2'-Methoxy-conocarpol

Details

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Internal ID 5b844807-722e-4ac5-b511-3cc5b73b829d
Taxonomy Lignans, neolignans and related compounds > Dibenzylbutane lignans
IUPAC Name 4-[4-(4-hydroxyphenyl)-2,3-dimethylbutyl]-3-methoxyphenol
SMILES (Canonical) CC(CC1=CC=C(C=C1)O)C(C)CC2=C(C=C(C=C2)O)OC
SMILES (Isomeric) CC(CC1=CC=C(C=C1)O)C(C)CC2=C(C=C(C=C2)O)OC
InChI InChI=1S/C19H24O3/c1-13(10-15-4-7-17(20)8-5-15)14(2)11-16-6-9-18(21)12-19(16)22-3/h4-9,12-14,20-21H,10-11H2,1-3H3
InChI Key LZSBDAAZSUIPOM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O3
Molecular Weight 300.40 g/mol
Exact Mass 300.17254462 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.16
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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NSC727407
NSC-727407

2D Structure

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2D Structure of 2'-Methoxy-conocarpol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.7985 79.85%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8720 87.20%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8957 89.57%
OATP1B3 inhibitior + 0.8554 85.54%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7353 73.53%
P-glycoprotein inhibitior - 0.6523 65.23%
P-glycoprotein substrate - 0.5887 58.87%
CYP3A4 substrate - 0.6030 60.30%
CYP2C9 substrate + 0.5965 59.65%
CYP2D6 substrate + 0.4548 45.48%
CYP3A4 inhibition - 0.8319 83.19%
CYP2C9 inhibition - 0.7120 71.20%
CYP2C19 inhibition + 0.6790 67.90%
CYP2D6 inhibition - 0.6880 68.80%
CYP1A2 inhibition + 0.6891 68.91%
CYP2C8 inhibition + 0.5921 59.21%
CYP inhibitory promiscuity + 0.6493 64.93%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6475 64.75%
Carcinogenicity (trinary) Non-required 0.6244 62.44%
Eye corrosion - 0.9774 97.74%
Eye irritation - 0.8491 84.91%
Skin irritation - 0.8244 82.44%
Skin corrosion - 0.9237 92.37%
Ames mutagenesis - 0.7837 78.37%
Human Ether-a-go-go-Related Gene inhibition + 0.9063 90.63%
Micronuclear - 0.6500 65.00%
Hepatotoxicity - 0.6234 62.34%
skin sensitisation - 0.7416 74.16%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.6979 69.79%
Acute Oral Toxicity (c) III 0.7326 73.26%
Estrogen receptor binding + 0.7017 70.17%
Androgen receptor binding + 0.5391 53.91%
Thyroid receptor binding + 0.7265 72.65%
Glucocorticoid receptor binding + 0.5524 55.24%
Aromatase binding + 0.7857 78.57%
PPAR gamma - 0.5271 52.71%
Honey bee toxicity - 0.8499 84.99%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5451 54.51%
Fish aquatic toxicity + 0.9957 99.57%

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
CHEMBL2581 P07339 Cathepsin D 97.18% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.89% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 93.10% 90.20%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.67% 91.11%
CHEMBL2535 P11166 Glucose transporter 91.91% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.12% 99.17%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.69% 95.89%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.42% 90.24%
CHEMBL4208 P20618 Proteasome component C5 87.07% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.51% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.35% 94.45%
CHEMBL5896 O75164 Lysine-specific demethylase 4A 83.32% 99.09%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.72% 89.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.20% 99.15%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.47% 91.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.99% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.17% 95.50%

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.
Conocarpus erectus

Cross-Links

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PubChem 45027841
LOTUS LTS0120201
wikiData Q105160098