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Naphthols

Naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position. They are often used in dyes and pigments, as antioxidants for rubber, fats, and oils, as insecticides, in pharmaceuticals, and in numerous other applications.
Also Known As:
Hydroxynaphthalene; Hydroxynaphthalenes; Naphthol
Networked: 64 relevant articles (2 outcomes, 13 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Munson-McGee, Stuart H: 2 articles (10/2022 - 08/2022)
2. Niemann, Danielle: 2 articles (10/2022 - 08/2022)
3. Rahman, Humairat H: 2 articles (10/2022 - 08/2022)
4. Carson, Sean C: 1 article (01/2022)
5. Colley, Susan B: 1 article (01/2022)
6. Faia, Celeste: 1 article (01/2022)
7. Ingraham Iv, Charles H: 1 article (01/2022)
8. Jursic, Branko S: 1 article (01/2022)
9. Lassak, Adam: 1 article (01/2022)
10. Peruzzi, Francesca: 1 article (01/2022)

Related Diseases

1. Neoplasms (Cancer)
2. Breast Neoplasms (Breast Cancer)
08/01/2012 - "EE2 had a K(i) of 10 nM for inhibiting p-nitrophenol and β-naphthol sulfation and inhibited 17β-estradiol (E2) sulfation in intact human MCF-7 breast cancer cells with a K(i) of 19 nM. In contrast, the K(m) for EE2 sulfation by SULT1A1 was 700 nM. The K(d) for EE2 binding of pure SULT1A1 was 0.5 ± 0.15 μM; however, the K(d) for EE2 binding to the SULT1A1-PAP complex was >100-fold lower (4.3 ± 1.7 nM). "
01/01/2018 - "N-substituted hydroxynaphthalene imino-oxindole derivatives as new class of PI3-kinase inhibitor and breast cancer drug: Molecular validation and structure-activity relationship studies."
12/26/2012 - "The one-pot, three-component reaction of α or β-naphthol, malonitrile and an aromatic aldehyde in the presence of diammonium hydrogen phosphate was afforded the corresponding 2-amino-4-aryl-4H-benzo[h or f]chromene-3-carbonitrile derivatives, All target compounds were evaluated for inhibition of Src kinase and cell proliferation in breast carcinoma (BT-20) cell lines. "
06/06/2014 - "The convergent total synthesis of polycarcin V, a gilvocarcin-type natural product that shows significant cytotoxicity with selectivity for nonsmall-cell lung cancer, breast cancer, and melanoma cells, has been achieved in 13 steps from 7, 8, and 22; the sequence features a stereoselective α-C-glycosylation reaction for the union of protected carbohydrate 7 and naphthol 8. The association constant for the binding of polycarcin V to duplex DNA is similar to that previously reported for gilvocarcin V. "
05/15/2019 - "In the aqueous solvent, excited state proton transfer (ESPT) competes with the abovementioned processes, giving rise to naphtholates, but the process is inefficient and can only be observed in the buffered aqueous solution at pH > 7. Since the dehydration of bis-naphthols delivers QMs, their potential antiproliferative activity was investigated by an MTT test on three human cancer cell lines (NCI-H1299, lung carcinoma; MCF-7, breast adenocarcinoma; and SUM159, pleomorphic breast carcinoma). "
3. Hyperthermia
4. Lymphoma (Lymphomas)
5. Krukenberg Tumor

Related Drugs and Biologics

1. Pyrans
2. beta-lapachone
3. Oxidoreductases (Dehydrogenase)
4. NAD (NADH)
5. quinone (benzoquinone)
6. Esterases
7. Hematoxylin (Haematoxylon)
8. Eosine Yellowish-(YS) (Eosin)
9. Periodic Acid
10. Pyronine

Related Therapies and Procedures

1. Transdermal Patch