2-Heptadec-10-enyl-6-methoxybenzene-1,4-diol

Details

Top
Internal ID 1a0b8ae8-cf0a-4d58-a8bf-1f9ec5051cd9
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 2-heptadec-10-enyl-6-methoxybenzene-1,4-diol
SMILES (Canonical) CCCCCCC=CCCCCCCCCCC1=C(C(=CC(=C1)O)OC)O
SMILES (Isomeric) CCCCCCC=CCCCCCCCCCC1=C(C(=CC(=C1)O)OC)O
InChI InChI=1S/C24H40O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-21-19-22(25)20-23(27-2)24(21)26/h8-9,19-20,25-26H,3-7,10-18H2,1-2H3
InChI Key BDWQNYPENCTULP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C24H40O3
Molecular Weight 376.60 g/mol
Exact Mass 376.29774513 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 9.20
Atomic LogP (AlogP) 7.30
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 16

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-Heptadec-10-enyl-6-methoxybenzene-1,4-diol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 - 0.5459 54.59%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8488 84.88%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.7519 75.19%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7467 74.67%
P-glycoprotein inhibitior - 0.4369 43.69%
P-glycoprotein substrate - 0.6879 68.79%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.3925 39.25%
CYP3A4 inhibition - 0.6474 64.74%
CYP2C9 inhibition - 0.7063 70.63%
CYP2C19 inhibition - 0.5099 50.99%
CYP2D6 inhibition - 0.7077 70.77%
CYP1A2 inhibition + 0.7310 73.10%
CYP2C8 inhibition + 0.8513 85.13%
CYP inhibitory promiscuity + 0.5794 57.94%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7786 77.86%
Carcinogenicity (trinary) Non-required 0.6577 65.77%
Eye corrosion - 0.9265 92.65%
Eye irritation + 0.5513 55.13%
Skin irritation - 0.5890 58.90%
Skin corrosion - 0.7584 75.84%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7439 74.39%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6381 63.81%
skin sensitisation + 0.6349 63.49%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7389 73.89%
Acute Oral Toxicity (c) III 0.7082 70.82%
Estrogen receptor binding + 0.8284 82.84%
Androgen receptor binding + 0.6837 68.37%
Thyroid receptor binding + 0.5669 56.69%
Glucocorticoid receptor binding + 0.5915 59.15%
Aromatase binding - 0.5611 56.11%
PPAR gamma + 0.7057 70.57%
Honey bee toxicity - 0.9658 96.58%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.8896 88.96%
Fish aquatic toxicity + 0.9954 99.54%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.55% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.90% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.55% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 96.10% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.60% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.85% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.62% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.01% 96.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 86.57% 89.62%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.96% 98.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.95% 95.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.93% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 84.68% 94.73%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.65% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.56% 96.00%
CHEMBL2885 P07451 Carbonic anhydrase III 83.51% 87.45%
CHEMBL3891 P07384 Calpain 1 82.07% 93.04%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.98% 91.81%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.32% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 81.16% 90.20%
CHEMBL1907 P15144 Aminopeptidase N 80.89% 93.31%

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.
Iris sibirica

Cross-Links

Top
PubChem 357303
LOTUS LTS0237562
wikiData Q104924823