Frondosin D

Details

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Internal ID 423ccc6b-9994-43a8-818f-173ab4eb33f8
Taxonomy Organoheterocyclic compounds > Pyrans
IUPAC Name (10S,14R)-14-hydroxy-6,6,10-trimethyl-13-oxatetracyclo[9.8.0.02,7.014,19]nonadeca-1(11),2(7),15,18-tetraen-17-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H26O3/c1-13-6-7-17-15(5-4-9-20(17,2)3)19-16(13)12-24-21(23)10-8-14(22)11-18(19)21/h8,10-11,13,23H,4-7,9,12H2,1-3H3/t13-,21+/m0/s1
InChI Key KVISAICAHCFDRV-YEJXKQKISA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C21H26O3
Molecular Weight 326.40 g/mol
Exact Mass 326.18819469 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 4.00
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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(10S,14R)-14-Hydroxy-6,6,10-trimethyl-13-oxatetracyclo[9.8.0.02,7.014,19]nonadeca-1(11),2(7),15,18-tetraen-17-one

2D Structure

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2D Structure of Frondosin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.8297 82.97%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7910 79.10%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8450 84.50%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.7270 72.70%
P-glycoprotein inhibitior - 0.6371 63.71%
P-glycoprotein substrate - 0.7471 74.71%
CYP3A4 substrate + 0.6482 64.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8674 86.74%
CYP3A4 inhibition - 0.8927 89.27%
CYP2C9 inhibition - 0.5991 59.91%
CYP2C19 inhibition - 0.6959 69.59%
CYP2D6 inhibition - 0.8955 89.55%
CYP1A2 inhibition - 0.6578 65.78%
CYP2C8 inhibition - 0.6263 62.63%
CYP inhibitory promiscuity - 0.9271 92.71%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6411 64.11%
Eye corrosion - 0.9864 98.64%
Eye irritation - 0.8426 84.26%
Skin irritation - 0.7070 70.70%
Skin corrosion - 0.9605 96.05%
Ames mutagenesis - 0.6149 61.49%
Human Ether-a-go-go-Related Gene inhibition + 0.6430 64.30%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5785 57.85%
skin sensitisation - 0.6163 61.63%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7265 72.65%
Acute Oral Toxicity (c) III 0.5691 56.91%
Estrogen receptor binding + 0.6796 67.96%
Androgen receptor binding + 0.6790 67.90%
Thyroid receptor binding + 0.7726 77.26%
Glucocorticoid receptor binding + 0.8803 88.03%
Aromatase binding + 0.5430 54.30%
PPAR gamma + 0.6949 69.49%
Honey bee toxicity - 0.7894 78.94%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9890 98.90%

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 99.20% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.91% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.30% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.66% 94.45%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.48% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.87% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.77% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.52% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.05% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.53% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.73% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.30% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.22% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.65% 89.00%
CHEMBL1871 P10275 Androgen Receptor 83.40% 96.43%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.21% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.76% 92.94%
CHEMBL1951 P21397 Monoamine oxidase A 82.50% 91.49%
CHEMBL1937 Q92769 Histone deacetylase 2 80.93% 94.75%

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 10087772
LOTUS LTS0262372
wikiData Q105146545