Petrocortyne F

Details

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Internal ID 649f48f5-d988-4d8c-88be-2f65b08ed03b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (3R,4E,14R,20E,27Z,43Z)-hexatetraconta-4,20,27,43-tetraen-1,12,15,45-tetrayne-3,14,22-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C46H70O3/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-26-30-35-40-45(48)42-37-32-28-33-38-43-46(49)41-36-31-27-24-23-25-29-34-39-44(47)4-2/h1-2,5-6,21-22,34,37,39,42,44-49H,7-20,23-33,35,40H2/b6-5-,22-21-,39-34+,42-37+/t44-,45?,46+/m0/s1
InChI Key KYOPDYZCISEEDJ-YFJJFFNOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C46H70O3
Molecular Weight 671.00 g/mol
Exact Mass 670.53249609 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 14.20
Atomic LogP (AlogP) 11.10
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 31

Synonyms

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CHEMBL503977

2D Structure

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2D Structure of Petrocortyne F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9495 94.95%
Caco-2 - 0.8447 84.47%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7468 74.68%
OATP2B1 inhibitior - 0.7141 71.41%
OATP1B1 inhibitior + 0.8497 84.97%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8989 89.89%
P-glycoprotein inhibitior + 0.6999 69.99%
P-glycoprotein substrate - 0.7982 79.82%
CYP3A4 substrate + 0.5331 53.31%
CYP2C9 substrate - 0.6095 60.95%
CYP2D6 substrate - 0.7375 73.75%
CYP3A4 inhibition - 0.8738 87.38%
CYP2C9 inhibition - 0.8061 80.61%
CYP2C19 inhibition - 0.8733 87.33%
CYP2D6 inhibition - 0.9519 95.19%
CYP1A2 inhibition - 0.6821 68.21%
CYP2C8 inhibition + 0.4504 45.04%
CYP inhibitory promiscuity - 0.7759 77.59%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6090 60.90%
Eye corrosion + 0.6870 68.70%
Eye irritation - 0.8873 88.73%
Skin irritation - 0.5533 55.33%
Skin corrosion - 0.7455 74.55%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8738 87.38%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5787 57.87%
skin sensitisation + 0.5783 57.83%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.9373 93.73%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7951 79.51%
Acute Oral Toxicity (c) III 0.5273 52.73%
Estrogen receptor binding + 0.7850 78.50%
Androgen receptor binding - 0.4896 48.96%
Thyroid receptor binding - 0.5139 51.39%
Glucocorticoid receptor binding - 0.4717 47.17%
Aromatase binding + 0.5905 59.05%
PPAR gamma + 0.5614 56.14%
Honey bee toxicity - 0.8648 86.48%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.5091 50.91%

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 95.24% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.91% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.04% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 90.50% 89.63%
CHEMBL2581 P07339 Cathepsin D 90.42% 98.95%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 88.93% 92.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.68% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.82% 96.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.15% 100.00%
CHEMBL1781 P11387 DNA topoisomerase I 80.75% 97.00%

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 10556398
LOTUS LTS0158272
wikiData Q105147827