Bisabola-1,3,5,7(14)-tetraene

Details

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Internal ID 89a735cc-196a-424f-b9cd-5e4632dbaa4c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-4-(6-methylhept-1-en-2-yl)benzene
SMILES (Canonical) CC1=CC=C(C=C1)C(=C)CCCC(C)C
SMILES (Isomeric) CC1=CC=C(C=C1)C(=C)CCCC(C)C
InChI InChI=1S/C15H22/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h8-12H,4-7H2,1-3H3
InChI Key OUOQVJYYZABQJT-UHFFFAOYSA-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 6.00
Atomic LogP (AlogP) 4.83
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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Bisabola-1,3,5,7(14)-tetraene

2D Structure

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2D Structure of Bisabola-1,3,5,7(14)-tetraene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 + 0.9798 97.98%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Nucleus 0.4195 41.95%
OATP2B1 inhibitior - 0.8591 85.91%
OATP1B1 inhibitior + 0.9377 93.77%
OATP1B3 inhibitior + 0.8851 88.51%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8099 80.99%
P-glycoprotein inhibitior - 0.9491 94.91%
P-glycoprotein substrate - 0.7733 77.33%
CYP3A4 substrate - 0.6645 66.45%
CYP2C9 substrate - 0.6417 64.17%
CYP2D6 substrate - 0.7063 70.63%
CYP3A4 inhibition - 0.8754 87.54%
CYP2C9 inhibition - 0.8866 88.66%
CYP2C19 inhibition - 0.8149 81.49%
CYP2D6 inhibition - 0.8961 89.61%
CYP1A2 inhibition - 0.6849 68.49%
CYP2C8 inhibition - 0.9121 91.21%
CYP inhibitory promiscuity - 0.5481 54.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Warning 0.4947 49.47%
Eye corrosion - 0.6561 65.61%
Eye irritation + 0.9557 95.57%
Skin irritation + 0.8062 80.62%
Skin corrosion - 0.9136 91.36%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3667 36.67%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.9455 94.55%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.7521 75.21%
Acute Oral Toxicity (c) III 0.9300 93.00%
Estrogen receptor binding - 0.7201 72.01%
Androgen receptor binding - 0.6487 64.87%
Thyroid receptor binding - 0.6527 65.27%
Glucocorticoid receptor binding - 0.8180 81.80%
Aromatase binding + 0.5600 56.00%
PPAR gamma - 0.5838 58.38%
Honey bee toxicity - 0.9805 98.05%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9968 99.68%

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 93.24% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 89.63% 91.49%
CHEMBL1907 P15144 Aminopeptidase N 88.54% 93.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.23% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 87.17% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.42% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.27% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.12% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.56% 90.71%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.87% 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.
Plagiochila asplenioides

Cross-Links

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PubChem 21580497
LOTUS LTS0111414
wikiData Q105200333