5-(Methoxymethyl)-1H-pyrrole-2-carbaldehyde

Details

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Internal ID 651a4a57-e1ea-4df0-a2e4-ef7566daf732
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 5-(methoxymethyl)-1H-pyrrole-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9NO2/c1-10-5-7-3-2-6(4-9)8-7/h2-4,8H,5H2,1H3
InChI Key BOXJWCCJFRQJLV-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9NO2
Molecular Weight 139.15 g/mol
Exact Mass 139.063328530 g/mol
Topological Polar Surface Area (TPSA) 42.10 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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RefChem:101811
862599-39-1
SCHEMBL29188607

2D Structure

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2D Structure of 5-(Methoxymethyl)-1H-pyrrole-2-carbaldehyde

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 + 0.5223 52.23%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.4710 47.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8913 89.13%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8862 88.62%
P-glycoprotein inhibitior - 0.9894 98.94%
P-glycoprotein substrate - 0.9304 93.04%
CYP3A4 substrate - 0.6166 61.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7834 78.34%
CYP3A4 inhibition - 0.9745 97.45%
CYP2C9 inhibition - 0.8324 83.24%
CYP2C19 inhibition - 0.8384 83.84%
CYP2D6 inhibition - 0.9239 92.39%
CYP1A2 inhibition + 0.5413 54.13%
CYP2C8 inhibition - 0.7953 79.53%
CYP inhibitory promiscuity - 0.8863 88.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7910 79.10%
Carcinogenicity (trinary) Non-required 0.6053 60.53%
Eye corrosion - 0.9090 90.90%
Eye irritation + 0.9926 99.26%
Skin irritation - 0.5245 52.45%
Skin corrosion - 0.6886 68.86%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7413 74.13%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.5659 56.59%
skin sensitisation - 0.7915 79.15%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.6886 68.86%
Acute Oral Toxicity (c) III 0.5582 55.82%
Estrogen receptor binding - 0.9231 92.31%
Androgen receptor binding - 0.8727 87.27%
Thyroid receptor binding - 0.8727 87.27%
Glucocorticoid receptor binding - 0.8400 84.00%
Aromatase binding - 0.8432 84.32%
PPAR gamma - 0.8713 87.13%
Honey bee toxicity - 0.9069 90.69%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.9365 93.65%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.41% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.82% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.14% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.32% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.49% 94.73%
CHEMBL4208 P20618 Proteasome component C5 80.27% 90.00%

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.
Salvia miltiorrhiza

Cross-Links

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PubChem 86063753
NPASS NPC78408
LOTUS LTS0074678
wikiData Q104940977