Alliin structure
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Common Name | Alliin | ||
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CAS Number | 556-27-4 | Molecular Weight | 177.221 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | 416.1±45.0 °C at 760 mmHg | |
Molecular Formula | C6H11NO3S | Melting Point | 165ºC | |
MSDS | Chinese USA | Flash Point | 205.5±28.7 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of AlliinAlliin, an orally active sulfoxide compound derived from garlic, exhibits hypoglycemic, antioxidant and anti-inflammatory activities[1][2]. |
Name | (S)-3-(Allylsulphinyl)-L-alanine |
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Synonym | More Synonyms |
Description | Alliin, an orally active sulfoxide compound derived from garlic, exhibits hypoglycemic, antioxidant and anti-inflammatory activities[1][2]. |
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Related Catalog | |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 416.1±45.0 °C at 760 mmHg |
Melting Point | 165ºC |
Molecular Formula | C6H11NO3S |
Molecular Weight | 177.221 |
Flash Point | 205.5±28.7 °C |
Exact Mass | 177.045959 |
PSA | 99.60000 |
LogP | -0.48 |
Vapour Pressure | 0.0±2.1 mmHg at 25°C |
Index of Refraction | 1.579 |
Storage condition | −20°C |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2942000000 |
~47% Alliin CAS#:556-27-4 |
Literature: Ripp, Sharon L.; Overby, Lila H.; Philpot, Richard M.; Elfarra, Adnan A. Molecular Pharmacology, 1997 , vol. 51, # 3 p. 507 - 515 |
~% Alliin CAS#:556-27-4 |
Literature: Helvetica Chimica Acta, , vol. 34, p. 481,486 Helvetica Chimica Acta, , vol. 31, p. 189,207 |
HS Code | 2942000000 |
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Metabolism, excretion, and pharmacokinetics of S-allyl-L-cysteine in rats and dogs.
Drug Metab. Dispos. 43(5) , 749-55, (2015) The metabolism, excretion, and pharmacokinetics of S-allyl-l-cysteine (SAC), an active key component of garlic supplements, were examined in rats and dogs. A single dose of SAC was administered orally... |
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Combination of aqueous two-phase extraction and cation-exchange chromatography: New strategies for separation and purification of alliin from garlic powder
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 957 , 60-7, (2014) In this study, a two-step process combining aqueous two-phase extraction (ATPE) with chromatography was developed for extraction and purification of alliin from garlic powder. The partition coefficien... |
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Fluorescent magnetic iron oxide nanoparticles for cardiac precursor cell selection from stromal vascular fraction and optimization for magnetic resonance imaging.
Int. J. Nanomedicine 10 , 711-26, (2015) Fluorescent magnetic iron oxide nanoparticles have been used to label cells for imaging as well as for therapeutic purposes. The purpose of this study was to modify the approach to develop a nanoprobe... |
MFCD01311056 |
(+)-L-Alliin |
(2R)-3-(Allylsulfinyl)-2-aminopropanoic acid |
(+/-)-S-2-propenyl-L-cysteine sulfoxide |
alliin |
3-((S)-allylsulfinyl)-L-alanine |
3-(Allylsulfinyl)-L-alanine |
Einecs 209-118-9 |
L-Alanine, 3-[(S)-(1S)-2-propen-1-ylsulfinyl]- |
L-Alanine, 3-(2-propenylsulfinyl)-, (S)- |
alliin zwitterion |
3-(2-Propèn-1-ylsulfinyl)-L-alanine |
Alliin (25 mg) |
3-(prop-2-en-1-ylsulfinyl)-L-alanine |
S-Allyl-L-cysteine Sulfoxide |
(S)-3-(Allylsulphiny |
3-[(S)-Allylsulfinyl]-L-alanine |
L-(+)-S-2-(propenyl)cysteine sulfoxide |
L-Alanine, 3-[(S)-2-propenylsulfinyl]- |
ALLIIN(P) |
3-(2-Propenylsulfinyl)-L-alanine |
L-Alanine, 3-(2-propen-1-ylsulfinyl)- |
(2R)-2-amino-3-[(S)-prop-2-enylsulfinyl]propanoic acid |