Acide DL-4-Hydroxyphényllactique - Moligand™, ≥98%(HPLC)(T) , CAS No.306-23-0

CAS: 306-23-0 Cat. No.: S160986 Formule: C₉H₁₀O₄ Poids moléculaire: 182.18 Beilstein Registry Number: 10(3)1524 Numéro CE: 679-910-0 PubChem CID: 9378

GRADE & PURITY Moligand™, ≥98%(HPLC)(T)

Synonyms

4-ISOTHIOCYANATOBENZOYL-DL-HOMOSERINELACTONE | Benzenepropanoic acid, alpha,4-dihydroxy- | .beta.-(4-Hydroxyphenyl)lactic acid | AKOS000283821 | 3-(4-Hydroxyphenyl)-DL-lactic acid | beta-(p-Hydroxyphenyl)-DL-lactate | .BETA.-(P-HYDROXYPHENYL)-DL-LACTIC AC

Storage

A conserver entre 2 et 8°C

Shipped In

Glace humide

Vue d’ensemble

L'acide DL-p-Hydroxyphényllactique est un précurseur dans la synthèse de l'acide rosmarinique qui peut être utilisé pour des applications pharmaceutiques et nutraceutiques. Il présente également une activité antifongique.

Specifications

Synonymes

4-ISOTHIOCYANATOBENZOYL-DL-HOMOSERINELACTONE | Benzenepropanoic acid, alpha,4-dihydroxy- | .beta.-(4-Hydroxyphenyl)lactic acid | AKOS000283821 | 3-(4-Hydroxyphenyl)-DL-lactic acid | beta-(p-Hydroxyphenyl)-DL-lactate | .BETA.-(P-HYDROXYPHENYL)-DL-LACTIC AC

Spécifications et pureté

Moligand™, ≥98%(HPLC)(T)

Conditions de stockage de stockage

A conserver entre 2 et 8°C

Expédié en

Glace humide

Grade

Moligand™

Type d'action

INHIBITOR

Pureté

≥98%(HPLC)(T)

Noms et identifiants

• Pubchem Sid: 488180970
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180970
• Sourires canoniques: C1=CC(=CC=C1CC(C(=O)O)O)O
• IUPAC Name: 2-hydroxy-3-(4-hydroxyphenyl)propanoic acid
• InChIKey: JVGVDSSUAVXRDY-UHFFFAOYSA-N
• INCHI: 1S/C9H10O4/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8,10-11H,5H2,(H,12,13)
• Isomères SMILES: C1=CC(=CC=C1CC(C(=O)O)O)O
• WGK Allemagne: 3
• CAS alternatif: 6482-98-0
• PubChem CID: 9378
• Poids moléculaire: 182.18
• Beilstein: 10(3)1524
• Reaxy-Rn: 2693719

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Phenylpropanoids and polyketides
    • Classe Phenylpropanoic acids

• Kingdom: Organic compounds
• Superclass: Phenylpropanoids and polyketides
• Classe: Phenylpropanoic acids
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylpropanoic acids
• Alternative Parents: 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Alpha hydroxy acids and derivatives Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: 3-phenylpropanoic-acid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alpha-hydroxy acid - Monocyclic benzene moiety - Benzenoid - Hydroxy acid - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Alcohol - Organooxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as phenylpropanoic acids. These are compounds with a structure containing a benzene ring conjugated to a propanoic acid.
• External Descriptors: phenols - 2-hydroxy carboxylic acid

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Cibles associées (non humaines)

Slc22a20 Solute carrier family 22 member 20 (86 Activities)

Discover Target: Slc22a20

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive
• Poids moléculaire: 182.170 g/mol
• XLogP3: 0.300
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 182.058 Da
• Monoisotopic Mass: 182.058 Da
• Topological Polar Surface Area: 77.800 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 172.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Références

1. Xiaomin Yuan, Biqing Chen, Zhenglan Duan, Ziqian Xia, Yang Ding, Tuo Chen, Huize Liu, Baosheng Wang, Bolin Yang, Xiaoyong Wang, Shijia Liu, Jin-Yong Zhou, Yajun Liu, Qiong Wang, Zhaofeng Shen, Jun Xiao, Hongtao Shang, Weiwei Liu, Guoping Shi, Lei Zhu, Yugen Chen.  (2021)  Depression and anxiety in patients with active ulcerative colitis: crosstalk of gut microbiota, metabolomics and proteomics.  Gut Microbes,      [PMID:34806521] [10.1080/19490976.2021.1987779]

2. Zhuang Yibin, Jiang Jingjie, Bi Huiping, Yin Hua, Liu Shaowei, Liu Tao.  (2015)  Synthesis of rosmarinic acid analogues in Escherichia coli.  BIOTECHNOLOGY LETTERS,  38  (4): (619-627).  [PMID:26667131] [10.1007/s10529-015-2011-1]

3. Qiang Wang, Feng Zhang, Yuhong Zhang, Yu Zhang, Hongwei Wang, Jiajia Song, Huayi Suo.  (2024)  A novel strain Lactiplantibacillus plantarum LPP95 isolated from Chinese pickles: Antifungal effect, mechanism, and potential application in yogurt.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.103640]

4. Kai Yang, Zhenjie Tang, Chong Zhang, Ruide Zhang, Sheng Hu, Changjiang Lv, Jun Huang, Jiaqi Mei, Weirui Zhao, Lehe Mei.  (2025)  Developing a highly efficient 4-hydroxyphenylacetate-3-hydroxylase for salvianic acid A synthesis by computer-aided molecular modification.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39864709] [10.1016/j.ijbiomac.2025.140313]