Montiporyne G

Details

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Internal ID 62e2dac5-740c-4925-b775-57d7dac08dd1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name dodec-11-en-2,4-diyn-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2,13H,1,3-7,12H2
InChI Key LGNSCSQFQCDGPG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O
Molecular Weight 176.25 g/mol
Exact Mass 176.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CHEMBL443245

2D Structure

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2D Structure of Montiporyne G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9774 97.74%
Caco-2 + 0.6156 61.56%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.3912 39.12%
OATP2B1 inhibitior - 0.8618 86.18%
OATP1B1 inhibitior + 0.9246 92.46%
OATP1B3 inhibitior + 0.9510 95.10%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9060 90.60%
P-glycoprotein inhibitior - 0.9767 97.67%
P-glycoprotein substrate - 0.9504 95.04%
CYP3A4 substrate - 0.6008 60.08%
CYP2C9 substrate - 0.8104 81.04%
CYP2D6 substrate - 0.7409 74.09%
CYP3A4 inhibition - 0.8955 89.55%
CYP2C9 inhibition - 0.8150 81.50%
CYP2C19 inhibition - 0.8482 84.82%
CYP2D6 inhibition - 0.9521 95.21%
CYP1A2 inhibition - 0.6815 68.15%
CYP2C8 inhibition - 0.8025 80.25%
CYP inhibitory promiscuity - 0.7590 75.90%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6320 63.20%
Eye corrosion + 0.9655 96.55%
Eye irritation + 0.8061 80.61%
Skin irritation + 0.6838 68.38%
Skin corrosion - 0.6845 68.45%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6424 64.24%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5766 57.66%
skin sensitisation + 0.7475 74.75%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5822 58.22%
Acute Oral Toxicity (c) III 0.3112 31.12%
Estrogen receptor binding - 0.8421 84.21%
Androgen receptor binding - 0.7573 75.73%
Thyroid receptor binding - 0.5960 59.60%
Glucocorticoid receptor binding - 0.7088 70.88%
Aromatase binding - 0.6427 64.27%
PPAR gamma - 0.6597 65.97%
Honey bee toxicity - 0.8020 80.20%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6529 65.29%
Fish aquatic toxicity + 0.7605 76.05%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.99% 91.11%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 85.94% 85.40%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.36% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.99% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 84.54% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.31% 97.29%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.07% 94.45%
CHEMBL1977 P11473 Vitamin D receptor 81.80% 99.43%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.77% 83.57%
CHEMBL1824 P04626 Receptor protein-tyrosine kinase erbB-2 80.56% 95.29%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 80.30% 92.95%

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.
There are no matching plants.

Cross-Links

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PubChem 11126805
LOTUS LTS0075589
wikiData Q105151477