Carfentanil

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NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C24H30N2O3
Molecular Weight	394.5066
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of Carfentanil

Structure Search

SMILES

CCC(=O)N(C1=CC=CC=C1)C2(CCN(CCC3=CC=CC=C3)CC2)C(=O)OC

InChI

InChIKey=YDSDEBIZUNNPOB-UHFFFAOYSA-N

InChI=1S/C24H30N2O3/c1-3-22(27)26(21-12-8-5-9-13-21)24(23(28)29-2)15-18-25(19-16-24)17-14-20-10-6-4-7-11-20/h4-13H,3,14-19H2,1-2H3

HIDE SMILES / InChI

Molecular Formula	C24H30N2O3
Molecular Weight	394.5066
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:10:30 UTC 2023` Edited by `admin` on `Fri Dec 15 16:10:30 UTC 2023`
Record UNII	LA9DTA2L8F
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

Carfentanil

Official Name

English

R 31833

Code

English

CARFENTANYL

Common Name

English

(4-CARBOMETHOXY FENTANYL)

Common Name

English

carfentanil [INN]

Common Name

English

4-PIPERIDINECARBOXYLIC ACID, 4-((1-OXOPROPYL)PHENYLAMINO)-1-(2-PHENYLETHYL)-, METHYL ESTER

Common Name

English

4-CARBOMETHOXYFENTANYL

Common Name

English

METHYL 1-PHENETHYL-4-(N-PHENYLPROPIONAMIDO)ISONIPECOTATE

Systematic Name

English

Classification Tree Code System Code

DEA NO.

9743

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

WIKIPEDIA

List_of_fentanyl_analogues

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

NCI_THESAURUS

C67413

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

Code System Code Type Description

EVMPD

SUB06626MIG

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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DRUG BANK

DB01535

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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WIKIPEDIA

CARFENTANIL

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

PRIMARY

Side effects of carfentanil are similar to those of fentanyl, which include itching, nausea and respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear. Carfentanil is classified as Schedule II under the Controlled Substances Act in the United States with a DEA ACSCN of 9743 and a 2016 annual aggregate manufacturing quota of 19 grams. In 2016, carfentanil was identified as an additive in heroin sold in Ohio, leading to a spike in the number of overdose cases.

SMS_ID

100000084592

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

PRIMARY

MESH

C017114

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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PUBCHEM

62156

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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FDA UNII

LA9DTA2L8F

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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NCI_THESAURUS

C80574

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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CHEBI

61084

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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ChEMBL

CHEMBL290429

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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INN

4430

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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EPA CompTox

DTXSID40208427

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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CAS

59708-52-0

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

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WEB RESOURCE

CARFENTANIL

Created by admin on Fri Dec 15 16:10:30 UTC 2023 , Edited by admin on Fri Dec 15 16:10:30 UTC 2023

PRIMARY

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METABOLITE ACTIVE -> PARENT

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Liver microsomes many CYP Enzymes catalyze reaction.

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METABOLITE ACTIVE -> PARENT

Comments:

More active than Carfentanil.

Interaction Type:

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METABOLITE ACTIVE -> PARENT

Comments:

Liver microsomes many CYP Enzymes catalyze reaction.

Interaction Type:

MAJOR

Amount:

Related Record Type Details


					LA9DTA2L8F

ACTIVE MOIETY

Amount: