4-(2-Formyl-1H-pyrrol-1-yl)butanoic acid

Details

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Internal ID b7f8a7e7-1294-4490-98ee-d08df853b074
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 4-(2-formylpyrrol-1-yl)butanoic acid
SMILES (Canonical) C1=CN(C(=C1)C=O)CCCC(=O)O
SMILES (Isomeric) C1=CN(C(=C1)C=O)CCCC(=O)O
InChI InChI=1S/C9H11NO3/c11-7-8-3-1-5-10(8)6-2-4-9(12)13/h1,3,5,7H,2,4,6H2,(H,12,13)
InChI Key HHLWLLWBHBDZGK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C9H11NO3
Molecular Weight 181.19 g/mol
Exact Mass 181.07389321 g/mol
Topological Polar Surface Area (TPSA) 59.30 Ų
XlogP 0.20
Atomic LogP (AlogP) 1.17
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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61837-38-5
4-(2-FORMYLPYRROL-1-YL)BUTANOIC ACID
SCHEMBL11562036
DTXSID40614781
2-formyl-1h-pyrrole-1-butanoic acid

2D Structure

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2D Structure of 4-(2-Formyl-1H-pyrrol-1-yl)butanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9428 94.28%
Caco-2 + 0.7407 74.07%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.8467 84.67%
OATP2B1 inhibitior - 0.8634 86.34%
OATP1B1 inhibitior + 0.8914 89.14%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6860 68.60%
BSEP inhibitior - 0.9149 91.49%
P-glycoprotein inhibitior - 0.9887 98.87%
P-glycoprotein substrate - 0.9121 91.21%
CYP3A4 substrate - 0.6313 63.13%
CYP2C9 substrate - 0.8278 82.78%
CYP2D6 substrate - 0.9029 90.29%
CYP3A4 inhibition - 0.9557 95.57%
CYP2C9 inhibition - 0.9469 94.69%
CYP2C19 inhibition - 0.9421 94.21%
CYP2D6 inhibition - 0.9637 96.37%
CYP1A2 inhibition - 0.9097 90.97%
CYP2C8 inhibition - 0.9059 90.59%
CYP inhibitory promiscuity - 0.9675 96.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6312 63.12%
Eye corrosion - 0.9700 97.00%
Eye irritation + 0.8884 88.84%
Skin irritation - 0.6304 63.04%
Skin corrosion - 0.7744 77.44%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8598 85.98%
Micronuclear + 0.5100 51.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.9214 92.14%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8697 86.97%
Acute Oral Toxicity (c) III 0.5317 53.17%
Estrogen receptor binding - 0.8079 80.79%
Androgen receptor binding - 0.7076 70.76%
Thyroid receptor binding - 0.8025 80.25%
Glucocorticoid receptor binding - 0.6525 65.25%
Aromatase binding - 0.7438 74.38%
PPAR gamma - 0.5287 52.87%
Honey bee toxicity - 0.9823 98.23%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.7946 79.46%

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 96.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.57% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.31% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.10% 99.17%
CHEMBL3891 P07384 Calpain 1 85.69% 93.04%
CHEMBL4330 Q9NS75 Cysteinyl leukotriene receptor 2 83.58% 98.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.57% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.87% 93.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.79% 96.00%

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.
Morus alba

Cross-Links

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PubChem 21491039
LOTUS LTS0095322
wikiData Q82516025