4-Benzoyl-6-(3-methylbut-2-enyl)-2,2-bis(5-methyl-2-prop-1-en-2-ylhex-4-enyl)cyclohexane-1,3,5-trione

Details

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Internal ID ea9e6509-6e2d-42e9-8ad7-5959db755c97
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones > Benzoylcyclohexane-1,3-diones
IUPAC Name 4-benzoyl-6-(3-methylbut-2-enyl)-2,2-bis(5-methyl-2-prop-1-en-2-ylhex-4-enyl)cyclohexane-1,3,5-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H50O4/c1-24(2)16-19-30(27(7)8)22-38(23-31(28(9)10)20-17-25(3)4)36(41)32(21-18-26(5)6)35(40)33(37(38)42)34(39)29-14-12-11-13-15-29/h11-18,30-33H,7,9,19-23H2,1-6,8,10H3
InChI Key JOHZHMWCVNCICX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C38H50O4
Molecular Weight 570.80 g/mol
Exact Mass 570.37091007 g/mol
Topological Polar Surface Area (TPSA) 68.30 Ų
XlogP 11.00
Atomic LogP (AlogP) 9.04
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Benzoyl-6-(3-methylbut-2-enyl)-2,2-bis(5-methyl-2-prop-1-en-2-ylhex-4-enyl)cyclohexane-1,3,5-trione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 - 0.7727 77.27%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8284 82.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8704 87.04%
OATP1B3 inhibitior + 0.9049 90.49%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9655 96.55%
P-glycoprotein inhibitior + 0.7803 78.03%
P-glycoprotein substrate - 0.6102 61.02%
CYP3A4 substrate + 0.5429 54.29%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8084 80.84%
CYP3A4 inhibition - 0.7077 70.77%
CYP2C9 inhibition + 0.5084 50.84%
CYP2C19 inhibition + 0.6340 63.40%
CYP2D6 inhibition - 0.8943 89.43%
CYP1A2 inhibition - 0.7551 75.51%
CYP2C8 inhibition - 0.6036 60.36%
CYP inhibitory promiscuity + 0.5723 57.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6453 64.53%
Carcinogenicity (trinary) Non-required 0.6809 68.09%
Eye corrosion - 0.9660 96.60%
Eye irritation - 0.8416 84.16%
Skin irritation - 0.6810 68.10%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8873 88.73%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.6932 69.32%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6143 61.43%
Acute Oral Toxicity (c) III 0.6106 61.06%
Estrogen receptor binding + 0.7434 74.34%
Androgen receptor binding + 0.7202 72.02%
Thyroid receptor binding + 0.6110 61.10%
Glucocorticoid receptor binding + 0.7312 73.12%
Aromatase binding + 0.5889 58.89%
PPAR gamma + 0.6739 67.39%
Honey bee toxicity - 0.8025 80.25%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.38% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.18% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 95.97% 90.17%
CHEMBL2581 P07339 Cathepsin D 94.10% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.41% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.47% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.37% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.16% 94.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.12% 99.23%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.30% 94.23%

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.
Clusia panapanari

Cross-Links

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PubChem 101420432
LOTUS LTS0244660
wikiData Q104399429