3-Chloro-4-(3-chloro-4-fluoro-2-nitrophenyl)-1H-pyrrole

Details

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Internal ID f467bec4-903c-45dd-bb6a-b8744795bc08
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles > Phenylpyrroles
IUPAC Name 3-chloro-4-(3-chloro-4-fluoro-2-nitrophenyl)-1H-pyrrole
SMILES (Canonical) C1=CC(=C(C(=C1C2=CNC=C2Cl)[N+](=O)[O-])Cl)F
SMILES (Isomeric) C1=CC(=C(C(=C1C2=CNC=C2Cl)[N+](=O)[O-])Cl)F
InChI InChI=1S/C10H5Cl2FN2O2/c11-7-4-14-3-6(7)5-1-2-8(13)9(12)10(5)15(16)17/h1-4,14H
InChI Key ICUDVCSRICMBIV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H5Cl2FN2O2
Molecular Weight 275.06 g/mol
Exact Mass 273.9712110 g/mol
Topological Polar Surface Area (TPSA) 61.60 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.04
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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17307-19-6
3-Chloro-4-(3-chloro-4-fluoro-2-nitrophenyl)-1H-pyrrole
DTXSID00515508

2D Structure

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2D Structure of 3-Chloro-4-(3-chloro-4-fluoro-2-nitrophenyl)-1H-pyrrole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.8856 88.56%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7237 72.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9059 90.59%
OATP1B3 inhibitior + 0.9420 94.20%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5202 52.02%
P-glycoprotein inhibitior - 0.9669 96.69%
P-glycoprotein substrate - 0.9343 93.43%
CYP3A4 substrate + 0.5608 56.08%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8396 83.96%
CYP3A4 inhibition - 0.8471 84.71%
CYP2C9 inhibition + 0.6370 63.70%
CYP2C19 inhibition + 0.9270 92.70%
CYP2D6 inhibition - 0.7199 71.99%
CYP1A2 inhibition + 0.9306 93.06%
CYP2C8 inhibition - 0.7890 78.90%
CYP inhibitory promiscuity + 0.8842 88.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5219 52.19%
Carcinogenicity (trinary) Non-required 0.6943 69.43%
Eye corrosion - 0.8873 88.73%
Eye irritation + 0.7013 70.13%
Skin irritation - 0.6299 62.99%
Skin corrosion - 0.9480 94.80%
Ames mutagenesis + 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6783 67.83%
Micronuclear + 0.9700 97.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation - 0.6061 60.61%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6364 63.64%
Acute Oral Toxicity (c) III 0.5855 58.55%
Estrogen receptor binding + 0.8345 83.45%
Androgen receptor binding + 0.6910 69.10%
Thyroid receptor binding + 0.7270 72.70%
Glucocorticoid receptor binding + 0.8999 89.99%
Aromatase binding + 0.7504 75.04%
PPAR gamma + 0.8560 85.60%
Honey bee toxicity - 0.9627 96.27%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6431 64.31%
Fish aquatic toxicity + 0.9400 94.00%

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
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 98.45% 85.94%
CHEMBL221 P23219 Cyclooxygenase-1 92.26% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.56% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 90.14% 94.80%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 89.85% 92.88%
CHEMBL3038469 P24941 CDK2/Cyclin A 88.22% 91.38%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 87.39% 91.24%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 85.77% 88.84%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.75% 95.56%
CHEMBL2581 P07339 Cathepsin D 84.99% 98.95%
CHEMBL217 P14416 Dopamine D2 receptor 84.62% 95.62%
CHEMBL3902 P09211 Glutathione S-transferase Pi 84.59% 93.81%
CHEMBL3401 O75469 Pregnane X receptor 84.57% 94.73%
CHEMBL4660 P28907 Lymphocyte differentiation antigen CD38 84.21% 95.27%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.02% 89.62%
CHEMBL240 Q12809 HERG 83.05% 89.76%
CHEMBL1811 P34995 Prostanoid EP1 receptor 82.45% 95.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.04% 86.92%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.86% 92.29%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.75% 90.24%
CHEMBL222 P23975 Norepinephrine transporter 80.27% 96.06%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.13% 82.69%

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.
Aglaia tomentosa
Backhousia citriodora
Capraria biflora
Centipeda minima
Mentha suaveolens subsp. timija
Senecio macrocephalus
Upuna borneensis

Cross-Links

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PubChem 13024187
NPASS NPC49561