Isolongifolen-5-one

Details

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Internal ID 40812f72-1bf5-4e77-901b-8b7829461482
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids
IUPAC Name 2,2,7,7-tetramethyltricyclo[6.2.1.01,6]undec-5-en-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-13(2)7-5-6-11-14(3,4)10-8-12(16)15(11,13)9-10/h6,10H,5,7-9H2,1-4H3
InChI Key HJIXDFZKWWWXSC-UHFFFAOYSA-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 3.20
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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HJIXDFZKWWWXSC-UHFFFAOYSA-N
Q67879960

2D Structure

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2D Structure of Isolongifolen-5-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 + 0.9317 93.17%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.5053 50.53%
OATP2B1 inhibitior - 0.8483 84.83%
OATP1B1 inhibitior + 0.9423 94.23%
OATP1B3 inhibitior + 0.9842 98.42%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.9124 91.24%
P-glycoprotein inhibitior - 0.9349 93.49%
P-glycoprotein substrate - 0.8505 85.05%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7912 79.12%
CYP2D6 substrate - 0.7902 79.02%
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 - 0.9345 93.45%
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 + 0.6876 68.76%
Skin irritation + 0.6189 61.89%
Skin corrosion - 0.9747 97.47%
Ames mutagenesis - 0.7137 71.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5477 54.77%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5482 54.82%
skin sensitisation + 0.8147 81.47%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.7014 70.14%
Acute Oral Toxicity (c) III 0.8019 80.19%
Estrogen receptor binding - 0.9176 91.76%
Androgen receptor binding - 0.5202 52.02%
Thyroid receptor binding - 0.7277 72.77%
Glucocorticoid receptor binding - 0.8607 86.07%
Aromatase binding + 0.5363 53.63%
PPAR gamma - 0.8231 82.31%
Honey bee toxicity - 0.9238 92.38%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6204 62.04%
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 91.42% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.41% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.67% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.81% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.32% 82.69%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.89% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 81.30% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.04% 97.09%

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.
Acorus calamus var. angustatus
Cyperus rotundus

Cross-Links

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PubChem 600416
NPASS NPC84953
LOTUS LTS0007204
wikiData Q67879960