(2E,8Z)-N-(2-methylpropyl)deca-2,8-dien-4,6-diynamide

Details

Top
Internal ID 853ffe28-c97b-4a5d-88f8-f5c740eca38b
Taxonomy Organic acids and derivatives > Carboximidic acids and derivatives > Carboximidic acids
IUPAC Name (2E,8Z)-N-(2-methylpropyl)deca-2,8-dien-4,6-diynamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H17NO/c1-4-5-6-7-8-9-10-11-14(16)15-12-13(2)3/h4-5,10-11,13H,12H2,1-3H3,(H,15,16)/b5-4-,11-10+
InChI Key WYWJSGONLKGLJA-JWPKELMXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H17NO
Molecular Weight 215.29 g/mol
Exact Mass 215.131014166 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 1.90
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2E,8Z)-N-(2-methylpropyl)deca-2,8-dien-4,6-diynamide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9895 98.95%
Caco-2 - 0.7249 72.49%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Lysosomes 0.4321 43.21%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9091 90.91%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7554 75.54%
P-glycoprotein inhibitior - 0.8884 88.84%
P-glycoprotein substrate - 0.7831 78.31%
CYP3A4 substrate - 0.5803 58.03%
CYP2C9 substrate - 0.8131 81.31%
CYP2D6 substrate - 0.8812 88.12%
CYP3A4 inhibition - 0.9647 96.47%
CYP2C9 inhibition - 0.8334 83.34%
CYP2C19 inhibition - 0.8384 83.84%
CYP2D6 inhibition - 0.9477 94.77%
CYP1A2 inhibition - 0.7411 74.11%
CYP2C8 inhibition - 0.9520 95.20%
CYP inhibitory promiscuity - 0.7985 79.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.4431 44.31%
Eye corrosion + 0.8129 81.29%
Eye irritation - 0.9328 93.28%
Skin irritation - 0.6922 69.22%
Skin corrosion - 0.7990 79.90%
Ames mutagenesis - 0.6774 67.74%
Human Ether-a-go-go-Related Gene inhibition - 0.5465 54.65%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation - 0.8530 85.30%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.5576 55.76%
Acute Oral Toxicity (c) III 0.6896 68.96%
Estrogen receptor binding - 0.6649 66.49%
Androgen receptor binding - 0.7086 70.86%
Thyroid receptor binding + 0.5274 52.74%
Glucocorticoid receptor binding - 0.5516 55.16%
Aromatase binding + 0.5398 53.98%
PPAR gamma - 0.7745 77.45%
Honey bee toxicity - 0.8906 89.06%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.6009 60.09%

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
CHEMBL2581 P07339 Cathepsin D 93.48% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.00% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 90.66% 83.82%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.88% 89.34%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.57% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 84.80% 90.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.83% 90.24%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.59% 97.29%
CHEMBL3401 O75469 Pregnane X receptor 83.25% 94.73%
CHEMBL226 P30542 Adenosine A1 receptor 82.60% 95.93%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 82.26% 95.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.85% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.72% 96.00%

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.
Achillea santolinoides subsp. wilhelmsii

Cross-Links

Top
PubChem 14015862
LOTUS LTS0059696
wikiData Q105322771