29-Hydroxyhentriaconta-4,17,20,27-tetraen-2,30-diynoic acid

Details

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Internal ID cdcb7513-709c-4177-b996-66a458badc5a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Very long-chain fatty acids
IUPAC Name 29-hydroxyhentriaconta-4,17,20,27-tetraen-2,30-diynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H46O3/c1-2-30(32)28-26-24-22-20-18-16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31(33)34/h1,6,8,12,14,23,25-26,28,30,32H,3-5,7,9-11,13,15-22,24H2,(H,33,34)
InChI Key MEFLVKKDPXTSHP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H46O3
Molecular Weight 466.70 g/mol
Exact Mass 466.34469533 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 10.40
Atomic LogP (AlogP) 7.93
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 29-Hydroxyhentriaconta-4,17,20,27-tetraen-2,30-diynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9343 93.43%
Caco-2 - 0.8152 81.52%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6815 68.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7514 75.14%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6265 62.65%
P-glycoprotein inhibitior + 0.6548 65.48%
P-glycoprotein substrate - 0.8897 88.97%
CYP3A4 substrate - 0.5388 53.88%
CYP2C9 substrate - 0.7914 79.14%
CYP2D6 substrate - 0.8447 84.47%
CYP3A4 inhibition - 0.8888 88.88%
CYP2C9 inhibition - 0.7431 74.31%
CYP2C19 inhibition - 0.8783 87.83%
CYP2D6 inhibition - 0.9544 95.44%
CYP1A2 inhibition - 0.7693 76.93%
CYP2C8 inhibition - 0.7549 75.49%
CYP inhibitory promiscuity - 0.8235 82.35%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6458 64.58%
Carcinogenicity (trinary) Non-required 0.6449 64.49%
Eye corrosion + 0.8636 86.36%
Eye irritation - 0.8540 85.40%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.7674 76.74%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8153 81.53%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.5534 55.34%
skin sensitisation + 0.5301 53.01%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.7742 77.42%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.7604 76.04%
Acute Oral Toxicity (c) III 0.7127 71.27%
Estrogen receptor binding + 0.7517 75.17%
Androgen receptor binding - 0.6524 65.24%
Thyroid receptor binding + 0.5326 53.26%
Glucocorticoid receptor binding - 0.5058 50.58%
Aromatase binding + 0.5187 51.87%
PPAR gamma + 0.5949 59.49%
Honey bee toxicity - 0.8988 89.88%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8696 86.96%

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 94.28% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 91.72% 83.82%
CHEMBL2581 P07339 Cathepsin D 91.47% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.06% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 89.89% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.62% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.98% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.45% 95.50%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 80.35% 92.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.31% 86.33%

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 73806732
LOTUS LTS0033188
wikiData Q105162205