Defucogilvocarcin V

Details

Top
Internal ID d1425eba-d14c-4700-8a35-3524a7e936eb
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name 8-ethenyl-1-hydroxy-10,12-dimethoxynaphtho[1,2-c]isochromen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H16O5/c1-4-11-8-14-18(16(9-11)24-2)13-10-17(25-3)19-12(6-5-7-15(19)22)20(13)26-21(14)23/h4-10,22H,1H2,2-3H3
InChI Key CZOCDNQYMADMLK-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H16O5
Molecular Weight 348.30 g/mol
Exact Mass 348.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.47
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
80155-95-9
Gilvocarcin V aglycone
DTXSID40230107
8-ethenyl-1-hydroxy-10,12-dimethoxynaphtho[1,2-c]isochromen-6-one
1-Hydroxy-10,12-dimethoxy-8-vinyl-6H-benzo(d)naphthol(1,2b)pyran-6-one
8-ethenyl-1-hydroxy-10,12-dimethoxynaphtho(1,2-c)isochromen-6-one
RefChem:131429
DTXCID00152598
6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 8-ethenyl-1-hydroxy-10,12-dimethoxy-
orb3023096
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Defucogilvocarcin V

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9820 98.20%
Caco-2 + 0.6191 61.91%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5706 57.06%
OATP2B1 inhibitior - 0.5819 58.19%
OATP1B1 inhibitior + 0.9282 92.82%
OATP1B3 inhibitior + 0.9646 96.46%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.5579 55.79%
P-glycoprotein inhibitior + 0.8079 80.79%
P-glycoprotein substrate - 0.8101 81.01%
CYP3A4 substrate + 0.5852 58.52%
CYP2C9 substrate - 0.8283 82.83%
CYP2D6 substrate - 0.8181 81.81%
CYP3A4 inhibition + 0.8770 87.70%
CYP2C9 inhibition - 0.7876 78.76%
CYP2C19 inhibition - 0.5768 57.68%
CYP2D6 inhibition - 0.8704 87.04%
CYP1A2 inhibition + 0.6562 65.62%
CYP2C8 inhibition + 0.5727 57.27%
CYP inhibitory promiscuity - 0.5638 56.38%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.4914 49.14%
Eye corrosion - 0.9404 94.04%
Eye irritation + 0.6376 63.76%
Skin irritation - 0.6714 67.14%
Skin corrosion - 0.9819 98.19%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6275 62.75%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8603 86.03%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.8217 82.17%
Acute Oral Toxicity (c) II 0.5741 57.41%
Estrogen receptor binding + 0.8713 87.13%
Androgen receptor binding + 0.7401 74.01%
Thyroid receptor binding + 0.7115 71.15%
Glucocorticoid receptor binding + 0.8509 85.09%
Aromatase binding + 0.7765 77.65%
PPAR gamma + 0.8577 85.77%
Honey bee toxicity - 0.8185 81.85%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9710 97.10%

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 98.94% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.25% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 95.57% 83.82%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.55% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.74% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 91.76% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.28% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 90.75% 94.73%
CHEMBL2581 P07339 Cathepsin D 90.43% 98.95%
CHEMBL2535 P11166 Glucose transporter 90.08% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.25% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.48% 99.23%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 84.67% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 84.31% 93.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.33% 85.14%
CHEMBL3194 P02766 Transthyretin 83.11% 90.71%
CHEMBL1255126 O15151 Protein Mdm4 82.91% 90.20%
CHEMBL1937 Q92769 Histone deacetylase 2 82.80% 94.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.64% 92.62%
CHEMBL4530 P00488 Coagulation factor XIII 82.00% 96.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.90% 98.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.52% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.34% 93.99%

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 133386
LOTUS LTS0068614
wikiData Q83110504