BTT 3033 - ≥98%(HPLC), high purity , CAS No.1259028-99-3, Inhibitor of integrin α2β1

Item Number
B288291
Grouped product items
SKUSizeAvailabilityPrice Qty
B288291-5mg
5mg
In stock
$147.90
B288291-10mg
10mg
In stock
$246.90
B288291-25mg
25mg
In stock
$494.90
B288291-50mg
50mg
In stock
$791.90
B288291-100mg
100mg
In stock
$1,425.90

Selective inhibitor of integrin α2β1

Basic Description

Specifications & PurityMoligand™, ≥98%(HPLC)
Biochemical and Physiological MechanismsSelective inhibitor of integrinα2β1(EC50= 130 nM forα2β1binding to collagen I). Binds to theα2I domain. Exhibits selectivity forα2β1over integrinsα3β1,α4β1,α5β1andαv. Inhibits platelet aggregation to collagen I coated capillaries under flow. Also inhibits
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of integrin α2β1
Product Description

Product description

BTT-3033 is an orally active conformation-selective inhibitor of α2β1 (EC50: 130 nM) by binding to the α2I domain. BTT-3033 inhibits platelet binding to collagen Ⅰ and cell proliferation, and induces cell apoptosis. BTT-3033 can be used in the research of prostate cancer, inflammation and cardiovascular disease.


Associated Targets(Human)

ITGA2 Tbio Integrin alpha-2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ITGB1 Tclin Integrin beta-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ITGB1 Tclin Integrin alpha2/beta1 (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 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-[4-[[1-(4-fluorophenyl)pyrazol-4-yl]sulfonyl-methylamino]phenyl]-3-phenylurea
INCHI InChI=1S/C23H20FN5O3S/c1-28(33(31,32)22-15-25-29(16-22)21-11-7-17(24)8-12-21)20-13-9-19(10-14-20)27-23(30)26-18-5-3-2-4-6-18/h2-16H,1H3,(H2,26,27,30)
InChi Key NSLIQOPYDUKWTA-UHFFFAOYSA-N
Canonical SMILES CN(C1=CC=C(C=C1)NC(=O)NC2=CC=CC=C2)S(=O)(=O)C3=CN(N=C3)C4=CC=C(C=C4)F
Isomeric SMILES CN(C1=CC=C(C=C1)NC(=O)NC2=CC=CC=C2)S(=O)(=O)C3=CN(N=C3)C4=CC=C(C=C4)F
PubChem CID 49841251
Molecular Weight 465.5

Certificates

Certificate of Analysis(COA)

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10 results found

Lot NumberCertificate TypeDateItem
F23141009Certificate of AnalysisMay 30, 2023 B288291
F23141010Certificate of AnalysisMay 30, 2023 B288291
F23141024Certificate of AnalysisMay 30, 2023 B288291
F23141026Certificate of AnalysisMay 30, 2023 B288291
F23141085Certificate of AnalysisMay 30, 2023 B288291
F23141119Certificate of AnalysisMay 30, 2023 B288291
F2314885Certificate of AnalysisMay 30, 2023 B288291
F2314931Certificate of AnalysisMay 30, 2023 B288291
F2314987Certificate of AnalysisMay 30, 2023 B288291
F2314989Certificate of AnalysisMay 30, 2023 B288291

Chemical and Physical Properties

SolubilitySolvent:DMSO, Max Conc. mg/mL: 46.55, Max Conc. mM: 100

Related Documents

References

1. Nissinen L, Koivunen J, Käpylä J, Salmela M, Nieminen J, Jokinen J, Sipilä K, Pihlavisto M, Pentikäinen OT, Marjamäki A et al..  (2012)  Novel α2β1 integrin inhibitors reveal that integrin binding to collagen under shear stress conditions does not require receptor preactivation..  J Biol Chem,  287  (53): (44694-702).  [PMID:23132859] [10.1021/op500134e]

Solution Calculators