 31 18:56:41 GMT 2025
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CAS
49637-08-3
Created by admin on Mon Mar 31 18:56:41 GMT 2025 , Edited by admin on Mon Mar 31 18:56:41 GMT 2025
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EPA CompTox
DTXSID20964312
Created by admin on Mon Mar 31 18:56:41 GMT 2025 , Edited by admin on Mon Mar 31 18:56:41 GMT 2025
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