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Merck

SML0334

Sigma-Aldrich

DMPQ dihydrochloride

≥98% (HPLC)

Synonym(e):

5,7-Dimethoxy-3-(4-pyridinyl)quinoline dihydrochloride

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About This Item

Empirische Formel (Hill-System):
C16H14N2O2 · 2HCl
CAS-Nummer:
Molekulargewicht:
339.22
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
NACRES:
NA.77

Qualitätsniveau

Assay

≥98% (HPLC)

Form

powder

Lagerbedingungen

desiccated

Farbe

white to beige

Löslichkeit

H2O: >10 mg/mL

Lagertemp.

room temp

SMILES String

Cl.Cl.COc1cc(OC)c2cc(cnc2c1)-c3ccncc3

InChI

1S/C16H14N2O2.2ClH/c1-19-13-8-15-14(16(9-13)20-2)7-12(10-18-15)11-3-5-17-6-4-11;;/h3-10H,1-2H3;2*1H

InChIKey

YBBAOKYVJCNJIV-UHFFFAOYSA-N

Biochem./physiol. Wirkung

DMPQ is a potent selective inhibitor of human vascular beta-type platelet derived growth factor receptor tyrosine kinase (PDGFR?) with IC50 = 80 nM. It is > 100-fold selective over EGFR, erbB2, p56, protein kinase A and protein kinase C.

Leistungsmerkmale und Vorteile

This compound is a featured product for Kinase Phosphatase Biology research. Click here to discover more featured Kinase Phosphatase Biology products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the PDGFR page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

Wafa Altalhi et al.
Biomaterials, 119, 23-32 (2016-12-19)
Cell-based tissue engineering is a potential treatment alternative for organ replacement. However, the lack of a robust vasculature, especially in the context of diseases such as diabetes, is a major hindrance to its success. Despite extensive research on the effects
Akshaya Srinivasan et al.
Biomaterials, 167, 153-167 (2018-03-24)
Mesenchymal stem cells (MSCs) have been isolated from various mesodermal and ectodermal tissues. While the phenotypic and functional heterogeneity of MSCs stemming from their developmental origins has been acknowledged, the genetic and environmental factors underpinning these differences are not well-understood.

Artikel

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