(1S,3E,5S)-2,8-dimethylidene-5-propan-2-ylcyclodec-3-en-1-ol

Details

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Internal ID 35927a72-5e1c-4170-987b-685a561c41ae
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Germacrane sesquiterpenoids
IUPAC Name (1S,3E,5S)-2,8-dimethylidene-5-propan-2-ylcyclodec-3-en-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-11(2)14-8-5-12(3)6-10-15(16)13(4)7-9-14/h7,9,11,14-16H,3-6,8,10H2,1-2H3/b9-7+/t14-,15+/m1/s1
InChI Key HHSHDKYRXLFJMS-MMCPSDEHSA-N
Popularity 3 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 3.70
Atomic LogP (AlogP) 3.86
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,3E,5S)-2,8-dimethylidene-5-propan-2-ylcyclodec-3-en-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7602 76.02%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5282 52.82%
OATP2B1 inhibitior - 0.8554 85.54%
OATP1B1 inhibitior + 0.9368 93.68%
OATP1B3 inhibitior + 0.9124 91.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.9386 93.86%
P-glycoprotein inhibitior - 0.9623 96.23%
P-glycoprotein substrate - 0.8710 87.10%
CYP3A4 substrate - 0.6034 60.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7555 75.55%
CYP3A4 inhibition - 0.8836 88.36%
CYP2C9 inhibition - 0.9036 90.36%
CYP2C19 inhibition - 0.8676 86.76%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition - 0.7669 76.69%
CYP2C8 inhibition - 0.9404 94.04%
CYP inhibitory promiscuity - 0.8813 88.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.6704 67.04%
Eye corrosion - 0.8145 81.45%
Eye irritation - 0.5159 51.59%
Skin irritation + 0.6014 60.14%
Skin corrosion - 0.9124 91.24%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4365 43.65%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.8139 81.39%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5941 59.41%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7801 78.01%
Acute Oral Toxicity (c) III 0.6934 69.34%
Estrogen receptor binding - 0.7816 78.16%
Androgen receptor binding - 0.8268 82.68%
Thyroid receptor binding - 0.6173 61.73%
Glucocorticoid receptor binding + 0.6107 61.07%
Aromatase binding - 0.8337 83.37%
PPAR gamma - 0.7079 70.79%
Honey bee toxicity - 0.9146 91.46%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9460 94.60%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.94% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.77% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.83% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.87% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.65% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 81.55% 95.93%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.51% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.37% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.07% 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.
Inulanthera dregeana
Senecio subsessilis

Cross-Links

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PubChem 162893981
LOTUS LTS0150661
wikiData Q105028535