10259 Results for "

from

" in MedChemExpress (MCE) Product Catalog:
Products (10259)

10259 Results for "from" in MCE Product Catalog:

22
22 Cited Publications
Cat. No.: HY-14538A
CAS No.: 1511-16-6
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease Cancer

Haloperidol hydrochloride is a potent dopamine D2 receptor antagonist, widely used as an antipsychotic agent. Haloperidol hydrochloride can be used in the study of schizophrenia, tics in Tourette syndrome, mania in bipolar disorder, delirium, agitation, acute psychosis, and hallucinations from alcohol withdrawal.
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22
22 Cited Publications
Cat. No.: HY-16261
CAS No.: 1361644-26-9
Synonyms: INNO-206; DOXO-EMCH
Research Areas:  

Cancer

Aldoxorubicin (INNO-206) is an albumin-binding proagent of Doxorubicin (DNA topoisomerase II inhibitor), which is released from albumin under acidic conditions. Aldoxorubicin (INNO-206) has potent antitumor activities in various cancer cell lines and in murine tumor models.
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21
21 Cited Publications
Cat. No.: HY-K1060

MCE Mitochondria Isolation Kit for Cultured Cells enables the fast and efficient isolation of intact mitochondria from cells using differential centrifugation.


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21
21 Cited Publications
Cat. No.: HY-N0776
CAS No.: 480-19-3
Synonyms: 3'-Methylquercetin
Isorhamnetin is a flavonoid compound extracted from the Chinese herb Hippophae rhamnoides L.. Isorhamnetin suppresses skin cancer through direct inhibition of MEK1 and PI3K.
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21
21 Cited Publications
Cat. No.: HY-K6001

MCE Basement Membrane Matrix (Phenol Red) is primarily composed of a natural basement membrane matrix derived from mouse tumors. This product is mainly for studies of tumor invasion, angiogenesis, and organoid culture.

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21
21 Cited Publications
Cat. No.: HY-N0020
CAS No.: 82854-37-3
Echinacoside, one of the phenylethanoids isolated from the stems of Cistanche deserticola, effectively inhibits Wnt/β-catenin signaling. Echinacoside elicits neuroprotection by activating Trk receptors and their downstream signal pathways. Antiosteoporotic activity .
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21
21 Cited Publications
Cat. No.: HY-B0101
CAS No.: 86386-73-4
Synonyms: UK-49858
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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20
20 Cited Publications
Cat. No.: HY-N0114
CAS No.: 518-17-2
Synonyms: (+)-Evodiamine; d-Evodiamine
Evodiamine is an alkaloid isolated from the fruit of Evodia rutaecarpa Bentham with diverse biological activities including anti-inflammatory, anti-obesity, and antitumor.
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20
20 Cited Publications
Cat. No.: HY-N0009
CAS No.: 24512-63-8
Geniposide is an iridoid glucoside extracted from Gardenia jasminoidesEllis fruits; exhibits a varity of biological activities such as anti-diabetic, antioxidative, antiproliferative and neuroprotective activities.
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20
20 Cited Publications
Cat. No.: HY-15515
CAS No.: 223104-29-8
Purity:  99.95%
Target:  

Na+/Ca2+ Exchanger

Research Areas:  

Cardiovascular Disease

SEA0400 is a novel and selective inhibitor of the Na +-Ca 2+ exchanger (NCX), inhibiting Na +-dependent Ca 2+ uptake in cultured neurons, astrocytes, and microglia with IC50s of from 5 to 33 nM.
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20
20 Cited Publications
Cat. No.: HY-12048
CAS No.: 3895-92-9
Purity:  99.11%
Chelerythrine chloride is a potent, cell-permeable inhibitor of protein kinase C, with an IC50 of 660 nM. Chelerythrine chloride inhibits the Bcl-XL-Bak BH3 peptide binding with IC50 of 1.5 μM and displaces Bax from Bcl-XL. Chelerythrine chloride induces apoptosis and autophagy.
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19
19 Cited Publications
Cat. No.: HY-P0216
CAS No.: 159432-28-7
A 779 is a specific antagonist of G-protein coupled receptor (Mas receptor), which is an Ang1-7 receptor distinct from the classical AngII.
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19
19 Cited Publications
Cat. No.: HY-N0439
CAS No.: 16830-15-2
Asiaticoside, a trisaccaride triterpene from Centella asiatica, suppresses TGF-β/Smad signaling through inducing Smad7 and inhibiting TGF-βRI and TGF-βRII in keloid fibroblasts; Asiaticoside shows antioxidant, anti-inflammatory, and anti-ulcer properties.
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19
19 Cited Publications
Cat. No.: HY-R04602
Target:  

MicroRNA

Research Areas:  

Cancer

MicroRNA Mimic Negative Control is a miRNA mimic of 21-nucleotides, and can be used as a negative control. The sequence of MicroRNA Mimic Negative Control is derived from cel-mir-239b. It has minimal sequence identity with miRNAs in human, mouse, and rat.
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18
18 Cited Publications
Cat. No.: HY-N0011
CAS No.: 113558-15-9
Synonyms: Icariin-II; Icariside-II
Baohuoside I, a flavonoid isolated from Epimedium koreanum Nakai, acts as an inhibitor of CXCR4, downregulates CXCR4 expression, induces apoptosis and shows anti-tumor activity.
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18
18 Cited Publications
Cat. No.: HY-112218
CAS No.: 1799631-75-6
Purity:  99.11%
Synonyms: S-64315
Target:  

Bcl-2 Family

Research Areas:  

Cancer

MIK665 (S-64315), derived from S63845, is a myeloid cell leukemia sequence 1 (MCL1) inhibitor . MIK665 has an IC50 of 1.81 nM for MCL1 .
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18
18 Cited Publications
Cat. No.: HY-N0144
CAS No.: 94-62-2
Synonyms: Bioperine; 1-Piperoylpiperidine
Piperine is an alkaloid, can be isolated from pepper. Piperine can inhibit the activity of P-glycoprotein and CYP3A4. Piperine inhibits HeLa cells with an IC50 of 61.94±0.054 μg/mL .
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17
17 Cited Publications
Cat. No.: HY-19332
CAS No.: 109944-15-2
Synonyms: FR-900494
Kifunensine, a potent and selective inhibitor of class I α-mannosidases isolated from Actinomycete, prevents α-mannosidases I from trimming mannose residues on glycoproteins. Kifunensine inhibits ERAD .
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17
17 Cited Publications
Cat. No.: HY-K1002

MCE NP-40 Lysis Buffer is a relatively mild reliable buffers used to lyse cells from animal, plant tissue and fungi, bacteria etc.

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17
17 Cited Publications
Cat. No.: HY-B0639
CAS No.: 20537-88-6
Synonyms: WR2721
Research Areas:  

Cancer

Amifostine (WR2721) is a broad-spectrum cytoprotective agent and a radioprotector. Amifostine selectively protects normal tissues from damage caused by radiation and chemotherapy. Amifostine is potent hypoxia-inducible factor-α1 (HIF-α1) and p53 inducer. Amifostine protects cells from damage by scavenging oxygen-derived free radicals. Amifostine reduces renal toxicity and has antiangiogenic action .
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