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749886-87-1

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749886-87-1 Usage

Description

4-METHYL-N1-(3-PHENYLPROPYL)BENZENE-1,2-DIAMINE, also known as JSH-23, is a cell-permeable diamino compound that selectively blocks nuclear translocation of NF-κB p65 and its transcription activity. It has an IC50 of 7.1 μM in a NF-κB reporter assay using RAW 264.7 cells and does not affect IκB degradation. JSH-23 has been shown to suppress DNA-binding of NF-κB and downregulate LPS-induced gene expression and apoptotic chromatin condensation.

Uses

Used in Pharmaceutical Industry:
4-METHYL-N1-(3-PHENYLPROPYL)BENZENE-1,2-DIAMINE is used as a nuclear factor κB (NF-κB) p65 inhibitor for its ability to selectively block nuclear translocation of NF-κB p65 and suppress its transcription activity. This makes it a potential candidate for the development of drugs targeting inflammatory and immune response pathways.
Used in Research Applications:
4-METHYL-N1-(3-PHENYLPROPYL)BENZENE-1,2-DIAMINE is used as a research tool for studying the role of NF-κB in various cellular processes, including inflammation, immune response, and cell survival. Its ability to selectively block NF-κB p65 translocation and suppress its transcription activity makes it a valuable compound for investigating the molecular mechanisms underlying these processes.

Biological Activity

jsh-23 is an inhibitor of nf-κb transcriptional activity with ic50 value of 7.1μm [1].jsh-23 is developed to inhibit nf-κb transcriptional activity in lps-stimulated macrophages raw 264.7. it shows a dose-dependent inhibition. this effect is not due to its cytotoxicity. in the same condition, jsh-23 is found to significantly decrease the lps-induced dna binding activity of nf-κb while decrease nuclear amount of nf-κb p65. jsh-23 plays these roles without affecting iκb degradation. in addition, jsh-23 also shows inhibition effects on the expression of the pro-inflammatory transcripts and enzymes, including il-6, il-1β, cox-2 and tnf-α. furthermore, jsh-23 inhibits lps-induced apoptotic chromatin condensation [1].

Biochem/physiol Actions

Primary TargetBlocks nuclear translocation of NF-κB p65 and its transcription activity

references

[1] shin hm, kim mh, kim bh, jung sh, kim ys, park hj, hong jt, min kr, kim y. inhibitory action of novel aromatic diamine compound on lipopolysaccharide-induced nuclear translocation of nf-kappab without affecting ikappab degradation. febs lett. 2004 jul 30;571(1-3):50-4.

Check Digit Verification of cas no

The CAS Registry Mumber 749886-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,9,8,8 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 749886-87:
(8*7)+(7*4)+(6*9)+(5*8)+(4*8)+(3*6)+(2*8)+(1*7)=251
251 % 10 = 1
So 749886-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H20N2/c1-13-9-10-16(15(17)12-13)18-11-5-8-14-6-3-2-4-7-14/h2-4,6-7,9-10,12,18H,5,8,11,17H2,1H3

749886-87-1 Well-known Company Product Price

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  • Sigma

  • (J4455)  JSH-23  ≥98% (HPLC), solid

  • 749886-87-1

  • J4455-5MG

  • 1,494.09CNY

  • Detail
  • Sigma

  • (J4455)  JSH-23  ≥98% (HPLC), solid

  • 749886-87-1

  • J4455-25MG

  • 6,019.65CNY

  • Detail

749886-87-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1-N-(3-phenylpropyl)benzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names IN1201

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:749886-87-1 SDS

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