CAS 132201-33-3
:(2R,3S)-N-Benzoyl-3-phenylisoserine
Description:
(2R,3S)-N-Benzoyl-3-phenylisoserine is an organic compound characterized by its specific stereochemistry and functional groups. It features a benzoyl group, which is a carbonyl group attached to a phenyl ring, indicating its potential for interactions typical of aromatic compounds. The presence of the isoserine moiety suggests that it contains both an amino group and a hydroxyl group, contributing to its polar nature and potential solubility in polar solvents. The stereochemistry, denoted by the (2R,3S) configuration, implies that the compound has specific spatial arrangements that can influence its biological activity and reactivity. This compound may exhibit properties typical of amino acids, such as participating in peptide bond formation or acting as a chiral building block in organic synthesis. Its unique structure may also suggest potential applications in pharmaceuticals or as a biochemical probe, although specific biological activities would depend on further empirical studies. Overall, the compound's characteristics are defined by its functional groups, stereochemistry, and potential interactions in various chemical environments.
Formula:C16H15NO4
InChI: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
InChI key:InChIKey=HYJVYOWKYPNSTK-UONOGXRCSA-N
SMILES:[C@@H](NC(=O)C1=CC=CC=C1)([C@H](C(O)=O)O)C2=CC=CC=C2
Synonyms:- (2R,3S)-2-hydroxy-3-phenyl-3-[(phenylcarbonyl)amino]propanoic acid
- (2R,3S)-3-(Benzoylamino)-2-hydroxy-3-phenylpropanoic acid
- (2R,3S)-3-(Benzoylamino)-2-hydroxy-3-phenylpropionic acid
- (2R,3S)-N-Benzoyl-3-phenylisoserine
- (αR,βS)-β-(Benzoylamino)-α-hydroxybenzenepropanoic acid
- Benzenepropanoic acid, β-(benzoylamino)-α-hydroxy-, (αR,βS)-
- Benzenepropanoic acid, β-(benzoylamino)-α-hydroxy-, [R-(R*,S*)]-
- N-benzoyl-(3S,2R)-3-phenylisoserine
- benzenepropanoic acid, beta-(benzoylamino)-alpha-hydroxy-, (alphaR,betaS)-
- N-Benzoyl-(2R,3S)-3-phenylisoserine
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Found 11 products.
Benzenepropanoic acid, β-(benzoylamino)-α-hydroxy-, (αR,βS)-
CAS:Formula:C16H15NO4Purity:97%Color and Shape:SolidMolecular weight:285.2946N-Benzoyl-(2R,3S)-3-phenylisoserine
CAS:N-Benzoyl-(2R,3S)-3-phenylisoserinePurity:≥98%Molecular weight:285.29g/mol(2R,3S)-3-(Benzoylamino)-2-hydroxy-3-phenylpropanoic Acid ((2R,3S)-N-Benzoyl-3-phenylisoserine)
CAS:Controlled ProductFormula:C16H15NO4Color and Shape:NeatMolecular weight:285.29N-Benzoyl-(2R,3S)-3-phenylisoserine
CAS:<p>N-Benzoyl-(2R,3S)-3-phenylisoserine (taxol side chain) is an intermediate in the preparation of potent anticancer drug Paclitaxel, used to study the location of</p>Formula:C16H15NO4Purity:99.10%Color and Shape:White PowderMolecular weight:285.29(2R,3S)-N-Benzoyl-3-phenyl Isoserine
CAS:Controlled Product<p>Impurity Paclitaxel Side Chain Impurity 1<br>Applications (2R,3S)-N-Benzoyl-3-phenylisoserine is an intermediate in the preparation of potent anticancer drug Paclitaxel (P132500) used to study the location of the binding sites. (2R,3S)-N-Benzoyl-3-phenylisoserine shows cytotoxic, antiviral and immunomodulatory activity. Paclitaxel Side Chain Impurity 1.<br>References Paal, K. et al.: Bioorg. Med. Chem., 15, 1323 (2007); Krawczyk, E. et al.: J. Pharm. Pharmacol., 57, 791 (2005);<br></p>Formula:C16H15NO4Color and Shape:NeatMolecular weight:285.29(2R,3S)-3-Benzamido-2-hydroxy-3-phenylpropanoic acid
CAS:Formula:C16H15NO4Purity:98%Molecular weight:285.299N-Benzoyl-(2R,3S)-3-amino-2-hydroxy-3-phenyl-propionicacid
CAS:<p>N-Benzoyl-(2R,3S)-3-amino-2-hydroxy-3-phenylpropionic acid (BAPA) is a substance that is used in the manufacture of various drugs. It is also a potent anticancer drug that can be used for the treatment of cancer. BAPA has been shown to be an effective chemotherapeutic agent against many types of cancer cells. This drug is synthesized through an asymmetric synthesis process and has been shown to have potent cytotoxic effects against cancer cells with low levels of glutathione peroxide reductase. BAPA also inhibits the growth of bacteria by hydrolyzing or oxidizing proteins or by binding to DNA and RNA.</p>Formula:C16H15NO4Purity:Min. 95%Molecular weight:285.29 g/mol










