Kinetin - suitable for plant cell culture, ≥99%(HPLC) , CAS No.525-79-1

CAS: 525-79-1 Cat. No.: K108959 Formule: C₁₀H₉N₅O Poids moléculaire: 215.21 Beilstein Registry Number: 21703 Numéro CE: 208-382-2

QUALITÉ & PURETÉ Suitable for plant cell culture, ≥99%(HPLC)

Synonyms

DivK1c_000011 | US9144538, Kinetin | DTXCID7015175 | N-(2-furylmethyl)-1H-purin-6-amine | 6-[(Furan-2-ylmethyl)amino]-9H-purine | KBio2_001544 | Kinetin (VAN) | N-(furan-2-ylmethyl)-9H-purin-6-amine | 2uy5 | HMS1570C19 | HMS561M13 | N6-(Furfurylamino)puri

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Vue d’ensemble

Kinetin is an adenine-type cytokinin phytohormone that is used in plant culture media such as Murashige & Skoog media in conjunction with auxins such as indole-3-acetic acid (IAA), indole-3-butyric acid (IBA), 1-napthaleneacetic acid (NAA) or others to induce the fomation of callus and to regenerate plant tissues from callus.

Spécifications

Synonymes

DivK1c_000011 | US9144538, Kinetin | DTXCID7015175 | N-(2-furylmethyl)-1H-purin-6-amine | 6-[(Furan-2-ylmethyl)amino]-9H-purine | KBio2_001544 | Kinetin (VAN) | N-(furan-2-ylmethyl)-9H-purin-6-amine | 2uy5 | HMS1570C19 | HMS561M13 | N6-(Furfurylamino)puri

Spécifications et pureté

suitable for plant cell culture, ≥99%(HPLC)

Mécanismes biochimiques et physiologiques

IC50 value: Not applicable. Kinetin (N6-furfurylaminopurine) belongs to a class of plant growth hormones, involved in cell division, differentiation, and other physiological processes. Estradiol is one of the widely used ingredients in numerous skincare

Conditions de stockage de stockage

Store at -20°C

Expédié en

Ice chest + Ice pads

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Suitable for plant cell culture

Pureté

≥99%(HPLC)

Noms et identifiants

Pubchem Sid

488179800

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488179800

Sourires canoniques

C1=COC(=C1)CNC2=NC=NC3=C2NC=N3

IUPAC Name

N-(furan-2-ylmethyl)-7H-purin-6-amine

InChIKey

QANMHLXAZMSUEX-UHFFFAOYSA-N

INCHI

1S/C10H9N5O/c1-2-7(16-3-1)4-11-9-8-10(13-5-12-8)15-6-14-9/h1-3,5-6H,4H2,(H2,11,12,13,14,15)

Isomères SMILES

C1=COC(=C1)CNC2=NC=NC3=C2NC=N3

WGK Allemagne

3

RTECS

AU6270000

Poids moléculaire

215.21

Beilstein

21703

Reaxy-Rn

21703

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=21703&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Imidazopyrimidines
      • Subclass Purines and purine derivatives
        • Level5 6-aminopurines
          • Level6 6-alkylaminopurines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Imidazopyrimidines
• Subclass: Purines and purine derivatives
• Intermediate Tree Nodes: 6-aminopurines
• Direct Parent: 6-alkylaminopurines
• Alternative Parents: Secondary alkylarylamines Aminopyrimidines and derivatives Imidolactams Imidazoles Heteroaromatic compounds Furans Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 6-alkylaminopurine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Pyrimidine - Imidolactam - Azole - Furan - Imidazole - Heteroaromatic compound - Secondary amine - Azacycle - Oxacycle - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as 6-alkylaminopurines. These are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
• External Descriptors: a small molecule

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

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water (<1 mg/ml) at 25°C, Acetic acid (49.00-51.00 mg/ml), DMSO (43 mg/ml) at 25°C, ethanol (<1 mg/ml) at 25°C, 0.1 N Sodium hydroxide (1% w/v), methanol (slightly), and dilute aqueous hydrochloric acid or sodium hydroxide (freely).
• Poids moléculaire: 215.210 g/mol
• XLogP3: 1.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 215.081 Da
• Monoisotopic Mass: 215.081 Da
• Topological Polar Surface Area: 79.600 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 239.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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