trans-Zeatin - Moligand™,10mM in DMSO , CAS No.1637-39-4

CAS: 1637-39-4 Cat. No.: T422013 Formula: C₁₀H₁₃N₅O Peso molecolare: 219.24 Beilstein Registry Number: 616241 Numero EC: 605-343-5

GRADE & PURITY Moligand™, 10mM in DMSO

Synonyms

CHEBI:5583 | AKOS037643348 | HY-19700A | (2Z)-2-methyl-4-[(7H-purin-6-yl)amino]but-2-en-1-ol | A806205 | CCG-266716 | (2Z)-2-methyl-4-(9H-purin-6-ylamino)-2-buten-1-ol | AC-22388 | MFCD00213654 | 7I6OOJ9GR6 | BCP13132 | (2E)-2-methyl-4-[(7H-purin-6-yl)ami

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Panoramica

trans-Zeatin contains a hydroxylated isoprenoid side chain.

Specifications

Sinonimi

CHEBI:5583 | AKOS037643348 | HY-19700A | (2Z)-2-methyl-4-[(7H-purin-6-yl)amino]but-2-en-1-ol | A806205 | CCG-266716 | (2Z)-2-methyl-4-(9H-purin-6-ylamino)-2-buten-1-ol | AC-22388 | MFCD00213654 | 7I6OOJ9GR6 | BCP13132 | (2E)-2-methyl-4-[(7H-purin-6-yl)ami

Specifiche e purezza

Moligand™,10mM in DMSO

Meccanismi biochimici e fisiologici

trans-Zeatin-riboside is a plant cytokinin.Endogenous plant growth hormone. Cytokinin. Potent AHK3 ligand (K i = 1.3 nM). Senescence-delaying hormone. Acts as a positional cue regulating lateral root spacing. Mediates plant growth and development in vivo.

Condizioni di conservazione di stoccaggio

Store at -80°C

Spedito in

Dry ice packs + Cold packs

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Tipo di azione

INHIBITOR

Nomi e identificatori

Pubchem Sid

528770561

Sorrisi canonici

CC(=CCNC1=NC=NC2=C1NC=N2)CO

IUPAC Name

(E)-2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol

InChIKey

UZKQTCBAMSWPJD-FARCUNLSSA-N

INCHI

1S/C10H13N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h2,5-6,16H,3-4H2,1H3,(H2,11,12,13,14,15)/b7-2+

Isomeri SMILES

C/C(=C\CNC1=NC=NC2=C1NC=N2)/CO

WGK Germania

3

RTECS

EM9506000

Peso molecolare

219.24

Beilstein

616241

Reaxy-Rn

18499478

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=18499478&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 Azacyclic compounds Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 6-alkylaminopurine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Secondary amine - Azacycle - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Descrizione: 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: zeatin

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

Obiettivi associati (umani)

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

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

PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

Discover Target: PTH1R

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

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

Discover Target: APEX1

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

BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)

Discover Target: BRD4

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

RECQL Tbio ATP-dependent DNA helicase Q1 (5575 Activities)

Discover Target: RECQL

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

Obiettivi associati (non umani)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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

Amaranthus (163 Activities)

Explore this target

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

Nicotiana tabacum (382 Activities)

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

Triticum aestivum (1582 Activities)

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

lef Anthrax lethal factor (7585 Activities)

Discover Target: lef

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

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

AHK4 Histidine kinase (36 Activities)

Discover Target: AHK4

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

CKX2 Cytokinin dehydrogenase 2 (21 Activities)

Discover Target: CKX2

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Light sensitive；Air sensitive
• Punto di fusione (°C): 210°C
• Peso molecolare: 219.240 g/mol
• XLogP3: 0.700
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 219.112 Da
• Monoisotopic Mass: 219.112 Da
• Topological Polar Surface Area: 86.700 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 258.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1