Brasilenol

Details

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Internal ID 724b2b98-dba3-4ed2-9c2b-a34ee37a1ae4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3R,4S,7R)-3,5,5-trimethyl-7-propan-2-yl-1,2,3,4,6,7-hexahydroinden-4-ol
SMILES (Canonical) CC1CCC2=C1C(C(CC2C(C)C)(C)C)O
SMILES (Isomeric) C[C@@H]1CCC2=C1[C@H](C(C[C@@H]2C(C)C)(C)C)O
InChI InChI=1S/C15H26O/c1-9(2)12-8-15(4,5)14(16)13-10(3)6-7-11(12)13/h9-10,12,14,16H,6-8H2,1-5H3/t10-,12-,14-/m1/s1
InChI Key YAYULTVMGYOHHF-MPKXVKKWSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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70000-39-4

2D Structure

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2D Structure of Brasilenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.5782 57.82%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.4502 45.02%
OATP2B1 inhibitior - 0.8450 84.50%
OATP1B1 inhibitior + 0.9422 94.22%
OATP1B3 inhibitior + 0.9169 91.69%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9592 95.92%
P-glycoprotein inhibitior - 0.9089 90.89%
P-glycoprotein substrate - 0.7204 72.04%
CYP3A4 substrate - 0.5305 53.05%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8492 84.92%
CYP2C9 inhibition - 0.6984 69.84%
CYP2C19 inhibition - 0.7043 70.43%
CYP2D6 inhibition - 0.9318 93.18%
CYP1A2 inhibition - 0.6668 66.68%
CYP2C8 inhibition - 0.9433 94.33%
CYP inhibitory promiscuity - 0.6445 64.45%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5516 55.16%
Eye corrosion - 0.9726 97.26%
Eye irritation + 0.9059 90.59%
Skin irritation + 0.7306 73.06%
Skin corrosion - 0.9427 94.27%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4458 44.58%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5552 55.52%
skin sensitisation + 0.7048 70.48%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7530 75.30%
Acute Oral Toxicity (c) III 0.6284 62.84%
Estrogen receptor binding - 0.6421 64.21%
Androgen receptor binding - 0.6450 64.50%
Thyroid receptor binding - 0.5806 58.06%
Glucocorticoid receptor binding - 0.6625 66.25%
Aromatase binding - 0.7961 79.61%
PPAR gamma - 0.8291 82.91%
Honey bee toxicity - 0.9151 91.51%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9932 99.32%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.24% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.91% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 92.23% 95.93%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.32% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.01% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.78% 95.89%
CHEMBL2581 P07339 Cathepsin D 84.08% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.29% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.26% 92.94%
CHEMBL221 P23219 Cyclooxygenase-1 82.14% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.08% 97.09%
CHEMBL1871 P10275 Androgen Receptor 81.82% 96.43%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.79% 91.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.35% 93.56%

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.
Anethum graveolens
Cymbidium aloifolium
Delphinium dictyocarpum
Ladeania juncea
Ligularia atroviolacea
Scutellaria glabra
Trifolium pannonicum

Cross-Links

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PubChem 14758694
NPASS NPC44666
LOTUS LTS0081272
wikiData Q104401060