Arecoic acid E

Details

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Internal ID 86149931-fdb7-41ce-94cb-ca44a6f52959
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name (1S,4aS,7S,8aR)-7-hydroxy-1,4a,6-trimethyl-2,3,4,7,8,8a-hexahydronaphthalene-1,5-dicarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O5/c1-8-9(16)7-10-14(2,11(8)12(17)18)5-4-6-15(10,3)13(19)20/h9-10,16H,4-7H2,1-3H3,(H,17,18)(H,19,20)/t9-,10+,14-,15-/m0/s1
InChI Key CEIDCYCXCMFPMO-OWLDWWDNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O5
Molecular Weight 282.33 g/mol
Exact Mass 282.14672380 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Arecoic acid E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9897 98.97%
Caco-2 + 0.6876 68.76%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8519 85.19%
OATP2B1 inhibitior - 0.8503 85.03%
OATP1B1 inhibitior + 0.9094 90.94%
OATP1B3 inhibitior - 0.2952 29.52%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5842 58.42%
BSEP inhibitior - 0.8795 87.95%
P-glycoprotein inhibitior - 0.9595 95.95%
P-glycoprotein substrate - 0.8918 89.18%
CYP3A4 substrate + 0.5146 51.46%
CYP2C9 substrate - 0.7928 79.28%
CYP2D6 substrate - 0.9050 90.50%
CYP3A4 inhibition - 0.7510 75.10%
CYP2C9 inhibition - 0.9561 95.61%
CYP2C19 inhibition - 0.9665 96.65%
CYP2D6 inhibition - 0.9534 95.34%
CYP1A2 inhibition - 0.9227 92.27%
CYP2C8 inhibition - 0.7886 78.86%
CYP inhibitory promiscuity - 0.9674 96.74%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6564 65.64%
Eye corrosion - 0.9955 99.55%
Eye irritation - 0.5291 52.91%
Skin irritation + 0.6993 69.93%
Skin corrosion - 0.9575 95.75%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7310 73.10%
Micronuclear - 0.7900 79.00%
Hepatotoxicity + 0.5166 51.66%
skin sensitisation - 0.5323 53.23%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.4754 47.54%
Acute Oral Toxicity (c) III 0.7243 72.43%
Estrogen receptor binding - 0.6382 63.82%
Androgen receptor binding - 0.6723 67.23%
Thyroid receptor binding - 0.5432 54.32%
Glucocorticoid receptor binding - 0.4845 48.45%
Aromatase binding - 0.6443 64.43%
PPAR gamma - 0.6846 68.46%
Honey bee toxicity - 0.9044 90.44%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9961 99.61%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.44% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.39% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.48% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.56% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 84.94% 90.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.87% 93.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.29% 91.19%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.75% 97.25%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.02% 95.50%

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 71545928
LOTUS LTS0137964
wikiData Q75057934