NEOTAME

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C20H30N2O5
Molecular Weight	378.4626
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of NEOTAME

Structure Search

SMILES

COC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@H](CC(O)=O)NCCC(C)(C)C

InChI

InChIKey=HLIAVLHNDJUHFG-HOTGVXAUSA-N

InChI=1S/C20H30N2O5/c1-20(2,3)10-11-21-15(13-17(23)24)18(25)22-16(19(26)27-4)12-14-8-6-5-7-9-14/h5-9,15-16,21H,10-13H2,1-4H3,(H,22,25)(H,23,24)/t15-,16-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C20H30N2O5
Molecular Weight	378.4626
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 17:36:00 UTC 2023` Edited by `admin` on `Fri Dec 15 17:36:00 UTC 2023`
Record UNII	VJ597D52EX
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

NEOTAME

Official Name

English

NEOTAME [FHFI]

Common Name

English

N-(N-(3,3-DIMETHYLBUTYL)-L-.ALPHA.-ASPARTYL)-L-PHENYLALANINE 1-METHYL ESTER

Common Name

English

E 961

Code

English

NC-00723

Code

English

INS-961

Code

English

NEOTAME [USP-RS]

Common Name

English

INS NO.961

Code

English

NEOTAME [MI]

Common Name

English

NEOTAME [MART.]

Common Name

English

L-PHENYLALANINE, N-(N-(3,3-DIMETHYLBUTYL)-L-.ALPHA.-ASPARTYL)-1-METHYL ESTER

Common Name

English

NEOTAME [INCI]

Common Name

English

NEOTAME [II]

Common Name

English

MIRASEE 200

Common Name

English

NEOTAME [FCC]

Common Name

English

E-961

Code

English

Classification Tree Code System Code

CODEX ALIMENTARIUS (GSFA)

INS-961

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

JECFA EVALUATION

INS-961

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

NCI_THESAURUS

C283

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

CFR

21 CFR 172.829

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

Code System Code Type Description

EVMPD

SUB119863

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

WIKIPEDIA

NEOTAME

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

RS_ITEM_NUM

1460204

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

FDA UNII

VJ597D52EX

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

EPA CompTox

DTXSID50167950

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

SMS_ID

100000143306

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

DAILYMED

VJ597D52EX

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

MERCK INDEX

m7820

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

Merck Index

PUBCHEM

9810996

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

HSDB

7965

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

CAS

165450-17-9

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

NCI_THESAURUS

C81625

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

RXCUI

1367111

Created by admin on Fri Dec 15 17:36:00 UTC 2023 , Edited by admin on Fri Dec 15 17:36:00 UTC 2023

PRIMARY

RxNorm

Related Record Type Details


					5MI7P9AI4A

TASTE RECEPTOR TYPE 1 MEMBER 2

TARGET -> AGONIST

Amount: