N-Benzoyl-(2R,3S)-3-phenylisoserine - 10mM in DMSO , CAS No.132201-33-3

CAS: 132201-33-3 Cat. No.: N421242 Peso molecular: 285.29 Número EC: 631-348-7

GRADE & PURITY 10mM in DMSO

Synonyms

Q27276267 | s9395 | SCHEMBL6277 | (2R,3S)-3-BENZOYLAMINO-2-HYDROXY-3-PHENYLPROPIONIC ACID | (2R,3S)-3-Benzoylamino-2-hydroxy-3-phenyl-propionic acid | HYJVYOWKYPNSTK-UONOGXRCSA-N | BP-22968 | D998Q2WJCM | F14253 | AC-9033 | BENZENEPROPANOIC ACID, .BETA.-(

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

It has been proven that the presence of this chiral side chain is essential for the biological activity of paclitaxel. The complex synthesis process of paclitaxel has attracted attention to attaching C-13 side chains to naturally derived taxanes (for example, baccatin III).

Specifications

Sinónimos

Q27276267 | s9395 | SCHEMBL6277 | (2R, 3S)-3-BENZOYLAMINO-2-HYDROXY-3-PHENYLPROPIONIC ACID | (2R, 3S)-3-Benzoylamino-2-hydroxy-3-phenyl-propionic acid | HYJVYOWKYPNSTK-UONOGXRCSA-N | BP-22968 | D998Q2WJCM | F14253 | AC-9033 | BENZENEPROPANOIC ACID, .BETA.-(

Especificaciones y pureza

10mM in DMSO

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 canónicas: C1=CC=C(C=C1)C(C(C(=O)O)O)NC(=O)C2=CC=CC=C2
• IUPAC Name: (2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoic acid
• InChIKey: HYJVYOWKYPNSTK-UONOGXRCSA-N
• INCHI: 1S/C16H15NO4/c18-14(16(20)21)13(11-7-3-1-4-8-11)17-15(19)12-9-5-2-6-10-12/h1-10,13-14,18H,(H,17,19)(H,20,21)/t13-,14+/m0/s1
• Isómeros SMILES: C1=CC=C(C=C1)[C@@H]([C@H](C(=O)O)O)NC(=O)C2=CC=CC=C2
• WGK Alemania: 3
• Peso molecular: 285.29
• Reaxy-Rn: 3383978
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3383978&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives
        • Level5 Benzamides
          • Level6 N-benzylbenzamides

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Benzamides
• Direct Parent: N-benzylbenzamides
• Alternative Parents: Phenylpropanoic acids Beta amino acids and derivatives Benzoyl derivatives Monosaccharides Alpha hydroxy acids and derivatives Secondary carboxylic acid amides Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: N-benzylbenzamide - Beta amino acid or derivatives - 3-phenylpropanoic-acid - Benzoyl - Alpha-hydroxy acid - Hydroxy acid - Monosaccharide - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as n-benzylbenzamides. These are compounds containing a benzamide moiety that is N-linked to a benzyl group.
• External Descriptors: Not available

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

Objetivos asociados (no humanos)

Plasmodium falciparum (966862 Activities)

Explore this target

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

B16 (5829 Activities)

Explore this target

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

L6 (7924 Activities)

Explore this target

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

Mecanismos de acción

Propiedades químicas y físicas

• Rotación específica [α]: -40°, c = 1.0 in ethanol
• Punto de fusión (°C): 169-172°C
• Peso molecular: 285.290 g/mol
• XLogP3: 1.700
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 285.1 Da
• Monoisotopic Mass: 285.1 Da
• Topological Polar Surface Area: 86.600 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 359.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Kui Zhang, Liangqin Zhou, Fan Chen, Yuanwei Chen, Xianglin Luo.  (2019)  Injectable gel self-assembled by paclitaxel itself for in situ inhibition of tumor growth.  JOURNAL OF CONTROLLED RELEASE,      [PMID:31669210] [10.1016/j.jconrel.2019.10.002]