RANOLAZINE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C24H33N3O4
Molecular Weight	427.5365
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of RANOLAZINE

Structure Search

SMILES

COC1=C(OCC(O)CN2CCN(CC(=O)NC3=C(C)C=CC=C3C)CC2)C=CC=C1

InChI

InChIKey=XKLMZUWKNUAPSZ-UHFFFAOYSA-N

InChI=1S/C24H33N3O4/c1-18-7-6-8-19(2)24(18)25-23(29)16-27-13-11-26(12-14-27)15-20(28)17-31-22-10-5-4-9-21(22)30-3/h4-10,20,28H,11-17H2,1-3H3,(H,25,29)

HIDE SMILES / InChI

Approval Year

Name

Type

Language

RANOLAZINE

Official Name

English

RANOLAZINE [USP-RS]

Common Name

English

CVT-303

Code

English

RAN D

Common Name

English

RAN4

Common Name

English

RANEXA

Brand Name

English

(±)-N-(2,6-DIMETHYLPHENYL)-4-(2-HYDROXY-3-(2-METHOXYPHENOXY)PROPYL)-1-PIPERAZINEACETAMIDE

Systematic Name

English

1-PIPERAZINEACETAMIDE, N-(2,6-DIMETHYLPHENYL)-4-(2-HYDROXY-3-(2-METHOXYPHENOXY)PROPYL)-, (±)-

Common Name

English

Ranolazine [WHO-DD]

Common Name

English

RANOLAZINE [EMA EPAR]

Common Name

English

NSC-759100

Code

English

N-(2,6-DIMETHYLPHENYL)-2-(4-((2RS)-2-HYDROXY-3-(2-METHOXYPHENOXY)PROPYL)PIPERAZIN-1-YL)ACETAMIDE

Systematic Name

English

1-PIPERAZINEACETAMIDE, N-(2,6-DIMETHYLPHENYL)-4-(2-HYDROXY-3-(2-METHOXYPHENOXY)PROPYL)-

Systematic Name

English

ASPRUZYO

Brand Name

English

RS-43285-003

Code

English

RANOLAZINE [VANDF]

Common Name

English

RANOLAZINE [USAN]

Common Name

English

RANOLAZINE [ORANGE BOOK]

Common Name

English

ranolazine [INN]

Common Name

English

RANOLAZINE [MART.]

Common Name

English

RANOLAZINE [MI]

Common Name

English

Classification Tree Code System Code

LIVERTOX

NBK547932

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

WHO-VATC

QC01EB18

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

EMA ASSESSMENT REPORTS

RANEXA (AUTHORIZED: ANGINA PECTORIS)

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

NDF-RT

N0000175427

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

WHO-ATC

C01EB18

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

NCI_THESAURUS

C93038

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

NCI_THESAURUS

C78322

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

Code System Code Type Description

ChEMBL

CHEMBL1404

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

RXCUI

35829

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

RxNorm

CAS

95635-55-5

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

USAN

QQ-33

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

SMS_ID

100000089164

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

FDA UNII

A6IEZ5M406

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

PUBCHEM

56959

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

INN

5946

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

DRUG CENTRAL

2359

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

EVMPD

SUB10259MIG

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

NSC

759100

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

RS_ITEM_NUM

1598744

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

NDF-RT

N0000182137

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

Cytochrome P450 2D6 Inhibitors [MoA]

MERCK INDEX

m9499

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

Merck Index

IUPHAR

7291

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

HSDB

7924

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

MESH

C055512

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

NDF-RT

N0000185503

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

P-Glycoprotein Inhibitors [MoA]

DAILYMED

A6IEZ5M406

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

NDF-RT

N0000187061

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

Organic Cation Transporter 2 Inhibitors [MoA]

CAS

142387-99-3

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

SUPERSEDED

NCI_THESAURUS

C66507

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

EPA CompTox

DTXSID3045196

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

CHEBI

87681

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

NDF-RT

N0000190114

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

Cytochrome P450 3A Inhibitors [MoA]

WIKIPEDIA

RANOLAZINE

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

DRUG BANK

DB00243

Created by admin on Fri Dec 15 16:29:48 UTC 2023 , Edited by admin on Fri Dec 15 16:29:48 UTC 2023

PRIMARY

ACTIVE MOIETY


					A6IEZ5M406

METABOLITE (PARENT)


					94VR6V6NA3

CVT-2513

METABOLITE (PARENT)


					EIU92KG3IM

2',6'-GLYCOLOXYLIDIDE

METABOLITE (PARENT)


					L58PM3303I

CVT-3248

METABOLITE (PARENT)


					J7KKT84Z1Z

N-(2,6-DIMETHYLPHENYL)OXAMIC ACID

METABOLITE (PARENT)


					495W7451VQ

METABOLITE (PARENT)


					ZV6358217Q

CVT-2551

METABOLITE (PARENT)


					39DGL7S53X

.BETA.-(2-METHOXYPHENOXY)LACTIC ACID

METABOLITE (PARENT)


					ZX4GQK5858

CVT-3369

METABOLITE (PARENT)


					NYS3I6283H

CVT-2738

METABOLITE (PARENT)


					UWX2BK4PFS

DES-O-METHYL-O-SULFATE-RANOLAZINE

METABOLITE (PARENT)


					04210SF62M

CVT-2512

SALT/SOLVATE (PARENT)


					F71253DJUN

RANOLAZINE HYDROCHLORIDE