Peyronetide B

Details

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Internal ID c1b3cbed-b994-42a5-b9ec-d5bbaae32595
Taxonomy Organoheterocyclic compounds > Naphthofurans
IUPAC Name (7S)-5,7-dihydroxy-8-methoxy-2-[(E,4S)-4-methylhex-2-en-2-yl]-6-oxo-7-(2-oxopropyl)benzo[g][1]benzofuran-4-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26O7/c1-6-12(2)7-13(3)18-8-15-17(11-25)21(27)20-16(22(15)31-18)9-19(30-5)24(29,23(20)28)10-14(4)26/h7-9,11-12,27,29H,6,10H2,1-5H3/b13-7+/t12-,24-/m0/s1
InChI Key QVZJKUGRRBTCQO-XUHHNZALSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O7
Molecular Weight 426.50 g/mol
Exact Mass 426.16785316 g/mol
Topological Polar Surface Area (TPSA) 114.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.29
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Peyronetide B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 - 0.6214 62.14%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6223 62.23%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.6889 68.89%
OATP1B3 inhibitior + 0.9172 91.72%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9510 95.10%
P-glycoprotein inhibitior + 0.7123 71.23%
P-glycoprotein substrate - 0.5190 51.90%
CYP3A4 substrate + 0.6563 65.63%
CYP2C9 substrate + 0.6076 60.76%
CYP2D6 substrate - 0.8490 84.90%
CYP3A4 inhibition - 0.5910 59.10%
CYP2C9 inhibition - 0.5715 57.15%
CYP2C19 inhibition - 0.6501 65.01%
CYP2D6 inhibition - 0.8908 89.08%
CYP1A2 inhibition - 0.5368 53.68%
CYP2C8 inhibition + 0.5974 59.74%
CYP inhibitory promiscuity + 0.6724 67.24%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Danger 0.4074 40.74%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.9110 91.10%
Skin irritation - 0.7531 75.31%
Skin corrosion - 0.9407 94.07%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7756 77.56%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.6387 63.87%
skin sensitisation - 0.7253 72.53%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8459 84.59%
Acute Oral Toxicity (c) III 0.3926 39.26%
Estrogen receptor binding + 0.7587 75.87%
Androgen receptor binding + 0.7598 75.98%
Thyroid receptor binding + 0.5372 53.72%
Glucocorticoid receptor binding + 0.8017 80.17%
Aromatase binding + 0.7374 73.74%
PPAR gamma + 0.7711 77.11%
Honey bee toxicity - 0.7183 71.83%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9879 98.79%

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 99.59% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.05% 94.45%
CHEMBL2581 P07339 Cathepsin D 97.89% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.63% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.51% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.32% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.47% 96.09%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 89.12% 98.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.95% 94.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.77% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.05% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 84.68% 91.19%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 84.27% 83.10%
CHEMBL3401 O75469 Pregnane X receptor 83.68% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.95% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.88% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.78% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.12% 92.62%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.61% 82.38%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.26% 99.15%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 146682608
LOTUS LTS0026482
wikiData Q105229026