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Details

Stereochemistry ACHIRAL
Molecular Formula C22H26O4
Molecular Weight 354.4394
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AM-1714

SMILES

CCCCCCC(C)(C)C1=CC(O)=C2C(OC(=O)C3=C2C=C(O)C=C3)=C1

InChI

InChIKey=BWKBVEVEQOCSCF-UHFFFAOYSA-N
InChI=1S/C22H26O4/c1-4-5-6-7-10-22(2,3)14-11-18(24)20-17-13-15(23)8-9-16(17)21(25)26-19(20)12-14/h8-9,11-13,23-24H,4-7,10H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C22H26O4
Molecular Weight 354.4394
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Selective activation of cannabinoid CB2 receptors suppresses neuropathic nociception induced by treatment with the chemotherapeutic agent paclitaxel in rats.
2008-11
Species comparison and pharmacological characterization of rat and human CB2 cannabinoid receptors.
2004-11-28
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:49:30 GMT 2025
Edited
by admin
on Mon Mar 31 21:49:30 GMT 2025
Record UNII
E3OY6PCU04
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AM-1714
Common Name English
6H-DIBENZO(B,D)PYRAN-6-ONE, 3-(1,1-DIMETHYLHEPTYL)-1,9-DIHYDROXY-
Preferred Name English
Code System Code Type Description
WIKIPEDIA
AM-1714
Created by admin on Mon Mar 31 21:49:30 GMT 2025 , Edited by admin on Mon Mar 31 21:49:30 GMT 2025
PRIMARY
FDA UNII
E3OY6PCU04
Created by admin on Mon Mar 31 21:49:30 GMT 2025 , Edited by admin on Mon Mar 31 21:49:30 GMT 2025
PRIMARY
CAS
335371-37-4
Created by admin on Mon Mar 31 21:49:30 GMT 2025 , Edited by admin on Mon Mar 31 21:49:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID801045362
Created by admin on Mon Mar 31 21:49:30 GMT 2025 , Edited by admin on Mon Mar 31 21:49:30 GMT 2025
PRIMARY
PUBCHEM
9950486
Created by admin on Mon Mar 31 21:49:30 GMT 2025 , Edited by admin on Mon Mar 31 21:49:30 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY