Myxotrichin A

Details

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Internal ID 47ce848c-b128-49df-b344-9212712cc52f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 3-butoxy-7,8-dihydroxy-3-methyl-10-oxo-1,4-dihydropyrano[4,3-b]chromene-9-carboxylic acid
SMILES (Canonical) CCCCOC1(CC2=C(CO1)C(=O)C3=C(O2)C=C(C(=C3C(=O)O)O)O)C
SMILES (Isomeric) CCCCOC1(CC2=C(CO1)C(=O)C3=C(O2)C=C(C(=C3C(=O)O)O)O)C
InChI InChI=1S/C18H20O8/c1-3-4-5-24-18(2)7-12-9(8-25-18)15(20)13-11(26-12)6-10(19)16(21)14(13)17(22)23/h6,19,21H,3-5,7-8H2,1-2H3,(H,22,23)
InChI Key LOABGLJUPQNVRX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H20O8
Molecular Weight 364.30 g/mol
Exact Mass 364.11581759 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Myxotrichin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5704 57.04%
Caco-2 + 0.5435 54.35%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8184 81.84%
OATP2B1 inhibitior - 0.5690 56.90%
OATP1B1 inhibitior + 0.8662 86.62%
OATP1B3 inhibitior + 0.8803 88.03%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7315 73.15%
P-glycoprotein inhibitior - 0.7991 79.91%
P-glycoprotein substrate - 0.5055 50.55%
CYP3A4 substrate + 0.6162 61.62%
CYP2C9 substrate + 0.6151 61.51%
CYP2D6 substrate - 0.8932 89.32%
CYP3A4 inhibition - 0.7710 77.10%
CYP2C9 inhibition - 0.9153 91.53%
CYP2C19 inhibition - 0.6686 66.86%
CYP2D6 inhibition - 0.9471 94.71%
CYP1A2 inhibition - 0.6726 67.26%
CYP2C8 inhibition + 0.6406 64.06%
CYP inhibitory promiscuity - 0.9169 91.69%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7093 70.93%
Eye corrosion - 0.9911 99.11%
Eye irritation + 0.6226 62.26%
Skin irritation - 0.8230 82.30%
Skin corrosion - 0.9514 95.14%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7458 74.58%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8893 88.93%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5437 54.37%
Acute Oral Toxicity (c) III 0.6040 60.40%
Estrogen receptor binding + 0.7866 78.66%
Androgen receptor binding + 0.7670 76.70%
Thyroid receptor binding - 0.6233 62.33%
Glucocorticoid receptor binding + 0.8799 87.99%
Aromatase binding + 0.7574 75.74%
PPAR gamma + 0.7447 74.47%
Honey bee toxicity - 0.9397 93.97%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9938 99.38%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.78% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.66% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.66% 99.17%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 91.48% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.41% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.14% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.67% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.44% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.78% 96.09%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 85.59% 95.64%
CHEMBL1811 P34995 Prostanoid EP1 receptor 82.66% 95.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.48% 99.23%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 81.69% 85.40%
CHEMBL3194 P02766 Transthyretin 81.66% 90.71%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 81.57% 80.78%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 81.56% 82.38%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.47% 96.77%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 81.06% 95.34%
CHEMBL3401 O75469 Pregnane X receptor 80.28% 94.73%

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.
There are no matching plants.

Cross-Links

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PubChem 139585261
LOTUS LTS0242509
wikiData Q77387138