S-Allyl-L-cysteine - 10mM in Water , CAS No.21593-77-1

CAS: 21593-77-1 Cat. No.: S422599 Peso molecular: 161.22 Número EC: 639-018-4
Disponible para pedir
GRADE & PURITY 10mM in Water
Synonyms
DTXCID901324424 | AC-31029 | Pyrazolone Red (Yellowish) R-6258 | S-ALLYL-L-CYSTEINE (USP-RS) | 3-(ALLYLTHIO)-L-ALANINE | DS-3406 | S-ALLYL-L-CYSTEINE (CONSTITUENT OF GARLIC) [DSC] | 81R3X99M15 | DEOXYALLIIN | NSC 16723 | S-Allylcysteine | DTXSID4067640 |
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
S422599-1ml
1

58,90US$

69,90US$
Guardar 11,00 US$ (15.74%)
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Why this grade

10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

L-Deoxyalliin is a water-soluble organosulfur obtained from garlic. L-Deoxyalliin is a proven candidate for chemoprevention in a clinical trial.
A water-soluble organosulfur

Specifications

Sinónimos
DTXCID901324424 | AC-31029 | Pyrazolone Red (Yellowish) R-6258 | S-ALLYL-L-CYSTEINE (USP-RS) | 3-(ALLYLTHIO)-L-ALANINE | DS-3406 | S-ALLYL-L-CYSTEINE (CONSTITUENT OF GARLIC) [DSC] | 81R3X99M15 | DEOXYALLIIN | NSC 16723 | S-Allylcysteine | DTXSID4067640 |
Especificaciones y pureza
10mM in Water
Mecanismos bioquímicos y fisiológicos
Antioxidant agent. Inhibits reperfusion-induced HIF-1α, VEGF, and MMP-9 upregulation. Shows selective neuroprotective effects against amyloid β-protein-induced cell death. Shows anti-ischemic effects in vivo. Orally active.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasC=CCSCC(C(=O)O)N
IUPAC Name(2R)-2-amino-3-prop-2-enylsulfanylpropanoic acid
InChIKeyZFAHNWWNDFHPOH-YFKPBYRVSA-N
INCHI1S/C6H11NO2S/c1-2-3-10-4-5(7)6(8)9/h2,5H,1,3-4,7H2,(H,8,9)/t5-/m0/s1
Isómeros SMILES C=CCSC[C@@H](C(=O)O)N
WGK Alemania 3
RTECS HA2466200
Peso molecular 161.22
Reaxy-Rn 2205501
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2205501&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Cysteine and derivatives
Direct ParentL-cysteine-S-conjugates
Alternative Parents L-alpha-amino acids  Amino acids  Allyl sulfur compounds  Sulfenyl compounds  Monocarboxylic acids and derivatives  Dialkylthioethers  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents L-cysteine-s-conjugate - Alpha-amino acid - L-alpha-amino acid - Amino acid - Allyl sulfur compound - Carboxylic acid - Monocarboxylic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Carbonyl group - Amine - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Organic oxygen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as l-cysteine-s-conjugates. These are compounds containing L-cysteine where the thio-group is conjugated.
External Descriptors S-hydrocarbyl-L-cysteine
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
TLR2 Tchem Toll-like receptor 2 (975 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadAir sensitive
Rotación específica [α]-15° (C=1,H2O)
Peso molecular161.220 g/mol
XLogP3-2.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count5
Exact Mass161.051 Da
Monoisotopic Mass161.051 Da
Topological Polar Surface Area88.600 Ų
Heavy Atom Count10
Formal Charge0
Complexity127.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Miaomiao Liu, Siqi Jing, Tiantian Xie, Haiyan Liu, Ligai Bai.  (2023)  Fabrication of a bio-based polymer adsorbent and its application for extraction and determination of glycosides from Huangqi Liuyi decoction.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:38181557] [10.1016/j.jpba.2023.115947]
2. Jing Nie, Rui Weng, Chunlin Li, Xiuhua Liu, Fang Wang, Karyne M. Rogers, Yongzhong Qian, Yongzhi Zhang, Yuwei Yuan.  (2022)  Chemometric origin classification of Chinese garlic using sulfur-containing compounds, assisted by stable isotopes and bioelements.  FOOD CHEMISTRY,      [PMID:35759834] [10.1016/j.foodchem.2022.133557]
3. Rong Xu, Siyan Qiu, Jie Zhang, Xiaoli Liu, Ling Zhang, Haizhu Xing, Min You, Man Wang, Yuting Lu, Peng Zhang, Jing Zhu.  (2022)  Silibinin Schiff Base Derivatives Counteract CCl4-Induced Acute Liver Injury by Enhancing Anti-Inflammatory and Antiapoptotic Bioactivities.  Drug Design Development and Therapy,      [PMID:35601675] [10.2147/DDDT.S356847]
4. Qiang Chen, Chunjing Guo, Xiudi Zhou, Yanguo Su, Huimin Guo, Min Cao, Jing Li, Yue Zhang, Weiyi Zhao, Xin Gao, Shuqi Mi, Daquan Chen.  (2022)  N-acetylneuraminic acid and chondroitin sulfate modified nanomicelles with ROS-sensitive H2S donor via targeting E-selectin receptor and CD44 receptor for the efficient therapy of atherosclerosis.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:35513096] [10.1016/j.ijbiomac.2022.04.180]
5. Xiaoying Zhang, Cuifeng Wang, Jiamin Wu, Yajun Liu, Zeping Yang, Ye Zhang, Xiaofeng Sui, Min Li, Min Feng.  (2017)  An acid-seeking carrier-free drug achieves high antitumor activity via a “solution-particle” transition.  JOURNAL OF CONTROLLED RELEASE,      [PMID:28797579] [10.1016/j.jconrel.2017.08.008]
6. Guqing Luo, Zhenghao Wu, Qiang Fan, Chihao Zhang, Jiayun Lin, Hongjie Li, Jinbo Zhao, Haizhong Huo, Xiaoliang Qi, Guangbo Wu, Min Chen, Jiwei Yu, Lei Zheng, Meng Luo.  (2025)  S-Allyl-Cysteine Ameliorates Cirrhotic Portal Hypertension by Enhancing Lymphangiogenesis via a VEGF-C-Independent Manner.  LIVER INTERNATIONAL,  45  (3): (e70024).  [PMID:39967382] [10.1111/liv.70024]
7. Liu Zihao, Huang Yahui, Chen Xiaoming, Zhu Jie, Tang Fanzhou, Zhu Wenkun, Wang Qing, Huang Zhaohui, Zhu Bo.  (2026)  Promotion of root Cd enrichment and inhibition of its translocation through integrated strategies.  PLANT AND SOIL,      [PMID:] [10.1007/s11104-025-08241-5]
8. Xu Zhang, Lei Wang, Xutang Tao, Huimin Li, Yaqian Qu, Peizhuo Han, Weiguo Song.  (2026)  Selected food additives for inhibiting the metastable polymorphic transformation of baricitinib: a novel and safe strategy.  INTERNATIONAL JOURNAL OF PHARMACEUTICS,      [PMID:] [10.1016/j.ijpharm.2026.126823]
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