3110 Results for "

active compound

" in MedChemExpress (MCE) Product Catalog:
Products (3110)

3110 Results for "active compound" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-N0526
CAS No.: 53209-27-1
2''-O-Galloylhyperin is an active natural compound with anti‑inflammatory, antioxidant, anti‑adipogenic, antifibrotic, and cytostatic activities. 2''-O-Galloylhyperin upregulates SIRT1/Nrf2 signaling, inhibits NF-κB and MAPK (ERK1/2, p38, JNK) phosphorylation, suppresses TSHR activation, reduces ROS accumulation, and enhances SOD and GSH-Px activities. 2''-O-Galloylhyperin protects against LPS-induced tissue injury, enhances survival, and inhibits adipogenesis and fibrosis. 2"-O-Galloylhyperin can be used for the research of sepsis, acute lung injury, and thyroid eye disease .
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2
2 Cited Publications
Cat. No.: HY-N10549
CAS No.: 83088-28-2
Gigantol is an orally active bibenzyl compound. Gigantol targets MYC to promote its ubiquitin-proteasomal degradation and inhibit the growth of lung cancer cells. Gigantol exerts anti-lung cancer activity by inducing ferroptosis (Ferroptosis) via the SLC7A11-GPX4 axis. Gigantol restores the sensitivity of mcr-harboring multidrug-resistant bacteria to colistin. Gigantol ameliorates carbon tetrachloride-induced liver injury by inhibiting the activation of the JNK/cPLA2/12-LOX inflammatory pathway. Gigantol promotes cholesterol metabolism and progesterone biosynthesis in Leydig cells. Gigantol can be used in studies related to diseases such as lung cancer, multidrug-resistant Gram-negative bacterial infections, and acute liver injury .
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1 Cited Publications
Cat. No.: HY-148263
Purity:  ≥98.0%
Target:  

Fluorescent Dye

Research Areas:  

Cancer

Biotin-PEG2000-Thiol is an active compound. Biotin-PEG2000-Thiol is pegylated by binding to streptavidin or antibiotin with high affinity and specificity. Biotin-PEG2000-Thiol can modify biomolecules, proteins, peptides and other small molecule materials. Biotin-PEG2000-Thiol is widely used in the research of agent release and nano new materials .
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1 Cited Publications
Cat. No.: HY-N6988
CAS No.: 3779-59-7
Cimigenol is an active compound isolated from Cimicifuga, with potent anti-tumor activity .
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1 Cited Publications
Cat. No.: HY-19764
CAS No.: 1423186-80-4
Target:  

RIP kinase

Research Areas:  

Cancer

GSK2983559 active metabolite is an active metabolite of GSK2983559. GSK2983559 active metabolite is a receptor interacting protein-2 (RIP2) kinase inhibitor extracted from patent WO/2014043446 A1, compound example 1.
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1 Cited Publications
Cat. No.: HY-32681
CAS No.: 1573-91-7
Target:  

Drug Intermediate

Research Areas:  

Others

4-Hydroxy-2-naphthoic acid is a drug intermediate for synthesis of various active compounds.
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1 Cited Publications
Cat. No.: HY-59243
CAS No.: 86-98-6
4,7-Dichloroquinoline is a dichloro-substituted quinoline that can be used for the synthesis of other active compounds .
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1 Cited Publications
Cat. No.: HY-N8651
CAS No.: 86383-39-3
Target:  

Drug Intermediate

Research Areas:  

Others

2'-Hydroxy-3,4-dimethoxydihydrochalcone is a drug intermediate for synthesis of various active compounds.
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1 Cited Publications
Cat. No.: HY-B1442
CAS No.: 99-15-0
Synonyms: N-Acetyl-DL-leucine
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

Acetylleucine (N-Acetyl-DL-leucine), orally active compound, can be used for the research of acute vestibular vertigo, cerebellar ataxia and nystagmus .
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1 Cited Publications
Cat. No.: HY-137573
CAS No.: 1706738-98-8
Purity:  99.74%
Synonyms: CC-90010
Research Areas:  

Cancer

CC-90010 (compound 1) is a reversible and orally active BET inhibitor. CC-90010 is applied in the study for advanced solid tumors .
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1 Cited Publications
Cat. No.: HY-N2518
CAS No.: 11027-63-7
Synonyms: Agnoside
Agnuside is used in the study of asthma, inflammation, and angiogenic diseases. Agnuside is an orally active compound that can be extracted from Vitex negundo .
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1 Cited Publications
Cat. No.: HY-N2543
CAS No.: 23696-85-7
Synonyms: (E/Z)-Damascenone
Damascenone ((E/Z)-Damascenone) is an active compound of Epipremnum pinnatum with anti-inflammatory activity . Damascenone is a mixture complex of E-isomer-Damascenone and Z-isomer Damascenone.
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1 Cited Publications
Cat. No.: HY-U00076
CAS No.: 862309-06-6
Target:  

Histamine Receptor

Research Areas:  

Neurological Disease Endocrinology

MK-0249 (Compound 1) is a potent, selective and orally active histamine H3 receptor antagonist, with an IC50 of 1.7 nM for human H3 .
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1 Cited Publications
Cat. No.: HY-109081
CAS No.: 1141397-80-9
Purity:  ≥98.0%
Synonyms: E7727
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Cedazuridine (E7727) (Compound 7a) is an orally active cytidine deaminase (CDA) inhibitor with an IC50 value of 0.4 μM. Cedazuridine can be used for cancer research .
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1 Cited Publications
Cat. No.: HY-41514
CAS No.: 1627924-19-9
Target:  

Drug Intermediate

Research Areas:  

Others

3-Iodo-1-tetrahydropyran-2-yl-pyrazole-4-carbaldehyde is a drug intermediate for synthesis of various active compounds.
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1 Cited Publications
Cat. No.: HY-I0198
CAS No.: 385425-15-0
Synonyms: 1-(4-Iodophenyl)piperidin-2-one
Target:  

Drug Intermediate

Research Areas:  

Others

1-(4-Iodophenyl)-2-piperidinone (1-(4-Iodophenyl)piperidin-2-one) is a drug intermediate for synthesis of various active compounds.
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1 Cited Publications
Cat. No.: HY-W002011
CAS No.: 93-10-7
Quinoline-2-carboxylic acid exhibits antidiabetic activity. Quinoline-2-carboxylic acid can be used as drug intermediate for synthesis of various active compounds .
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1 Cited Publications
Cat. No.: HY-W105804
CAS No.: 3542-13-0
Research Areas:  

Others

Selenocystamine dihydrochloride is a selenocysteine derivative that can be used in the synthesis of other active compounds. Selenocystamine dihydrochloride can also induce the aggregation of amphiphilic p-sulfonatocalixarene to form supramolecular nanoparticles .
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1 Cited Publications
Cat. No.: HY-125748
CAS No.: 902146-11-6
Purity:  99.4%
Research Areas:  

Cardiovascular Disease

CBM-301940 (compound 5) is an orally active malonate CoA decarboxylase (MCD) inhibitor with IC50 value of 23 nM. CBM-301940 can be used in the study of cardiovascular diseases .
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1 Cited Publications
Cat. No.: HY-131338
CAS No.: 2170477-75-3
Purity:  98.13%
Target:  

ROR

Research Areas:  

Inflammation/Immunology

RORγt inverse agonist 13 (Compound 3i) is a potent, orally active and selective RORγt inverse agonist, with improved agent-like properties, with an IC50 of 63.8 nM .
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