Bisabola-2,10-diene 1,9-oxide

Details

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Internal ID 08fe8d80-3a3f-48da-a609-56673424723c
Taxonomy Organoheterocyclic compounds > Benzopyrans
IUPAC Name 4,7-dimethyl-2-(2-methylprop-1-enyl)-3,4,4a,5,6,8a-hexahydro-2H-chromene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-10(2)7-13-9-12(4)14-6-5-11(3)8-15(14)16-13/h7-8,12-15H,5-6,9H2,1-4H3
InChI Key SUZWJCBHQIOYCF-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) 9.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.10
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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Bisabola-2,10-diene 1,9-oxide

2D Structure

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2D Structure of Bisabola-2,10-diene 1,9-oxide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.8448 84.48%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Plasma membrane 0.3562 35.62%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9173 91.73%
OATP1B3 inhibitior + 0.9587 95.87%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8777 87.77%
P-glycoprotein inhibitior - 0.9401 94.01%
P-glycoprotein substrate - 0.8752 87.52%
CYP3A4 substrate + 0.5380 53.80%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6798 67.98%
CYP3A4 inhibition - 0.8229 82.29%
CYP2C9 inhibition - 0.7488 74.88%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9205 92.05%
CYP1A2 inhibition + 0.5359 53.59%
CYP2C8 inhibition - 0.7913 79.13%
CYP inhibitory promiscuity - 0.7246 72.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6025 60.25%
Eye corrosion - 0.9254 92.54%
Eye irritation - 0.8373 83.73%
Skin irritation - 0.5569 55.69%
Skin corrosion - 0.9543 95.43%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5705 57.05%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5783 57.83%
skin sensitisation + 0.7238 72.38%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.7232 72.32%
Acute Oral Toxicity (c) III 0.7886 78.86%
Estrogen receptor binding - 0.8607 86.07%
Androgen receptor binding - 0.6344 63.44%
Thyroid receptor binding - 0.7353 73.53%
Glucocorticoid receptor binding - 0.7464 74.64%
Aromatase binding - 0.7889 78.89%
PPAR gamma - 0.8078 80.78%
Honey bee toxicity - 0.7766 77.66%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9392 93.92%

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 93.10% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.70% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.40% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.26% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.21% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.26% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.48% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.58% 94.80%

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.
Calypogeia suecica

Cross-Links

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PubChem 91750183
LOTUS LTS0274631
wikiData Q105261734