4338-47-0,MFCD00037987
Catalog No.:AA0034ZX

4338-47-0 | Kinetin riboside

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
≥98%
in stock  
$118.00   $82.00
- +
5g
≥98%
in stock  
$289.00   $202.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0034ZX
Chemical Name:
Kinetin riboside
CAS Number:
4338-47-0
Molecular Formula:
C15H17N5O5
Molecular Weight:
347.3260
MDL Number:
MFCD00037987
SMILES:
OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cnc2c1ncnc2NCc1ccco1
Properties
Properties
 
BP:
683.7°C at 760 mmHg  
Form:
Solid  
MP:
>129°C (dec.)  
Storage:
2-8℃;  

Computed Properties
 
Complexity:
460  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.2  

Downstream Synthesis Route

[1]Hamptonetal.[JournaloftheAmericanChemicalSociety,1956,vol.78,p.5695]

[1]Kissmann;Weiss[JournalofOrganicChemistry,1956,vol.21,p.1053]

[1]Sattsangi,PremD.;Barrio,JorgeR.;Leonard,NelsonJ.[JournaloftheAmericanChemicalSociety,1980,vol.102,#2,p.770-774]

(2R,3R,4S,5R)-2-{6-(Benzotriazol-1-yl-furan-2-yl-methyl)-amino-purin-9-yl}-5-hydroxymethyl-tetrahydro-furan-3,4-diol 
  4338-47-0 

[1]Afify,HananM.N.M.;Pedersen,ErikB.;Zahran,MagdyA.[JournalofHeterocyclicChemistry,2000,vol.37,#2,p.339-341]

Literature

Title: A small molecule screening strategy with validation on human leukemia stem cells uncovers the therapeutic efficacy of kinetin riboside.

Journal: Blood 20120202

Title: Antiproliferative activity of kinetin riboside on HCT-15 colon cancer cell line.

Journal: Nucleosides, nucleotides & nucleic acids 20120101

Title: Simultaneous determination of different endogenetic plant growth regulators in common green seaweeds using dispersive liquid-liquid microextraction method.

Journal: Plant physiology and biochemistry : PPB 20111101

Title: Effects of kinetin riboside on proliferation and proapoptotic activities in human normal and cancer cell lines.

Journal: Journal of cellular biochemistry 20110801

Title: Anticancer activity of natural cytokinins: a structure-activity relationship study.

Journal: Phytochemistry 20100801

Title: FKBP38 protects Bcl-2 from caspase-dependent degradation.

Journal: The Journal of biological chemistry 20100326

Title: The experimental chemotherapeutic N6-furfuryladenosine (kinetin-riboside) induces rapid ATP depletion, genotoxic stress, and CDKN1A(p21) upregulation in human cancer cell lines.

Journal: Biochemical pharmacology 20090401

Title: Inhibitory effect of kinetin riboside in human heptamoa, HepG2.

Journal: Molecular bioSystems 20090101

Title: Ribose-modified purine nucleosides as ribonucleotide reductase inhibitors. Synthesis, antitumor activity, and molecular modeling of N6-substituted 3'-C-methyladenosine derivatives.

Journal: Journal of medicinal chemistry 20080724

Title: Constrained NBMPR analogue synthesis, pharmacophore mapping and 3D-QSAR modeling of equilibrative nucleoside transporter 1 (ENT1) inhibitory activity.

Journal: Bioorganic & medicinal chemistry 20080401

Title: Kinetin riboside preferentially induces apoptosis by modulating Bcl-2 family proteins and caspase-3 in cancer cells.

Journal: Cancer letters 20080308

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: Rajabi M, et al. Antiproliferative activity of kinetin riboside on HCT-15 colon cancer cell line. Nucleosides Nucleotides Nucleic Acids. 2012;31(6):474-81.

Title: Choi BH, et al. Kinetin riboside preferentially induces apoptosis by modulating Bcl-2 family proteins and caspase-3 in cancer cells. Cancer Lett. 2008 Mar 8;261(1):37-45.

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Additional Info:
SDS
Tags:4338-47-0 Molecular Formula|4338-47-0 MDL|4338-47-0 SMILES|4338-47-0 Kinetin riboside
Catalog No.: AA0034ZX
4338-47-0,MFCD00037987
4338-47-0 | Kinetin riboside
Pack Size: 1g
Purity: ≥98%
in stock
$118.00 $82.00
Pack Size: 5g
Purity: ≥98%
in stock
$289.00 $202.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0034ZX
Chemical Name: Kinetin riboside
CAS Number: 4338-47-0
Molecular Formula: C15H17N5O5
Molecular Weight: 347.3260
MDL Number: MFCD00037987
SMILES: OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cnc2c1ncnc2NCc1ccco1
Properties
BP: 683.7°C at 760 mmHg  
Form: Solid  
MP: >129°C (dec.)  
Storage: 2-8℃;  
Complexity: 460  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 4  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 25  
Hydrogen Bond Acceptor Count: 9  
Hydrogen Bond Donor Count: 4  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.2  
Downstream Synthesis Route
617-89-0    342-69-8    4338-47-0 

[1]Hamptonetal.[JournaloftheAmericanChemicalSociety,1956,vol.78,p.5695]

617-89-0    3510-73-4    4338-47-0 

[1]Kissmann;Weiss[JournalofOrganicChemistry,1956,vol.21,p.1053]

98-01-1    58-61-7    4338-47-0 

[1]Sattsangi,PremD.;Barrio,JorgeR.;Leonard,NelsonJ.[JournaloftheAmericanChemicalSociety,1980,vol.102,#2,p.770-774]

(2R,3R,4S,5R)-2-{6-(Benzotriazol-1-yl-furan-2-yl-methyl)-amino-purin-9-yl}-5-hydroxymethyl-tetrahydro-furan-3,4-diol 
  4338-47-0 

[1]Afify,HananM.N.M.;Pedersen,ErikB.;Zahran,MagdyA.[JournalofHeterocyclicChemistry,2000,vol.37,#2,p.339-341]

Literature fold

Title: A small molecule screening strategy with validation on human leukemia stem cells uncovers the therapeutic efficacy of kinetin riboside.

Journal: Blood20120202

Title: Antiproliferative activity of kinetin riboside on HCT-15 colon cancer cell line.

Journal: Nucleosides, nucleotides & nucleic acids20120101

Title: Simultaneous determination of different endogenetic plant growth regulators in common green seaweeds using dispersive liquid-liquid microextraction method.

Journal: Plant physiology and biochemistry : PPB20111101

Title: Effects of kinetin riboside on proliferation and proapoptotic activities in human normal and cancer cell lines.

Journal: Journal of cellular biochemistry20110801

Title: Anticancer activity of natural cytokinins: a structure-activity relationship study.

Journal: Phytochemistry20100801

Title: FKBP38 protects Bcl-2 from caspase-dependent degradation.

Journal: The Journal of biological chemistry20100326

Title: The experimental chemotherapeutic N6-furfuryladenosine (kinetin-riboside) induces rapid ATP depletion, genotoxic stress, and CDKN1A(p21) upregulation in human cancer cell lines.

Journal: Biochemical pharmacology20090401

Title: Inhibitory effect of kinetin riboside in human heptamoa, HepG2.

Journal: Molecular bioSystems20090101

Title: Ribose-modified purine nucleosides as ribonucleotide reductase inhibitors. Synthesis, antitumor activity, and molecular modeling of N6-substituted 3'-C-methyladenosine derivatives.

Journal: Journal of medicinal chemistry20080724

Title: Constrained NBMPR analogue synthesis, pharmacophore mapping and 3D-QSAR modeling of equilibrative nucleoside transporter 1 (ENT1) inhibitory activity.

Journal: Bioorganic & medicinal chemistry20080401

Title: Kinetin riboside preferentially induces apoptosis by modulating Bcl-2 family proteins and caspase-3 in cancer cells.

Journal: Cancer letters20080308

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology20060501

Title: Rajabi M, et al. Antiproliferative activity of kinetin riboside on HCT-15 colon cancer cell line. Nucleosides Nucleotides Nucleic Acids. 2012;31(6):474-81.

Title: Choi BH, et al. Kinetin riboside preferentially induces apoptosis by modulating Bcl-2 family proteins and caspase-3 in cancer cells. Cancer Lett. 2008 Mar 8;261(1):37-45.

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