Aristola-1(10),8-dien-2-one

Details

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Internal ID 48c2f1d6-3ca3-4ac4-ba33-94b40d295887
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Aristolane sesquiterpenoids
IUPAC Name (1aR,7R,7aR,7bS)-1,1,7,7a-tetramethyl-1a,6,7,7b-tetrahydrocyclopropa[a]naphthalen-5-one
SMILES (Canonical) CC1CC(=O)C=C2C1(C3C(C3(C)C)C=C2)C
SMILES (Isomeric) C[C@@H]1CC(=O)C=C2[C@]1([C@H]3[C@H](C3(C)C)C=C2)C
InChI InChI=1S/C15H20O/c1-9-7-11(16)8-10-5-6-12-13(14(12,2)3)15(9,10)4/h5-6,8-9,12-13H,7H2,1-4H3/t9-,12-,13+,15+/m1/s1
InChI Key FAGPISMIHLVLSK-JWFUOXDNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O
Molecular Weight 216.32 g/mol
Exact Mass 216.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.37
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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22391-34-0
1(10),8-Aristoladien-2-one
(1Ar,7R,7aR,7bS)-1,1,7,7a-tetramethyl-1a,6,7,7b-tetrahydrocyclopropa[a]naphthalen-5-one
FAGPISMIHLVLSK-JWFUOXDNSA-N
AKOS040761372
E89057

2D Structure

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2D Structure of Aristola-1(10),8-dien-2-one

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 + 0.8266 82.66%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.5241 52.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8897 88.97%
OATP1B3 inhibitior + 0.9694 96.94%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9179 91.79%
P-glycoprotein inhibitior - 0.9144 91.44%
P-glycoprotein substrate - 0.8024 80.24%
CYP3A4 substrate + 0.5258 52.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8840 88.40%
CYP3A4 inhibition - 0.7064 70.64%
CYP2C9 inhibition - 0.7632 76.32%
CYP2C19 inhibition + 0.5540 55.40%
CYP2D6 inhibition - 0.8651 86.51%
CYP1A2 inhibition - 0.6724 67.24%
CYP2C8 inhibition - 0.9587 95.87%
CYP inhibitory promiscuity - 0.5703 57.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.4925 49.25%
Eye corrosion - 0.9733 97.33%
Eye irritation - 0.7728 77.28%
Skin irritation + 0.5082 50.82%
Skin corrosion - 0.9417 94.17%
Ames mutagenesis - 0.7583 75.83%
Human Ether-a-go-go-Related Gene inhibition - 0.4733 47.33%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.7587 75.87%
skin sensitisation + 0.7958 79.58%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6447 64.47%
Acute Oral Toxicity (c) III 0.6618 66.18%
Estrogen receptor binding - 0.6927 69.27%
Androgen receptor binding + 0.5912 59.12%
Thyroid receptor binding - 0.6818 68.18%
Glucocorticoid receptor binding - 0.7757 77.57%
Aromatase binding - 0.6856 68.56%
PPAR gamma - 0.6085 60.85%
Honey bee toxicity - 0.8600 86.00%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.9768 97.68%

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 92.88% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.72% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 90.81% 86.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.97% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.55% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.20% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.37% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.31% 95.56%
CHEMBL3045 P05771 Protein kinase C beta 83.73% 97.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.22% 86.33%

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.
Humulus scandens
Kopsia flavida
Nardostachys jatamansi
Ribes sanguineum
Stachys chinensis

Cross-Links

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PubChem 101297625
NPASS NPC74214
LOTUS LTS0179272
wikiData Q104992252