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ScientificNameLabel
3-p-coumaroylquinic acid
PHCD compound ID : 4179
Chemical Names :
5-p-Coumaroyl quinic acid , 3-p-coumaroylquinic acid
Molecular Formula : C16H18O8
Molecular Weight : 338.100168
More Details :
Names & Synonyms: (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-cyclohexanecarboxylic acid , (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)-1-oxoprop-2-enoxy]-1-cyclohexanecarboxylic acid , (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxycyclohexane-1-carboxylic acid , (1R,3R,4S,5R)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,4,5-tris(oxidanyl)cyclohexane-1-carboxylic acid , (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)acryloyl]oxy-cyclohexanecarboxylic acid
Smiles: O=C(O[C@@H]1C[C@](O)(C[C@H]([C@@H]1O)O)C(=O)O)/C=C/c1ccc(cc1)O
InChi : InChI=1S/C16H18O8/c17-10-4-1-9(2-5-10)3-6-13(19)24-12-8-16(23,15(21)22)7-11(18)14(12)20/h1-6,11-12,14,17-18,20,23H,7-8H2,(H,21,22)/b6-3+/t11-,12-,14+,16-/m1/s1
InChi Key : InChIKey=BMRSEYFENKXDIS-QHAYPTCMSA-N
PubChem ID : 9945785
Rotatable bond count : 5 Rule of five : 0
Hydrogen bond acceptor count : 8 Ionization potential : 9.382374
Hydrogen bond donor count : 5 Electric dipole moment : 2.082
XLogP : -0.837 VDW volume : 304.182357
Molecular weight : 338.100168 HOMO-LUMO gap : 8.366000
Herb list :
Refrences & Litretures:
  
583.      Journal:'Food Chemistry'      Year:'2012'      Volume:'132'      Page:'261'      DOI:'10.1016/j.foodchem.2011.10.074'      Title:'The anticarcinogenic potential of essential oil and aqueous infusion from caper (Capparis spinosa L.)'
613.      Journal:'Food and Chemical Toxicology'      Year:'2007'      Volume:'45'      Page:'2287'      DOI:'10.1016/j.fct.2007.06.004'      Title:'Walnut (Juglans regia L.) leaves: Phenolic compounds, antibacterial activity and antioxidant potential of di?erent cultivars'
645.      Journal:'J. Agric. Food Chem'      Year:'2013'      Volume:'61'      Page:'801'      DOI:'10.1021/jf304002h'      Title:'Chemical Composition, Antioxidative and Anti-In?ammatory Activity of Extracts Prepared from Aerial Parts of Oenothera biennis L. and Oenothera paradoxa Hudziok Obtained after Seeds Cultivation'
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