Tricosa-14,20-dien-3,5,10,12,22-pentayne-1,2,16-triol

Details

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Internal ID cea1ae62-e4bc-42f5-960c-6dd551c85975
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name tricosa-14,20-dien-3,5,10,12,22-pentayne-1,2,16-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O3/c1-2-3-4-12-15-18-22(25)19-16-13-10-8-6-5-7-9-11-14-17-20-23(26)21-24/h1,3-4,16,19,22-26H,5,7,9,12,15,18,21H2
InChI Key LJVSFZWRHGCGBU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O3
Molecular Weight 348.40 g/mol
Exact Mass 348.17254462 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 3.20
Atomic LogP (AlogP) 1.80
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tricosa-14,20-dien-3,5,10,12,22-pentayne-1,2,16-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8709 87.09%
Caco-2 - 0.8316 83.16%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7094 70.94%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.8511 85.11%
OATP1B3 inhibitior + 0.9522 95.22%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7593 75.93%
P-glycoprotein inhibitior - 0.6406 64.06%
P-glycoprotein substrate - 0.7463 74.63%
CYP3A4 substrate + 0.5385 53.85%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.7723 77.23%
CYP3A4 inhibition - 0.8520 85.20%
CYP2C9 inhibition - 0.8570 85.70%
CYP2C19 inhibition - 0.8672 86.72%
CYP2D6 inhibition - 0.9397 93.97%
CYP1A2 inhibition - 0.7487 74.87%
CYP2C8 inhibition - 0.7191 71.91%
CYP inhibitory promiscuity - 0.8810 88.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.7015 70.15%
Eye corrosion - 0.6604 66.04%
Eye irritation - 0.9291 92.91%
Skin irritation + 0.4918 49.18%
Skin corrosion + 0.5619 56.19%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7654 76.54%
Micronuclear - 0.9268 92.68%
Hepatotoxicity - 0.6321 63.21%
skin sensitisation - 0.5772 57.72%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.7130 71.30%
Acute Oral Toxicity (c) III 0.4256 42.56%
Estrogen receptor binding + 0.7293 72.93%
Androgen receptor binding - 0.6336 63.36%
Thyroid receptor binding + 0.6882 68.82%
Glucocorticoid receptor binding + 0.5739 57.39%
Aromatase binding + 0.5318 53.18%
PPAR gamma + 0.7635 76.35%
Honey bee toxicity - 0.8357 83.57%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.9344 93.44%

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 94.58% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.38% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.12% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.44% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 82.50% 90.17%
CHEMBL2581 P07339 Cathepsin D 82.37% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.39% 94.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85189037
LOTUS LTS0021698
wikiData Q105152848