Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H24N2O8S2 |
| Molecular Weight | 364.436 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CS(=O)(=O)OCCNC[C@H](O)[C@H](O)CNCCOS(C)(=O)=O
InChI
InChIKey=BYZJBHCTZJGJFV-AOOOYVTPSA-N
InChI=1S/C10H24N2O8S2/c1-21(15,16)19-5-3-11-7-9(13)10(14)8-12-4-6-20-22(2,17)18/h9-14H,3-8H2,1-2H3/t9-,10+
| Molecular Formula | C10H24N2O8S2 |
| Molecular Weight | 364.436 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Ritrosulfan (also known as R-74 and Lycurim) is a sulfonate-based alkylation agent that might exert antineoplastic activity, acting to stop the development of a tumor. By alkylating DNA and producing crosslinks, ritrosulfan is thought to cause tumor cell cycle arrest. However, no alkylating activity could be demonstrated in the plasma of cancer patients, using intracavitary application of ritrosulfan. Other studies in the 1980’s have confirmed some immunodepressive properties of ritrosulfan in cancer patients, but no information is available on current development of ritrosulfan.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:33:27 GMT 2025
by
admin
on
Wed Apr 02 09:33:27 GMT 2025
|
| Record UNII |
YIY0662KX9
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C1590
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
100000080265
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
YIY0662KX9
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
C75294
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
3789
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
122402
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
C000288
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
4148-16-7
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
DTXSID801023469
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
142773
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
CHEMBL455711
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY | |||
|
SUB10344MIG
Created by
admin on Wed Apr 02 09:33:27 GMT 2025 , Edited by admin on Wed Apr 02 09:33:27 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |