Cis-4-Hydroxy-L-proline - ≥98% , CAS No.618-27-9

CAS: 618-27-9 Cat. No.: H110730 Molecular Weight: 131.13 Beilstein Registry Number: 81440 EC Number: 210-542-1

GRADE & PURITY ≥98%

Synonyms

C01015 | 3-(5-Oxo-1-phenyl-2-thioxo-4-imidazolidinyl)propanoic acid # | BDBM50357209 | Hydroxyproline, cis- | PMMYEEVYMWASQN-IMJSIDKUSA-N | (4s)-hydroxyproline | A8558 | AS-15085 | cis-4-Hydroxy-L-proline, collagen synthesis inhibitor | L-Proline, 4-hydro

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

C01015 | 3-(5-Oxo-1-phenyl-2-thioxo-4-imidazolidinyl)propanoic acid # | BDBM50357209 | Hydroxyproline, cis- | PMMYEEVYMWASQN-IMJSIDKUSA-N | (4s)-hydroxyproline | A8558 | AS-15085 | cis-4-Hydroxy-L-proline, collagen synthesis inhibitor | L-Proline, 4-hydro

Specifications & Purity

≥98%

Biochemical and Physiological Mechanisms

cis-4-Hydroxy-L-proline (CHP) and its derivatives may have anticancer activity. cis-4-Hydroxy-L-proline and other hydrosyl-L-prolines are important intermediates for chiral synthesis of potential drugs.

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504758726
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504758726
• Canonical Smiles: C1C(CNC1C(=O)O)O
• IUPAC Name: (2S,4S)-4-hydroxypyrrolidine-2-carboxylic acid
• InChIKey: PMMYEEVYMWASQN-IMJSIDKUSA-N
• INCHI: 1S/C5H9NO3/c7-3-1-4(5(8)9)6-2-3/h3-4,6-7H,1-2H2,(H,8,9)/t3-,4-/m0/s1
• Isomeric SMILES: C1[C@@H](CN[C@@H]1C(=O)O)O
• WGK Germany: 3
• Molecular Weight: 131.13
• Beilstein: 81440
• Reaxy-Rn: 81437
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=81437&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Proline and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Proline and derivatives
• Alternative Parents: L-alpha-amino acids Pyrrolidine carboxylic acids Secondary alcohols Amino acids 1,2-aminoalcohols Monocarboxylic acids and derivatives Dialkylamines Carboxylic acids Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Proline or derivatives - Alpha-amino acid - L-alpha-amino acid - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine - 1,2-aminoalcohol - Amino acid - Secondary alcohol - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Azacycle - Secondary amine - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Amine - Carbonyl group - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as proline and derivatives. These are compounds containing proline or a derivative thereof resulting from reaction of proline at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• External Descriptors: non-proteinogenic L-alpha-amino acid - 4-hydroxyproline

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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in water.
• Sensitivity: Air Sensitive
• Specific Rotation[α]: -59 ° (C=2, H2O)
• Melt Point(°C): 241°C
• Molecular Weight: 131.130 g/mol
• XLogP3: -3.300
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 131.058 Da
• Monoisotopic Mass: 131.058 Da
• Topological Polar Surface Area: 69.600 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 125.000
• 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