Pyrocatechol
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Basic Info
Common Name | Pyrocatechol(F05459) |
2D Structure | |
Description | Pyrocatechol, often known as catechol or benzene-1,2-diol, is a benzenediol, with formula C6H4(OH)2. It was first prepared in 1839 by H. Reinsch by distilling catechin (the juice of Mimosa catechu). This colourless compound occurs naturally, but about 20000 tons are manufactured each year, mainly as precursors to pesticides, flavors, and fragrances. Its sulfonic acid is often present in the urine of many mammals. Small amounts of catechol occur naturally in fruits and vegetables, along with the enzyme polyphenol oxidase. Upon mixing the enzyme with the substrate and exposure to oxygen (as when a potato or apple is cut), the colorless catechol oxidizes to reddish-brown benzoquinone derivatives. The enzyme is inactivated by adding an acid, such as lemon juice, or by refrigeration. Excluding oxygen also prevents the browning reaction. Catechol melts at 28 oC and boils at 250 oC. It is employed in medicine as an expectorant. The dimethyl ether or veratrol is also used in medicine. Many other pyrocatechin derivatives have been suggested for therapeutic application. |
FRCD ID | F05459 |
CAS Number | 120-80-9 |
PubChem CID | 289 |
Formula | C6H6O2 |
IUPAC Name | benzene-1,2-diol |
InChI Key | YCIMNLLNPGFGHC-UHFFFAOYSA-N |
InChI | InChI=1S/C6H6O2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H |
Canonical SMILES | C1=CC=C(C(=C1)O)O |
Isomeric SMILES | C1=CC=C(C(=C1)O)O |
Wikipedia | Pyrocatechol |
Synonyms | benzene-1,2-diol pyrocatechol catechol 120-80-9 1,2-dihydroxybenzene 1,2-benzenediol pyrocatechin 2-hydroxyphenol o-Benzenediol Pyrocatechine |
Classifies | Pollutant Pesticide |
Update Date | Nov 13, 2018 17:07 |
Chemical Taxonomy
Kingdom | Organic compounds |
Superclass | Benzenoids |
Class | Phenols |
Subclass | Benzenediols |
Intermediate Tree Nodes | Not available |
Direct Parent | Catechols |
Alternative Parents | |
Molecular Framework | Aromatic homomonocyclic compounds |
Substituents | Catechol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
Description | This compound belongs to the class of organic compounds known as catechols. These are compounds containing a 1,2-benzenediol moiety. |
Properties
Property Name | Property Value |
---|---|
Molecular Weight | 110.112 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 0 |
Complexity | 62.9 |
Monoisotopic Mass | 110.037 |
Exact Mass | 110.037 |
XLogP | 0.9 |
Formal Charge | 0 |
Heavy Atom Count | 8 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Isotope Atom Count | 0 |
Covalently-Bonded Unit Count | 1 |
ADMET
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB+ | 0.5000 |
Human Intestinal Absorption | HIA+ | 0.9782 |
Caco-2 Permeability | Caco2+ | 0.8824 |
P-glycoprotein Substrate | Non-substrate | 0.7207 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9705 |
Non-inhibitor | 0.9926 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.9134 |
Distribution | ||
Subcellular localization | Mitochondria | 0.8082 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8247 |
CYP450 2D6 Substrate | Non-substrate | 0.8574 |
CYP450 3A4 Substrate | Non-substrate | 0.7305 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.8949 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9070 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.9579 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.9348 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9570 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7461 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9322 |
Non-inhibitor | 0.8953 | |
AMES Toxicity | Non AMES toxic | 0.6674 |
Carcinogens | Non-carcinogens | 0.8689 |
Fish Toxicity | High FHMT | 0.7424 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9702 |
Honey Bee Toxicity | High HBT | 0.6926 |
Biodegradation | Ready biodegradable | 0.6877 |
Acute Oral Toxicity | II | 0.7741 |
Carcinogenicity (Three-class) | Warning | 0.5621 |
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -0.0276 | LogS |
Caco-2 Permeability | 1.1463 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.5957 | LD50, mol/kg |
Fish Toxicity | 1.0318 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.6327 | pIGC50, ug/L |
References
Title | Journal | Date | Pubmed ID |
---|---|---|---|
Chromatographic fingerprinting through chemometric techniques for herbal slimming pills: A way of adulterant identification. | Forensic Sci Int | 2018 May | 29602149 |
Influence of inherent hierarchical porous char with alkali and alkaline earthmetallic species on lignin pyrolysis. | Bioresour Technol | 2018 Jul 25 | 30092486 |
Phenolic root exudate and tissue compounds vary widely among temperate forest tree species and have contrasting effects on soil microbial respiration. | New Phytol | 2018 Apr | 29473651 |
Molecular characterization and phylogenetic analysis of highly pathogenic Vibrio alginolyticus strains isolated during mortality outbreaks in cultured Ruditapesdecussatus juvenile. | Microb Pathog | 2017 Oct | 28923608 |
Multiple metabolic pathways for metabolism of l-tryptophan in Fusarium graminearum. | Can J Microbiol | 2017 Nov | 28926717 |
Antioxidant capacity of (+)-catechin visible-light photoirradiated in thepresence of vitamin B2. | Redox Rep | 2017 Nov | 27712465 |
Phenolic compounds isolated from fermented blueberry juice decrease hepatocellular glucose output and enhance muscle glucose uptake in cultured murine and human cells. | BMC Complement Altern Med | 2017 Mar 4 | 28259166 |
Bacteria Associated to Plants Naturally Selected in a Historical PCB PollutedSoil Show Potential to Sustain Natural Attenuation. | Front Microbiol | 2017 Jul 25 | 28790991 |
Efficacy of free and encapsulated Bacillus lichenformis strain SL10 on degradation of phenol: A comparative study of degradation kinetics. | J Environ Manage | 2017 Jul 15 | 28407600 |
Antioxidant and ion-induced gelation functions of pectins enabled by polyphenolconjugation. | Int J Biol Macromol | 2017 Aug | 28366850 |
Antioxidant activity of commercial food grade tannins exemplified in a winemodel. | Food Addit Contam Part A Chem Anal Control Expo Risk Assess | 2016Dec | 27696959 |
Nutrient retention and fate of iron-binding phenolic compounds during the injera processing of tannin-free and high-tannin sorghum. | J Sci Food Agric | 2016 Mar 30 | 25951136 |
Retaining Oxidative Stability of Emulsified Foods by Novel NonmigratoryPolyphenol Coated Active Packaging. | J Agric Food Chem | 2016 Jul 13 | 27310107 |
Evaluation of metal concentration and antioxidant, antimicrobial, and anticancer potentials of two edible mushrooms Lactarius deliciosus and Macrolepiota procera. | J Food Drug Anal | 2016 Jul | 28911552 |
Efficient Binding of Heavy Metals by Black Sesame Pigment: Toward InnovativeDietary Strategies To Prevent Bioaccumulation. | J Agric Food Chem | 2016 Feb 3 | 26752477 |
Effect of Selected Plant Phenolics on Fe2+-EDTA-H₂O₂ System Mediated Deoxyribose Oxidation: Molecular Structure-Derived Relationships of Anti- and Pro-OxidantActions. | Molecules | 2016 Dec 31 | 28042856 |
Iron binding efficiency of polyphenols: Comparison of effect of ascorbic acid andethylenediaminetetraacetic acid on catechol and galloyl groups. | Food Chem | 2016 Apr 15 | 26675868 |
Neuraminidase inhibition of Dietary chlorogenic acids and derivatives - potentialantivirals from dietary sources. | Food Funct | 2016 Apr | 27010419 |
Dietary Catechols and their Relationship to Microbial Endocrinology. | Adv Exp Med Biol | 2016 | 26589215 |
Platinum Nanoparticles: Efficient and Stable Catechol Oxidase Mimetics. | ACS Appl Mater Interfaces | 2015 Sep 9 | 26305170 |
Targets
- General Function:
- Zinc ion binding
- Specific Function:
- Nuclear receptor that binds DNA as a monomer to ROR response elements (RORE) containing a single core motif half-site 5'-AGGTCA-3' preceded by a short A-T-rich sequence. Key regulator of cellular differentiation, immunity, peripheral circadian rhythm as well as lipid, steroid, xenobiotics and glucose metabolism. Considered to have intrinsic transcriptional activity, have some natural ligands like oxysterols that act as agonists (25-hydroxycholesterol) or inverse agonists (7-oxygenated sterols), enhancing or repressing the transcriptional activity, respectively. Recruits distinct combinations of cofactors to target gene regulatory regions to modulate their transcriptional expression, depending on the tissue, time and promoter contexts. Regulates the circadian expression of clock genes such as CRY1, ARNTL/BMAL1 and NR1D1 in peripheral tissues and in a tissue-selective manner. Competes with NR1D1 for binding to their shared DNA response element on some clock genes such as ARNTL/BMAL1, CRY1 and NR1D1 itself, resulting in NR1D1-mediated repression or RORC-mediated activation of the expression, leading to the circadian pattern of clock genes expression. Therefore influences the period length and stability of the clock. Involved in the regulation of the rhythmic expression of genes involved in glucose and lipid metabolism, including PLIN2 and AVPR1A. Negative regulator of adipocyte differentiation through the regulation of early phase genes expression, such as MMP3. Controls adipogenesis as well as adipocyte size and modulates insulin sensitivity in obesity. In liver, has specific and redundant functions with RORA as positive or negative modulator of expression of genes encoding phase I and Phase II proteins involved in the metabolism of lipids, steroids and xenobiotics, such as SULT1E1. Also plays also a role in the regulation of hepatocyte glucose metabolism through the regulation of G6PC and PCK1. Regulates the rhythmic expression of PROX1 and promotes its nuclear localization (By similarity). Plays an indispensable role in the induction of IFN-gamma dependent anti-mycobacterial systemic immunity (PubMed:26160376).Isoform 2: Essential for thymopoiesis and the development of several secondary lymphoid tissues, including lymph nodes and Peyer's patches. Required for the generation of LTi (lymphoid tissue inducer) cells. Regulates thymocyte survival through DNA-binding on ROREs of target gene promoter regions and recruitment of coactivaros via the AF-2. Also plays a key role, downstream of IL6 and TGFB and synergistically with RORA, for lineage specification of uncommitted CD4(+) T-helper (T(H)) cells into T(H)17 cells, antagonizing the T(H)1 program. Probably regulates IL17 and IL17F expression on T(H) by binding to the essential enhancer conserved non-coding sequence 2 (CNS2) in the IL17-IL17F locus. May also play a role in the pre-TCR activation cascade leading to the maturation of alpha/beta T-cells and may participate in the regulation of DNA accessibility in the TCR-J(alpha) locus.
- Gene Name:
- RORC
- Uniprot ID:
- P51449
- Molecular Weight:
- 58194.845 Da
References
- Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]