9,10-Diolhinokiic acid

Details

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Internal ID f6578c4f-950c-4f5d-8a91-856754dab509
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1aR,4aR,6R,7S,8aR)-6,7-dihydroxy-4a,8,8-trimethyl-1,1a,4,5,6,7-hexahydrocyclopropa[j]naphthalene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O4/c1-13(2)11(17)10(16)7-14(3)5-4-8(12(18)19)9-6-15(9,13)14/h4,9-11,16-17H,5-7H2,1-3H3,(H,18,19)/t9-,10+,11+,14+,15-/m0/s1
InChI Key XTUOMMWRCSZFGR-ILYYPIBPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O4
Molecular Weight 266.33 g/mol
Exact Mass 266.15180918 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.57
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9,10-Diolhinokiic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9889 98.89%
Caco-2 + 0.5879 58.79%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7769 77.69%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.9166 91.66%
OATP1B3 inhibitior + 0.8962 89.62%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8830 88.30%
P-glycoprotein inhibitior - 0.9519 95.19%
P-glycoprotein substrate - 0.9055 90.55%
CYP3A4 substrate - 0.5085 50.85%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8934 89.34%
CYP3A4 inhibition - 0.6883 68.83%
CYP2C9 inhibition - 0.8161 81.61%
CYP2C19 inhibition - 0.7949 79.49%
CYP2D6 inhibition - 0.9403 94.03%
CYP1A2 inhibition - 0.8414 84.14%
CYP2C8 inhibition - 0.9325 93.25%
CYP inhibitory promiscuity - 0.9470 94.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6526 65.26%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.8109 81.09%
Skin irritation - 0.5276 52.76%
Skin corrosion - 0.9435 94.35%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7877 78.77%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.6463 64.63%
skin sensitisation - 0.5772 57.72%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.4791 47.91%
Acute Oral Toxicity (c) III 0.6381 63.81%
Estrogen receptor binding - 0.4873 48.73%
Androgen receptor binding + 0.5458 54.58%
Thyroid receptor binding - 0.5826 58.26%
Glucocorticoid receptor binding - 0.4899 48.99%
Aromatase binding - 0.5161 51.61%
PPAR gamma - 0.5972 59.72%
Honey bee toxicity - 0.8758 87.58%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.9972 99.72%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.95% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.62% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.43% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.73% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.11% 94.45%
CHEMBL2581 P07339 Cathepsin D 83.32% 98.95%
CHEMBL1811 P34995 Prostanoid EP1 receptor 81.05% 95.71%

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 139590606
LOTUS LTS0146277
wikiData Q105341935