Cytospolide F

Details

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Internal ID 93867e1a-e2c6-4fba-9852-21b3aff7df93
Taxonomy Organoheterocyclic compounds > Oxocins
IUPAC Name (2R,3S,6E,8R,9R)-3,8-dihydroxy-2-[(4S)-4-hydroxypentyl]-9-methyl-2,3,4,5,8,9-hexahydrooxecin-10-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26O5/c1-10(16)6-5-9-14-13(18)8-4-3-7-12(17)11(2)15(19)20-14/h3,7,10-14,16-18H,4-6,8-9H2,1-2H3/b7-3+/t10-,11+,12+,13-,14+/m0/s1
InChI Key ATNGVHJGYIWYSL-BSJDXJPLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O5
Molecular Weight 286.36 g/mol
Exact Mass 286.17802393 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.16
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cytospolide F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9318 93.18%
Caco-2 + 0.5595 55.95%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6606 66.06%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9218 92.18%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8760 87.60%
P-glycoprotein inhibitior - 0.8747 87.47%
P-glycoprotein substrate - 0.6281 62.81%
CYP3A4 substrate + 0.5549 55.49%
CYP2C9 substrate - 0.8537 85.37%
CYP2D6 substrate - 0.8640 86.40%
CYP3A4 inhibition - 0.6051 60.51%
CYP2C9 inhibition - 0.9409 94.09%
CYP2C19 inhibition - 0.7757 77.57%
CYP2D6 inhibition - 0.9499 94.99%
CYP1A2 inhibition - 0.7264 72.64%
CYP2C8 inhibition - 0.9717 97.17%
CYP inhibitory promiscuity - 0.9646 96.46%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.7125 71.25%
Eye corrosion - 0.9782 97.82%
Eye irritation - 0.9673 96.73%
Skin irritation - 0.5397 53.97%
Skin corrosion - 0.9338 93.38%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5451 54.51%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5807 58.07%
skin sensitisation - 0.8045 80.45%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6188 61.88%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7115 71.15%
Acute Oral Toxicity (c) III 0.4717 47.17%
Estrogen receptor binding + 0.6517 65.17%
Androgen receptor binding - 0.7594 75.94%
Thyroid receptor binding - 0.5187 51.87%
Glucocorticoid receptor binding - 0.6402 64.02%
Aromatase binding - 0.8122 81.22%
PPAR gamma - 0.6551 65.51%
Honey bee toxicity - 0.8947 89.47%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9331 93.31%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.79% 83.82%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.57% 97.25%
CHEMBL2581 P07339 Cathepsin D 97.62% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.00% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.73% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.74% 85.14%
CHEMBL5103 Q969S8 Histone deacetylase 10 91.35% 90.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.02% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.89% 97.09%
CHEMBL4588 P22894 Matrix metalloproteinase 8 85.88% 94.66%
CHEMBL325 Q13547 Histone deacetylase 1 85.51% 95.92%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.28% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 82.84% 94.73%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.43% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.40% 95.89%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.11% 96.61%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 81.09% 96.37%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.25% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.20% 90.71%

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 53307440
LOTUS LTS0189409
wikiData Q77496378