Discoipyrrole C

Details

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Internal ID 46a3b20c-3f23-474e-a69a-4fa92366a26f
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 2-hydroxy-4,5-bis(4-hydroxyphenyl)-2-(2-methylpropyl)-1H-pyrrol-3-one
SMILES (Canonical) CC(C)CC1(C(=O)C(=C(N1)C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)O
SMILES (Isomeric) CC(C)CC1(C(=O)C(=C(N1)C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)O
InChI InChI=1S/C20H21NO4/c1-12(2)11-20(25)19(24)17(13-3-7-15(22)8-4-13)18(21-20)14-5-9-16(23)10-6-14/h3-10,12,21-23,25H,11H2,1-2H3
InChI Key DFJFMRMDRGUBQM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H21NO4
Molecular Weight 339.40 g/mol
Exact Mass 339.14705815 g/mol
Topological Polar Surface Area (TPSA) 89.80 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Discoipyrrole C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.5195 51.95%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6310 63.10%
OATP2B1 inhibitior - 0.7082 70.82%
OATP1B1 inhibitior + 0.9087 90.87%
OATP1B3 inhibitior + 0.9335 93.35%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7008 70.08%
P-glycoprotein inhibitior - 0.7809 78.09%
P-glycoprotein substrate - 0.7781 77.81%
CYP3A4 substrate - 0.5278 52.78%
CYP2C9 substrate - 0.5962 59.62%
CYP2D6 substrate - 0.8649 86.49%
CYP3A4 inhibition - 0.8050 80.50%
CYP2C9 inhibition - 0.5747 57.47%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.8726 87.26%
CYP1A2 inhibition - 0.7422 74.22%
CYP2C8 inhibition - 0.6463 64.63%
CYP inhibitory promiscuity + 0.6522 65.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8111 81.11%
Carcinogenicity (trinary) Non-required 0.5391 53.91%
Eye corrosion - 0.9907 99.07%
Eye irritation - 0.8942 89.42%
Skin irritation - 0.8006 80.06%
Skin corrosion - 0.9325 93.25%
Ames mutagenesis - 0.6437 64.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6889 68.89%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.7679 76.79%
skin sensitisation - 0.8050 80.50%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5436 54.36%
Acute Oral Toxicity (c) III 0.5974 59.74%
Estrogen receptor binding + 0.6829 68.29%
Androgen receptor binding + 0.8797 87.97%
Thyroid receptor binding + 0.5991 59.91%
Glucocorticoid receptor binding + 0.5913 59.13%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.8441 84.41%
Honey bee toxicity - 0.9106 91.06%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9086 90.86%

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 98.39% 98.95%
CHEMBL242 Q92731 Estrogen receptor beta 96.97% 98.35%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.75% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.67% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.82% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 88.71% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.37% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.93% 85.14%
CHEMBL1944 P08473 Neprilysin 84.57% 92.63%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 84.50% 93.10%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.41% 91.71%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 84.03% 90.93%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.72% 85.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.66% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.16% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.73% 94.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 80.51% 83.10%
CHEMBL4208 P20618 Proteasome component C5 80.04% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.01% 99.15%

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.
There are no matching plants.

Cross-Links

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PubChem 73426922
LOTUS LTS0067692
wikiData Q103818334