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S-(N-Phenylbutylthiocarbamoyl)-L-cysteine

S-(N-Phenylbutylthiocarbamoyl)-L-cysteine

Product ID P2516
Cas No.
Purity ≥98%
Product Unit SizeCostQuantityStock
5 mg $142.80 In stock
10 mg $214.00 In stock
25 mg $465.30 In stock
100 mg $1,459.10 In stock
Bulk Quote

Quicklinks

  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Custom Order

Description

S-(N-Phenylbutylthiocarbamoyl)-L-cysteine (PBITC) is a conjugate of phenylbutylisothiocyanate and cysteine. Isothiocyanates are typically found in plants of the Brassicaceae family, including broccoli, cabbage, and radish. Isothiocyanates are best known for their antioxidative, anticancer chemotherapeutic, chemopreventive, anti-angiogenic, and antibiotic properties. In vitro, PBITC increases caspase 3 activity and cleavage of poly(ADP)-ribose polymerase (PARP), inducing caspase-mediated apoptosis. PBITC also inhibits development of pancreatic ductal dysplasias and adenocarcinomas and decreases occurrence of lung tumors in animal models. This compound decreases oxidation of carcinogen NNK and increases activity of NADPH:quinone oxidoreductase and glutathione-S-transferase in vitro and in vivo.

Product Info

Purity

≥98%

Formula

C14H20N2O2S2

Formula Wt.

312.45

Chemical Name

S-(N-Phenylbutylthiocarbamoyl)-L-cysteine

Synonym

Phenylbutylisothiocyanate-L-cysteine

Appearance

White to off white powder

Shipping and Storage

Store Temp

-20°C

Ship Temp

Ambient

Downloads

MSDS

P2516 MSDS PDF

Info Sheet

P2516 Info Sheet PDF

References

Son HY, Nishikawa A, Furukawa F, et al. Modifying effects of 4-phenylbutyl isothiocyanate on N-nitrosobis(2-oxopropyl)amine-induced tumorigenesis in hamsters. Cancer Lett. 2000 Nov 28;160(2):141-7. PMID: 11053643.

Yu R, Mandlekar S, Harvey KJ, et al. Chemopreventive isothiocyanates induce apoptosis and caspase-3-like protease activity. Cancer Res. 1998 Feb 1;58(3):402-8. PMID: 9458080.

Guo Z, Smith TJ, Wang E, et al. Structure-activity relationships of arylalkyl isothiocyanates for the inhibition of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone metabolism and the modulation of xenobiotic-metabolizing enzymes in rats and mice. Carcinogenesis. 1993 Jun;14(6):1167-73. PMID: 8508504.

Custom Order

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