18 Results for "

Paederota lutea Scop.

" in MedChemExpress (MCE) Product Catalog:
Products (18)

18 Results for "Paederota lutea Scop." in MCE Product Catalog:

Cat. No.: HY-N8305
CAS No.: 25954-44-3
Gentianose is a predominant carbohydrate reserve found in the storage roots of perennial Gentiana lutea .
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Cat. No.: HY-W160679
CAS No.: 64700-15-8
Target:  

Bacterial Fungal

Research Areas:  

Infection

7-(Carboxymethoxy)-4-methylcoumarin (Compound VIIIa) is the antibacterial and antifungal agent that exhibits inhibitory activity against S. aureus, B. cereus, S. lutea, C. albicans, C. glabrata, and C. parapsilosis .
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Cat. No.: HY-N20675
CAS No.: 35536-70-0
Stachannin A is a 6-hydroxy-flavone glucoside that can be found in Paederota lutea .
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Cat. No.: HY-161783
CAS No.: 3048532-05-1
HDAC6-IN-45 (Compound 15) is a selective inhibitor for HDAC6 with IC50 of 15.2 nM. HDAC6-IN-45 exhibits neurotrophic through the upregulation of GAP43 and Beta-3 tubulin markers. HDAC6-IN-45 activates the Nrf2 signaling pathway, reduces H2O2-induced ROS production, inhibits apoptosis in PC12, and exhibits neuroprotective efficacy in SCOP-induced zebrafish Alzheimer's Disease models. HDAC6-IN-45 exhibits antioxidant activity and good blood-brain barrier (BBB) permeability .
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Cat. No.: HY-128222
CAS No.: 21198-79-8
Purity:  ≥95.0%
Synonyms: Hydrazinecarboselenoamide
Target:  

Bacterial

Research Areas:  

Infection Cancer

Selenosemicarbazide (Hydrazinecarboselenoamide) exhibits antimicrobial activity, that inhibits B. subtilis, S. aureus, Klebsiella pneumoniae, Sarcina lutea and Mycobacterium tuberculosis. Selenosemicarbazide forms complex with metal ions, and exhibits antitumor efficacy against cancer cells
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Cat. No.: HY-N8401
CAS No.: 907583-51-1
Musellactone is a lactone that can be isolated from Musella lasiocarpa. Musellactone is an antibiotic, that exhibits antibacterial activity against Bacillus megaterium and Sarcina lutea .
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Cat. No.: HY-P5562
Target:  

Bacterial

Research Areas:  

Infection

PP102 is an antimicrobial peptide is active against gram-positive B. subtilis (MIC: 25 uM), S. aureus (MIC: 13.3 uM), S. lutea (MIC: 63 uM), and B. pumilu (MIC: 23 uM) .
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Cat. No.: HY-P5563
Target:  

Bacterial

Research Areas:  

Infection

PP113 is an antimicrobial peptide is active against Gram-negative and Gram-positive bacteria, E.coli (MIC: 73.3 uM), B. subtilis (MIC: 23.3 uM), S. aureus (MIC: 13 uM), S. lutea (MIC: 16.7 uM), and B. pumilu (MIC: 23.3 uM) .
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Cat. No.: HY-P5560
CAS No.: 1099486-04-0
Target:  

Bacterial

Research Areas:  

Infection

PP13 is an antimicrobial peptide, and is active against Gram-negative and Gram-positive bacteria E.coli (MIC: 16.7 uM), B. subtilis (MIC: 13.3 uM), S. aureus (MIC: 23.3 uM), S. lutea (MIC: 8.0 uM), and B. pumilu (MIC: 9.0 uM) .
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Cat. No.: HY-165154
CAS No.: 35663-85-5
Synonyms: Desdanine; Pyracrimycin A
Cyclamidomycin (Desdanine) is an acrylamide antibiotic with antibacterial activity. Cyclamidomycin inhibits nucleoside diphosphate kinase and pyruvate kinase (in E. coli) and oxidative phosphorylation in rat liver mitochondria. Cyclamidomycin is active against S. aureus, M. flavus, S. lutea, B. subtilis, E. coli, S. flexneri, S. typhosa, P. vulgaris, and K. pneumoniae (MICs=3.12-25 mg/ml) .
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Cat. No.: HY-127020
CAS No.: 108605-51-2
Target:  

Bacterial

Research Areas:  

Infection

Deoxyenterocin is a bacterial metabolite originally isolated from Streptomyces that has diverse biological activities, including antibiotic, antiviral, and antioxidant properties. It inhibits the growth of S. lutea, S. aureus, K. pneumoniae, and V. percolans in vitro when used at a concentration of 500 μg/mL. Deoxyenterocin (50 μg/mL) inhibits the cytopathic effect of influenza A H1N1 virus by 60.6% in vitro. It also prevents hydrogen peroxide-induced decreases in glutathione (GSH) levels and in the mitochondrial membrane potential in mouse primary cortical neuronal cultures when used at a concentration of 1 μM.
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Cat. No.: HY-155330
Research Areas:  

Neurological Disease

PZ-1922 (Compound 16) is a BBB-penetrable 5-HT6R/5-HT3R antagonist (Ki: 17 nM, 0.45 nM for 5-HT6R/5-HT3R respectively). PZ-1922 reversibly inhibits MAO-B (pIC50: 8.93). PZ-1922 reverses Scopolamine (SCOP) (HY-N0296) induced memory deficits in the novel object recognition (NOR) test in rats. PZ-1922 prevents Aβ-induced memory decline in the T-maze test .
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Cat. No.: HY-155330A
CAS No.: 1648745-65-6
Research Areas:  

Neurological Disease

PZ-1922 free base is a BBB-penetrable 5-HT6R/5-HT3R antagonist (Ki: 17 nM, 0.45 nM for 5-HT6R/5-HT3R respectively). PZ-1922 free base reversibly inhibits MAO-B (pIC50: 8.93). PZ-1922 free base reverses Scopolamine (SCOP) (HY-N0296) induced memory deficits in the novel object recognition (NOR) test in rats. PZ-1922 free base prevents Aβ-induced memory decline in the T-maze test .
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Cat. No.: HY-N19634
CAS No.: 19942-05-3
Betulatriterpene C is a dammarane triterpene found in the glandular trichome exudates of Ibicella lutea .
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Cat. No.: HY-N11717
CAS No.: 352312-68-6
Bracteoside is a flavonoid glycoside found in the flowering aerial parts of Centaurea bracteata Scop. (Asteraceae) .
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Cat. No.: HY-184800
CAS No.: 38115-21-8
Research Areas:  

Infection

Desacetyl cephapirin is the active metabolite of Cephapirin (HY-A0153). Desacetyl cephapirin retains bactericidal activity by disrupting bacterial cell wall synthesis, but exhibits reduced antimicrobial activity, longer in vivo residual time, and high tissue retention. Desacetyl cephapirin can be used in studies related to Gram-positive bacterial infections .
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Cat. No.: HY-122301
CAS No.: 11031-47-3
Target:  

Drug Derivative

Sarcinaxanthin is a carotenoid present in various bacteria with antioxidant activity. Sarcinaxanthin scavenges singlet oxygen, thereby inhibiting oxidative degradation in the β-carotene/linoleic acid system. Sarcinaxanthin acts as a photoprotective agent against UVB radiation that induces erythema. Sarcinaxanthin can be applied in studies related to antioxidation and radiation resistance .
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Cat. No.: HY-182535
CAS No.: 33137-73-4
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Tuberactinomycin-O is a peptide antibiotic belonging to the tuberactinomycin family. Tuberactinomycin-O inhibits the growth of various bacteria, including Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and Mycobacterium ATCC 607. Tuberactinomycin-O exhibits acute toxicity in male mice when administered intravenously. Tuberactinomycin-O can be used in the research of tuberculosis .
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