6-(3-Chloro-2-hydroxy-3-methylbutyl)-5,7-dimethoxycoumarin

Details

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Internal ID 8df97add-81e3-48f4-b136-02606342ccf5
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 6-(3-chloro-2-hydroxy-3-methylbutyl)-5,7-dimethoxychromen-2-one
SMILES (Canonical) CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)Cl
SMILES (Isomeric) CC(C)(C(CC1=C(C=C2C(=C1OC)C=CC(=O)O2)OC)O)Cl
InChI InChI=1S/C16H19ClO5/c1-16(2,17)13(18)7-10-11(20-3)8-12-9(15(10)21-4)5-6-14(19)22-12/h5-6,8,13,18H,7H2,1-4H3
InChI Key JDYJPQNEOXWJQN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H19ClO5
Molecular Weight 326.77 g/mol
Exact Mass 326.0921014 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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15575-50-5

2D Structure

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2D Structure of 6-(3-Chloro-2-hydroxy-3-methylbutyl)-5,7-dimethoxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.8244 82.44%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5161 51.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9106 91.06%
OATP1B3 inhibitior + 0.9121 91.21%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5161 51.61%
P-glycoprotein inhibitior - 0.8269 82.69%
P-glycoprotein substrate - 0.6836 68.36%
CYP3A4 substrate + 0.5315 53.15%
CYP2C9 substrate - 0.6435 64.35%
CYP2D6 substrate - 0.7857 78.57%
CYP3A4 inhibition - 0.8689 86.89%
CYP2C9 inhibition - 0.8208 82.08%
CYP2C19 inhibition - 0.7878 78.78%
CYP2D6 inhibition - 0.9141 91.41%
CYP1A2 inhibition - 0.6833 68.33%
CYP2C8 inhibition + 0.4655 46.55%
CYP inhibitory promiscuity - 0.8135 81.35%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8074 80.74%
Carcinogenicity (trinary) Non-required 0.5461 54.61%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.8335 83.35%
Skin irritation - 0.7484 74.84%
Skin corrosion - 0.9268 92.68%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7473 74.73%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8463 84.63%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8494 84.94%
Acute Oral Toxicity (c) III 0.5223 52.23%
Estrogen receptor binding + 0.8588 85.88%
Androgen receptor binding + 0.6016 60.16%
Thyroid receptor binding + 0.6726 67.26%
Glucocorticoid receptor binding + 0.6724 67.24%
Aromatase binding - 0.4900 49.00%
PPAR gamma + 0.9222 92.22%
Honey bee toxicity - 0.7897 78.97%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5253 52.53%
Fish aquatic toxicity + 0.9711 97.11%

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 97.99% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.93% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.69% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.48% 94.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.14% 89.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.77% 95.56%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 89.41% 94.03%
CHEMBL2535 P11166 Glucose transporter 87.71% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.19% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 86.16% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.03% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.39% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.58% 86.92%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.53% 97.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.13% 96.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.44% 92.62%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.17% 100.00%

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.
Zanthoxylum asiaticum

Cross-Links

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PubChem 15071018
LOTUS LTS0026797
wikiData Q105125860