Vinrosidine sulfate

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C46H58N4O9.H2O4S
Molecular Weight	909.053
Optical Activity	UNSPECIFIED
Defined Stereocenters	10 / 10
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OS(O)(=O)=O.CC[C@@]1(O)C[C@@H]2C[N@](C1)CCC3=C(NC4=CC=CC=C34)[C@@](C2)(C(=O)OC)C5=C(OC)C=C6N(C)[C@@H]7[C@]8(CCN9CC=C[C@](CC)([C@@H]89)[C@@H](OC(C)=O)[C@]7(O)C(=O)OC)C6=C5

InChI

InChIKey=KDQAABAKXDWYSZ-SDCRJXSCSA-N

InChI=1S/C46H58N4O9.H2O4S/c1-8-42(54)23-28-24-45(40(52)57-6,36-30(15-19-49(25-28)26-42)29-13-10-11-14-33(29)47-36)32-21-31-34(22-35(32)56-5)48(4)38-44(31)17-20-50-18-12-16-43(9-2,37(44)50)39(59-27(3)51)46(38,55)41(53)58-7;1-5(2,3)4/h10-14,16,21-22,28,37-39,47,54-55H,8-9,15,17-20,23-26H2,1-7H3;(H2,1,2,3,4)/t28-,37-,38+,39+,42+,43+,44+,45-,46-;/m0./s1

HIDE SMILES / InChI

Molecular Formula	H2O4S
Molecular Weight	98.078
Charge	0
Count

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

Molecular Formula	C46H58N4O9
Molecular Weight	810.9741
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	9 / 9
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14070392

Vinrosidine (leurosidine) is a leurosine-like alkaloid originally isolated from Vinca rosea Linn. Vinrosidine exerts antitumor activity in animal models.

Originator

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
Tubulin 69 Target ID: CHEMBL2095182 Sources: http://www.genome.jp/dbget-bin/www_bget?dr:D06308	Inhibitor 8504

Conditions

Condition	Modality	Targets	Highest Phase	Product
Cancer 609 Sources: https://www.ncbi.nlm.nih.gov/pubmed/14070392	Primary		Preclinical	Unknown Approved Use Unknown

PubMed

Title	Date	PubMed
Total synthesis of vinblastine, vincristine, related natural products, and key structural analogues.	2009-04-08	19292450
The syntheses of 16a'-homo-leurosidine and 16a'-homo-vinblastine. Generation of atropisomers.	2001-08-10	11485450
Catharanthus alkaloids. XXXV. Isolation of leurosidine N'b-oxide from Catharanthus roseus.	1981-09-01	7320741
A reduction in energy-dependent amino acid transport by microtubular inhibitors in Ehrlich ascites tumor cells.	1975-10	1194361
STUDIES ON CATHARANTHUS ALKALOIDS. 3. SEPARATION OF VINCALEUKOBLASTINE, LEUROCRISTINE, LEUROSINE AND LEUROSIDINE BY THIN-LAYER CHROMATOGRAPHY.	1965-04	14334202
THE VINCA ALKALOIDS: A NEW CLASS OF ONCOLYTIC AGENTS.	1963-09	14070392

Patents

Sample Use Guides

In Vivo Use Guide

mice: 2-10 mg/kg/day

Route of Administration: Intraperitoneal

In Vitro Use Guide

Unknown

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:47:44 GMT 2025` Edited by `admin` on `Mon Mar 31 18:47:44 GMT 2025`
Record UNII	4944BQ2GBF
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

Vinrosidine sulfate

Official Name

English

(+)-LEUROSIDINE, SULFATE

Preferred Name

English

VINROSIDINE SULPHATE

Common Name

English

VINCALEUKOBLASTINE, (4'.ALPHA.)-,SULPHATE

Common Name

English

(+)-LEUROSIDINE, SULPHATE

Common Name

English

VINCALEUKOBLASTINE, (4'.ALPHA.)-,SULFATE

Common Name

English

VINROSIDINE SULFATE [USAN]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C932