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

Pyrimethamine; sulfadoxine

HCID 65404
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
37338-39-9
Standard SMILES
CCc1nc(N)nc(N)c1-c1ccc(Cl)cc1.COc1ncnc(NS(=O)(=O)c2ccc(N)cc2)c1OC
InChIKey
LUBUTTBEBGYNJN-UHFFFAOYSA-N
Molecular formula
C24H27ClN8O4S
Average molar mass
559 g/mol
Monoisotopic mass
558.1564502

Overview

Pyrimethamine-Sulfadoxine is a combination product containing pyrimethamine and sulfadoxine. Pyrimethamine is a competitive inhibitor of dihydrofolate reductase (DHFR). DHFR is a key enzyme in the redox cycle for production of tetrahydrofolate, a cofactor that is required for the synthesis of DNA and proteins. Sulfadoxine competitively antagonizes paraaminobenzoic acid (PABA), resulting in disruption of folic acid synthesis and ultimately DNA synthesis. Sulfadoxine acts synergistically with pyrimethamine. (NCI04)

Names & identifiers

Preferred name
Pyrimethamine; sulfadoxine
IUPAC
4-amino-N-(5,6-dimethoxypyrimidin-4-yl)benzenesulfonamide;5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine
English name
sulfadoxine-pyrimethamine
Molecular formula
C12H14N4O4S.C12H13ClN4
Molecular weight
559.048

Names & synonyms

FansidarPyrimethamine-sulfadoxineNSC618943RefChem:58925Pyrimethamine SulfadoxinePyrimethamine; sulfadoxinesulfadoxine & pyrimethaminesulfadoxine + pyrimethamine37338-39-9fanasil - pyrimethamineSuldoxsulfadoxine-pyrimethamine
Show more names
Ro-6-4753Combination with sulfadoxine
4-amino-N-(5,6-dimethoxypyrimidin-4-yl)benzenesulfonamide;5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diaminesulphadoxine-pyrimethamineFansidar (TN)Sulphadoxyne-pyrimethaminesulfadoxine / pyrimethaminePyrimethamine / sulfadoxineSulphadoxine / pyrimethaminePyrimethamine combination with sulfadoxine

Database identifiers

CAS
37338-39-9
PubChem CID
65404
DTXSID
DTXSID70190780
ChEMBL
CHEMBL3137690

Properties

Computed structural properties

Topological polar surface area
203 Ų
Hydrogen bond donors
4
Hydrogen bond acceptors
12
Rotatable bonds
7
Heavy atoms
38
Formal charge
0
Complexity
662

Experimental & physicochemical properties

Human Drugs · 3 items

Breast Feeding; Lactation; Anti-Infective Agents; Antiparasitic Agents; Antimalarials; Antiprotozoal Agents; Sulfonamides

FDA approved drugs -> Active ingredient

Antimalarial medicines > Medicines for chemoprevention

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Toxicology

Effects During Pregnancy and Lactation◉ Summary of Use during Lactation

Chemistry & industry

Pharmacology

ATC CodeP01BD51

Suppliers2 total

Bhumit Pharma Pvt. Ltd.—
CHEMICAL LAND21[email protected]

Related reactions

0 records
New reaction record

No reaction records under the current filter.

Compound notes

Loading…

On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes