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PLX647

CAS No.
873786-09-5
Chemical Name:
PLX647
Synonyms
PLC647;PLX647;CS-1696;PLX 647;PLX-647;[5-[(1H-Pyrrolo[2,3-b]pyridin-3-yl)methyl]pyridin-2-yl](4-trifluoromethylbenzyl)amine;5-(1H-Pyrrolo[2,3-b]pyridin-3-ylmethyl)-N-[[4-(trifluoromethyl)phenyl]methyl]-2-pyridinamine;2-Pyridinamine, 5-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-N-[[4-(trifluoromethyl)phenyl]methyl]-
CBNumber:
CB72667277
Molecular Formula:
C21H17F3N4
Molecular Weight:
382.38
MDL Number:
MFCD28100808
MOL File:
873786-09-5.mol
MSDS File:
SDS
Last updated:2023-07-12 16:57:28

PLX647 Properties

Density 1.358±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO: soluble20mg/mL, clear
form powder
pka 13.73±0.40(Predicted)
color white to beige

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319-H315-H335
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  36/37/39
WGK Germany  3
NFPA 704
0
2 0

PLX647 price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 18012 PLX647 ≥95% 873786-09-5 5mg $97 2024-03-01 Buy
Cayman Chemical 18012 PLX647 ≥95% 873786-09-5 10mg $184 2024-03-01 Buy
Cayman Chemical 18012 PLX647 ≥95% 873786-09-5 25mg $433 2024-03-01 Buy
Cayman Chemical 18012 PLX647 ≥95% 873786-09-5 50mg $768 2024-03-01 Buy
TRC P635003 PLX647 873786-09-5 10mg $100 2021-12-16 Buy
Product number Packaging Price Buy
18012 5mg $97 Buy
18012 10mg $184 Buy
18012 25mg $433 Buy
18012 50mg $768 Buy
P635003 10mg $100 Buy

PLX647 Chemical Properties,Uses,Production

Description

PLX647 is a dual inhibitor of the receptor tyrosine kinases FMS and KIT (IC50s = 28 and 16 nM, respectively). It is selective for FMS and KIT but does inhibit FLT3 and KDR (IC50s = 91 and 130 nM, respectively) in a panel of 400 kinases at a concentration of 1 μM. PLX647 inhibits proliferation of Ba/F3 cells expressing constitutively active FMS or KIT (IC50s = 92 and 180 nM, respectively) as well as ligand-dependent growth of M-NFS-60 and M-07e cells that express endogenous FMS and KIT, respectively (IC50s = 380 and 230 nM, respectively). It has no effect on HEK293T or HepG2 cells that lack FMS and KIT (IC50 = >50 μM) or Ba/F3 cells overexpressing KDR (IC50 = >5 μM). PLX647 also inhibits differentiation of human osteoclast precursor cells (IC50 = 170 nM). In vivo, PLX647 (40 mg/kg) reduces TNF-α and IL-6 release in a rat model of LPS-induced cytokine release. It reduces mast cell degranulation in a mouse model of passive cutaneous anaphylaxis (PCA) and inhibits bone destruction and delays disease progression in a mouse model of collagen-induced arthritis (CIA). PLX647 also reverses bone osteolysis and allodynia in a syngeneic rat model of cancer-induced bone pain.

Uses

PLX647 is a novel tyrosine kinase (TK) inhibitor, which selectively targets c-Kit and c-Fms.

References

[1]. zhang c, ibrahim pn, zhang j, et al. design and pharmacology of a highly specific dual fms and kit kinase inhibitor. proc natl acad sci u s a, 2013, 110(14): 5689-5694.

PLX647 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 58)Suppliers
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ATK CHEMICAL COMPANY LIMITED
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Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131981 58

PLX647 Spectrum

873786-09-5(PLX647)Related Search:

PLX647 PLC647 5-(1H-Pyrrolo[2,3-b]pyridin-3-ylmethyl)-N-[[4-(trifluoromethyl)phenyl]methyl]-2-pyridinamine [5-[(1H-Pyrrolo[2,3-b]pyridin-3-yl)methyl]pyridin-2-yl](4-trifluoromethylbenzyl)amine 2-Pyridinamine, 5-(1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-N-[[4-(trifluoromethyl)phenyl]methyl]- PLX 647;PLX-647 CS-1696 873786-09-5 C21H17F3N4 Inhibitors