Dendrolasin

Details

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Internal ID 7946bad7-01d9-4f29-97d2-30ad083a55ba
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 3-[(3E)-4,8-dimethylnona-3,7-dienyl]furan
SMILES (Canonical) CC(=CCCC(=CCCC1=COC=C1)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CCC1=COC=C1)/C)C
InChI InChI=1S/C15H22O/c1-13(2)6-4-7-14(3)8-5-9-15-10-11-16-12-15/h6,8,10-12H,4-5,7,9H2,1-3H3/b14-8+
InChI Key LZBXPXAOYQVZEC-RIYZIHGNSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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Denderalasin
23262-34-2
Dendrasaline
Furan, 3-(4,8-dimethyl-3,7-nonadienyl)-, (E)-
3-(4,8-Dimethyl-3,7-nonadienyl)furan
SCHEMBL11886113
CHEBI:80721
LZBXPXAOYQVZEC-RIYZIHGNSA-N
DTXSID501318273
AKOS015905136
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dendrolasin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.9531 95.31%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Nucleus 0.4321 43.21%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.7933 79.33%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.5987 59.87%
P-glycoprotein inhibitior - 0.9383 93.83%
P-glycoprotein substrate - 0.9114 91.14%
CYP3A4 substrate - 0.5577 55.77%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.6885 68.85%
CYP3A4 inhibition - 0.9172 91.72%
CYP2C9 inhibition - 0.7389 73.89%
CYP2C19 inhibition - 0.6220 62.20%
CYP2D6 inhibition - 0.8916 89.16%
CYP1A2 inhibition + 0.5126 51.26%
CYP2C8 inhibition - 0.7986 79.86%
CYP inhibitory promiscuity + 0.5714 57.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4191 41.91%
Eye corrosion - 0.7359 73.59%
Eye irritation + 0.7948 79.48%
Skin irritation + 0.6517 65.17%
Skin corrosion - 0.9254 92.54%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6856 68.56%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.8158 81.58%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5841 58.41%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.5628 56.28%
Acute Oral Toxicity (c) III 0.8464 84.64%
Estrogen receptor binding - 0.7544 75.44%
Androgen receptor binding - 0.7469 74.69%
Thyroid receptor binding - 0.7350 73.50%
Glucocorticoid receptor binding - 0.5516 55.16%
Aromatase binding - 0.6538 65.38%
PPAR gamma + 0.6946 69.46%
Honey bee toxicity - 0.9278 92.78%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6232 62.32%
Fish aquatic toxicity + 0.9887 98.87%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 97.67% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 93.44% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.07% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.57% 94.45%
CHEMBL2581 P07339 Cathepsin D 91.12% 98.95%
CHEMBL2039 P27338 Monoamine oxidase B 88.04% 92.51%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.34% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.21% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.83% 86.33%

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.
Callicarpa macrophylla
Capsicum annuum
Santalum album
Santalum spicatum
Teucrium leucocladum
Torreya nucifera
Virola surinamensis

Cross-Links

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PubChem 5316534
NPASS NPC155129
LOTUS LTS0012692
wikiData Q27149763