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228266-40-8,MFCD07772353
Catalog No.:AA00BF22

228266-40-8 | Taltobulin

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$82.00   $57.00
- +
5mg
99%
in stock  
$333.00   $233.00
- +
10mg
99%
in stock  
$488.00   $342.00
- +
25mg
99%
in stock  
$1,040.00   $728.00
- +
50mg
99%
in stock  
$1,577.00   $1,104.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00BF22
Chemical Name:
Taltobulin
CAS Number:
228266-40-8
Molecular Formula:
C27H43N3O4
Molecular Weight:
473.6480
MDL Number:
MFCD07772353
SMILES:
CN[C@@H](C(c1ccccc1)(C)C)C(=O)N[C@@H](C(C)(C)C)C(=O)N([C@@H](C(C)C)/C=C(/C(=O)O)\C)C
Properties
Computed Properties
 
Complexity:
746  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Defined Bond Stereocenter Count:
1  
Heavy Atom Count:
34  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
11  
XLogP3:
2.6  

Literature

Title: Mitochondrial dysfunction confers resistance to multiple drugs in Caenorhabditis elegans.

Journal: Molecular biology of the cell 20100315

Title: Absolute configurations of tubulin inhibitors taltobulin (HTI-286) and HTI-042 characterized by X-ray diffraction analysis and NMR studies.

Journal: Bioorganic & medicinal chemistry letters 20100301

Title: Total synthesis and biological evaluation of tubulysin U, tubulysin V, and their analogues.

Journal: Journal of medicinal chemistry 20090122

Title: Targeting prostate cancer with HTI-286, a synthetic analog of the marine sponge product hemiasterlin.

Journal: International journal of cancer 20080515

Title: Tubulysin analogs incorporating desmethyl and dimethyl tubuphenylalanine derivatives.

Journal: Bioorganic & medicinal chemistry letters 20080501

Title: Inhibition of hepatic tumor cell proliferation in vitro and tumor growth in vivo by taltobulin, a synthetic analogue of the tripeptide hemiasterlin.

Journal: World journal of gastroenterology 20061114

Title: Two photoaffinity analogues of the tripeptide, hemiasterlin, exclusively label alpha-tubulin.

Journal: Biochemistry 20050510

Title: Tumor cells resistant to a microtubule-depolymerizing hemiasterlin analogue, HTI-286, have mutations in alpha- or beta-tubulin and increased microtubule stability.

Journal: Biochemistry 20041109

Title: Cells resistant to HTI-286 do not overexpress P-glycoprotein but have reduced drug accumulation and a point mutation in alpha-tubulin.

Journal: Molecular cancer therapeutics 20041001

Title: Synthesis and biological activity of analogues of the antimicrotubule agent N,beta,beta-trimethyl-L-phenylalanyl-N(1)-[(1S,2E)-3-carboxy-1-isopropylbut-2-enyl]- N(1),3-dimethyl-L-valinamide (HTI-286).

Journal: Journal of medicinal chemistry 20040909

Title: Probing the interaction of HTI-286 with tubulin using a stilbene analogue.

Journal: Journal of the American Chemical Society 20040818

Title: D-piece modifications of the hemiasterlin analog HTI-286 produce potent tubulin inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20040816

Title: Targeting vascular and avascular compartments of tumors with C. novyi-NT and anti-microtubule agents.

Journal: Cancer biology & therapy 20040301

Title: Biophysical characterization of the interactions of HTI-286 with tubulin heterodimer and microtubules.

Journal: Biochemistry 20031125

Title: HTI-286, a synthetic analogue of the tripeptide hemiasterlin, is a potent antimicrotubule agent that circumvents P-glycoprotein-mediated resistance in vitro and in vivo.

Journal: Cancer research 20030415

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