Formanilide

Details

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Internal ID f6be5fa9-d5e8-40a3-aae4-dfb5941767e2
Taxonomy Benzenoids > Benzene and substituted derivatives > Anilides
IUPAC Name N-phenylformamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H7NO/c9-6-8-7-4-2-1-3-5-7/h1-6H,(H,8,9)
InChI Key DYDNPESBYVVLBO-UHFFFAOYSA-N
Popularity 388 references in papers

Physical and Chemical Properties

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Molecular Formula C7H7NO
Molecular Weight 121.14 g/mol
Exact Mass 121.052763847 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.25
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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N-PHENYLFORMAMIDE
103-70-8
N-Formylaniline
Formamide, N-phenyl-
Phenyl formamide
Formylaniline
Formamidobenzene
Carbanilaldehyde
Aniline, N-formyl-
N-phenyl-formamide
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Formanilide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 + 0.9438 94.38%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.4349 43.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9320 93.20%
OATP1B3 inhibitior + 0.9617 96.17%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9237 92.37%
P-glycoprotein inhibitior - 0.9902 99.02%
P-glycoprotein substrate - 0.9892 98.92%
CYP3A4 substrate - 0.7942 79.42%
CYP2C9 substrate - 0.6265 62.65%
CYP2D6 substrate - 0.8068 80.68%
CYP3A4 inhibition - 0.9808 98.08%
CYP2C9 inhibition - 0.8947 89.47%
CYP2C19 inhibition - 0.7198 71.98%
CYP2D6 inhibition - 0.7650 76.50%
CYP1A2 inhibition + 0.5588 55.88%
CYP2C8 inhibition - 0.8919 89.19%
CYP inhibitory promiscuity - 0.7730 77.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6948 69.48%
Eye corrosion + 0.9538 95.38%
Eye irritation + 0.9967 99.67%
Skin irritation + 0.6591 65.91%
Skin corrosion - 0.7362 73.62%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8522 85.22%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.5893 58.93%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.6156 61.56%
Acute Oral Toxicity (c) III 0.8431 84.31%
Estrogen receptor binding - 0.8352 83.52%
Androgen receptor binding - 0.8007 80.07%
Thyroid receptor binding - 0.6846 68.46%
Glucocorticoid receptor binding - 0.7889 78.89%
Aromatase binding - 0.7279 72.79%
PPAR gamma - 0.7673 76.73%
Honey bee toxicity - 0.9243 92.43%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity - 0.3911 39.11%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.17% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.71% 94.62%
CHEMBL3401 O75469 Pregnane X receptor 82.86% 94.73%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.43% 94.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.05% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 81.82% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.19% 86.33%

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.
Citrus × aurantium

Cross-Links

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PubChem 7671
LOTUS LTS0143643
wikiData Q2689660