5-[[(2R,3S)-7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]methyl]-1,3-benzodioxole

Details

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Internal ID a0f68923-b4a7-4f47-94df-e159ca75ea2f
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 5-[[(2R,3S)-7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]methyl]-1,3-benzodioxole
SMILES (Canonical) CC=CC1=CC2=C(C(=C1)OC)OC(C2C)CC3=CC4=C(C=C3)OCO4
SMILES (Isomeric) C/C=C/C1=CC2=C(C(=C1)OC)O[C@@H]([C@H]2C)CC3=CC4=C(C=C3)OCO4
InChI InChI=1S/C21H22O4/c1-4-5-14-8-16-13(2)18(25-21(16)20(11-14)22-3)9-15-6-7-17-19(10-15)24-12-23-17/h4-8,10-11,13,18H,9,12H2,1-3H3/b5-4+/t13-,18+/m0/s1
InChI Key TVUKAZBHCZRCLV-AJALSWGYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O4
Molecular Weight 338.40 g/mol
Exact Mass 338.15180918 g/mol
Topological Polar Surface Area (TPSA) 36.90 Ų
XlogP 5.10
Atomic LogP (AlogP) 4.56
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-[[(2R,3S)-7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-2,3-dihydro-1-benzofuran-2-yl]methyl]-1,3-benzodioxole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.8787 87.87%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6418 64.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9022 90.22%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8870 88.70%
P-glycoprotein inhibitior + 0.7847 78.47%
P-glycoprotein substrate - 0.5990 59.90%
CYP3A4 substrate + 0.5578 55.78%
CYP2C9 substrate - 0.6259 62.59%
CYP2D6 substrate - 0.6984 69.84%
CYP3A4 inhibition + 0.8276 82.76%
CYP2C9 inhibition + 0.5779 57.79%
CYP2C19 inhibition + 0.8144 81.44%
CYP2D6 inhibition + 0.6100 61.00%
CYP1A2 inhibition + 0.5153 51.53%
CYP2C8 inhibition + 0.5322 53.22%
CYP inhibitory promiscuity + 0.9352 93.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9408 94.08%
Carcinogenicity (trinary) Non-required 0.3927 39.27%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9398 93.98%
Skin irritation - 0.7806 78.06%
Skin corrosion - 0.9643 96.43%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8637 86.37%
Micronuclear + 0.5218 52.18%
Hepatotoxicity + 0.5552 55.52%
skin sensitisation - 0.5960 59.60%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7638 76.38%
Acute Oral Toxicity (c) III 0.6488 64.88%
Estrogen receptor binding + 0.7747 77.47%
Androgen receptor binding + 0.5877 58.77%
Thyroid receptor binding + 0.6447 64.47%
Glucocorticoid receptor binding + 0.6811 68.11%
Aromatase binding - 0.5640 56.40%
PPAR gamma + 0.6105 61.05%
Honey bee toxicity - 0.7205 72.05%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9795 97.95%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.01% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.83% 96.09%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.73% 94.80%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.12% 96.77%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.71% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.27% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.47% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.86% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.86% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.69% 95.56%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.87% 95.89%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 87.65% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.30% 90.24%
CHEMBL261 P00915 Carbonic anhydrase I 86.76% 96.76%
CHEMBL2581 P07339 Cathepsin D 85.06% 98.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.98% 97.14%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 84.68% 82.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.38% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.96% 89.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.98% 96.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.47% 89.62%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.91% 89.50%
CHEMBL3401 O75469 Pregnane X receptor 80.42% 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.
Ocotea porosa

Cross-Links

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PubChem 163189305
LOTUS LTS0030483
wikiData Q105265557