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Alvespimycin

Base Information Edit
  • Chemical Name:Alvespimycin
  • CAS No.:467214-20-6
  • Molecular Formula:C32H48N4O8
  • Molecular Weight:616.755
  • Hs Code.:29419090
  • UNII:001L2FE0M3
  • DSSTox Substance ID:DTXSID00963646
  • Wikipedia:17-Dimethylaminoethylamino-17-demethoxygeldanamycin
  • Wikidata:Q4552287
  • NCI Thesaurus Code:C38142
  • Pharos Ligand ID:8A2P6WKTAK4Z,8A2VKSZVVLNF
  • Metabolomics Workbench ID:153429
  • ChEMBL ID:CHEMBL383824
  • Mol file:467214-20-6.mol
Alvespimycin

Synonyms:17-(dimethylaminoethylamino)-17-demethoxy-geldanamycin;17-(dimethylaminoethylamino)-17-demethoxygeldanamycin;17-desmethoxy-17-n,n-dimethylaminoethylamino-geldanamycin;17-dimethylaminoethylamino-17-demethoxy-geldanamycin;17-DMAG;17DMAG;alvespimycin;KOS 1022;KOS-1022;KOS1022;NSC 707545;NSC707545

Suppliers and Price of Alvespimycin
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • 17-DMAG
  • 100ug
  • $ 273.00
  • Usbiological
  • 17-DMAG hydrochloride
  • 100mg
  • $ 506.00
  • Usbiological
  • 17-DMAG Hydrochloride
  • 250mg
  • $ 422.00
  • TRC
  • 17-N-(2-Dimethylaminoethylamino)-17-demethoxyGeldanamycin-d6
  • 1mg
  • $ 155.00
  • TRC
  • 17-DMAG
  • 2.5mg
  • $ 315.00
  • Tocris
  • 17-DMAGhydrochloride ≥99%(HPLC)
  • 1
  • $ 255.00
  • Crysdot
  • 17-DMAG 98+%
  • 25mg
  • $ 70.00
  • Crysdot
  • 17-DMAG 98+%
  • 10mg
  • $ 49.00
  • Crysdot
  • 17-DMAG 98+%
  • 100mg
  • $ 191.00
  • Cayman Chemical
  • 17-DMAG ≥98%
  • 10mg
  • $ 173.00
Total 65 raw suppliers
Chemical Property of Alvespimycin Edit
Chemical Property:
  • PSA:169.52000 
  • Density:1.2 
  • LogP:3.33320 
  • Storage Temp.:Desiccate at -20°C 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • XLogP3:2
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:8
  • Exact Mass:616.34721450
  • Heavy Atom Count:44
  • Complexity:1230
Purity/Quality:

98%,99%, *data from raw suppliers

17-DMAG *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1CC(C(C(C=C(C(C(C=CC=C(C(=O)NC2=CC(=O)C(=C(C1)C2=O)NCCN(C)C)C)OC)OC(=O)N)C)C)O)OC
  • Isomeric SMILES:C[C@H]1C[C@@H]([C@@H]([C@H](/C=C(/[C@@H]([C@H](/C=C\C=C(\C(=O)NC2=CC(=O)C(=C(C1)C2=O)NCCN(C)C)/C)OC)OC(=O)N)\C)C)O)OC
  • Recent ClinicalTrials:Clinical Trial of Intravenous Alvespimycin in Patients With Her2 Positive Breast Cancer
  • Description Geldanamycin is a potent inhibitor of Hsp90 that has poor water solubility. 17-DMAG is a water-soluble derivative of geldanamycin which potently inhibits Hsp90 (IC50 = 24 nM) and has excellent bioavailability and tissue distribution in animals. Like other Hsp90 inhibitors, 17-DMAG has diverse anti-tumor actions and has potential in treating certain types of cancer. This compound also suppresses inflammation by interfering with signaling through the NF-κB pathway. 17-DMAG also ameliorates high fat diet-induced renal failure in a mouse model of diabetes.
  • Uses 17-DMAG is an analogue of Gelamycin (G304500) and 17-(Allylamino)geldanamycin (A549650). 17-DMAG acts as a Hsp90 inhibitor and displays more potent antitumor activity than 17-AAG. The labelled derivative of the analogue of Gelamycin (G304500) and 17-(Allylamino)geldanamycin (A549650). It acts as a Hsp90 inhibitor and displays more potent antitumor activity than 17-AAG. 17-DMAG is a synthetic Geldanamycin derivative and inhibitor of Hsp90.
Technology Process of Alvespimycin

There total 1 articles about Alvespimycin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In chloroform; at 20 ℃; for 4h;
Guidance literature:
With dmap; In 1,2-dichloro-ethane; at 20 ℃; for 48h;
DOI:10.1021/jm900098v
Refernces Edit
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