N-Acetyl-L-farnesylcysteine

Modify Date: 2024-01-02 10:51:23

N-Acetyl-L-farnesylcysteine Structure
N-Acetyl-L-farnesylcysteine structure
Common Name N-Acetyl-L-farnesylcysteine
CAS Number 135304-07-3 Molecular Weight 367.546
Density 1.0±0.1 g/cm3 Boiling Point 566.1±50.0 °C at 760 mmHg
Molecular Formula C20H33NO3S Melting Point N/A
MSDS N/A Flash Point 296.1±30.1 °C

 Use of N-Acetyl-L-farnesylcysteine


Arazine (N-Acetyl-S-farnesyl-L-cysteine) is a cell-permeable modulator of G protein and G-protein coupled receptor signaling. Arazine can be a a substrate for isoprenylcysteine methyltransferase by competing with prenylated G protein or its receptors site[1].

 Names

Name Ac-Cys(farnesyl)-OH
Synonym More Synonyms

 N-Acetyl-L-farnesylcysteine Biological Activity

Description Arazine (N-Acetyl-S-farnesyl-L-cysteine) is a cell-permeable modulator of G protein and G-protein coupled receptor signaling. Arazine can be a a substrate for isoprenylcysteine methyltransferase by competing with prenylated G protein or its receptors site[1].
Related Catalog
In Vitro Arazine (2 hours) inhibits ATPγS induced CXCL1, CXCL8 and CCL2 production as a dose-dependent manner in HMEC-1 cell[1]. Arazine (10–100 μM;8 hours) significantly affects the HMEC-1 cell viability as measured by trypan blue exclusion in HMEC-1 cell[1].
In Vivo Arazine (AFC) (2,000 μg/20 μl; applied on ear) produces a dose-dependent inhibition of the TPA-induced edema, with the maximal reduction of edema approaching 73%, with a 50% effective dose (ED50) of 55±12 μg/20 μl[1]. Animal Model: TPA-induced ear acute inflammation in mouse[1] Dosage: 2000 μg/20 μl Administration: 2000 μg/20 μl; Applied on ear Result: Inhibited ear edema, as measured by ear weight.
References

[1]. Gordon JS, et al. Topical N-acetyl-S-farnesyl-L-cysteine inhibits mouse skin inflammation, and unlike dexamethasone, its effects are restricted to the application site.J Invest Dermatol. 2008 Mar;128(3):643-54. Epub 2007 Sep 20.

[2]. Adhami K, et al. N-acetyl-S-farnesyl-l-cysteine suppresses chemokine production by human dermal microvascular endothelial cells.Exp Dermatol. 2012 Sep;21(9):700-5.

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 566.1±50.0 °C at 760 mmHg
Molecular Formula C20H33NO3S
Molecular Weight 367.546
Flash Point 296.1±30.1 °C
Exact Mass 367.218109
PSA 91.70000
LogP 5.86
Vapour Pressure 0.0±3.3 mmHg at 25°C
Index of Refraction 1.520
Storage condition -15°C

 Safety Information

HS Code 2930909090

 Customs

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Synonyms

L-Cysteine, N-acetyl-S-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl]-
N-Acetyl-S-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl]-L-cysteine
N-Acetylfarnesylcysteine
N-acetyl-S-farnesyl-L-Cysteine
N-acetyl-S-farnesylcysteine
Arazine
N-Acetyl-S-trans,trans-farnesyl-L-cysteine
N-AFC
afc
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Price: ¥3700/5 mg (27.2 mM * 500  μL in Methyl Acetate)

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