Cucumin D

Details

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Internal ID cd81697e-6149-47f7-b8f9-0b498d145d0d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Triquinane sesquiterpenoids > Linear triquinanes
IUPAC Name (3R,3aR,4R)-4-hydroxy-3,3a,5,5-tetramethyl-4,7-dihydro-3H-cyclopenta[a]pentalene-2,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18O3/c1-7-10(16)6-8-5-9-11(15(7,8)4)13(18)14(2,3)12(9)17/h6-7,13,18H,5H2,1-4H3/t7-,13+,15+/m0/s1
InChI Key ZJQBSHFABOKMJU-SBPMXOOQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O3
Molecular Weight 246.30 g/mol
Exact Mass 246.125594432 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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InChI=1/C15H18O3/c1-7-10(16)6-8-5-9-11(15(7,8)4)13(18)14(2,3)12(9)17/h6-7,13,18H,5H2,1-4H3/t7-,13+,15+/m0/s

2D Structure

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2D Structure of Cucumin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.7004 70.04%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6977 69.77%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8509 85.09%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8143 81.43%
P-glycoprotein inhibitior - 0.9461 94.61%
P-glycoprotein substrate - 0.8377 83.77%
CYP3A4 substrate + 0.5256 52.56%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.8653 86.53%
CYP3A4 inhibition - 0.9015 90.15%
CYP2C9 inhibition - 0.7561 75.61%
CYP2C19 inhibition - 0.8368 83.68%
CYP2D6 inhibition - 0.9118 91.18%
CYP1A2 inhibition - 0.6300 63.00%
CYP2C8 inhibition - 0.8896 88.96%
CYP inhibitory promiscuity - 0.7917 79.17%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4870 48.70%
Eye corrosion - 0.9555 95.55%
Eye irritation - 0.7415 74.15%
Skin irritation + 0.6598 65.98%
Skin corrosion - 0.8275 82.75%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5594 55.94%
Micronuclear - 0.7000 70.00%
Hepatotoxicity + 0.6491 64.91%
skin sensitisation + 0.5439 54.39%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.6316 63.16%
Acute Oral Toxicity (c) III 0.4574 45.74%
Estrogen receptor binding + 0.5320 53.20%
Androgen receptor binding - 0.6232 62.32%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.5368 53.68%
PPAR gamma - 0.5779 57.79%
Honey bee toxicity - 0.8321 83.21%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9579 95.79%

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 93.29% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 92.98% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.87% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.84% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.54% 99.23%
CHEMBL2581 P07339 Cathepsin D 87.47% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.08% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.69% 90.71%
CHEMBL230 P35354 Cyclooxygenase-2 82.69% 89.63%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.90% 85.14%

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 10490644
LOTUS LTS0251932
wikiData Q75062400