1-Ethyl-2-pyrrolecarboxaldehyde

Details

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Internal ID 98397e2d-fdc3-4692-a834-8a5bdb0f753c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 1-ethylpyrrole-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9NO/c1-2-8-5-3-4-7(8)6-9/h3-6H,2H2,1H3
InChI Key DVLGEHCERRWDIX-UHFFFAOYSA-N
Popularity 17 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9NO
Molecular Weight 123.15 g/mol
Exact Mass 123.068413911 g/mol
Topological Polar Surface Area (TPSA) 22.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.32
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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1-Ethyl-1H-pyrrole-2-carboxaldehyde
1H-Pyrrole-2-carboxaldehyde, 1-ethyl-
1-Ethyl-2-formylpyrrole
Tea pyrrole
1-Ethyl-2-pyrrolecarboxaldehyde
1-Ethylpyrrole-2-aldehyde
UNII-51J1CE738Y
1-Ethyl-2-formyl-1H-pyrrole
FEMA No. 4317
N-ETHYL-2-FORMYLPYRROLE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Ethyl-2-pyrrolecarboxaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.9749 97.49%
Blood Brain Barrier + 0.9570 95.70%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.6671 66.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9019 90.19%
OATP1B3 inhibitior + 0.9529 95.29%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7664 76.64%
BSEP inhibitior - 0.9377 93.77%
P-glycoprotein inhibitior - 0.9878 98.78%
P-glycoprotein substrate - 0.9432 94.32%
CYP3A4 substrate - 0.7186 71.86%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.8737 87.37%
CYP3A4 inhibition - 0.9563 95.63%
CYP2C9 inhibition - 0.8589 85.89%
CYP2C19 inhibition - 0.6899 68.99%
CYP2D6 inhibition - 0.9399 93.99%
CYP1A2 inhibition + 0.5798 57.98%
CYP2C8 inhibition - 0.9166 91.66%
CYP inhibitory promiscuity + 0.7246 72.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4858 48.58%
Eye corrosion - 0.6817 68.17%
Eye irritation + 0.9803 98.03%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.6558 65.58%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7987 79.87%
Micronuclear + 0.5900 59.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8155 81.55%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.5923 59.23%
Acute Oral Toxicity (c) III 0.6178 61.78%
Estrogen receptor binding - 0.9142 91.42%
Androgen receptor binding - 0.7516 75.16%
Thyroid receptor binding - 0.8408 84.08%
Glucocorticoid receptor binding - 0.9172 91.72%
Aromatase binding - 0.8321 83.21%
PPAR gamma - 0.8326 83.26%
Honey bee toxicity - 0.9666 96.66%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.7175 71.75%

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 95.24% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.69% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.45% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.61% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.11% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 81.44% 94.73%

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.
Ficus carica

Cross-Links

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PubChem 579338
NPASS NPC164230