(2Z,9Z)-octadeca-2,9-dien-4,6-diyne-1,18-diol

Details

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Internal ID 9b63dcff-9a21-47e3-b5cb-ccd4f442685b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (2Z,9Z)-octadeca-2,9-dien-4,6-diyne-1,18-diol
SMILES (Canonical) C(CCCCO)CCCC=CCC#CC#CC=CCO
SMILES (Isomeric) C(CCCCO)CCC/C=C\CC#CC#C/C=C\CO
InChI InChI=1S/C18H26O2/c19-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-18-20/h1-2,14,16,19-20H,3-5,7,9,11,13,15,17-18H2/b2-1-,16-14-
InChI Key LETMGPQSRWMBMO-FBOKGXLDSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H26O2
Molecular Weight 274.40 g/mol
Exact Mass 274.193280068 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2Z,9Z)-octadeca-2,9-dien-4,6-diyne-1,18-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9447 94.47%
Caco-2 - 0.7059 70.59%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.5269 52.69%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.8428 84.28%
OATP1B3 inhibitior + 0.9402 94.02%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7972 79.72%
P-glycoprotein inhibitior - 0.8460 84.60%
P-glycoprotein substrate - 0.8802 88.02%
CYP3A4 substrate - 0.5287 52.87%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.7593 75.93%
CYP3A4 inhibition - 0.8981 89.81%
CYP2C9 inhibition - 0.8333 83.33%
CYP2C19 inhibition - 0.9093 90.93%
CYP2D6 inhibition - 0.9574 95.74%
CYP1A2 inhibition - 0.7345 73.45%
CYP2C8 inhibition - 0.6971 69.71%
CYP inhibitory promiscuity - 0.8549 85.49%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5787 57.87%
Eye corrosion + 0.9084 90.84%
Eye irritation - 0.5200 52.00%
Skin irritation - 0.5408 54.08%
Skin corrosion - 0.8598 85.98%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7340 73.40%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6818 68.18%
skin sensitisation + 0.6331 63.31%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5707 57.07%
Acute Oral Toxicity (c) III 0.7279 72.79%
Estrogen receptor binding + 0.5732 57.32%
Androgen receptor binding - 0.6558 65.58%
Thyroid receptor binding + 0.7149 71.49%
Glucocorticoid receptor binding - 0.4690 46.90%
Aromatase binding + 0.5378 53.78%
PPAR gamma + 0.6555 65.55%
Honey bee toxicity - 0.8801 88.01%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6658 66.58%
Fish aquatic toxicity - 0.7086 70.86%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 92.13% 99.17%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 88.77% 92.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.46% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 85.22% 87.45%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 84.42% 95.52%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.57% 94.45%
CHEMBL1781 P11387 DNA topoisomerase I 81.21% 97.00%

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.
Bupleurum longiradiatum

Cross-Links

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PubChem 44613552
LOTUS LTS0144207
wikiData Q105150785