Onychine

Details

Top
Internal ID 2bcfe5c7-44ec-4473-9c1b-4941ea5d0205
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones
IUPAC Name 4-methylindeno[1,2-b]pyridin-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H9NO/c1-8-6-7-14-12-9-4-2-3-5-10(9)13(15)11(8)12/h2-7H,1H3
InChI Key LTVBTVOAUQJJEV-UHFFFAOYSA-N
Popularity 52 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H9NO
Molecular Weight 195.22 g/mol
Exact Mass 195.068413911 g/mol
Topological Polar Surface Area (TPSA) 30.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

Top
58787-04-5
4-methylindeno[1,2-b]pyridin-5-one
DTXSID80207515
4-methylindeno(1,2-b)pyridin-5-one
RefChem:928231
DTXCID30130006
1-methyl-4-azafluoren-9-one
Onychin
4-Methyl-5H-indeno[1,2-b]pyridin-5-one
5H-Indeno(1,2-b)pyridin-5-one, 4-methyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Onychine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5709 57.09%
Blood Brain Barrier + 0.8129 81.29%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.6898 68.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9742 97.42%
OATP1B3 inhibitior + 0.9757 97.57%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5451 54.51%
P-glycoprotein inhibitior - 0.9511 95.11%
P-glycoprotein substrate - 0.9472 94.72%
CYP3A4 substrate - 0.5968 59.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8632 86.32%
CYP3A4 inhibition - 0.5378 53.78%
CYP2C9 inhibition - 0.6504 65.04%
CYP2C19 inhibition + 0.7609 76.09%
CYP2D6 inhibition - 0.6787 67.87%
CYP1A2 inhibition + 0.9573 95.73%
CYP2C8 inhibition - 0.7908 79.08%
CYP inhibitory promiscuity - 0.6597 65.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5690 56.90%
Eye corrosion - 0.9875 98.75%
Eye irritation + 0.5717 57.17%
Skin irritation - 0.6027 60.27%
Skin corrosion - 0.9834 98.34%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6702 67.02%
Micronuclear + 0.5959 59.59%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.7104 71.04%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.4594 45.94%
Acute Oral Toxicity (c) III 0.8204 82.04%
Estrogen receptor binding + 0.6432 64.32%
Androgen receptor binding + 0.5966 59.66%
Thyroid receptor binding + 0.6055 60.55%
Glucocorticoid receptor binding + 0.6649 66.49%
Aromatase binding + 0.7600 76.00%
PPAR gamma - 0.6005 60.05%
Honey bee toxicity - 0.9240 92.40%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.7243 72.43%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.28% 91.49%
CHEMBL2581 P07339 Cathepsin D 95.49% 98.95%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 93.11% 96.67%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 90.82% 93.65%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.75% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.12% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 89.82% 94.73%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 86.89% 96.47%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.13% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.76% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 84.49% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.28% 86.33%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 82.26% 96.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.03% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.98% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.33% 96.09%
CHEMBL3524 P56524 Histone deacetylase 4 80.19% 92.97%

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.
Cibotium barometz
Cleistopholis patens
Guatteria blepharophylla
Onychium japonicum
Onychium lucidum
Porcelia macrocarpa
Unonopsis spectabilis

Cross-Links

Top
PubChem 72584
NPASS NPC265100
LOTUS LTS0062903
wikiData Q6050997