1,4-Methanoazulen-7(1H)-one, octahydro-4,8,8,9-tetramethyl-, (+)-

Details

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Internal ID 6e29e5d4-cd7c-48f2-817a-270698e74998
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,3,7,8-tetramethyltricyclo[5.4.0.02,9]undecan-4-one
SMILES (Canonical) CC1C2CCC3C2C(C(=O)CCC13C)(C)C
SMILES (Isomeric) CC1C2CCC3C2C(C(=O)CCC13C)(C)C
InChI InChI=1S/C15H24O/c1-9-10-5-6-11-13(10)14(2,3)12(16)7-8-15(9,11)4/h9-11,13H,5-8H2,1-4H3
InChI Key IDGOUUWCFVZDEL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1,4-Methanoazulen-7(1H)-one, octahydro-4,8,8,9-tetramethyl-, (+)-

2D Structure

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2D Structure of 1,4-Methanoazulen-7(1H)-one, octahydro-4,8,8,9-tetramethyl-, (+)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8158 81.58%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4838 48.38%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9219 92.19%
OATP1B3 inhibitior + 0.9732 97.32%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8630 86.30%
P-glycoprotein inhibitior - 0.9061 90.61%
P-glycoprotein substrate - 0.9315 93.15%
CYP3A4 substrate + 0.5658 56.58%
CYP2C9 substrate - 0.7483 74.83%
CYP2D6 substrate - 0.7683 76.83%
CYP3A4 inhibition - 0.9389 93.89%
CYP2C9 inhibition - 0.8669 86.69%
CYP2C19 inhibition - 0.9063 90.63%
CYP2D6 inhibition - 0.9668 96.68%
CYP1A2 inhibition - 0.7937 79.37%
CYP2C8 inhibition - 0.9308 93.08%
CYP inhibitory promiscuity - 0.9674 96.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6302 63.02%
Eye corrosion - 0.9074 90.74%
Eye irritation + 0.5515 55.15%
Skin irritation + 0.7802 78.02%
Skin corrosion - 0.9181 91.81%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5450 54.50%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6996 69.96%
skin sensitisation + 0.8714 87.14%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6537 65.37%
Estrogen receptor binding + 0.5632 56.32%
Androgen receptor binding + 0.5587 55.87%
Thyroid receptor binding - 0.7174 71.74%
Glucocorticoid receptor binding - 0.7698 76.98%
Aromatase binding - 0.7284 72.84%
PPAR gamma - 0.7779 77.79%
Honey bee toxicity - 0.7944 79.44%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9471 94.71%

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
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.70% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.19% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.15% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 87.17% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.75% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.29% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.20% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.77% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.68% 93.04%
CHEMBL4370 P16662 UDP-glucuronosyltransferase 2B7 82.00% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.90% 99.23%
CHEMBL1871 P10275 Androgen Receptor 80.84% 96.43%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 572868
LOTUS LTS0217515
wikiData Q105111348