Nlcamzutwgfusw-uhfffaoysa-

Details

Top
Internal ID fc8e9c6c-6593-4f8a-bd6c-a878293d5322
Taxonomy Organoheterocyclic compounds > Coumarans > 1-phenylcoumarans
IUPAC Name 8-methoxy-7-(4-methoxyphenyl)-7H-furo[2,3-f][1,3]benzodioxol-6-one
SMILES (Canonical) COC1=CC=C(C=C1)C2C3=C(C4=C(C=C3OC2=O)OCO4)OC
SMILES (Isomeric) COC1=CC=C(C=C1)C2C3=C(C4=C(C=C3OC2=O)OCO4)OC
InChI InChI=1S/C17H14O6/c1-19-10-5-3-9(4-6-10)13-14-11(23-17(13)18)7-12-15(16(14)20-2)22-8-21-12/h3-7,13H,8H2,1-2H3
InChI Key NLCAMZUTWGFUSW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H14O6
Molecular Weight 314.29 g/mol
Exact Mass 314.07903816 g/mol
Topological Polar Surface Area (TPSA) 63.20 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.48
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
NLCAMZUTWGFUSW-UHFFFAOYSA-
DTXSID501164604
1027995-86-3
8-Methoxy-7-(4-methoxyphenyl)furo[2,3-f]-1,3-benzodioxol-6(7H)-one
InChI=1/C17H14O6/c1-19-10-5-3-9(4-6-10)13-14-11(23-17(13)18)7-12-15(16(14)20-2)22-8-21-12/h3-7,13H,8H2,1-2H3

2D Structure

Top
2D Structure of Nlcamzutwgfusw-uhfffaoysa-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.8822 88.22%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7446 74.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9516 95.16%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.6200 62.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5666 56.66%
P-glycoprotein inhibitior - 0.4564 45.64%
P-glycoprotein substrate - 0.9403 94.03%
CYP3A4 substrate + 0.5065 50.65%
CYP2C9 substrate - 0.6054 60.54%
CYP2D6 substrate - 0.7972 79.72%
CYP3A4 inhibition + 0.9372 93.72%
CYP2C9 inhibition + 0.9629 96.29%
CYP2C19 inhibition + 0.9683 96.83%
CYP2D6 inhibition + 0.7226 72.26%
CYP1A2 inhibition - 0.5197 51.97%
CYP2C8 inhibition - 0.8210 82.10%
CYP inhibitory promiscuity + 0.9476 94.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4308 43.08%
Eye corrosion - 0.9790 97.90%
Eye irritation - 0.6695 66.95%
Skin irritation - 0.7666 76.66%
Skin corrosion - 0.9708 97.08%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4689 46.89%
Micronuclear + 0.7974 79.74%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.6643 66.43%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.8046 80.46%
Acute Oral Toxicity (c) III 0.6548 65.48%
Estrogen receptor binding + 0.8661 86.61%
Androgen receptor binding + 0.7419 74.19%
Thyroid receptor binding + 0.5759 57.59%
Glucocorticoid receptor binding + 0.7353 73.53%
Aromatase binding - 0.5061 50.61%
PPAR gamma - 0.6317 63.17%
Honey bee toxicity - 0.8954 89.54%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9722 97.22%

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 98.60% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.07% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.16% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.04% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.25% 96.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.19% 94.80%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.99% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.36% 92.62%
CHEMBL4208 P20618 Proteasome component C5 88.14% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.87% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.67% 86.33%
CHEMBL2581 P07339 Cathepsin D 83.94% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.89% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.42% 99.15%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.00% 96.00%
CHEMBL2535 P11166 Glucose transporter 81.89% 98.75%
CHEMBL4581 P52732 Kinesin-like protein 1 81.10% 93.18%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.02% 95.89%
CHEMBL1907 P15144 Aminopeptidase N 80.19% 93.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.07% 85.14%

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.
Aglaia edulis
Aglaia elaeagnoidea

Cross-Links

Top
PubChem 10591326
LOTUS LTS0007560
wikiData Q105181260