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Compound InformationSONAR Target prediction
Name:

CHLOROGENIC ACID

Unique Identifier:SPE00210800
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:336.166 g/mol
X log p:8.313  (online calculus)
Lipinksi Failures1
TPSA43.37
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:9
Rotatable Bond Count:5
Canonical Smiles:OC1CC(O)(CC(OC(=O)C=Cc2ccc(O)c(O)c2)C1O)C(O)=O
Class:aromatic
Source:occurence in many plants
Reference:Phytochemistry 15: 703 (1976); Biochem J 361: 57 (2002)
Therapeutics:antioxidant, free radical scavenger

Found: 205 nonactive as graph: single | with analogs [1] << Back 101 102 103 104 105 106 107 108 109 110  Next >> [205]
Species: 4932
Condition: ASF1
Replicates: 2
Raw OD Value: r im 0.5969±0.000353553
Normalized OD Score: sc h 0.9924±0.00707314
Z-Score: -0.3255±0.30298
p-Value: 0.750386
Z-Factor: -15.0234
Fitness Defect: 0.2872
Bioactivity Statement: Nonactive
Experimental Conditions
Library:SPECMTS3
Plate Number and Position:12|H5
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:23.80 Celcius
Date:2008-01-30 YYYY-MM-DD
Plate CH Control (+):0.043625±0.00040
Plate DMSO Control (-):0.5763750000000001±0.01732
Plate Z-Factor:0.9023
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DBLink | Rows returned: 23<< Back 1 2 3 4 Next >> 
5280633 (1S,3R,4R,5R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxy-cyclohexane-1-carboxylic
acid
5315832 3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxy-cyclohexane-1-carboxylic acid
5317239 ethyl 3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxy-cyclohexane-1-carboxylate
5318529 (1R,3R,4R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxy-cyclohexane-1-carboxylic acid
6325638 methyl
(1R,3R,4R,5R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxy-cyclohexane-1-carboxylate
6436237 (1R,3R,4R,5R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxy-cyclohexane-1-carboxylic
acid

internal high similarity DBLink | Rows returned: 0

active | Cluster 6023 | Additional Members: 3 | Rows returned: 0

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