(+)-Isolongifolene-9-one

Details

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Internal ID ff44c1ff-b17d-4bf2-a48c-2c349efd9499
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids
IUPAC Name (1S,8R)-2,2,7,7-tetramethyltricyclo[6.2.1.01,6]undec-5-en-4-one
SMILES (Canonical) CC1(CC(=O)C=C2C13CCC(C3)C2(C)C)C
SMILES (Isomeric) CC1(CC(=O)C=C2[C@]13CC[C@H](C3)C2(C)C)C
InChI InChI=1S/C15H22O/c1-13(2)9-11(16)7-12-14(3,4)10-5-6-15(12,13)8-10/h7,10H,5-6,8-9H2,1-4H3/t10-,15-/m1/s1
InChI Key LGSKOQUJWNADCQ-MEBBXXQBSA-N
Popularity 0 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 3.60
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (+)-Isolongifolene-9-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 + 0.9526 95.26%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.9000 90.00%
Subcellular localzation Mitochondria 0.5053 50.53%
OATP2B1 inhibitior - 0.8486 84.86%
OATP1B1 inhibitior + 0.9268 92.68%
OATP1B3 inhibitior + 0.9842 98.42%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.9312 93.12%
P-glycoprotein inhibitior - 0.9402 94.02%
P-glycoprotein substrate - 0.8480 84.80%
CYP3A4 substrate + 0.5813 58.13%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.8478 84.78%
CYP3A4 inhibition - 0.9021 90.21%
CYP2C9 inhibition - 0.8130 81.30%
CYP2C19 inhibition - 0.5609 56.09%
CYP2D6 inhibition - 0.9461 94.61%
CYP1A2 inhibition - 0.8901 89.01%
CYP2C8 inhibition - 0.9555 95.55%
CYP inhibitory promiscuity - 0.7899 78.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4627 46.27%
Eye corrosion - 0.9764 97.64%
Eye irritation + 0.6398 63.98%
Skin irritation + 0.6189 61.89%
Skin corrosion - 0.9747 97.47%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4648 46.48%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5573 55.73%
skin sensitisation + 0.8147 81.47%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.4903 49.03%
Acute Oral Toxicity (c) III 0.8019 80.19%
Estrogen receptor binding - 0.8619 86.19%
Androgen receptor binding - 0.5345 53.45%
Thyroid receptor binding - 0.7128 71.28%
Glucocorticoid receptor binding - 0.8125 81.25%
Aromatase binding + 0.5876 58.76%
PPAR gamma - 0.8376 83.76%
Honey bee toxicity - 0.9151 91.51%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9862 98.62%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.13% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.91% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 91.52% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.46% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.14% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.97% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.93% 97.09%
CHEMBL2581 P07339 Cathepsin D 84.12% 98.95%
CHEMBL1871 P10275 Androgen Receptor 83.31% 96.43%
CHEMBL1951 P21397 Monoamine oxidase A 82.21% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.03% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.42% 99.23%

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.
Pogostemon cablin

Cross-Links

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PubChem 92278848
NPASS NPC162264