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Page 1
Showing results for quinols
Search for Quiñoa S instead (1 results)
Natural sesquiterpene quinone/quinols: chemistry, biological activity, and synthesis.
Tian XH, Hong LL, Jiao WH, Lin HW. Tian XH, et al. Nat Prod Rep. 2023 Mar 22;40(3):718-749. doi: 10.1039/d2np00045h. Nat Prod Rep. 2023. PMID: 36636914 Review.
Covering: 2010 to 2021Sesquiterpene quinone/quinols (SQs) are characterized by a C15-sesquiterpenoid unit incorporating a C6-benzoquinone/quinol moiety. ...
Covering: 2010 to 2021Sesquiterpene quinone/quinols (SQs) are characterized by a C15-sesquiterpenoid unit incorporating a C6-benzoqui …
Interaction of membrane-embedded cytochrome b-complexes with quinols: Classical Q-cycle and murburn model.
Manoj KM, Gideon DA, Jaeken L. Manoj KM, et al. Cell Biochem Funct. 2022 Mar;40(2):118-126. doi: 10.1002/cbf.3682. Epub 2022 Jan 13. Cell Biochem Funct. 2022. PMID: 35026863 Review.
We recently proposed a diffusible reactive (oxygen) species (DRS/DROS) based function for cytochrome b complexes (CBC) and quinones (Q)/quinols (QH(2) ) in the murburn model of bioenergetics. This proposal is in direct conflict with the classical purview of Q-cycle. ...New …
We recently proposed a diffusible reactive (oxygen) species (DRS/DROS) based function for cytochrome b complexes (CBC) and quinones (Q)/q …
Reductive Aromatization of Quinols with B(2) pin(2) as Deoxidizing Agent.
Liu B, Xu Y, Luo Z, Xie J. Liu B, et al. Chem Asian J. 2020 Apr 1;15(7):1022-1024. doi: 10.1002/asia.202000064. Epub 2020 Mar 5. Chem Asian J. 2020. PMID: 32034862
We have demonstrated B(2) pin(2) as superior deoxidizing agent for the reductive deoxygenation of quinol derivatives under basic conditions. A wide range of highly functionalized phenols were obtained in good yields including a complex drug molecule, which revealed the hig …
We have demonstrated B(2) pin(2) as superior deoxidizing agent for the reductive deoxygenation of quinol derivatives under basic cond …
Predicting pK(a) Values of Quinols and Related Aromatic Compounds with Multiple OH Groups.
Morency M, Néron S, Iftimie R, Wuest JD. Morency M, et al. J Org Chem. 2021 Nov 5;86(21):14444-14460. doi: 10.1021/acs.joc.1c01279. Epub 2021 Oct 6. J Org Chem. 2021. PMID: 34613729
Our approach has been validated by showing that predicted and experimental values for over 100 quinols and related compounds differ by an average of only 0.3 units. This accuracy makes it possible to select proper pK(a) values when experimental data vary, predict the acidi …
Our approach has been validated by showing that predicted and experimental values for over 100 quinols and related compounds differ b …
History of hydroquinone.
Banodkar PD, Banodkar KP. Banodkar PD, et al. Indian J Dermatol Venereol Leprol. 2022 Sep-Oct;88(5):696-699. doi: 10.25259/IJDVL_657_2021. Indian J Dermatol Venereol Leprol. 2022. PMID: 35841353 Free article. No abstract available.
Hydroquinone: myths and reality.
Searle T, Al-Niaimi F, Ali FR. Searle T, et al. Clin Exp Dermatol. 2021 Jun;46(4):636-640. doi: 10.1111/ced.14480. Epub 2020 Nov 7. Clin Exp Dermatol. 2021. PMID: 33159818 Review.
Hydroquinone.
[No authors listed] [No authors listed] IARC Monogr Eval Carcinog Risks Hum. 1999;71 Pt 2(PT 2):691-719. IARC Monogr Eval Carcinog Risks Hum. 1999. PMID: 10476468 Free PMC article. Review. No abstract available.
One-Pot Synthesis of 1-Hydroxyacridones from para-Quinols and ortho-Methoxycarbonylaryl Isocyanates.
Wu J, Zhang J, Soto-Acosta R, Mao L, Lian J, Chen K, Pillon G, Zhang G, Geraghty RJ, Zheng S. Wu J, et al. J Org Chem. 2020 Mar 20;85(6):4515-4524. doi: 10.1021/acs.joc.9b03307. Epub 2020 Feb 27. J Org Chem. 2020. PMID: 32070098
A variety of substituted acridones were synthesized via a one-pot, metal-free cascade reaction. In this event, the DBU-mediated addition between quinols and ortho-methoxycarbonylaryl isocyanates formed a bicyclic oxazolidinone, followed by a sequence of intramolecular cond …
A variety of substituted acridones were synthesized via a one-pot, metal-free cascade reaction. In this event, the DBU-mediated addition bet …
Cytotoxic Sesquiterpenoid Quinones and Quinols, and an 11-Membered Heterocycle, Kauamide, from the Hawaiian Marine Sponge Dactylospongia elegans.
Neupane RP, Parrish SM, Neupane JB, Yoshida WY, Yip MLR, Turkson J, Harper MK, Head JD, Williams PG. Neupane RP, et al. Mar Drugs. 2019 Jul 19;17(7):423. doi: 10.3390/md17070423. Mar Drugs. 2019. PMID: 31331110 Free PMC article.
Several known sesquiterpenoid quinones and quinols (1-9), and kauamide (10), a new polyketide-peptide containing an 11-membered heterocycle, were isolated from the extracts of the Hawaiian marine sponge Dactylospongia elegans. ...
Several known sesquiterpenoid quinones and quinols (1-9), and kauamide (10), a new polyketide-peptide containing an 11-membered heter …
Treatment of hyperpigmentation.
Woolery-Lloyd H, Kammer JN. Woolery-Lloyd H, et al. Semin Cutan Med Surg. 2011 Sep;30(3):171-5. doi: 10.1016/j.sder.2011.06.004. Semin Cutan Med Surg. 2011. PMID: 21925372 Review.
6,713 results