Eupenifeldin

Details

Top
Internal ID 6dcf0c83-5ecc-4d0a-8bb0-f9b338601c36
Taxonomy Hydrocarbon derivatives > Tropones > Tropolones
IUPAC Name 3,9,25-trihydroxy-4,11,16,16,20,27-hexamethyl-5,21-dioxapentacyclo[18.9.0.04,14.06,12.022,28]nonacosa-6,9,11,17,22,25,27-heptaene-8,24-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H40O7/c1-18-10-24(34)26(36)15-28-22(18)12-20-14-30(38)33(6)21(17-31(3,4)8-7-9-32(20,5)39-28)13-23-19(2)11-25(35)27(37)16-29(23)40-33/h7-8,10-11,15-16,20-21,30,38H,9,12-14,17H2,1-6H3,(H,34,36)(H,35,37)
InChI Key BWTQHPFSWXJOGP-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C33H40O7
Molecular Weight 548.70 g/mol
Exact Mass 548.27740361 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Eupenifeldin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9770 97.70%
Caco-2 - 0.6839 68.39%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6554 65.54%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.8849 88.49%
OATP1B3 inhibitior + 0.9495 94.95%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9064 90.64%
BSEP inhibitior + 0.9945 99.45%
P-glycoprotein inhibitior + 0.8077 80.77%
P-glycoprotein substrate - 0.5758 57.58%
CYP3A4 substrate + 0.6458 64.58%
CYP2C9 substrate - 0.7936 79.36%
CYP2D6 substrate - 0.7475 74.75%
CYP3A4 inhibition - 0.6808 68.08%
CYP2C9 inhibition - 0.8503 85.03%
CYP2C19 inhibition - 0.7995 79.95%
CYP2D6 inhibition - 0.8971 89.71%
CYP1A2 inhibition - 0.5429 54.29%
CYP2C8 inhibition + 0.4908 49.08%
CYP inhibitory promiscuity - 0.9334 93.34%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6018 60.18%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.8841 88.41%
Skin irritation - 0.6999 69.99%
Skin corrosion - 0.9252 92.52%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8664 86.64%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.5013 50.13%
skin sensitisation - 0.8091 80.91%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5330 53.30%
Acute Oral Toxicity (c) III 0.4050 40.50%
Estrogen receptor binding + 0.8507 85.07%
Androgen receptor binding + 0.6612 66.12%
Thyroid receptor binding + 0.7011 70.11%
Glucocorticoid receptor binding + 0.8721 87.21%
Aromatase binding + 0.7939 79.39%
PPAR gamma + 0.6275 62.75%
Honey bee toxicity - 0.8400 84.00%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9967 99.67%

Targets

Top

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 99.19% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 96.50% 83.82%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 95.20% 93.40%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.70% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.38% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.76% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.71% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 91.66% 91.49%
CHEMBL2581 P07339 Cathepsin D 90.94% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.18% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.09% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.06% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.84% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.82% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.86% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.06% 92.94%
CHEMBL3038469 P24941 CDK2/Cyclin A 82.89% 91.38%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.15% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.12% 94.00%

Plants that contains it

Top
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

Top
PubChem 139587675
LOTUS LTS0251038
wikiData Q103817087