Pentatetraconta-4,21,27,42-tetraen-1,12,15,44-tetrayne-3,14-diol

Details

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Internal ID 2b308e30-6f5f-4393-9bbb-518fde07fcb1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name pentatetraconta-4,21,27,42-tetraen-1,12,15,44-tetrayne-3,14-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C45H68O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-33-36-39-42-45(47)43-40-37-34-31-30-32-35-38-41-44(46)4-2/h1-2,5-6,20-21,26-27,38,41,44-47H,7-19,22-25,28-37H2
InChI Key MRQZYVOSYAHCBX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C45H68O2
Molecular Weight 641.00 g/mol
Exact Mass 640.52193141 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 15.20
Atomic LogP (AlogP) 11.74
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 30

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pentatetraconta-4,21,27,42-tetraen-1,12,15,44-tetrayne-3,14-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9586 95.86%
Caco-2 - 0.8269 82.69%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.5171 51.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8447 84.47%
OATP1B3 inhibitior + 0.9422 94.22%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9152 91.52%
P-glycoprotein inhibitior + 0.6902 69.02%
P-glycoprotein substrate - 0.8923 89.23%
CYP3A4 substrate - 0.5311 53.11%
CYP2C9 substrate - 0.6095 60.95%
CYP2D6 substrate - 0.7375 73.75%
CYP3A4 inhibition - 0.8675 86.75%
CYP2C9 inhibition - 0.7073 70.73%
CYP2C19 inhibition - 0.8378 83.78%
CYP2D6 inhibition - 0.9471 94.71%
CYP1A2 inhibition - 0.6135 61.35%
CYP2C8 inhibition - 0.6245 62.45%
CYP inhibitory promiscuity - 0.5258 52.58%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.5405 54.05%
Eye corrosion + 0.9050 90.50%
Eye irritation - 0.8680 86.80%
Skin irritation + 0.6030 60.30%
Skin corrosion - 0.5844 58.44%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8377 83.77%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5412 54.12%
skin sensitisation + 0.7441 74.41%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7465 74.65%
Acute Oral Toxicity (c) III 0.6172 61.72%
Estrogen receptor binding + 0.8099 80.99%
Androgen receptor binding + 0.5351 53.51%
Thyroid receptor binding + 0.5553 55.53%
Glucocorticoid receptor binding + 0.5418 54.18%
Aromatase binding + 0.6420 64.20%
PPAR gamma + 0.5943 59.43%
Honey bee toxicity - 0.8780 87.80%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity - 0.3910 39.10%

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 94.40% 91.11%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 92.79% 92.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.33% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 91.05% 90.17%
CHEMBL2581 P07339 Cathepsin D 89.96% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.18% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.02% 96.00%

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 85137190
LOTUS LTS0270955
wikiData Q105170844