Bisabola-1,3,5,7-tetraene

Details

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Internal ID 72b39880-a9ff-4d30-9300-1d971d9d08ed
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-4-[(Z)-6-methylhept-2-en-2-yl]benzene
SMILES (Canonical) CC1=CC=C(C=C1)C(=CCCC(C)C)C
SMILES (Isomeric) CC1=CC=C(C=C1)/C(=C\CCC(C)C)/C
InChI InChI=1S/C15H22/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h7-12H,5-6H2,1-4H3/b14-7-
InChI Key YKWOHCWVJMGYOF-AUWJEWJLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22
Molecular Weight 202.33 g/mol
Exact Mass 202.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 5.70
Atomic LogP (AlogP) 4.83
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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YKWOHCWVJMGYOF-AUWJEWJLSA-N

2D Structure

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2D Structure of Bisabola-1,3,5,7-tetraene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.9804 98.04%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Nucleus 0.4561 45.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9036 90.36%
OATP1B3 inhibitior + 0.8870 88.70%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6841 68.41%
P-glycoprotein inhibitior - 0.9569 95.69%
P-glycoprotein substrate - 0.8771 87.71%
CYP3A4 substrate - 0.6898 68.98%
CYP2C9 substrate - 0.6417 64.17%
CYP2D6 substrate - 0.7063 70.63%
CYP3A4 inhibition - 0.9140 91.40%
CYP2C9 inhibition - 0.9018 90.18%
CYP2C19 inhibition - 0.8633 86.33%
CYP2D6 inhibition - 0.8894 88.94%
CYP1A2 inhibition - 0.6895 68.95%
CYP2C8 inhibition - 0.9356 93.56%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Warning 0.4736 47.36%
Eye corrosion - 0.7162 71.62%
Eye irritation + 0.9440 94.40%
Skin irritation + 0.8403 84.03%
Skin corrosion - 0.8341 83.41%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7091 70.91%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5838 58.38%
skin sensitisation + 0.9596 95.96%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6647 66.47%
Acute Oral Toxicity (c) III 0.9346 93.46%
Estrogen receptor binding - 0.7645 76.45%
Androgen receptor binding - 0.7432 74.32%
Thyroid receptor binding - 0.7508 75.08%
Glucocorticoid receptor binding - 0.8504 85.04%
Aromatase binding - 0.5289 52.89%
PPAR gamma - 0.7170 71.70%
Honey bee toxicity - 0.9767 97.67%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9931 99.31%

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
CHEMBL2581 P07339 Cathepsin D 91.13% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 87.72% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.69% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 86.72% 91.49%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.39% 93.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.80% 96.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.03% 97.21%
CHEMBL1907 P15144 Aminopeptidase N 80.46% 93.31%

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.
Plagiochila asplenioides

Cross-Links

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PubChem 91749821
LOTUS LTS0100573
wikiData Q105349928