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SML0837

FAK Inhibitor 14

≥95% (HPLC)

Synonym(s):

1,2,4,5-Benzene tetraamine tetrahydrochloride, 1,2,4,5-Benzenetetraamine 4HCl, 1,2,4,5-Benzenetetraamine tetrahydrochloride, Benzene-1,2,4,5-tetramine tetrahydrochloride, NSC 667249, Y15

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About This Item

Empirical Formula (Hill Notation):
C6H10N4 · 4HCl
CAS Number:
Molecular Weight:
284.01
UNSPSC Code:
12352200
EC Number:
224-822-6
NACRES:
NA.77
Assay:
≥95% (HPLC)
Form:
powder
Storage condition:
desiccated
Pricing and availability is not currently available.
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Quality Segment

assay

≥95% (HPLC)

form

powder

storage condition

desiccated

color

, faint purple to dark brown

solubility

H2O: 20 mg/mL, clear

storage temp.

room temp

SMILES string

[Cl-].[Cl-].[Cl-].[Cl-].Nc1c(cc(c(c1)N)N)N.[H+].[H+].[H+].[H+]

InChI

1S/C6H10N4.4ClH/c7-3-1-4(8)6(10)2-5(3)9;;;;/h1-2H,7-10H2;4*1H

InChI key

BZDGCIJWPWHAOF-UHFFFAOYSA-N

Application

FAK Inhibitor 14 has been used in the metastasis assay. It is also used to study its effect on bone morphogenetic protein 7 (BMP-7)-induced cell crawling and adhesion.

Biochem/physiol Actions

1,2,4,5-Benzenetetraamine tetrahydrochloride (FAK Inhibitor 14; Y15) is a cell-permeable, selective focal adhesion kinase (FAK) inhibitor.
1,2,4,5-Benzenetetraamine tetrahydrochloride (FAK Inhibitor 14; Y15) is a cell-permeable, selective focal adhesion kinase (FAK) inhibitor. Focal adhesion kinase (FAK) is essential in regulating integrin signaling pathways responsible for cell survival, cell proliferation and motility. Phosphorylation of FAK tyrosine 397 (Y397) forms a high affinity binding site for the SH2 domain of the Src family kinases and PI3 kinase. FAK is overexpressed in a number of human tumors. 1,2,4,5-Benzenetetraamine tetrahydrochloride (FAK Inhibitor 14, Y15) blocks phosphorylation of Y397-FAK, which results in neuroblastoma cell detachment and apoptosis.

Features and Benefits

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 Fak page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

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This Item
305065D5905S2876
description

≥95% (HPLC)

description

≥95%

description

tablet, 10 mg substrate per tablet

description

powder or crystals

form

powder

form

-

form

tablet

form

powder or crystals

assay

≥95% (HPLC)

assay

≥95.0% (AT), ≥95%

assay

-

assay

-

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

200

storage temp.

room temp

storage temp.

-

storage temp.

−20°C

storage temp.

room temp

solubility

H2O: 20 mg/mL, clear

solubility

-

solubility

water: 1 tablet/15 mL (may contain small insoluble particles)

solubility

water, high purity: 100 mg/ml

storage condition

desiccated

storage condition

-

storage condition

-

storage condition

-


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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