Mannosulfan
Appearance
From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Clinical data | |
---|---|
Other names | [(2R,3S,4S,5R)-3,4-dihydroxy-2,5,6-tris(methylsulfonyloxy)hexyl] methanesulfonate |
ATC code | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
Chemical and physical data | |
Formula | C10H22O14S4 |
Molar mass | 494.51 g·mol−1 |
3D model (JSmol) | |
| |
| |
(verify) |
Mannosulfan (INN) is an alkylating agent with the potential for the treatment of cancer. It is not approved by the United States FDA for cancer treatment. Research suggests it is less toxic than the alkyl sulfonate Busulfan.[1]
References
[edit]- ^ Jeswani G, Paul SD (2017). "Recent Advances in the Delivery of Chemotherapeutic Agents". Nano- and Microscale Drug Delivery Systems. pp. 281–98. doi:10.1016/B978-0-323-52727-9.00015-7. ISBN 978-0-323-52727-9.
External links
[edit]- Media related to Mannosulfan at Wikimedia Commons
By consumption |
| ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Primary alcohols (1°) |
| ||||||||||||||||
Secondary alcohols (2°) | |||||||||||||||||
Tertiary alcohols (3°) | |||||||||||||||||
Hydric alcohols |
| ||||||||||||||||
Amyl alcohols | |||||||||||||||||
Aromatic alcohols | |||||||||||||||||
Saturated fatty alcohols | |||||||||||||||||
Branched and unsaturated fatty alcohols | |||||||||||||||||
Sugar alcohols |
| ||||||||||||||||
Terpene alcohols |
| ||||||||||||||||
Dialcohols | |||||||||||||||||
Trialcohols | |||||||||||||||||
Sterols | |||||||||||||||||
Fluoroalcohols | |||||||||||||||||
Preparations | |||||||||||||||||
Reactions | |||||||||||||||||
This antineoplastic or immunomodulatory drug article is a stub. You can help Wikipedia by expanding it. |
Hidden categories: