Chondrosterin O

Details

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Internal ID 7e462d69-0e6d-4145-9b10-05868de308ae
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Triquinane sesquiterpenoids > Linear triquinanes
IUPAC Name (2S,3R,3aR,6R,7aS)-2,6-dihydroxy-3,3a,5,5-tetramethyl-1,2,3,4,6,7a-hexahydrocyclopenta[a]pentalen-7-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O3/c1-7-10(16)5-8-12(17)11-9(15(7,8)4)6-14(2,3)13(11)18/h7-8,10,13,16,18H,5-6H2,1-4H3/t7-,8+,10-,13-,15+/m0/s1
InChI Key VXKRUQOEWHSKEZ-CAZPLRKFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O3
Molecular Weight 250.33 g/mol
Exact Mass 250.15689456 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Chondrosterin O

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5301 53.01%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6621 66.21%
OATP2B1 inhibitior - 0.8480 84.80%
OATP1B1 inhibitior + 0.8944 89.44%
OATP1B3 inhibitior + 0.9566 95.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8221 82.21%
P-glycoprotein inhibitior - 0.9194 91.94%
P-glycoprotein substrate - 0.8018 80.18%
CYP3A4 substrate + 0.5486 54.86%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.8653 86.53%
CYP3A4 inhibition - 0.8953 89.53%
CYP2C9 inhibition - 0.8272 82.72%
CYP2C19 inhibition - 0.7842 78.42%
CYP2D6 inhibition - 0.9439 94.39%
CYP1A2 inhibition - 0.8035 80.35%
CYP2C8 inhibition - 0.9808 98.08%
CYP inhibitory promiscuity - 0.8575 85.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Warning 0.4548 45.48%
Eye corrosion - 0.9853 98.53%
Eye irritation - 0.6441 64.41%
Skin irritation + 0.5761 57.61%
Skin corrosion - 0.9173 91.73%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7721 77.21%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.5870 58.70%
skin sensitisation - 0.5396 53.96%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.7197 71.97%
Acute Oral Toxicity (c) I 0.3716 37.16%
Estrogen receptor binding - 0.6291 62.91%
Androgen receptor binding - 0.5562 55.62%
Thyroid receptor binding + 0.5702 57.02%
Glucocorticoid receptor binding - 0.5797 57.97%
Aromatase binding - 0.6341 63.41%
PPAR gamma - 0.6835 68.35%
Honey bee toxicity - 0.8552 85.52%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9594 95.94%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.55% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.39% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.84% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.22% 97.09%
CHEMBL2581 P07339 Cathepsin D 84.99% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 84.08% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.35% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.93% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.37% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.30% 100.00%

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 139591699
LOTUS LTS0067570
wikiData Q105298548