2-Phenyl-5-sec-butyl-1H-pyrrole

Details

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Internal ID 839c8637-8c68-4867-9610-f1807fa442ea
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles > Phenylpyrroles
IUPAC Name 2-butan-2-yl-5-phenyl-1H-pyrrole
SMILES (Canonical) CCC(C)C1=CC=C(N1)C2=CC=CC=C2
SMILES (Isomeric) CCC(C)C1=CC=C(N1)C2=CC=CC=C2
InChI InChI=1S/C14H17N/c1-3-11(2)13-9-10-14(15-13)12-7-5-4-6-8-12/h4-11,15H,3H2,1-2H3
InChI Key CKOPPECBTCHMPP-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H17N
Molecular Weight 199.29 g/mol
Exact Mass 199.136099547 g/mol
Topological Polar Surface Area (TPSA) 15.80 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.20
H-Bond Acceptor 0
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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2-(sec-Butyl)-5-phenyl-1H-pyrrole
1422518-32-8
SCHEMBL22734771
2-butan-2-yl-5-phenyl-1H-pyrrole
MFCD29067372

2D Structure

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2D Structure of 2-Phenyl-5-sec-butyl-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 + 1.0000 100.00%
Caco-2 + 0.8695 86.95%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.4545 45.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8964 89.64%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.5536 55.36%
P-glycoprotein inhibitior - 0.9741 97.41%
P-glycoprotein substrate - 0.8148 81.48%
CYP3A4 substrate - 0.7382 73.82%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.6649 66.49%
CYP3A4 inhibition - 0.9161 91.61%
CYP2C9 inhibition - 0.5612 56.12%
CYP2C19 inhibition + 0.6951 69.51%
CYP2D6 inhibition + 0.5000 50.00%
CYP1A2 inhibition + 0.7670 76.70%
CYP2C8 inhibition - 0.8450 84.50%
CYP inhibitory promiscuity + 0.6906 69.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.4980 49.80%
Eye corrosion - 0.9460 94.60%
Eye irritation - 0.4906 49.06%
Skin irritation - 0.5883 58.83%
Skin corrosion - 0.8621 86.21%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8263 82.63%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.5804 58.04%
skin sensitisation - 0.5678 56.78%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7509 75.09%
Acute Oral Toxicity (c) III 0.6477 64.77%
Estrogen receptor binding + 0.7313 73.13%
Androgen receptor binding - 0.5357 53.57%
Thyroid receptor binding - 0.6467 64.67%
Glucocorticoid receptor binding - 0.8559 85.59%
Aromatase binding + 0.5586 55.86%
PPAR gamma - 0.7846 78.46%
Honey bee toxicity - 0.9586 95.86%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8874 88.74%

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 98.15% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 95.67% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.90% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.36% 95.56%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 86.37% 97.23%
CHEMBL1937 Q92769 Histone deacetylase 2 85.70% 94.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.77% 93.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.93% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 80.71% 94.73%

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 70680088
LOTUS LTS0206748
wikiData Q104962636