2-Propynyl-L-proline hydrochloride
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2-Propynyl-L-proline hydrochloride

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Category
Alkynyl Amino Acids
Catalog number
BAT-006764
CAS number
1049733-10-9
Molecular Formula
C8H12ClNO2
Molecular Weight
189.64
2-Propynyl-L-proline hydrochloride
IUPAC Name
(2R)-2-prop-2-ynylpyrrolidine-2-carboxylic acid;hydrochloride
Synonyms
H-(Propynyl)Pro-OH HCl; (R)-α-Propynyl-proline HCl; (R)-2-Propynylpyrrolidine-2-carboxylic acid hydrochloride
Related CAS
1049977-79-8 (free base)
Appearance
White powder
Purity
≥ 98% (HPLC)
Storage
Store at -20 °C
InChI
InChI=1S/C8H11NO2.ClH/c1-2-4-8(7(10)11)5-3-6-9-8;/h1,9H,3-6H2,(H,10,11);1H/t8-;/m0./s1
InChI Key
HUPSJXIFWSWGFS-QRPNPIFTSA-N
Canonical SMILES
C#CCC1(CCCN1)C(=O)O.Cl
1.Simultaneous determination of timolol maleate in combination with some other anti-glaucoma drugs in rabbit aqueous humor by high performance liquid chromatography-tandem mass spectroscopy.
Hassib ST1, Elkady EF1, Sayed RM2. J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Apr 7;1022:109-117. doi: 10.1016/j.jchromb.2016.04.012. [Epub ahead of print]
In this work, a sensitive, selective, accurate and precise LC-MS/MS method has been developed for the simultaneous determination of an anti-glaucoma ß-blocker, timolol maleate (TIM) with other co-administered anti-glaucoma drugs of different classes, namely; dorzolamide hydrochloride (DOR), brinzolamide (BRZ) and brimonidine tartrate (BRM) in rabbit aqueous humor (AH) using eslicarbazepine as an internal standard (IS). Liquid-liquid extraction was used for the purification and pre-concentration of analytes from rabbit AH matrix. The chromatographic separation was achieved using a mobile phase consisting of 10mM ammonium formate pH=7: methanol: acetonitrile (5: 50: 45, v/v/v) in isocratic mode of elution at a flow rate of 0.8mL/min on an INERTSIL® C18 ODS-3 column (150mm×4.6mm, 3.5μm). The method was operated using electrospray ionization source in the positive ionization mode prior to detection by multiple reaction monitoring (MRM) at the following transitions: m/z 317.
2.Terbinafine hydrochloride nanovesicular gel: In vitro characterization, ex vivo permeation and clinical investigation.
AbdelSamie SM1, Kamel AO2, Sammour OA1, Ibrahim SM3. Eur J Pharm Sci. 2016 Apr 9;88:91-100. doi: 10.1016/j.ejps.2016.04.004. [Epub ahead of print]
In this work, nanovesicular chitosan gels were prepared for dermal delivery of terbinafine hydrochloride (TBN HCl). Ethosomes and vesicles containing different types of penetration enhancers (PEs) viz. Terpenes (cineole and limonene), labrasol and transcutol were developed. The prepared vesicles were evaluated for physical characteristics as well as skin interaction. The selected vesicles were incorporated into chitosan gel. An in vivo animal study was done on rat induced superficial Candida infection model. Moreover, randomized double blind clinical study was done on patients to compare the effect of the selected nanovesicular gel against the market product. Results showed the formation of nearly spherical, mostly deformable vesicular systems with size range of 95.5-530nm, zeta potential range of -0.1 to 15mV and entrapment efficiency range of 20-96.7%. Penetration enhancer vesicles (PEVs) prepared with 4% limonene (ELI4) showed the highest percent of drug deposition in the skin (53%) and the highest local accumulation efficiency value (35.
3.Long-term stability of ketamine hydrochloride 50mg/ml injection in 3ml syringes.
Huvelle S1, Godet M2, Hecq JD3, Gillet P4, Bihin B5, Jamart J5, Galanti L2. Ann Pharm Fr. 2016 Apr 20. pii: S0003-4509(16)30001-3. doi: 10.1016/j.pharma.2016.03.003. [Epub ahead of print]
INTRODUCTION: Ketamine hydrochloride (Ketalar®) injection is often used as a general anesthetic agent. It is particularly suited to short-term interventions. It can also be used as an inducer of anesthesia before the administration of other anesthetic agents. The aim of this study was to evaluate the stability of ketamine hydrochloride in 3ml polypropylene syringes after storage for up to 180days at room temperature.
4.Treatment of experimental autoimmune uveoretinitis with different natural compounds.
Li M1, Chen X1, Liu J2, Wang D2, Gan L1, Lv X1, Qiao Y2. Mol Med Rep. 2016 Apr 8. doi: 10.3892/mmr.2016.5096. [Epub ahead of print]
Uveitis is an important eye disease that potentially causes loss of sight. Although extensive studies have been conducted on uveitis, the exact pathogenesis remains to be determined. The effects of treatment with natural compounds on an experimental autoimmune uveoretinitis (EAU) rat model were examined in the present study. A total of 25 rats were divided into 5 groups: Alkaloids (n=5), saponins (n=5), flavonoids (n=5), phenols (n=5), and the normal saline group (n=5). The rats in each group were treated with an intraperitoneal injection of proper alkaloids (berberine hydrochloride), saponins (steroidal saponins), flavonoids (baicalein), or phenols (chlorogenic acid) or physiological saline, respectively. The rats' aqueous humour and crystalline lens was then observed under the slit lamp periodically, looking for signs of inflammation. After 2 weeks, the rats were sacrificed and the degree of pathological changes on their eyeballs under different treatment methods were determined using an optical microscope.
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