(+)-delta-Araneosene

Details

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Internal ID 49387493-8b47-405e-8515-28b59d7a5830
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Dolabellane and neodolabellane diterpenoids
IUPAC Name (3aR,5Z,9Z)-3a,6,10-trimethyl-1-propan-2-yl-3,4,7,8,11,12-hexahydro-2H-cyclopenta[11]annulene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H32/c1-15(2)18-12-14-20(5)13-11-17(4)8-6-7-16(3)9-10-19(18)20/h7,11,15H,6,8-10,12-14H2,1-5H3/b16-7-,17-11-/t20-/m0/s1
InChI Key MCSCRBZMKVBNJL-CRQGJTKCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32
Molecular Weight 272.50 g/mol
Exact Mass 272.250401021 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 6.60
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-delta-Araneosene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.9568 95.68%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.6746 67.46%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9464 94.64%
OATP1B3 inhibitior + 0.9659 96.59%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.7502 75.02%
P-glycoprotein inhibitior - 0.8039 80.39%
P-glycoprotein substrate - 0.9072 90.72%
CYP3A4 substrate - 0.5335 53.35%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.9267 92.67%
CYP2C9 inhibition - 0.7215 72.15%
CYP2C19 inhibition - 0.6971 69.71%
CYP2D6 inhibition - 0.9340 93.40%
CYP1A2 inhibition - 0.7711 77.11%
CYP2C8 inhibition - 0.9121 91.21%
CYP inhibitory promiscuity - 0.7639 76.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Warning 0.4611 46.11%
Eye corrosion - 0.8903 89.03%
Eye irritation - 0.7615 76.15%
Skin irritation + 0.5644 56.44%
Skin corrosion - 0.9734 97.34%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8757 87.57%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5019 50.19%
skin sensitisation + 0.8633 86.33%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5311 53.11%
Acute Oral Toxicity (c) III 0.7493 74.93%
Estrogen receptor binding - 0.7279 72.79%
Androgen receptor binding - 0.6583 65.83%
Thyroid receptor binding - 0.5582 55.82%
Glucocorticoid receptor binding - 0.5160 51.60%
Aromatase binding + 0.6035 60.35%
PPAR gamma + 0.5752 57.52%
Honey bee toxicity - 0.8595 85.95%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9952 99.52%

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 94.50% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.08% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.95% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.89% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 83.35% 97.79%
CHEMBL221 P23219 Cyclooxygenase-1 81.91% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.60% 93.56%

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.
There are no matching plants.

Cross-Links

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PubChem 101921093
LOTUS LTS0136765
wikiData Q77424583