Vitexdoin C

Details

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Internal ID fb5d9810-fe9b-4c5f-837c-bd16986b3fef
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-6-methoxynaphthalene-2-carbaldehyde
SMILES (Canonical) COC1=C(C=CC(=C1)C2=C(C=CC3=CC(=C(C=C32)O)OC)C=O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C2=C(C=CC3=CC(=C(C=C32)O)OC)C=O)O
InChI InChI=1S/C19H16O5/c1-23-17-8-12(5-6-15(17)21)19-13(10-20)4-3-11-7-18(24-2)16(22)9-14(11)19/h3-10,21-22H,1-2H3
InChI Key TWPBLWBNALQAFO-UHFFFAOYSA-N
Popularity 1 reference 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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CHEMBL1079038

2D Structure

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2D Structure of Vitexdoin C

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 + 0.8574 85.74%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.9003 90.03%
OATP2B1 inhibitior - 0.5806 58.06%
OATP1B1 inhibitior + 0.8016 80.16%
OATP1B3 inhibitior + 0.9104 91.04%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5273 52.73%
P-glycoprotein inhibitior - 0.7524 75.24%
P-glycoprotein substrate - 0.8561 85.61%
CYP3A4 substrate - 0.5280 52.80%
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 + 0.8572 85.72%
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 + 0.9140 91.40%
Skin irritation - 0.5615 56.15%
Skin corrosion - 0.9718 97.18%
Ames mutagenesis + 0.5346 53.46%
Human Ether-a-go-go-Related Gene inhibition - 0.7224 72.24%
Micronuclear + 0.8100 81.00%
Hepatotoxicity - 0.5053 50.53%
skin sensitisation - 0.9229 92.29%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6009 60.09%
Acute Oral Toxicity (c) III 0.5933 59.33%
Estrogen receptor binding + 0.8550 85.50%
Androgen receptor binding + 0.7872 78.72%
Thyroid receptor binding + 0.8077 80.77%
Glucocorticoid receptor binding + 0.9232 92.32%
Aromatase binding + 0.6472 64.72%
PPAR gamma + 0.8163 81.63%
Honey bee toxicity - 0.9013 90.13%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5045 50.45%
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 99.60% 98.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.13% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.29% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.02% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 91.47% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.39% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.46% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.66% 94.45%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 89.48% 80.78%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.22% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.14% 96.00%
CHEMBL2581 P07339 Cathepsin D 88.97% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.03% 99.17%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 85.77% 89.32%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.33% 92.94%
CHEMBL1907 P15144 Aminopeptidase N 84.73% 93.31%
CHEMBL4208 P20618 Proteasome component C5 84.49% 90.00%
CHEMBL3194 P02766 Transthyretin 82.87% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.49% 92.62%
CHEMBL3438 Q05513 Protein kinase C zeta 80.75% 88.48%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.17% 89.00%

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.
Cota tinctoria
Vitex negundo

Cross-Links

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PubChem 44478949
NPASS NPC91694
ChEMBL CHEMBL1079038
LOTUS LTS0084329
wikiData Q104996753