(Z,6R)-hentriacont-28-en-2,4,16,30-tetrayne-1,6-diol

Details

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Internal ID 30e2a700-a20d-4254-9086-6868e1722f9b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (Z,6R)-hentriacont-28-en-2,4,16,30-tetrayne-1,6-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H46O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-25-28-31(33)29-26-24-27-30-32/h1,3-4,31-33H,5-14,17-23,25,28,30H2/b4-3-/t31-/m1/s1
InChI Key MJRYMHVVDZNHNP-WDKBPJLCSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C31H46O2
Molecular Weight 450.70 g/mol
Exact Mass 450.349780706 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 9.80
Atomic LogP (AlogP) 6.95
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z,6R)-hentriacont-28-en-2,4,16,30-tetrayne-1,6-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9694 96.94%
Caco-2 - 0.7902 79.02%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6669 66.69%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.8727 87.27%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4671 46.71%
P-glycoprotein inhibitior - 0.5517 55.17%
P-glycoprotein substrate - 0.7999 79.99%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.7581 75.81%
CYP3A4 inhibition - 0.8765 87.65%
CYP2C9 inhibition - 0.7869 78.69%
CYP2C19 inhibition - 0.8730 87.30%
CYP2D6 inhibition - 0.9325 93.25%
CYP1A2 inhibition - 0.6238 62.38%
CYP2C8 inhibition - 0.7201 72.01%
CYP inhibitory promiscuity - 0.7415 74.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6805 68.05%
Eye corrosion + 0.6497 64.97%
Eye irritation - 0.8483 84.83%
Skin irritation - 0.6025 60.25%
Skin corrosion - 0.8279 82.79%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7958 79.58%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6736 67.36%
skin sensitisation + 0.5704 57.04%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6205 62.05%
Acute Oral Toxicity (c) III 0.5500 55.00%
Estrogen receptor binding + 0.7618 76.18%
Androgen receptor binding + 0.5396 53.96%
Thyroid receptor binding + 0.6545 65.45%
Glucocorticoid receptor binding - 0.4942 49.42%
Aromatase binding + 0.6374 63.74%
PPAR gamma + 0.6140 61.40%
Honey bee toxicity - 0.9059 90.59%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5010 50.10%
Fish aquatic toxicity - 0.7856 78.56%

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 93.53% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.24% 97.29%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.91% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.65% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 88.05% 90.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.68% 92.86%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.00% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 82.21% 89.63%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 81.82% 92.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.30% 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 11465110
LOTUS LTS0174393
wikiData Q105165618