Gibberodione

Details

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Internal ID 6a1ee630-9f72-46d0-9d38-b76290e9fb46
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (6S,7S)-6-methyl-7-(3-oxobutyl)-3-propan-2-ylcyclohept-2-en-1-one
SMILES (Canonical) CC1CCC(=CC(=O)C1CCC(=O)C)C(C)C
SMILES (Isomeric) C[C@H]1CCC(=CC(=O)[C@H]1CCC(=O)C)C(C)C
InChI InChI=1S/C15H24O2/c1-10(2)13-7-5-11(3)14(15(17)9-13)8-6-12(4)16/h9-11,14H,5-8H2,1-4H3/t11-,14-/m0/s1
InChI Key PDXOECHKUSAMHE-FZMZJTMJSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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CHEMBL486794
(6S,7S)-6-methyl-7-(3-oxobutyl)-3-propan-2-ylcyclohept-2-en-1-one

2D Structure

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2D Structure of Gibberodione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.8713 87.13%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6709 67.09%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.9077 90.77%
OATP1B3 inhibitior + 0.9136 91.36%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7573 75.73%
P-glycoprotein inhibitior - 0.9216 92.16%
P-glycoprotein substrate - 0.8299 82.99%
CYP3A4 substrate - 0.5198 51.98%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8631 86.31%
CYP3A4 inhibition - 0.8975 89.75%
CYP2C9 inhibition - 0.8199 81.99%
CYP2C19 inhibition - 0.7928 79.28%
CYP2D6 inhibition - 0.9128 91.28%
CYP1A2 inhibition - 0.6469 64.69%
CYP2C8 inhibition - 0.9560 95.60%
CYP inhibitory promiscuity - 0.8743 87.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.6406 64.06%
Eye corrosion - 0.8812 88.12%
Eye irritation + 0.5438 54.38%
Skin irritation + 0.5499 54.99%
Skin corrosion - 0.9623 96.23%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4687 46.87%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7265 72.65%
skin sensitisation + 0.7949 79.49%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.6830 68.30%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.7609 76.09%
Acute Oral Toxicity (c) III 0.4857 48.57%
Estrogen receptor binding - 0.8593 85.93%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.6935 69.35%
Glucocorticoid receptor binding - 0.6535 65.35%
Aromatase binding - 0.9200 92.00%
PPAR gamma - 0.9038 90.38%
Honey bee toxicity - 0.9402 94.02%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9742 97.42%

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
CHEMBL2581 P07339 Cathepsin D 97.51% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.35% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.31% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.64% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.30% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.30% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.24% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.70% 95.56%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.51% 94.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.19% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.32% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.04% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.86% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 80.73% 91.19%
CHEMBL4040 P28482 MAP kinase ERK2 80.44% 83.82%

Cross-Links

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PubChem 11586727
NPASS NPC193695
LOTUS LTS0153787
wikiData Q105206811