1-(2,3-Dimethoxy-5-prop-2-enylphenyl)-2,3-dimethoxy-5-prop-2-enylbenzene

Details

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Internal ID b9b0572a-d08d-4650-803b-1b1895babbc6
Taxonomy Benzenoids > Benzene and substituted derivatives > Biphenyls and derivatives
IUPAC Name 1-(2,3-dimethoxy-5-prop-2-enylphenyl)-2,3-dimethoxy-5-prop-2-enylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26O4/c1-7-9-15-11-17(21(25-5)19(13-15)23-3)18-12-16(10-8-2)14-20(24-4)22(18)26-6/h7-8,11-14H,1-2,9-10H2,3-6H3
InChI Key FPLKPCUDKVEJDK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26O4
Molecular Weight 354.40 g/mol
Exact Mass 354.18310931 g/mol
Topological Polar Surface Area (TPSA) 36.90 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.85
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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C22H26O4

2D Structure

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2D Structure of 1-(2,3-Dimethoxy-5-prop-2-enylphenyl)-2,3-dimethoxy-5-prop-2-enylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.7989 79.89%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8128 81.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8536 85.36%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9432 94.32%
P-glycoprotein inhibitior + 0.7762 77.62%
P-glycoprotein substrate - 0.8853 88.53%
CYP3A4 substrate - 0.5612 56.12%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.4914 49.14%
CYP3A4 inhibition + 0.8580 85.80%
CYP2C9 inhibition - 0.6851 68.51%
CYP2C19 inhibition + 0.8881 88.81%
CYP2D6 inhibition - 0.8749 87.49%
CYP1A2 inhibition + 0.7471 74.71%
CYP2C8 inhibition + 0.6882 68.82%
CYP inhibitory promiscuity + 0.9362 93.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7438 74.38%
Carcinogenicity (trinary) Non-required 0.5103 51.03%
Eye corrosion - 0.9691 96.91%
Eye irritation - 0.4899 48.99%
Skin irritation - 0.8840 88.40%
Skin corrosion - 0.9727 97.27%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8320 83.20%
Micronuclear - 0.5508 55.08%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation - 0.8582 85.82%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6288 62.88%
Acute Oral Toxicity (c) III 0.7524 75.24%
Estrogen receptor binding + 0.8287 82.87%
Androgen receptor binding - 0.6505 65.05%
Thyroid receptor binding + 0.6566 65.66%
Glucocorticoid receptor binding + 0.8060 80.60%
Aromatase binding + 0.6547 65.47%
PPAR gamma + 0.7196 71.96%
Honey bee toxicity - 0.7922 79.22%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9954 99.54%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.75% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.07% 99.17%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.78% 95.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.35% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.21% 98.95%
CHEMBL5747 Q92793 CREB-binding protein 85.31% 95.12%
CHEMBL1255126 O15151 Protein Mdm4 82.65% 90.20%
CHEMBL4208 P20618 Proteasome component C5 80.37% 90.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.23% 89.62%

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.
Damburneya purpurea

Cross-Links

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PubChem 11121778
LOTUS LTS0171841
wikiData Q104999246