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14 results for “Cinnamaldehyde”
Data from: Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship
Cinnamaldehyde amino acid Schiff base (CAAS) is a new class of safe, bioactive compounds which could be developed as potential antifungal agents for fungal infections. To design new cinnamaldehyde amino acid Schiff base compounds with high bioactivity, the quantitative structure–activity relationships (QSARs) for CAAS compounds against Aspergillus niger (A. niger) and Penicillium citrinum (P. citrinum) were analysed. The QSAR models (R2 = 0.9346 for A. niger, R2 = 0.9590 for P. citrinum,) were constructed and validated. The models indicated that the molecular polarity and the Max atomic orbital electronic population had a significant effect on antifungal activity. Based on the best QSAR models, two new compounds were designed and synthesized. Antifungal activity tests proved that both of them have great bioactivity against the selected fungi.
The Effect of Capsaicin and Cinnamaldehyde on Intestinal Permeability
ClinicalTrials.gov study NCT01667523. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Data from: Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship
Open the record for dataset details and reuse information.
Gene expression response of Salmonella enterica serovar Enteritidis phage type 8 to subinhibitory concentrations of trans-cinnamaldehyde and eugenol
GEO Series GSE102477. Salmonella enterica; Salmonella enterica subsp. enterica serovar Enteritidis. 11 samples. Type: Expression profiling by array.
Transcriptomic Responses of Mycoplasma bovis upon Treatments of trans-Cinnamaldehyde, Carvacrol, and Eugenol
GEO Series GSE198086. Mycoplasmopsis bovis PG45. 24 samples. Type: Expression profiling by high throughput sequencing.
Transcriptomic Analysis of the Candida albicans Response to Treatment with Cinnamaldehyde
GEO Series GSE262904. Candida albicans SC5314. 6 samples. Type: Expression profiling by high throughput sequencing.
Desensitization of Nociceptive Afferents by Application of Topical Capsaicin, Trans-cinnamaldehyde and L-menthol
ClinicalTrials.gov study NCT03132142. IPD Sharing: NO. Countries: 1. Publications: 0.
Influence of Antipruritics on the Dermal Blood Flow Response to Histamine, Cinnamaldehyde and Capsaicin.
ClinicalTrials.gov study NCT04399148. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Influence of Ubrogepant and Sumatriptan on the Dermal Blood Flow Response to Histamine, Cinnamaldehyde and Capsaicin
ClinicalTrials.gov study NCT05654298. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Influence of H1-antihistamines on the Dermal Blood Flow Response to Histamine, Cinnamaldehyde and Capsaicin.
ClinicalTrials.gov study NCT04399525. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Antimicrobial action of t-cinnamaldehyde on Escherichia coli MG1655
GEO Series GSE252441. Escherichia coli. 12 samples. Type: Expression profiling by high throughput sequencing.
Modulation of inflammation and parasite infection by cinnamaldehyde
GEO Series GSE165377. Mus musculus. 24 samples. Type: Expression profiling by array.
Transcriptional response of Escherichia coli O157:H7 to cinnamaldehyde
GEO Series GSE40693. Escherichia coli; Escherichia coli O157:H7. 8 samples. Type: Expression profiling by array.
RelA influence on antimicrobial action of t-cinnamaldehyde on Escherichia coli MG1655
GEO Series GSE301628. Escherichia coli. 12 samples. Type: Expression profiling by high throughput sequencing.
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