Pyrayachinon-A

Details

Top
Internal ID 1a459336-edb3-4ce5-a3de-9c5136b8fc38
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 2,2,7-trimethyl-10H-pyrano[3,2-h]carbazole-6,9-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H15NO3/c1-9-6-13(20)16-15(17(9)21)11-7-10-4-5-18(2,3)22-14(10)8-12(11)19-16/h4-8,19H,1-3H3
InChI Key NFGNDUGWFOACRQ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H15NO3
Molecular Weight 293.30 g/mol
Exact Mass 293.10519334 g/mol
Topological Polar Surface Area (TPSA) 59.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.68
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Pyrayachinon-A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7490 74.90%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7972 79.72%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8814 88.14%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8227 82.27%
P-glycoprotein inhibitior - 0.6512 65.12%
P-glycoprotein substrate - 0.7244 72.44%
CYP3A4 substrate + 0.6121 61.21%
CYP2C9 substrate + 0.6035 60.35%
CYP2D6 substrate - 0.8560 85.60%
CYP3A4 inhibition + 0.5818 58.18%
CYP2C9 inhibition + 0.8575 85.75%
CYP2C19 inhibition + 0.8061 80.61%
CYP2D6 inhibition - 0.7556 75.56%
CYP1A2 inhibition + 0.8775 87.75%
CYP2C8 inhibition - 0.6048 60.48%
CYP inhibitory promiscuity + 0.9275 92.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4562 45.62%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.6011 60.11%
Skin irritation - 0.8187 81.87%
Skin corrosion - 0.9436 94.36%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5659 56.59%
Micronuclear + 0.7200 72.00%
Hepatotoxicity - 0.5376 53.76%
skin sensitisation - 0.7654 76.54%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5084 50.84%
Acute Oral Toxicity (c) III 0.6564 65.64%
Estrogen receptor binding + 0.8505 85.05%
Androgen receptor binding + 0.5792 57.92%
Thyroid receptor binding + 0.7669 76.69%
Glucocorticoid receptor binding + 0.7030 70.30%
Aromatase binding + 0.6359 63.59%
PPAR gamma + 0.6339 63.39%
Honey bee toxicity - 0.8860 88.60%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9507 95.07%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.55% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.18% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.10% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.61% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 94.19% 94.75%
CHEMBL2581 P07339 Cathepsin D 93.77% 98.95%
CHEMBL255 P29275 Adenosine A2b receptor 92.55% 98.59%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.80% 94.80%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 90.41% 80.96%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.33% 85.30%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.49% 93.99%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 88.73% 96.77%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.62% 99.23%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 85.99% 85.00%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 85.64% 85.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.22% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 84.12% 94.73%
CHEMBL3310 Q96DB2 Histone deacetylase 11 83.69% 88.56%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.37% 85.94%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.75% 96.67%
CHEMBL325 Q13547 Histone deacetylase 1 82.11% 95.92%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.96% 96.21%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.95% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.67% 94.00%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 81.10% 81.14%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.94% 91.71%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.80% 90.08%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 80.02% 89.44%

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 13966506
LOTUS LTS0090904
wikiData Q105178455