HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
Huagongshe Open Program:[email protected]AI access: llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.7.8
  1. Home
  2. /Compound

Neosar

HCID 89585
NotesReactions
Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
22068-88-8
Standard SMILES
COP(=S)(OC)SS(=O)(=O)c1ccccc1
InChIKey
ZVBGXSLDEJEETH-UHFFFAOYSA-N
Molecular formula
C8H11O4PS3
Average molar mass
298.3 g/mol
Monoisotopic mass
297.95570935

Overview

See also: Cyclophosphamide (broader).

Names & identifiers

Preferred name
Neosar
IUPAC
benzenesulfonylsulfanyl-dimethoxy-sulfanylidene-λ5-phosphane

Names & synonyms

Benzenethiosulphonic acid, anhydrosulphide with O,O-dimethyl hydrogen dithiophosphateDTXSID6017655822068-88-8RefChem:199757DTXCID8099049244-758-2NeosarSCHEMBL11509478EINECS 244-758-2NS00049188

Database identifiers

CAS
22068-88-8
PubChem CID
89585
DTXSID
DTXSID60176558
EC Number
244-758-2
Nikkaji
J285.425B

Properties

Computed structural properties

XLogP
2.8
Topological polar surface area
118 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
6
Rotatable bonds
5
Heavy atoms
16
Formal charge
0
Complexity
348

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 5 items

Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-CELLS or by inhibiting the activation of HELPER CELLS. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of INTERLEUKINS and other CYTOKINES are emerging.

Chemical agents that increase the rate of genetic mutation by interfering with the function of nucleic acids. A clastogen is a specific mutagen that causes breaks in chromosomes.

Drugs that are used to treat RHEUMATOID ARTHRITIS.

A class of drugs that differs from other alkylating agents used clinically in that they are monofunctional and thus unable to cross-link cellular macromolecules. Among their common properties are a requirement for metabolic activation to intermediates with antitumor efficacy and the presence in their chemical structures of N-methyl groups, that after metabolism, can covalently modify cellular DNA. The precise mechanisms by which each of these drugs acts to kill tumor cells are not completely understood. (From AMA, Drug Evaluations Annual, 1994, p2026)

Agents that destroy bone marrow activity. They are used to prepare patients for BONE MARROW TRANSPLANTATION or STEM CELL TRANSPLANTATION.

Related reactions

0 records
New reaction record

No reaction records under the current filter.

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes