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Adarotene

Base Information
  • Chemical Name:Adarotene
  • CAS No.:496868-77-0
  • Molecular Formula:C25H26O3
  • Molecular Weight:374.48
  • Hs Code.:
  • UNII:W6SU73VG8H
  • DSSTox Substance ID:DTXSID9040390
  • Nikkaji Number:J2.762.251H
  • Wikipedia:Adarotene
  • Wikidata:Q15633950
  • NCI Thesaurus Code:C96706
  • ChEMBL ID:CHEMBL442016
  • Mol file:496868-77-0.mol
Adarotene

Synonyms:adarotene

Suppliers and Price of Adarotene
Supply Marketing:
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
  • DC Chemicals
  • Adarotene >98%
  • 250 mg
  • $ 900.00
  • DC Chemicals
  • Adarotene >98%
  • 100 mg
  • $ 450.00
  • Cayman Chemical
  • Adarotene
  • 25mg
  • $ 254.00
  • Cayman Chemical
  • Adarotene
  • 10mg
  • $ 107.00
  • Cayman Chemical
  • Adarotene
  • 5mg
  • $ 60.00
  • Cayman Chemical
  • Adarotene
  • 50mg
  • $ 476.00
  • ApexBio Technology
  • Adarotene
  • 10mg
  • $ 127.00
  • ApexBio Technology
  • Adarotene
  • 5mg
  • $ 68.00
  • American Custom Chemicals Corporation
  • ADAROTENE 95.00%
  • 5MG
  • $ 220.00
  • AK Scientific
  • Adarotene
  • 25mg
  • $ 389.00
Total 11 raw suppliers
Chemical Property of Adarotene
Chemical Property:
  • Melting Point:>240 °C 
  • Boiling Point:574.1±50.0 °C(Predicted) 
  • PKA:-95.54±0.10(Predicted) 
  • PSA:57.53000 
  • Density:1.257 
  • LogP:5.62480 
  • Solubility.:≥37.4 mg/mL in DMSO; insoluble in H2O; ≥10.97 mg/mL in EtOH with gentle warming and ultrasonic 
  • XLogP3:6.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:374.18819469
  • Heavy Atom Count:28
  • Complexity:574
Purity/Quality:

97% *data from raw suppliers

Adarotene >98% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C2CC3CC1CC(C2)(C3)C4=C(C=CC(=C4)C5=CC=C(C=C5)C=CC(=O)O)O
  • Isomeric SMILES:C1C2CC3CC1CC(C2)(C3)C4=C(C=CC(=C4)C5=CC=C(C=C5)/C=C/C(=O)O)O
  • Uses Adarotene has been found to have antitumor activity against different types of cancer, including acute myeloid leukemia, primary effusion lymphoma, prostate cancer and glioma. It may also be useful in treating acute lung injury through inflammation and ROS suppression via inactivating TLR4?/NF-?κB and p38?/ERK1?/2 signaling pathways.
Technology Process of Adarotene

There total 17 articles about Adarotene 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:
With lithium hydroxide; In tetrahydrofuran; at 25 ℃;
DOI:10.1021/jm025593y
Guidance literature:
Multi-step reaction with 3 steps
1: 100 percent / AcOH; H2SO4 / 96 h / 20 °C
2: 98 percent / Pd(OAc)2; tri-o-tolylphosphine; Et3N / 4 h / 100 - 110 °C
3: 94 percent / aq. LiOH / tetrahydrofuran / 20 °C
With palladium diacetate; lithium hydroxide; sulfuric acid; acetic acid; triethylamine; tris-(o-tolyl)phosphine; In tetrahydrofuran; 2: Heck reaction;
DOI:10.1021/jm049440h
Guidance literature:
With water; In dimethyl sulfoxide; at 37 ℃; for 24h; pH=7.4; aq. buffer;
DOI:10.1016/j.bmc.2012.01.042
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