Norperistictic acid

Details

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Internal ID d004e8ca-47c7-4f40-bbbf-1c2239728023
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Phthalate esters > m-Phthalate esters
IUPAC Name 5,13,17-trihydroxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.03,8.014,18]octadeca-1(11),3(8),4,6,12,14(18)-hexaene-4-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H12O10/c1-4-3-6(19)8(15(21)22)13-7(4)16(23)27-12-5(2)11(20)9-10(14(12)26-13)18(25)28-17(9)24/h3,18-20,25H,1-2H3,(H,21,22)
InChI Key YGHQAMXBZNTFBI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H12O10
Molecular Weight 388.30 g/mol
Exact Mass 388.04304658 g/mol
Topological Polar Surface Area (TPSA) 160.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 1.90
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Norperistictic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9297 92.97%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6836 68.36%
OATP2B1 inhibitior - 0.7076 70.76%
OATP1B1 inhibitior - 0.4222 42.22%
OATP1B3 inhibitior - 0.5300 53.00%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8795 87.95%
P-glycoprotein inhibitior - 0.7810 78.10%
P-glycoprotein substrate - 0.8656 86.56%
CYP3A4 substrate - 0.5073 50.73%
CYP2C9 substrate + 0.7657 76.57%
CYP2D6 substrate - 0.8946 89.46%
CYP3A4 inhibition - 0.7158 71.58%
CYP2C9 inhibition + 0.5485 54.85%
CYP2C19 inhibition - 0.6391 63.91%
CYP2D6 inhibition - 0.9006 90.06%
CYP1A2 inhibition - 0.7218 72.18%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.6293 62.93%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9543 95.43%
Carcinogenicity (trinary) Non-required 0.4786 47.86%
Eye corrosion - 0.9889 98.89%
Eye irritation + 0.6270 62.70%
Skin irritation - 0.6168 61.68%
Skin corrosion - 0.9080 90.80%
Ames mutagenesis + 0.6663 66.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.9000 90.00%
Hepatotoxicity - 0.5573 55.73%
skin sensitisation - 0.7663 76.63%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7886 78.86%
Acute Oral Toxicity (c) II 0.3862 38.62%
Estrogen receptor binding + 0.8115 81.15%
Androgen receptor binding + 0.5803 58.03%
Thyroid receptor binding - 0.6462 64.62%
Glucocorticoid receptor binding + 0.5573 55.73%
Aromatase binding - 0.6051 60.51%
PPAR gamma + 0.5857 58.57%
Honey bee toxicity - 0.9300 93.00%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9824 98.24%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.15% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.36% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.30% 89.00%
CHEMBL2581 P07339 Cathepsin D 91.57% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.45% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 88.71% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.59% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 87.19% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.30% 86.33%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.99% 94.42%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.73% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101249643
LOTUS LTS0273977
wikiData Q104201672