3-Hydroxy-1-(5-methoxy-2,2-dimethylchromen-6-yl)-3-phenylprop-2-en-1-one

Details

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Internal ID a31107d1-2a3f-4dfe-b673-1a1a50ff1eb3
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > 2,2-dimethyl-1-benzopyrans
IUPAC Name 3-hydroxy-1-(5-methoxy-2,2-dimethylchromen-6-yl)-3-phenylprop-2-en-1-one
SMILES (Canonical) CC1(C=CC2=C(O1)C=CC(=C2OC)C(=O)C=C(C3=CC=CC=C3)O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C=CC(=C2OC)C(=O)C=C(C3=CC=CC=C3)O)C
InChI InChI=1S/C21H20O4/c1-21(2)12-11-16-19(25-21)10-9-15(20(16)24-3)18(23)13-17(22)14-7-5-4-6-8-14/h4-13,22H,1-3H3
InChI Key NTSLHMYMWQPYFF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O4
Molecular Weight 336.40 g/mol
Exact Mass 336.13615911 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.66
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Hydroxy-1-(5-methoxy-2,2-dimethylchromen-6-yl)-3-phenylprop-2-en-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8688 86.88%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7672 76.72%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9149 91.49%
OATP1B3 inhibitior + 0.9868 98.68%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9014 90.14%
P-glycoprotein inhibitior + 0.7536 75.36%
P-glycoprotein substrate - 0.8864 88.64%
CYP3A4 substrate + 0.5461 54.61%
CYP2C9 substrate - 0.7991 79.91%
CYP2D6 substrate - 0.8556 85.56%
CYP3A4 inhibition + 0.6237 62.37%
CYP2C9 inhibition - 0.6865 68.65%
CYP2C19 inhibition + 0.8657 86.57%
CYP2D6 inhibition - 0.7955 79.55%
CYP1A2 inhibition + 0.8477 84.77%
CYP2C8 inhibition + 0.5271 52.71%
CYP inhibitory promiscuity + 0.7513 75.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.5076 50.76%
Eye corrosion - 0.9852 98.52%
Eye irritation + 0.7544 75.44%
Skin irritation - 0.7489 74.89%
Skin corrosion - 0.9761 97.61%
Ames mutagenesis + 0.5930 59.30%
Human Ether-a-go-go-Related Gene inhibition + 0.6650 66.50%
Micronuclear + 0.6200 62.00%
Hepatotoxicity - 0.5841 58.41%
skin sensitisation - 0.8408 84.08%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.4525 45.25%
Acute Oral Toxicity (c) III 0.5470 54.70%
Estrogen receptor binding + 0.9385 93.85%
Androgen receptor binding + 0.8398 83.98%
Thyroid receptor binding + 0.8003 80.03%
Glucocorticoid receptor binding + 0.8246 82.46%
Aromatase binding + 0.6936 69.36%
PPAR gamma + 0.8868 88.68%
Honey bee toxicity - 0.8712 87.12%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5455 54.55%
Fish aquatic toxicity + 0.9781 97.81%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 96.04% 87.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.26% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.59% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.64% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 90.50% 90.20%
CHEMBL2535 P11166 Glucose transporter 89.44% 98.75%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.03% 81.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.31% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.46% 95.50%
CHEMBL4208 P20618 Proteasome component C5 87.01% 90.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.67% 97.14%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 86.57% 94.08%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.42% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.23% 99.23%
CHEMBL221 P23219 Cyclooxygenase-1 85.11% 90.17%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 84.37% 89.44%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.26% 94.62%
CHEMBL2581 P07339 Cathepsin D 82.68% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.33% 99.17%

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.
Millettia erythrocalyx
Tephrosia purpurea

Cross-Links

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PubChem 74819277
LOTUS LTS0025554
wikiData Q105185634