2-Fluoro-L-β-homophenylalanine hydrochloride
Need Assistance?
  • US & Canada:
    +
  • UK: +

2-Fluoro-L-β-homophenylalanine hydrochloride

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
Fluorinated amino acids
Catalog number
BAT-006745
CAS number
331763-61-2
Molecular Formula
C10H13ClFNO2
Molecular Weight
233.67
2-Fluoro-L-β-homophenylalanine hydrochloride
IUPAC Name
(3S)-3-amino-4-(2-fluorophenyl)butanoic acid;hydrochloride
Synonyms
H-Phe(2-F)-(C#CH2)OH HCl; (S)-3-Amino-4-(2-fluorophenyl)butanoic acid hydrochloride
Related CAS
246876-92-6 (free base)
Purity
95%
Storage
Store at 2-8 °C
InChI
InChI=1S/C10H12FNO2.ClH/c11-9-4-2-1-3-7(9)5-8(12)6-10(13)14;/h1-4,8H,5-6,12H2,(H,13,14);1H/t8-;/m0./s1
InChI Key
JZQZLHARRLTFJX-QRPNPIFTSA-N
Canonical SMILES
C1=CC=C(C(=C1)CC(CC(=O)O)N)F.Cl
1.Erlotinib-cisplatin combination inhibits growth and angiogenesis through c-MYC and HIF-1α in EGFR-mutated lung cancer in vitro and in vivo.
Lee JG1, Wu R2. Neoplasia. 2015 Feb;17(2):190-200. doi: 10.1016/j.neo.2014.12.008.
Combination treatment for non-small cell lung cancer (NSCLC) is becoming more popular due to the anticipation that it may be more effective than single drug treatment. In addition, there are efforts to genetically screen patients for specific mutations in light of attempting to administer specific anticancer agents that are most effective. In this study, we evaluate the anticancer and anti-angiogenic effects of low dose erlotinib-cisplatin combination in NSCLC in vitro and in vivo. In NSCLC cells harboring epidermal growth factor receptor (EGFR) mutations, combination erlotinib-cisplatin treatment led to synergistic cell death, but there was minimal efficacy in NSCLC cells with wild-type EGFR. In xenograft models, combination treatment also demonstrated greater inhibition of tumor growth compared to individual treatment. The anti-tumor effect observed was secondary to the targeting of angiogenesis, evidenced by decreased vascular endothelial growth factor (VEGF) levels and decreased levels of CD31 and microvessel density.
2.Inhibition of local blood flow control systems in the mammary glands of lactating cows affects uptakes of energy metabolites from blood.
Madsen TG1, Cieslar SR2, Trout DR3, Nielsen MO1, Cant JP4. J Dairy Sci. 2015 May;98(5):3046-58. doi: 10.3168/jds.2014-8200. Epub 2015 Mar 6.
To test the effect of mammary blood flow on net uptakes of milk precursors by the mammary glands, inhibitors of nitric oxide synthase (NOS) and cyclooxygenase (COX) were infused into the mammary circulation of 4 lactating cows. Inhibitors were infused in a 4×4 Latin square design, where treatments were infusion for 1 h of saline, NOS inhibitor (Nω-nitro-l-arginine methyl ester hydrochloride), COX inhibitor (indomethacin), or both NOS + COX inhibitors into one external iliac artery. Para-aminohippuric acid was also infused to allow for estimation of iliac plasma flow (IPF), of which approximately 80% flows to the mammary glands. Blood samples were collected before, during, and after inhibitor infusion from the contralateral external iliac artery and ipsilateral mammary vein. Inhibition of COX and NOS each produced a decrease in IPF, although the NOS effect was smaller and IPF continued to be depressed throughout the recovery period. The combination of COX and NOS inhibition produced a 50% depression in IPF and there was no carryover into the recovery period.
3.Chiral Separation of Ormeloxifene Hydrochloride, a Non-steroidal Contraceptive Agent.
Ahmad H1, Gupta V1, Dwivedi AP2, Katti SB2, Dwivedi AK3. J Chromatogr Sci. 2016 Feb;54(2):125-9. doi: 10.1093/chromsci/bmv109. Epub 2015 Aug 1.
Ormeloxifene hydrochloride (Centchroman) is once-a-week non-steroidal oral contraceptive agent marketed in India and other countries. In this study, we report a validated isocratic high-performance liquid chromatographic (HPLC) method for chiral separation of d- and l-ormeloxifene hydrochloride. This method is capable of baseline separation of its d- and l-isomers. HPLC separation was achieved on a Lux 5µ cellulose-1 with a mobile phase comprising hexane, isopropanol, methanol and triethylamine (90:10:1:0.5). Validation parameters such as limit of detection, limit of quantitation, linearity, precision, accuracy, specificity and preformulation studies were conducted according to new guidelines of International Conference on Harmonization.
4.The Effect of Systemic Tamsulosin Hydrochloride on Choroidal Thickness Measured by Enhanced Depth Imaging Spectral Domain Optical Coherence Tomography.
Sari E1, Sari ES2, Yazici A2, Koç A1, Bulbul E3, Koytak A4, Ermis SS2, Erol MK5. Curr Eye Res. 2015;40(10):1068-72. doi: 10.3109/02713683.2014.971935. Epub 2014 Dec 12.
BACKGROUND: To evaluate the effects of selective α1A-adrenoceptor antagonist tamsulosin hydrochloride on choroidal thickness using enhanced depth imaging spectral-domain optical coherence tomography (EDI-OCT).
Online Inquiry
Verification code
Inquiry Basket