(2R,3Z,6E)-1-bromo-3,7,11-trimethyldodeca-3,6,10-trien-2-ol

Details

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Internal ID 54311daf-c6b9-46f3-8d3b-75b0a91087ee
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2R,3Z,6E)-1-bromo-3,7,11-trimethyldodeca-3,6,10-trien-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H25BrO/c1-12(2)7-5-8-13(3)9-6-10-14(4)15(17)11-16/h7,9-10,15,17H,5-6,8,11H2,1-4H3/b13-9+,14-10-/t15-/m0/s1
InChI Key BMYRKAKGPSZRBG-DELIOSKOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H25BrO
Molecular Weight 301.26 g/mol
Exact Mass 300.10888 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.77
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3Z,6E)-1-bromo-3,7,11-trimethyldodeca-3,6,10-trien-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.7008 70.08%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.3755 37.55%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9172 91.72%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7052 70.52%
P-glycoprotein inhibitior - 0.9582 95.82%
P-glycoprotein substrate - 0.9457 94.57%
CYP3A4 substrate - 0.6120 61.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7093 70.93%
CYP3A4 inhibition - 0.8335 83.35%
CYP2C9 inhibition - 0.8611 86.11%
CYP2C19 inhibition - 0.8421 84.21%
CYP2D6 inhibition - 0.9152 91.52%
CYP1A2 inhibition - 0.7395 73.95%
CYP2C8 inhibition - 0.9710 97.10%
CYP inhibitory promiscuity - 0.8315 83.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5945 59.45%
Carcinogenicity (trinary) Non-required 0.6187 61.87%
Eye corrosion - 0.6477 64.77%
Eye irritation - 0.6576 65.76%
Skin irritation + 0.7235 72.35%
Skin corrosion - 0.9027 90.27%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5770 57.70%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5002 50.02%
skin sensitisation + 0.8903 89.03%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.8375 83.75%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.7343 73.43%
Acute Oral Toxicity (c) III 0.7964 79.64%
Estrogen receptor binding - 0.8070 80.70%
Androgen receptor binding - 0.8862 88.62%
Thyroid receptor binding - 0.4931 49.31%
Glucocorticoid receptor binding - 0.5777 57.77%
Aromatase binding - 0.6698 66.98%
PPAR gamma + 0.5950 59.50%
Honey bee toxicity - 0.8587 85.87%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9215 92.15%

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 93.14% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.67% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.74% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 89.39% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.83% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.00% 92.08%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162966743
LOTUS LTS0047949
wikiData Q104938652