Demethoxycacalohastine

Details

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Internal ID ec10bd5f-7d7c-40e9-b103-fe94f7bc1b5c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
IUPAC Name (5S)-3,4,5-trimethyl-5,6-dihydrobenzo[f][1]benzofuran
SMILES (Canonical) CC1CC=CC2=CC3=C(C(=CO3)C)C(=C12)C
SMILES (Isomeric) C[C@H]1CC=CC2=CC3=C(C(=CO3)C)C(=C12)C
InChI InChI=1S/C15H16O/c1-9-5-4-6-12-7-13-15(10(2)8-16-13)11(3)14(9)12/h4,6-9H,5H2,1-3H3/t9-/m0/s1
InChI Key IQVWMDXKYQHJMP-VIFPVBQESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O
Molecular Weight 212.29 g/mol
Exact Mass 212.120115130 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.57
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 Demethoxycacalohastine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.7883 78.83%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Plasma membrane 0.4380 43.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9265 92.65%
OATP1B3 inhibitior + 0.9607 96.07%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6846 68.46%
P-glycoprotein inhibitior - 0.9456 94.56%
P-glycoprotein substrate - 0.6841 68.41%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6140 61.40%
CYP2D6 substrate - 0.7265 72.65%
CYP3A4 inhibition - 0.8655 86.55%
CYP2C9 inhibition - 0.6803 68.03%
CYP2C19 inhibition + 0.7395 73.95%
CYP2D6 inhibition - 0.7894 78.94%
CYP1A2 inhibition + 0.8629 86.29%
CYP2C8 inhibition - 0.7315 73.15%
CYP inhibitory promiscuity + 0.8685 86.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Danger 0.6501 65.01%
Eye corrosion - 0.9636 96.36%
Eye irritation - 0.9305 93.05%
Skin irritation - 0.5846 58.46%
Skin corrosion - 0.9760 97.60%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4344 43.44%
Micronuclear - 0.6267 62.67%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.7177 71.77%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.8802 88.02%
Acute Oral Toxicity (c) III 0.6911 69.11%
Estrogen receptor binding + 0.5885 58.85%
Androgen receptor binding + 0.6781 67.81%
Thyroid receptor binding - 0.6403 64.03%
Glucocorticoid receptor binding - 0.6566 65.66%
Aromatase binding + 0.6120 61.20%
PPAR gamma - 0.6980 69.80%
Honey bee toxicity - 0.8888 88.88%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9775 97.75%

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 95.68% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 89.78% 83.82%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.03% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 87.49% 93.65%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.82% 89.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.66% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.92% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.81% 86.00%
CHEMBL2581 P07339 Cathepsin D 82.43% 98.95%

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.
Ammopiptanthus mongolicus
Arnebia ugamensis
Clausena lenis
Euryops arabicus
Launaea arborescens
Piptanthus nepalensis
Reichardia gaditana
Soehrensia spachiana

Cross-Links

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PubChem 638210
NPASS NPC208867
LOTUS LTS0022512
wikiData Q105118634