Euchrestifoline

Details

Top
Internal ID 494ca231-5173-4f7e-a75e-a6b3708a0a28
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 3,3,5-trimethyl-2,11-dihydropyrano[3,2-a]carbazol-1-one
SMILES (Canonical) CC1=CC2=C(C3=C1OC(CC3=O)(C)C)NC4=CC=CC=C42
SMILES (Isomeric) CC1=CC2=C(C3=C1OC(CC3=O)(C)C)NC4=CC=CC=C42
InChI InChI=1S/C18H17NO2/c1-10-8-12-11-6-4-5-7-13(11)19-16(12)15-14(20)9-18(2,3)21-17(10)15/h4-8,19H,9H2,1-3H3
InChI Key YIOPHGZRHZZMIM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H17NO2
Molecular Weight 279.30 g/mol
Exact Mass 279.125928785 g/mol
Topological Polar Surface Area (TPSA) 42.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.37
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
3,3,5-trimethyl-2,11-dihydropyrano(3,2-a)carbazol-1-one
3,3,5-trimethyl-2,11-dihydropyrano[3,2-a]carbazol-1-one
RefChem:139345
SCHEMBL30929798

2D Structure

Top
2D Structure of Euchrestifoline

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9966 99.66%
Caco-2 + 0.7882 78.82%
Blood Brain Barrier + 0.7879 78.79%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6365 63.65%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9668 96.68%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6953 69.53%
P-glycoprotein inhibitior - 0.6291 62.91%
P-glycoprotein substrate - 0.8687 86.87%
CYP3A4 substrate + 0.6035 60.35%
CYP2C9 substrate - 0.5773 57.73%
CYP2D6 substrate - 0.7917 79.17%
CYP3A4 inhibition - 0.8428 84.28%
CYP2C9 inhibition - 0.7206 72.06%
CYP2C19 inhibition + 0.5436 54.36%
CYP2D6 inhibition - 0.8085 80.85%
CYP1A2 inhibition + 0.7611 76.11%
CYP2C8 inhibition - 0.6011 60.11%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4355 43.55%
Eye corrosion - 0.9914 99.14%
Eye irritation - 0.5475 54.75%
Skin irritation - 0.8241 82.41%
Skin corrosion - 0.9374 93.74%
Ames mutagenesis + 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5715 57.15%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.7501 75.01%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.4539 45.39%
Acute Oral Toxicity (c) III 0.6121 61.21%
Estrogen receptor binding + 0.8323 83.23%
Androgen receptor binding + 0.7514 75.14%
Thyroid receptor binding + 0.7565 75.65%
Glucocorticoid receptor binding + 0.8516 85.16%
Aromatase binding + 0.8050 80.50%
PPAR gamma + 0.5624 56.24%
Honey bee toxicity - 0.8653 86.53%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity - 0.3623 36.23%

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 98.61% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.30% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.16% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.75% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.00% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 92.54% 94.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.76% 96.21%
CHEMBL240 Q12809 HERG 90.00% 89.76%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.93% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.17% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.87% 93.99%
CHEMBL3310 Q96DB2 Histone deacetylase 11 88.35% 88.56%
CHEMBL3401 O75469 Pregnane X receptor 87.55% 94.73%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 87.34% 85.49%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 85.80% 81.14%
CHEMBL255 P29275 Adenosine A2b receptor 85.77% 98.59%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.83% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.52% 86.33%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.44% 96.00%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 83.32% 85.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 82.64% 91.71%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.97% 92.67%
CHEMBL4208 P20618 Proteasome component C5 81.64% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.46% 96.09%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.91% 96.25%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 80.61% 95.70%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.39% 93.03%

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.
Bergera euchrestifolia

Cross-Links

Top
PubChem 25172103
LOTUS LTS0260123
wikiData Q105348945