3-(3,4-Dibromo-5-hydroxyphenyl)-3-hydroxy-1-octadecanoylpyrrolidin-2-one

Details

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Internal ID d83c45a0-ce71-4d31-a539-b521d058642c
Taxonomy Organoheterocyclic compounds > Pyrrolidines > Phenylpyrrolidines
IUPAC Name 3-(3,4-dibromo-5-hydroxyphenyl)-3-hydroxy-1-octadecanoylpyrrolidin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H43Br2NO4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-25(33)31-19-18-28(35,27(31)34)22-20-23(29)26(30)24(32)21-22/h20-21,32,35H,2-19H2,1H3
InChI Key HBSJNCNRIRVIQL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H43Br2NO4
Molecular Weight 617.50 g/mol
Exact Mass 617.15383 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 9.90
Atomic LogP (AlogP) 8.13
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(3,4-Dibromo-5-hydroxyphenyl)-3-hydroxy-1-octadecanoylpyrrolidin-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9798 97.98%
Caco-2 - 0.7892 78.92%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7669 76.69%
OATP2B1 inhibitior - 0.7181 71.81%
OATP1B1 inhibitior + 0.8918 89.18%
OATP1B3 inhibitior + 0.9276 92.76%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6863 68.63%
P-glycoprotein inhibitior - 0.5248 52.48%
P-glycoprotein substrate + 0.5621 56.21%
CYP3A4 substrate + 0.5568 55.68%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8074 80.74%
CYP3A4 inhibition - 0.8771 87.71%
CYP2C9 inhibition - 0.8118 81.18%
CYP2C19 inhibition - 0.7272 72.72%
CYP2D6 inhibition - 0.8281 82.81%
CYP1A2 inhibition - 0.7961 79.61%
CYP2C8 inhibition - 0.6977 69.77%
CYP inhibitory promiscuity - 0.7026 70.26%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7443 74.43%
Carcinogenicity (trinary) Non-required 0.5594 55.94%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.8384 83.84%
Skin irritation - 0.7737 77.37%
Skin corrosion - 0.9172 91.72%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5892 58.92%
Micronuclear + 0.7100 71.00%
Hepatotoxicity - 0.5114 51.14%
skin sensitisation - 0.8480 84.80%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.8039 80.39%
Acute Oral Toxicity (c) III 0.6323 63.23%
Estrogen receptor binding + 0.7871 78.71%
Androgen receptor binding + 0.7302 73.02%
Thyroid receptor binding - 0.5961 59.61%
Glucocorticoid receptor binding + 0.5374 53.74%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6351 63.51%
Honey bee toxicity - 0.9633 96.33%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.8170 81.70%
Fish aquatic toxicity + 0.9671 96.71%

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
CHEMBL230 P35354 Cyclooxygenase-2 99.47% 89.63%
CHEMBL2581 P07339 Cathepsin D 99.41% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.29% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.43% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.22% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.02% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.50% 90.71%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.28% 95.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.40% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.41% 94.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 84.78% 91.81%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 84.27% 90.24%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.96% 96.61%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.49% 93.03%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.23% 92.08%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.15% 93.40%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 82.09% 82.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.24% 82.69%
CHEMBL4208 P20618 Proteasome component C5 81.18% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.31% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.19% 89.00%
CHEMBL4588 P22894 Matrix metalloproteinase 8 80.14% 94.66%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 10100372
LOTUS LTS0008892
wikiData Q105025463