RAMELTEON

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C16H21NO2
Molecular Weight	259.3434
Optical Activity	( - )
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of RAMELTEON

Structure Search

SMILES

CCC(=O)NCC[C@@H]1CCC2=CC=C3OCCC3=C12

InChI

InChIKey=YLXDSYKOBKBWJQ-LBPRGKRZSA-N

InChI=1S/C16H21NO2/c1-2-15(18)17-9-7-12-4-3-11-5-6-14-13(16(11)12)8-10-19-14/h5-6,12H,2-4,7-10H2,1H3,(H,17,18)/t12-/m0/s1

HIDE SMILES / InChI

Approval Year

Name

Type

Language

RAMELTEON

Official Name

English

RAMELTEON [JAN]

Common Name

English

RAMELTEON [VANDF]

Common Name

English

ROZEREM

Brand Name

English

TAK375

Code

English

(-)-N-(2-(((8S)-1,6,7,8-TETRAHYDRO-2H-INDENO(5,4-.BETA.)FURAN-8-YL)ETHYL)PROPANAMIDE

Common Name

English

RAMELTEON [HSDB]

Common Name

English

RAMELTEON [MART.]

Common Name

English

RAMELTEON [ORANGE BOOK]

Common Name

English

RAMELTEON [USAN]

Common Name

English

TAK-375

Code

English

Ramelteon [WHO-DD]

Common Name

English

RAMELTEON [MI]

Common Name

English

PROPANAMIDE, N-(2-((8S)-1,6,7,8-TETRAHYDRO-2H-INDENO(5,4-.BETA.)FURAN-8-YL)ETHYL)-

Common Name

English

ramelteon [INN]

Common Name

English

Classification Tree Code System Code

WHO-ATC

N05CH02

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

LIVERTOX

NBK548437

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

NDF-RT

N0000000250

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

WHO-VATC

QN05CH02

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

NDF-RT

N0000175743

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

NCI_THESAURUS

C47795

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

Code System Code Type Description

NCI_THESAURUS

C66504

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

SMS_ID

100000085617

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

LACTMED

Ramelteon

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

WIKIPEDIA

RAMELTEON

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

FDA UNII

901AS54I69

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

CAS

196597-26-9

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

USAN

PP-50

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

RXCUI

596205

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

RxNorm

HSDB

7787

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

ChEMBL

CHEMBL1218

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

DRUG CENTRAL

2355

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

EVMPD

SUB21315

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

MERCK INDEX

m9489

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

Merck Index

DAILYMED

901AS54I69

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

INN

8447

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

EPA CompTox

DTXSID6045951

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

MESH

C495910

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

PUBCHEM

208902

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

IUPHAR

1356

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

DRUG BANK

DB00980

Created by admin on Fri Dec 15 16:00:48 UTC 2023 , Edited by admin on Fri Dec 15 16:00:48 UTC 2023

PRIMARY

ACTIVE MOIETY


					901AS54I69

RAMELTEON

METABOLITE (PARENT)


					7JTE6E6XVF

(S)-RAMELTEON M II GLUCURONIDE CONJUGATE

METABOLITE (PARENT)


					R2DS4VMX4K

(S)-RAMELTEON M IV GLUCURONIDE CONJUGATE

METABOLITE (PARENT)


					M5W3B96WDP

(S)-RAMELTEON GLUCURONIDE CONJUGATE

METABOLITE ACTIVE (PARENT)


					P4VWQ9NHF2

(S)-2-HYDROXY-RAMELTEON

METABOLITE ACTIVE (PARENT)


					EYC868P4VY

2-HYDROXY-RAMELTEON

METABOLITE INACTIVE (PARENT)


					ZQ45Z2DD7W

DES(1-OXOPROPYL)-(2-HYDROXY-1-OXOPROPYL)-6-OXO-RAMELTEON

METABOLITE INACTIVE (PARENT)


					R509OY341Z

6-OXO-RAMELTEON

METABOLITE INACTIVE (PARENT)


					TA6XQS4TL6

2,3-DIHYDRO-5-HYDROXY-3-(2-((1-OXOPROPYL)AMINO)ETHYL)-1H-INDENE-4-ACETIC ACID, (3S)-