(S)-Moluccanin

Details

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Internal ID f1bbad2e-3a6f-45d4-94a5-336e3d746855
Taxonomy Lignans, neolignans and related compounds > Coumarinolignans
IUPAC Name (2S,3S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-2,3-dihydropyrano[3,2-g][1,4]benzodioxin-7-one
SMILES (Canonical) COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=C4C(=C3)C=CC(=O)O4)CO
SMILES (Isomeric) COC1=CC(=CC(=C1O)OC)[C@H]2[C@@H](OC3=C(O2)C=C4C(=C3)C=CC(=O)O4)CO
InChI InChI=1S/C20H18O8/c1-24-15-6-11(7-16(25-2)19(15)23)20-17(9-21)26-13-5-10-3-4-18(22)27-12(10)8-14(13)28-20/h3-8,17,20-21,23H,9H2,1-2H3/t17-,20-/m0/s1
InChI Key GBLZBLJGCQTQMB-PXNSSMCTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O8
Molecular Weight 386.40 g/mol
Exact Mass 386.10016753 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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116521-73-4
121700-26-3
(2S,3S)-3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-2,3-dihydropyrano[3,2-g][1,4]benzodioxin-7-one
7H-Pyrano[2,3-g]-1,4-benzodioxin-7-one,2,3-dihydro-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-, trans- (9CI)
starbld0000794
HY-N3251
AKOS032961933
FS-10237
CS-0023719

2D Structure

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2D Structure of (S)-Moluccanin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9150 91.50%
Caco-2 - 0.5316 53.16%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8090 80.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8037 80.37%
OATP1B3 inhibitior - 0.2712 27.12%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8350 83.50%
P-glycoprotein inhibitior + 0.8087 80.87%
P-glycoprotein substrate - 0.7323 73.23%
CYP3A4 substrate + 0.5168 51.68%
CYP2C9 substrate - 0.8212 82.12%
CYP2D6 substrate - 0.8135 81.35%
CYP3A4 inhibition - 0.8224 82.24%
CYP2C9 inhibition - 0.5672 56.72%
CYP2C19 inhibition - 0.7656 76.56%
CYP2D6 inhibition - 0.9056 90.56%
CYP1A2 inhibition - 0.9197 91.97%
CYP2C8 inhibition + 0.4627 46.27%
CYP inhibitory promiscuity + 0.5722 57.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6925 69.25%
Eye corrosion - 0.9848 98.48%
Eye irritation - 0.7161 71.61%
Skin irritation - 0.8335 83.35%
Skin corrosion - 0.9739 97.39%
Ames mutagenesis - 0.6944 69.44%
Human Ether-a-go-go-Related Gene inhibition - 0.5322 53.22%
Micronuclear + 0.7133 71.33%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9143 91.43%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7547 75.47%
Acute Oral Toxicity (c) III 0.6661 66.61%
Estrogen receptor binding + 0.9016 90.16%
Androgen receptor binding + 0.7038 70.38%
Thyroid receptor binding + 0.6041 60.41%
Glucocorticoid receptor binding + 0.8754 87.54%
Aromatase binding - 0.6363 63.63%
PPAR gamma + 0.6979 69.79%
Honey bee toxicity - 0.8366 83.66%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.7289 72.89%

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 98.53% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.68% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.16% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.16% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.51% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.45% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.63% 86.92%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.42% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.12% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.34% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.23% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.42% 94.45%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.97% 94.03%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.58% 92.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.11% 97.09%

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.
Aleurites moluccanus

Cross-Links

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PubChem 91895364
LOTUS LTS0112665
wikiData Q105005938