Petrocortyne G

Details

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Internal ID 81ff7805-5039-402a-bec2-57cde5748b83
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (3R,4E,14R,21Z,28E,43Z)-hexatetraconta-4,21,28,43-tetraen-1,12,15,45-tetrayne-3,14,27-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C46H70O3/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-19-25-30-35-40-45(48)41-36-31-26-20-17-18-21-27-32-37-42-46(49)43-38-33-28-23-22-24-29-34-39-44(47)4-2/h1-2,5-6,17,20,34-35,39-40,44-49H,7-16,18-19,21-33,36,41H2/b6-5-,20-17-,39-34+,40-35+/t44-,45?,46-/m0/s1
InChI Key BBSNNCKQYMKHNA-YAZFTXODSA-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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CHEMBL454563

2D Structure

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2D Structure of Petrocortyne G

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 - 0.8382 83.82%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7468 74.68%
OATP2B1 inhibitior - 0.7148 71.48%
OATP1B1 inhibitior + 0.8527 85.27%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9624 96.24%
P-glycoprotein inhibitior + 0.6918 69.18%
P-glycoprotein substrate - 0.8107 81.07%
CYP3A4 substrate + 0.5234 52.34%
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 - 0.5785 57.85%
CYP inhibitory promiscuity - 0.7759 77.59%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6090 60.90%
Eye corrosion + 0.6870 68.70%
Eye irritation - 0.8926 89.26%
Skin irritation - 0.5533 55.33%
Skin corrosion - 0.7455 74.55%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8432 84.32%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5662 56.62%
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 - 0.8003 80.03%
Acute Oral Toxicity (c) III 0.5273 52.73%
Estrogen receptor binding + 0.8080 80.80%
Androgen receptor binding - 0.4896 48.96%
Thyroid receptor binding + 0.5307 53.07%
Glucocorticoid receptor binding + 0.5843 58.43%
Aromatase binding + 0.6059 60.59%
PPAR gamma + 0.5698 56.98%
Honey bee toxicity - 0.8565 85.65%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5800 58.00%
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 95.05% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.91% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.04% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.22% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 89.20% 89.63%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 88.93% 92.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.87% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.82% 96.00%
CHEMBL1781 P11387 DNA topoisomerase I 81.45% 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 10580327
LOTUS LTS0135747
wikiData Q104923022