Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C18H19N5O3S.ClH |
Molecular Weight | 421.901 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.COC(=O)NC1=NC2=C(N1)C=C(SC3=CC=C(NC(=O)[C@H](C)N)C=C3)C=C2
InChI
InChIKey=JUMSCXLBFWHCRA-PPHPATTJSA-N
InChI=1S/C18H19N5O3S.ClH/c1-10(19)16(24)20-11-3-5-12(6-4-11)27-13-7-8-14-15(9-13)22-17(21-14)23-18(25)26-2;/h3-10H,19H2,1-2H3,(H,20,24)(H2,21,22,23,25);1H/t10-;/m0./s1
Molecular Formula | ClH |
Molecular Weight | 36.461 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C18H19N5O3S |
Molecular Weight | 385.44 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Denibulin is a novel antineoplastic agent. Denibulin selectively targets and reversibly binds to the colchicine-binding site on tubulin and inhibits microtubule assembly. This results in the disruption of the cytoskeleton of tumor endothelial cells, ultimately leading to cell cycle arrest, blockage of cell division and apoptosis. This causes inadequate blood flow to the tumor and eventually leads to a decrease in tumor cell proliferation. Denibulin hydrochloride had been in phase I clinical trials for the treatment of solid tumours. It was generally well tolerated and showed decrease in tumor vascular parameters. However, no recent development has been reported.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21305290
Escalating doses 4.0-225 mg/m(2) administered at 3-week intervals
Route of Administration:
Intravenous
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:56:27 GMT 2023
by
admin
on
Fri Dec 15 15:56:27 GMT 2023
|
Record UNII |
0U575HR16Q
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C67421
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
300000044539
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY | |||
|
DTXSID20228587
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY | |||
|
779356-64-8
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY | |||
|
CHEMBL2111088
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY | |||
|
RR-90
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY | |||
|
DBSALT002606
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY | |||
|
C72736
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY | |||
|
11661757
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY | |||
|
0U575HR16Q
Created by
admin on Fri Dec 15 15:56:27 GMT 2023 , Edited by admin on Fri Dec 15 15:56:27 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |