Surfen dihydrochloride - ≥98%(HPLC), high purity , CAS No.5424-37-3

  • ≥98%(HPLC)
Item Number
S286940
Grouped product items
SKUSizeAvailabilityPrice Qty
S286940-1mg
1mg
In stock
$24.90
S286940-5mg
5mg
In stock
$102.90
S286940-10mg
10mg
In stock
$162.90

Heparin sulfate antagonist

Basic Description

SynonymsAKOS030527176 | EINECS 226-566-0 | Tox21_110013 | 1,3-Bis(4-amino-2-methyl-6-quinolyl)urea dihydrochloride | DTXSID1045083 | NSC 12155 | MFCD00051734 | Surfen dihydrochloride | Aminoquincarbamide dihydrochloride | Luminor Yellow Green 490RT | P2YT71SUIU |
Specifications & Purity≥98%(HPLC)
Biochemical and Physiological MechanismsHeparan sulfate antagonist. Inhibits heparan sulfate-mediated cell attachmentin vitro. Maintains hESCs in a pluripotent state by reversible inhibition of glycan-growth factor interactions.
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

Product Describtion:

Surfen dihydrochloride is a potent HS (heparan sulfate) antagonist. Surfen binds to glycosaminoglycans. Surfen neutralizes the anticoagulant activity of both unfractionated and low molecular weight heparins. Surfen affects sulfation of heparin and inhibits degradation by heparin lyases. Surfen inhibits FGF2 binding and signaling. Surfen inhibits cell attachment, and virus infection.

Associated Targets(Human)

KMT2A Tchem Histone-lysine N-methyltransferase 2A (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 1,3-bis(4-amino-2-methylquinolin-6-yl)urea;dihydrochloride
INCHI InChI=1S/C21H20N6O.2ClH/c1-11-7-17(22)15-9-13(3-5-19(15)24-11)26-21(28)27-14-4-6-20-16(10-14)18(23)8-12(2)25-20;;/h3-10H,1-2H3,(H2,22,24)(H2,23,25)(H2,26,27,28);2*1H
InChi Key GKQYGRWQCWWSHN-UHFFFAOYSA-N
Canonical SMILES CC1=CC(=C2C=C(C=CC2=N1)NC(=O)NC3=CC4=C(C=C(N=C4C=C3)C)N)N.Cl.Cl
Isomeric SMILES CC1=CC(=C2C=C(C=CC2=N1)NC(=O)NC3=CC4=C(C=C(N=C4C=C3)C)N)N.Cl.Cl
PubChem CID 79472
Molecular Weight 445.35

Certificates

Certificate of Analysis(COA)

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6 results found

Lot NumberCertificate TypeDateItem
G23201112Certificate of AnalysisJun 27, 2023 S286940
G23201113Certificate of AnalysisJun 27, 2023 S286940
G23201116Certificate of AnalysisJun 27, 2023 S286940
G23201118Certificate of AnalysisJun 27, 2023 S286940
G23201120Certificate of AnalysisJun 27, 2023 S286940
G23201125Certificate of AnalysisJun 27, 2023 S286940

Chemical and Physical Properties

SolubilitySolvent:water, Max Conc. mg/mL: 8.91, Max Conc. mM: 20; Solvent:DMSO, Max Conc. mg/mL: 8.91, Max Conc. mM: 20
Sensitivitylight sensitive;Moisture sensitive.

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Solution Calculators