(+)-Simulanol

Details

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Internal ID 3e387a6d-5454-44df-89fd-35e4f703619b
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name 4-[(2S,3R)-3-(hydroxymethyl)-5-[(E)-3-hydroxyprop-1-enyl]-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2,6-dimethoxyphenol
SMILES (Canonical) COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)C=CCO
SMILES (Isomeric) COC1=CC(=CC2=C1O[C@@H]([C@H]2CO)C3=CC(=C(C(=C3)OC)O)OC)/C=C/CO
InChI InChI=1S/C21H24O7/c1-25-16-9-13(10-17(26-2)19(16)24)20-15(11-23)14-7-12(5-4-6-22)8-18(27-3)21(14)28-20/h4-5,7-10,15,20,22-24H,6,11H2,1-3H3/b5-4+/t15-,20+/m0/s1
InChI Key SGRRPSBKBJVKJE-BMSLLPBFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H24O7
Molecular Weight 388.40 g/mol
Exact Mass 388.15220310 g/mol
Topological Polar Surface Area (TPSA) 97.60 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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CHEMBL1761711

2D Structure

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2D Structure of (+)-Simulanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9847 98.47%
Caco-2 + 0.6070 60.70%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6793 67.93%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.7550 75.50%
OATP1B3 inhibitior + 0.9216 92.16%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8048 80.48%
P-glycoprotein inhibitior + 0.7036 70.36%
P-glycoprotein substrate - 0.7653 76.53%
CYP3A4 substrate + 0.5484 54.84%
CYP2C9 substrate + 0.6095 60.95%
CYP2D6 substrate - 0.6654 66.54%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition + 0.7644 76.44%
CYP2C19 inhibition + 0.7840 78.40%
CYP2D6 inhibition - 0.8444 84.44%
CYP1A2 inhibition + 0.5566 55.66%
CYP2C8 inhibition + 0.6596 65.96%
CYP inhibitory promiscuity + 0.9539 95.39%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9308 93.08%
Carcinogenicity (trinary) Non-required 0.4544 45.44%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.8640 86.40%
Skin irritation - 0.8236 82.36%
Skin corrosion - 0.9599 95.99%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6286 62.86%
Micronuclear + 0.7100 71.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.7512 75.12%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5150 51.50%
Acute Oral Toxicity (c) III 0.5794 57.94%
Estrogen receptor binding + 0.8280 82.80%
Androgen receptor binding + 0.5848 58.48%
Thyroid receptor binding + 0.8132 81.32%
Glucocorticoid receptor binding + 0.7372 73.72%
Aromatase binding + 0.5328 53.28%
PPAR gamma + 0.5480 54.80%
Honey bee toxicity - 0.8576 85.76%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9356 93.56%

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 98.07% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.15% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.11% 85.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.90% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.69% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.85% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.78% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.63% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.98% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.32% 89.00%

Cross-Links

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PubChem 52918181
NPASS NPC87725
ChEMBL CHEMBL1761711
LOTUS LTS0249068
wikiData Q105252560