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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H35NO4
Molecular Weight 413.5497
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIHYDROETORPHINE

SMILES

[H][C@@]12OC3=C(O)C=CC4=C3[C@@]15CCN(C)[C@]([H])(C4)[C@]56CC[C@@]2(OC)[C@]([H])(C6)[C@](C)(O)CCC

InChI

InChIKey=BRTSNYPDACNMIP-FAWZKKEFSA-N
InChI=1S/C25H35NO4/c1-5-8-22(2,28)17-14-23-9-10-25(17,29-4)21-24(23)11-12-26(3)18(23)13-15-6-7-16(27)20(30-21)19(15)24/h6-7,17-18,21,27-28H,5,8-14H2,1-4H3/t17-,18-,21-,22-,23-,24+,25-/m1/s1

HIDE SMILES / InChI

Molecular Formula C25H35NO4
Molecular Weight 413.5497
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
A protective effect against undesirable increase of dihydroetorphine permeation through damaged skin by using pressure-sensitive adhesive tape with an ethylene-vinyl acetate co-polymer membrane.
2001 Jan
Tolerance to analgesia and dependence liability by topical application of dihydroetorphine to hairless rats.
2001 Jul 6
Cell death-inducing activity of opiates in human oral tumor cell lines.
2002 Jan-Feb
Biochemical characterisation of newly developed beta-etorphine and beta-dihydroetorphine derivatives.
2002 May 3
Dihydroetorphine: a potent analgesic: pharmacology, toxicology, pharmacokinetics, and clinical effects.
2002 Winter
Discriminative stimulus and antinociceptive effects of dihydroetorphine in rhesus monkeys.
2003 Apr
Binding affinity to and dependence on some opioids in Sf9 insect cells expressing human mu-opioid receptor.
2003 Sep
Synthesis and biological evaluation of 14-alkoxymorphinans. 20. 14-phenylpropoxymetopon: an extremely powerful analgesic.
2003 Sep 11
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:31:24 GMT 2023
Edited
by admin
on Sat Dec 16 10:31:24 GMT 2023
Record UNII
QQX8S479YV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIHYDROETORPHINE
WHO-DD  
Common Name English
TETRAHYDRO-7.ALPHA.-(1-HYDROXY-1-METHYLBUTYL)-6,14-ENDO-ETHANOORIPAVINE
Common Name English
Dihydroetorphine [WHO-DD]
Common Name English
IDS-ND-025
Code English
6,14-ETHENOMORPHINAN-7-METHANOL, 4,5-EPOXY-18,19-DIHYDRO-3-HYDROXY-6-METHOXY-.ALPHA.,17-DIMETHYL-.ALPHA.-PROPYL-, (.ALPHA.R,5.ALPHA.,7.ALPHA.)
Common Name English
7,8-DIHYDRO-7.ALPHA.-(1-(R)-HYDROXY-1-METHYLBUTYL)-6,14-ENDOETHANOTETRAHYDROORIPAVINE
Systematic Name English
Classification Tree Code System Code
DEA NO. 9334
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
Code System Code Type Description
PUBCHEM
107765
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
PRIMARY
EVMPD
SUB195347
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
PRIMARY
WIKIPEDIA
DIHYDROETORPHINE
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID60905082
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
PRIMARY
CAS
14357-76-7
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
PRIMARY
SMS_ID
100000181584
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
PRIMARY
DRUG BANK
DB01450
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
PRIMARY
FDA UNII
QQX8S479YV
Created by admin on Sat Dec 16 10:31:24 GMT 2023 , Edited by admin on Sat Dec 16 10:31:24 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> DERIVATIVE
7,8-dihydro-7α-[1-(R)-hydroxy-1-methylbutyl]-6,14-endoethanotetrahydrooripavine (derivative of etorphine) as per INCB
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY