Flemichapparin A

Details

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Internal ID 24dad1b2-06aa-43ca-a6ae-c56f201d143e
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > 2-Hydroxychalcones
IUPAC Name (E)-1-(5,8-dihydroxy-2,2-dimethylchromen-6-yl)-3-phenylprop-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H18O4/c1-20(2)11-10-14-18(23)15(12-17(22)19(14)24-20)16(21)9-8-13-6-4-3-5-7-13/h3-12,22-23H,1-2H3/b9-8+
InChI Key HZEJNIAQUFJSBF-CMDGGOBGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O4
Molecular Weight 322.40 g/mol
Exact Mass 322.12050905 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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RefChem:140682
(E)-1-(5,8-dihydroxy-2,2-dimethylchromen-6-yl)-3-phenylprop-2-en-1-one
32507-61-2,30880-56-9
LMPK12120134
32507-61-2

2D Structure

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2D Structure of Flemichapparin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9853 98.53%
Caco-2 - 0.5604 56.04%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7645 76.45%
OATP2B1 inhibitior - 0.5800 58.00%
OATP1B1 inhibitior + 0.8845 88.45%
OATP1B3 inhibitior + 0.9852 98.52%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8445 84.45%
P-glycoprotein inhibitior + 0.6419 64.19%
P-glycoprotein substrate - 0.8129 81.29%
CYP3A4 substrate + 0.5060 50.60%
CYP2C9 substrate - 0.7983 79.83%
CYP2D6 substrate - 0.8506 85.06%
CYP3A4 inhibition - 0.5677 56.77%
CYP2C9 inhibition + 0.6941 69.41%
CYP2C19 inhibition + 0.6356 63.56%
CYP2D6 inhibition - 0.7423 74.23%
CYP1A2 inhibition + 0.8277 82.77%
CYP2C8 inhibition + 0.7670 76.70%
CYP inhibitory promiscuity + 0.6385 63.85%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5833 58.33%
Eye corrosion - 0.9887 98.87%
Eye irritation + 0.8213 82.13%
Skin irritation - 0.6331 63.31%
Skin corrosion - 0.9102 91.02%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4870 48.70%
Micronuclear + 0.7400 74.00%
Hepatotoxicity - 0.6496 64.96%
skin sensitisation - 0.6786 67.86%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8518 85.18%
Acute Oral Toxicity (c) III 0.7129 71.29%
Estrogen receptor binding + 0.9511 95.11%
Androgen receptor binding + 0.8457 84.57%
Thyroid receptor binding + 0.7575 75.75%
Glucocorticoid receptor binding + 0.9245 92.45%
Aromatase binding + 0.7496 74.96%
PPAR gamma + 0.8726 87.26%
Honey bee toxicity - 0.8912 89.12%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9767 97.67%

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 99.49% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.61% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 90.97% 91.49%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.76% 95.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.43% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.17% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.74% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.39% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.96% 94.45%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.57% 91.71%
CHEMBL4208 P20618 Proteasome component C5 82.67% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.26% 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.
Abrus melanospermus subsp. melanospermus

Cross-Links

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PubChem 11110066
NPASS NPC226182