5,5,9-Trimethyl-1-methylidenespiro[5.5]undec-9-en-2-ol

Details

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Internal ID 72259171-993d-4739-ae8d-3847a7697694
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Chamigranes
IUPAC Name 5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-en-2-ol
SMILES (Canonical) CC1=CCC2(CC1)C(=C)C(CCC2(C)C)O
SMILES (Isomeric) CC1=CCC2(CC1)C(=C)C(CCC2(C)C)O
InChI InChI=1S/C15H24O/c1-11-5-9-15(10-6-11)12(2)13(16)7-8-14(15,3)4/h5,13,16H,2,6-10H2,1,3-4H3
InChI Key KSZBRCLNQKIVGH-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) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,5,9-Trimethyl-1-methylidenespiro[5.5]undec-9-en-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.8396 83.96%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4664 46.64%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.9166 91.66%
OATP1B3 inhibitior - 0.2296 22.96%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7293 72.93%
P-glycoprotein inhibitior - 0.9651 96.51%
P-glycoprotein substrate - 0.8690 86.90%
CYP3A4 substrate + 0.5451 54.51%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.7401 74.01%
CYP3A4 inhibition - 0.8223 82.23%
CYP2C9 inhibition - 0.7978 79.78%
CYP2C19 inhibition - 0.6556 65.56%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition - 0.8886 88.86%
CYP2C8 inhibition - 0.8197 81.97%
CYP inhibitory promiscuity - 0.8635 86.35%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6218 62.18%
Eye corrosion - 0.9768 97.68%
Eye irritation + 0.5232 52.32%
Skin irritation + 0.6855 68.55%
Skin corrosion - 0.9470 94.70%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4596 45.96%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5680 56.80%
skin sensitisation + 0.6914 69.14%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7000 70.00%
Acute Oral Toxicity (c) III 0.8769 87.69%
Estrogen receptor binding - 0.8973 89.73%
Androgen receptor binding - 0.4915 49.15%
Thyroid receptor binding - 0.7508 75.08%
Glucocorticoid receptor binding - 0.6956 69.56%
Aromatase binding - 0.6096 60.96%
PPAR gamma - 0.7531 75.31%
Honey bee toxicity - 0.8730 87.30%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9928 99.28%

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 93.11% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.18% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.78% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.93% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.33% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 85.64% 86.00%
CHEMBL1871 P10275 Androgen Receptor 84.62% 96.43%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.86% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.93% 92.94%

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.
Reboulia hemisphaerica

Cross-Links

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PubChem 73235300
LOTUS LTS0235978
wikiData Q105145658