Vitrofolal E

Details

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Internal ID 8f033ef7-10bf-473e-a1ef-c5a189ab5b35
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-7-methoxynaphthalene-2-carbaldehyde
SMILES (Canonical) COC1=C(C=CC(=C1)C2=CC(=CC3=CC(=C(C=C32)O)OC)C=O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C2=CC(=CC3=CC(=C(C=C32)O)OC)C=O)O
InChI InChI=1S/C19H16O5/c1-23-18-7-12(3-4-16(18)21)14-6-11(10-20)5-13-8-19(24-2)17(22)9-15(13)14/h3-10,21-22H,1-2H3
InChI Key ASJBFNXTDMUMBC-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C19H16O5
Molecular Weight 324.30 g/mol
Exact Mass 324.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.75
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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CHEMBL486412
SCHEMBL5424459

2D Structure

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2D Structure of Vitrofolal E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.8058 80.58%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.9003 90.03%
OATP2B1 inhibitior - 0.5780 57.80%
OATP1B1 inhibitior + 0.8816 88.16%
OATP1B3 inhibitior + 0.9104 91.04%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.7417 74.17%
P-glycoprotein substrate - 0.8088 80.88%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8076 80.76%
CYP2D6 substrate - 0.6598 65.98%
CYP3A4 inhibition - 0.5182 51.82%
CYP2C9 inhibition + 0.8798 87.98%
CYP2C19 inhibition + 0.7986 79.86%
CYP2D6 inhibition - 0.8092 80.92%
CYP1A2 inhibition + 0.8752 87.52%
CYP2C8 inhibition + 0.7614 76.14%
CYP inhibitory promiscuity + 0.6610 66.10%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8730 87.30%
Carcinogenicity (trinary) Non-required 0.4750 47.50%
Eye corrosion - 0.9813 98.13%
Eye irritation + 0.8485 84.85%
Skin irritation - 0.5615 56.15%
Skin corrosion - 0.9718 97.18%
Ames mutagenesis - 0.5454 54.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7181 71.81%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.9229 92.29%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4852 48.52%
Acute Oral Toxicity (c) III 0.5933 59.33%
Estrogen receptor binding + 0.8393 83.93%
Androgen receptor binding + 0.6467 64.67%
Thyroid receptor binding + 0.7255 72.55%
Glucocorticoid receptor binding + 0.9168 91.68%
Aromatase binding + 0.6324 63.24%
PPAR gamma + 0.7131 71.31%
Honey bee toxicity - 0.8777 87.77%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.9776 97.76%

Targets

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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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 98.40% 98.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.59% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.78% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.74% 91.11%
CHEMBL3438 Q05513 Protein kinase C zeta 93.44% 88.48%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.73% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.60% 99.15%
CHEMBL2581 P07339 Cathepsin D 91.49% 98.95%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 91.10% 80.78%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.14% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.84% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.47% 95.50%
CHEMBL1907 P15144 Aminopeptidase N 85.12% 93.31%
CHEMBL3194 P02766 Transthyretin 85.08% 90.71%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.63% 92.94%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.41% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.95% 96.00%
CHEMBL5747 Q92793 CREB-binding protein 81.49% 95.12%
CHEMBL1929 P47989 Xanthine dehydrogenase 81.13% 96.12%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.93% 85.14%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.60% 92.38%

Plants that contains it

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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.
Vitex negundo
Vitex trifolia subsp. litoralis

Cross-Links

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PubChem 10947295
NPASS NPC300603
ChEMBL CHEMBL486412
LOTUS LTS0271739
wikiData Q104399078