L-Histidinol dihydrochloride - 10mM in DMSO , CAS No.1596-64-1

CAS: 1596-64-1 Cat. No.: L421910 Peso molecular: 214.09 Beilstein Registry Number: 3914853 Número EC: 216-482-2

GRADE & PURITY 10mM in DMSO

Synonyms

FRCAFNBBXRWXQA-XRIGFGBMSA-N | L-Histidinol dihydrochloride, >=98 (TLC) | HY-W014233 | MFCD00078058 | 8,10-DIAZA-6-HYDROXY-5-METHYLENE-1-(2-METHYL-1,2,3-TRIHYDROXYPROPYL)-2-OXABICYCLO(4.2.2)DECAN-7,9-DIONE | EINECS 216-482-2 | l-histidinol 2hcl | CHEBI:135

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

Precursor of histamine,reversible inhibitor of protein synthesis.

Specifications

Sinónimos

FRCAFNBBXRWXQA-XRIGFGBMSA-N | L-Histidinol dihydrochloride, >=98 (TLC) | HY-W014233 | MFCD00078058 | 8, 10-DIAZA-6-HYDROXY-5-METHYLENE-1-(2-METHYL-1, 2, 3-TRIHYDROXYPROPYL)-2-OXABICYCLO(4.2.2)DECAN-7, 9-DIONE | EINECS 216-482-2 | l-histidinol 2hcl | CHEBI:135

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=C(NC=N1)CC(CO)N.Cl.Cl
• IUPAC Name: (2S)-2-amino-3-(1H-imidazol-5-yl)propan-1-ol;dihydrochloride
• InChIKey: FRCAFNBBXRWXQA-XRIGFGBMSA-N
• INCHI: 1S/C6H11N3O.2ClH/c7-5(3-10)1-6-2-8-4-9-6;;/h2,4-5,10H,1,3,7H2,(H,8,9);2*1H/t5-;;/m0../s1
• Isómeros SMILES: C1=C(NC=N1)C[C@@H](CO)N.Cl.Cl
• WGK Alemania: 3
• RTECS: NI8260000
• CAS alternativo: 4836-52-6
• Peso molecular: 214.09
• Beilstein: 3914853

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Amines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Not available
• Direct Parent: Aralkylamines
• Alternative Parents: Imidazoles Heteroaromatic compounds 1,2-aminoalcohols Azacyclic compounds Primary alcohols Organopnictogen compounds Monoalkylamines Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aralkylamine - Azole - Imidazole - Heteroaromatic compound - 1,2-aminoalcohol - Organoheterocyclic compound - Azacycle - Organic oxygen compound - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Hydrocarbon derivative - Organopnictogen compound - Alcohol - Hydrochloride - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl 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

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive.
• Peso molecular: 214.090 g/mol
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 213.044 Da
• Monoisotopic Mass: 213.044 Da
• Topological Polar Surface Area: 74.900 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 99.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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: 3

XLogP3

Referencias

1. Shuping Fei, Jiatong Zhao, Wenwen Wu, Chaoqun Lian, Wanggang Tang.  (2025)  Biochemical characterization of histidinol dehydrogenase from the human pathogen Neisseria gonorrhoeae.  PROTEIN EXPRESSION AND PURIFICATION,      [PMID:41016688] [10.1016/j.pep.2025.106824]