7-O-Methylaloesin

Details

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Internal ID 28c62ba0-9a55-476c-b4f0-3213c68060d5
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 7-methoxy-5-methyl-2-(2-oxopropyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one
SMILES (Canonical) CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(=O)C)C3C(C(C(C(O3)CO)O)O)O)OC
SMILES (Isomeric) CC1=CC(=C(C2=C1C(=O)C=C(O2)CC(=O)C)[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)OC
InChI InChI=1S/C20H24O9/c1-8-4-12(27-3)15(20-18(26)17(25)16(24)13(7-21)29-20)19-14(8)11(23)6-10(28-19)5-9(2)22/h4,6,13,16-18,20-21,24-26H,5,7H2,1-3H3/t13-,16-,17+,18-,20+/m1/s1
InChI Key CNMGVPHFWMWCGL-XGWLOPGHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O9
Molecular Weight 408.40 g/mol
Exact Mass 408.14203234 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -0.24
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-O-Methylaloesin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5847 58.47%
Caco-2 - 0.6942 69.42%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5646 56.46%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8756 87.56%
OATP1B3 inhibitior + 0.9575 95.75%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6487 64.87%
P-glycoprotein inhibitior - 0.6592 65.92%
P-glycoprotein substrate - 0.7468 74.68%
CYP3A4 substrate + 0.5794 57.94%
CYP2C9 substrate - 0.6035 60.35%
CYP2D6 substrate - 0.8179 81.79%
CYP3A4 inhibition - 0.8358 83.58%
CYP2C9 inhibition - 0.8922 89.22%
CYP2C19 inhibition - 0.8989 89.89%
CYP2D6 inhibition - 0.9361 93.61%
CYP1A2 inhibition - 0.7999 79.99%
CYP2C8 inhibition - 0.6537 65.37%
CYP inhibitory promiscuity - 0.8534 85.34%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7095 70.95%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9499 94.99%
Skin irritation - 0.8475 84.75%
Skin corrosion - 0.9545 95.45%
Ames mutagenesis + 0.5844 58.44%
Human Ether-a-go-go-Related Gene inhibition - 0.5682 56.82%
Micronuclear + 0.5600 56.00%
Hepatotoxicity - 0.6250 62.50%
skin sensitisation - 0.9200 92.00%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7027 70.27%
Acute Oral Toxicity (c) III 0.6233 62.33%
Estrogen receptor binding + 0.6472 64.72%
Androgen receptor binding + 0.6706 67.06%
Thyroid receptor binding - 0.6190 61.90%
Glucocorticoid receptor binding + 0.6478 64.78%
Aromatase binding - 0.5923 59.23%
PPAR gamma + 0.6070 60.70%
Honey bee toxicity - 0.7825 78.25%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.8377 83.77%

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 98.05% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.42% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.77% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.20% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.10% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.89% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.00% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 89.91% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.83% 99.17%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 86.97% 96.21%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.23% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.62% 96.09%

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.
Allium macrostemon
Allium sativum
Allium victorialis
Aloe cheranganiensis
Aloe marlothii
Aloe perryi

Cross-Links

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PubChem 5319505
NPASS NPC8288
LOTUS LTS0071023
wikiData Q104392993