8|A,9|A-Epoxycoleon-U-quinone

Details

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Internal ID f4276d4a-0c3b-4e73-9f53-c2ff7b3c1725
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (1S,2S,10R)-8,13-dihydroxy-2,6,6-trimethyl-12-propan-2-yl-15-oxatetracyclo[8.4.1.01,10.02,7]pentadeca-7,12-diene-9,11,14-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O6/c1-9(2)10-11(21)16(25)20-18(5)8-6-7-17(3,4)13(18)12(22)15(24)19(20,26-20)14(10)23/h9,21-22H,6-8H2,1-5H3/t18-,19+,20-/m0/s1
InChI Key AEXKDWVVGVHVQM-ZCNNSNEGSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O6
Molecular Weight 360.40 g/mol
Exact Mass 360.15728848 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL516515
HY-N10564
CS-0611084
93800-59-0

2D Structure

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2D Structure of 8|A,9|A-Epoxycoleon-U-quinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 + 0.6380 63.80%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6869 68.69%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.8357 83.57%
OATP1B3 inhibitior + 0.9674 96.74%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.8743 87.43%
P-glycoprotein inhibitior - 0.7695 76.95%
P-glycoprotein substrate - 0.9080 90.80%
CYP3A4 substrate + 0.5476 54.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8662 86.62%
CYP3A4 inhibition - 0.9005 90.05%
CYP2C9 inhibition - 0.7309 73.09%
CYP2C19 inhibition - 0.8170 81.70%
CYP2D6 inhibition - 0.9038 90.38%
CYP1A2 inhibition - 0.5543 55.43%
CYP2C8 inhibition - 0.8666 86.66%
CYP inhibitory promiscuity - 0.8382 83.82%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5761 57.61%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.7356 73.56%
Skin irritation - 0.5322 53.22%
Skin corrosion - 0.9124 91.24%
Ames mutagenesis + 0.5346 53.46%
Human Ether-a-go-go-Related Gene inhibition - 0.8048 80.48%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.5502 55.02%
skin sensitisation - 0.6544 65.44%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.4677 46.77%
Acute Oral Toxicity (c) III 0.5135 51.35%
Estrogen receptor binding + 0.7182 71.82%
Androgen receptor binding + 0.6662 66.62%
Thyroid receptor binding + 0.6494 64.94%
Glucocorticoid receptor binding + 0.7874 78.74%
Aromatase binding + 0.6860 68.60%
PPAR gamma + 0.6585 65.85%
Honey bee toxicity - 0.8895 88.95%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9886 98.86%

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 99.05% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.03% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.28% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 86.26% 94.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.25% 97.25%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.06% 99.15%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.64% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.54% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.04% 90.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.09% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Coleus sanguineus

Cross-Links

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PubChem 21595190
LOTUS LTS0265393
wikiData Q104910748