670 Results for "

Miconia albicans (Sw.) Steud.

" in MedChemExpress (MCE) Product Catalog:
Products (670)

670 Results for "Miconia albicans (Sw.) Steud." in MCE Product Catalog:

31
31 Publications Verification
Cat. No.: HY-P80137
Synonyms: GAPDH; GAPD; CDABP0047; OK/SW-cl.12; Glyceraldehyde-3-phosphate dehydrogenase; Peptidyl-cysteine S-nitrosylase GAPDH

Host:  

Rabbit

Application:  

WB, ICC/IF, IHC-P, FC, IP

Reactivity:  

Human, Mouse, Rat, Chicken

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21
21 Cited Publications
Cat. No.: HY-B0101
CAS No.: 86386-73-4
Synonyms: UK-49858
Domaines de recherche:  

Infection Cancer

Fluconazole (UK-49858) is a triazole antifungal agent with excellent activities against a broad range of fungi, especially against Candida albicans. Fluconazole inhibits C. albicans and Candida kefyr with IC99s range from 0.20 μg/mL to 0.39 μg/mL .
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10
10 Cited Publications
Cat. No.: HY-109049
CAS No.: 1467093-03-3
Pureté:  98.85%
Synonyms: SM04690; Lorecivivint
Target:  

Wnt

Domaines de recherche:  

Inflammation/Immunology Cancer

Adavivint (SM04690; Lorecivivint) is a potent and selective inhibitor of canonical Wnt signaling, with an EC50 of 19.5 nM via a high-throughput TCF/LEF-reporter assay in SW480 colon cancer cells .
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10
10 Cited Publications
Cat. No.: HY-P80670
Synonyms: FTH1; FTH; FTHL6; OK/SW-cl.84; PIG15; Ferritin heavy chain; Ferritin H subunit; Cell proliferation-inducing gene 15 protein

Host:  

Rabbit

Application:  

WB, ICC/IF

Reactivity:  

Human, Mouse, Rat, Hamster

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7
7 Cited Publications
Cat. No.: HY-16968
CAS No.: 459147-39-8
Target:  

15-PGDH

Domaines de recherche:  

Others

SW033291 is a potent and high-affinity inhibitor of 15-PGDH with a Ki of 0.1 nM. SW033291 increases prostaglandin PGE2 levels in bone marrow and other tissues. SW033291 also promotes tissue regeneration .
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7
7 Cited Publications
Cat. No.: HY-12032
CAS No.: 328543-09-5
Pureté:  99.44%
Target:  

PARP

Domaines de recherche:  

Cancer

AG14361 is a potent PARP-1 inhibitor, with a Ki of < 5 nM, and in permeabilized SW620 and intact SW620 cells, the IC50s are 29 nM and 14 nM, respectively.
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5
5 Cited Publications
Cat. No.: HY-115475
CAS No.: 2126744-35-0
Pureté:  99.93%
Target:  

HDAC

Domaines de recherche:  

Neurological Disease

SW-100, a selective histone deacetylase 6 (HDAC6) inhibitor with an IC50 of 2.3 nM, shows at least 1000-fold selectivity for HDAC6 relative to all other HDAC isozymes. SW-100 displays a significantly improved ability to cross the blood-brain-barrier .
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5
5 Cited Publications
Cat. No.: HY-B0919
CAS No.: 115-02-6
Synonyms: CI-337; O-Diazoacetyl-L-serine; P-165
Domaines de recherche:  

Infection Cancer

Azazerine (CI-337) is a competitive inhibitor of glutamine amidotransferase. Azaserine is an antibiotic, it shows antibacterial activities. Azazerine shows anti-tumor activities and it may also act as a tumor inducer. Azazerine can be used for the research of cancer and infection .
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5
5 Cited Publications
Cat. No.: HY-N2389
CAS No.: 50773-42-7
Formosanin C is a diosgenin saponin with multiple biological activities. Formosanin C possesses multiple anti-tumor mechanisms, including inducing apoptosis and autophagy, blocking the cell cycle, inhibiting metastasis and inducing ferroptosis. Formosanin C can inhibit the NF-κB signaling pathway to exert anti-inflammatory effects, and enhance the activity of immune cells. Formosanin C exhibits the inhibiting effect against C. albicans. Formosanin C can be used for the study of anti-inflammation, antifungal anti and anti-cancer (including lung cancer, liver cancer, breast cancer and colorectal cancer, etc.) .
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3
3 Cited Publications
Cat. No.: HY-19593
CAS No.: 59456-70-1
Target:  

Fungal

Domaines de recherche:  

Infection

Nikkomycin Z is a nucleoside peptide and an orally active antifungal agent. Nikkomycin Z inhibits chitin synthesis by acting as a competitive analogue of the chitin synthase substrate UDP-N-acetylglucosamine. Nikkomycin Z has antifungal activity .
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3
3 Cited Publications
Cat. No.: HY-P80487
Synonyms: TUBB5, OK/SW-cl.56, TUBB, Tubulin beta chain, Tubulin beta-5 chain

Host:  

Rabbit

Application:  

WB, ICC/IF, IHC-P, FC

Reactivity:  

Human, Mouse, Rat

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3
3 Cited Publications
Cat. No.: HY-P80954A
Synonyms: GAPDH; GAPD; CDABP0047; OK/SW-cl.12; Glyceraldehyde-3-phosphate dehydrogenase; Peptidyl-cysteine S-nitrosylase GAPDH

Host:  

Mouse

Application:  

WB, ELISA

Reactivity:  

Human, Mouse, Rat

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3
3 Cited Publications
Cat. No.: HY-B0852
CAS No.: 107534-96-3
Domaines de recherche:  

Infection

Tebuconazole is an orally active agricultural azole fungicide which can also inhibit CYP51 with IC50s of 0.9 and 1.3 μM for Candida albicans CYP51 (CaCYP51) and truncated Homo sapiens CYP51 (Δ60HsCYP51), respectively. Tebuconazole induces lipid accumulation and oxidative stress in HepG2 Cells. Tebuconazole decreases MAC-T cells viability and proliferation, induces ER-stress-mediated apoptosis and increases oxidative stress levels in MAC-T cells .
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3
3 Cited Publications
Cat. No.: HY-114495
CAS No.: 21802-37-9
Pureté:  ≥98.0%
Synonyms: Cerulomycin; Caerulomycin
Caerulomycin A is an orally active immunomodulator and antimicrobial agent. Caerulomycin A targets Smad3, STAT1 and GATA-3. Caerulomycin A downregulates GATA-3 expression, inhibits Th2 cell differentiation and Th2 cytokine production, reduces IgE levels, and alleviates pulmonary inflammatory responses and eosinophil infiltration. Caerulomycin A ameliorates collagen-induced arthritis symptoms, reduces joint inflammation and synovitis, and decreases the levels of proinflammatory cytokines in joints. Caerulomycin A inhibits the growth of some filamentous fungi, yeasts and specific bacteria. Caerulomycin A can be used in research related to arthritis and asthma .
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2
2 Cited Publications
Cat. No.: HY-A0148A
CAS No.: 36167-63-2
Synonyms: SKF-102886; WR-171669 hydrochloride
Halofantrine hydrochloride (SKF-102886 hydrochloride; WR-171669 hydrochloride) is a blocker that delays the delayed rectifier potassium current by inhibiting human ERG channels, and it is a potent antimalarial agent with oral activity. Halofantrine hydrochloride inhibits the Cap1-dependent oxidative stress response of Candida albicans, suppresses ROS responses, and enhances the antifungal (Fungal) activity of oxidative damage agents. Halofantrine hydrochloride exhibits antifungal activity in the Galleria mellonella model, and shows antimalarial activity against Plasmodium strains both in vitro and in animal models. Halofantrine hydrochloride can be used in studies related to invasive candidiasis, falciparum malaria, and vivax malaria .
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2
2 Cited Publications
Cat. No.: HY-Y0248A
CAS No.: 4602-84-0
Farnesol is a sesquiterpene alcohol that modulates cell-to-cell communication in Candida albicans, and has the activity in inhibiting bacteria.
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2
2 Cited Publications
Cat. No.: HY-W895978
CAS No.: 27523-40-6
Target:  

Fungal

Domaines de recherche:  

Infection

Isoconazole is an antifungal agent against Candida albicans. Isoconazole is a broad-spectrum antimicrobial azole that can be studied in research on dermatomycoses .
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2
2 Cited Publications
Cat. No.: HY-129523
CAS No.: 2378258-52-5
Pureté:  95.66%
Target:  

PROTACs Ras

Domaines de recherche:  

Cancer

PROTAC K-Ras Degrader-1 (Compound 518) is a PROTAC. PROTAC K-Ras Degrader-1 can effectively degrades K-Ras based on Cereblon E3 ligand, exhibits ≥70% degradation efficacy in SW1573 cells .
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2
2 Cited Publications
Cat. No.: HY-N6647
CAS No.: 20633-84-5
Luteolin-7-rutinoside has both anti-arthritic and antifungal activities, can result in a combination therapy for the treatment of fungal arthritis due to C. albicans infection.
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2
2 Cited Publications
Cat. No.: HY-B0293A
CAS No.: 64872-76-0
Target:  

Fungal

Domaines de recherche:  

Infection

Butoconazole, an imidazole antifungal agent, is active against Candida spp. and effective against vaginal infections due to Candida albicans. Butoconazole is presumed to function as other imidazole derivatives via inhibition of steroid synthesis .
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