TRIBENOSIDE

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NCATS

Details

Stereochemistry	EPIMERIC
Molecular Formula	C29H34O6
Molecular Weight	478.5767
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 5
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of TRIBENOSIDE

Structure Search

SMILES

[H][C@@]1(OC(OCC)[C@H](O)[C@H]1OCC2=CC=CC=C2)[C@@H](COCC3=CC=CC=C3)OCC4=CC=CC=C4

InChI

InChIKey=ULLNJSBQMBKOJH-VIVFLBMVSA-N

InChI=1S/C29H34O6/c1-2-32-29-26(30)28(34-20-24-16-10-5-11-17-24)27(35-29)25(33-19-23-14-8-4-9-15-23)21-31-18-22-12-6-3-7-13-22/h3-17,25-30H,2,18-21H2,1H3/t25-,26-,27-,28-,29?/m1/s1

HIDE SMILES / InChI

Molecular Formula	C29H34O6
Molecular Weight	478.5767
Charge	0
Count

Stereochemistry	EPIMERIC
Additional Stereochemistry	No
Defined Stereocenters	4 / 5
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:50:40 UTC 2023` Edited by `admin` on `Fri Dec 15 18:50:40 UTC 2023`
Record UNII	Z7N0Y673NU
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

TRIBENOSIDE

Official Name

English

TRIBENOSIDE [MART.]

Common Name

English

21401-BA

Code

English

tribenoside [INN]

Common Name

English

HEMOCURON

Brand Name

English

D-GLUCOFURANOSIDE, ETHYL 3,5,6-TRIS-O-(PHENYLMETHYL)-

Common Name

English

Tribenoside [WHO-DD]

Common Name

English

TRIBENOSIDE [EP MONOGRAPH]

Common Name

English

TRIBENOSIDE [JAN]

Common Name

English

TRIBENOSIDE [USAN]

Common Name

English

ETHYL 3,5,6-TRI-O-BENZYL-D-GLUCOFURANOSIDE

Common Name

English

TRIBENOSIDE [MI]

Common Name

English

Classification Tree Code System Code

WHO-VATC

QC05AX05

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

WHO-ATC

C05AX05

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

WHO-VATC

QC05CX01

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

WHO-ATC

C05CX01

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

NCI_THESAURUS

C123418

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

Code System Code Type Description

CAS

10310-32-4

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

ECHA (EC/EINECS)

233-687-2

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

DRUG BANK

DB13227

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

DRUG CENTRAL

2730

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

INN

2463

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

MERCK INDEX

m11039

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

Merck Index

EPA CompTox

DTXSID7023697

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

RXCUI

38557

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

RxNorm

FDA UNII

Z7N0Y673NU

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

SMS_ID

100000077513

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

MESH

C100302

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

NCI_THESAURUS

C152735

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

ChEMBL

CHEMBL3301681

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

PUBCHEM

196122

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

EVMPD

SUB11260MIG

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

WIKIPEDIA

TRIBENOSIDE

Created by admin on Fri Dec 15 18:50:41 UTC 2023 , Edited by admin on Fri Dec 15 18:50:41 UTC 2023

PRIMARY

Related Record Type Details


					TA269SD04T

IMPURITY -> PARENT

Comments:

impurity C: not more than twice the area of the corresponding peak in the chromatogram obtained with reference solution (a) (0.5 per cent); if the area of the peak due to impurity C in the chromatogram obtained with the test solution is greater than the area of the corresponding peak in the chromatogram obtained with reference solution (a) (0.25 per cent), dilute the test solution to obtain an area equal to or smaller than the area of the peak in the chromatogram obtained with reference solution (a); calculate the content of impurity C taking into account the dilution factor;

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP


					J63MA3RV3G

3,5,6-TRI-O-BENZYL-1,2-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOSE

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					UR9LBA3UTQ

.ALPHA.-D-GLUCOFURANOSE, 1,2-O-(1-METHYLETHYLIDENE)-3,5-BIS-O-(PHENYLMETHYL)-

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:


					2O6CNO27RJ

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:

Related Record Type Details


					Z7N0Y673NU

ACTIVE MOIETY