7-Keto-delta-cadinene

Details

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Internal ID 8cb9da6a-adb5-4672-b544-049aaa0a0536
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4aR,5S)-3,8-dimethyl-5-propan-2-yl-4a,5,6,7-tetrahydro-1H-naphthalen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-9(2)12-6-5-10(3)13-8-15(16)11(4)7-14(12)13/h7,9,12,14H,5-6,8H2,1-4H3/t12-,14-/m0/s1
InChI Key IZZYGYDERUCSAO-JSGCOSHPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
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 7-Keto-delta-cadinene

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 + 0.9071 90.71%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5551 55.51%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9555 95.55%
OATP1B3 inhibitior + 0.9722 97.22%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8441 84.41%
P-glycoprotein inhibitior - 0.9032 90.32%
P-glycoprotein substrate - 0.8852 88.52%
CYP3A4 substrate - 0.5755 57.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.8963 89.63%
CYP2C9 inhibition - 0.8109 81.09%
CYP2C19 inhibition - 0.6407 64.07%
CYP2D6 inhibition - 0.9479 94.79%
CYP1A2 inhibition - 0.6876 68.76%
CYP2C8 inhibition - 0.9810 98.10%
CYP inhibitory promiscuity - 0.7442 74.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5288 52.88%
Eye corrosion - 0.9659 96.59%
Eye irritation - 0.5483 54.83%
Skin irritation + 0.5650 56.50%
Skin corrosion - 0.9633 96.33%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4034 40.34%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.8842 88.42%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5566 55.66%
Acute Oral Toxicity (c) III 0.5507 55.07%
Estrogen receptor binding - 0.9381 93.81%
Androgen receptor binding - 0.5548 55.48%
Thyroid receptor binding - 0.6515 65.15%
Glucocorticoid receptor binding - 0.7758 77.58%
Aromatase binding - 0.8608 86.08%
PPAR gamma - 0.6115 61.15%
Honey bee toxicity - 0.8940 89.40%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9922 99.22%

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 93.24% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.72% 95.56%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.63% 93.40%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.94% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.44% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.34% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.26% 96.09%
CHEMBL1871 P10275 Androgen Receptor 81.88% 96.43%
CHEMBL1937 Q92769 Histone deacetylase 2 80.47% 94.75%

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.
Heterotheca grandiflora

Cross-Links

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PubChem 145714661
LOTUS LTS0131908
wikiData Q105123616