trans-Lachnophyllol

Details

Top
Internal ID a8fc9603-fa6c-4af4-9983-e863d74dd0e5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (E)-dec-2-en-4,6-diyn-1-ol
SMILES (Canonical) CCCC#CC#CC=CCO
SMILES (Isomeric) CCCC#CC#C/C=C/CO
InChI InChI=1S/C10H12O/c1-2-3-4-5-6-7-8-9-10-11/h8-9,11H,2-3,10H2,1H3/b9-8+
InChI Key UVYOXYJPADNJRE-CMDGGOBGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H12O
Molecular Weight 148.20 g/mol
Exact Mass 148.088815002 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.34
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
23180-62-3
2-Decene-4,6-diyn-1-ol, (E)-
2-Decene-4,6-diyne-1-ol
CHEBI:81417
DTXSID001310600
(2E)-2-Decene-4,6-diyn-1-ol
C17965
Q27155349

2D Structure

Top
2D Structure of trans-Lachnophyllol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9878 98.78%
Caco-2 + 0.6662 66.62%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4340 43.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8742 87.42%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9178 91.78%
P-glycoprotein inhibitior - 0.9771 97.71%
P-glycoprotein substrate - 0.8946 89.46%
CYP3A4 substrate - 0.6125 61.25%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7877 78.77%
CYP3A4 inhibition - 0.9355 93.55%
CYP2C9 inhibition - 0.8810 88.10%
CYP2C19 inhibition - 0.8490 84.90%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.5864 58.64%
CYP2C8 inhibition - 0.9375 93.75%
CYP inhibitory promiscuity - 0.7448 74.48%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5282 52.82%
Eye corrosion + 0.9195 91.95%
Eye irritation + 0.7400 74.00%
Skin irritation + 0.7472 74.72%
Skin corrosion - 0.8736 87.36%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5621 56.21%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5198 51.98%
skin sensitisation + 0.7468 74.68%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5975 59.75%
Acute Oral Toxicity (c) I 0.5163 51.63%
Estrogen receptor binding - 0.8825 88.25%
Androgen receptor binding - 0.7501 75.01%
Thyroid receptor binding - 0.6967 69.67%
Glucocorticoid receptor binding - 0.8128 81.28%
Aromatase binding - 0.7655 76.55%
PPAR gamma - 0.6337 63.37%
Honey bee toxicity - 0.9339 93.39%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8348 83.48%
Fish aquatic toxicity - 0.5250 52.50%

Targets

Top

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 90.29% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 87.10% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.22% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.02% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.65% 89.34%

Plants that contains it

Top
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.
Aster tataricus
Plagiocheilus bogotensis
Toxicodendron succedaneum

Cross-Links

Top
PubChem 5318913
NPASS NPC96767
LOTUS LTS0092668
wikiData Q27155349