3103 Results for "

active compound

" in MedChemExpress (MCE) Product Catalog:
Products (3103)

3103 Results for "active compound" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-N0573
CAS No.: 93-35-6
Synonyms: 7-Hydroxycoumarin; Hydrangin; NSC 19790
Umbelliferone (7-Hydroxycoumarin), a natural orally active product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent. Umbelliferone induces cell cycle arrest, apoptosis and DNA fragmentation in HepG2 cells. Umbelliferone exhibits significant anticancer effects. Umbelliferone attenuates the alteration characteristics of allergic airway inflammation. Umbelliferone displays the neuroprotective effects and cross the blood-brain barrier. Umbelliferone exhibits anti-inflammatory and antioxidant effects in chronic alcohol-fed rats .
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5
5 Cited Publications
Cat. No.: HY-N0853
CAS No.: 19885-10-0
Alisol A is an orally active tetracyclic triterpenoid compound of the prototerpane type. Alisol A can be extracted from the rhizome of Alisma orientale. Alisol A activates AMPK/ACC/SREBP-1c, SIRT1, PPARα, inhibits MMP-2/-9, decreases inflammatory cytokine expression (IL-1β, IL-6, IL-8). Alisol A has anti-tumor activity against breast cancer and colorectal cancer. Alisol A has anti-obesity and anti-atherosclerotic activities. Alisol A can be used in the research of hepatitis B, breast cancer, colorectal cancer, atherosclerosis, and obesity .
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5
5 Cited Publications
Cat. No.: HY-151527
CAS No.: 2708177-73-3
Purity:  98.64%
Research Areas:  

Neurological Disease

PI3K/Akt/CREB activator 1 (compound AE-18) is a potent, orally active PI3K/Akt/CREB activator. PI3K/Akt/CREB activator 1 promotes neuronal proliferation, induced differentiation of Neuro-2a cells into a neuron-like morphology, and accelerated the establishment of axon-dendrite polarization of primary hippocampal neurons through upregulating brain-derived neurotrophic factor via the PI3K/Akt/CREB pathway. PI3K/Akt/CREB activator 1 can be used in research of vascular dementia (VaD) .
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4
4 Cited Publications
Cat. No.: HY-147010
CAS No.: 2259624-71-8
Purity:  98.26%
Target:  

STING

Research Areas:  

Inflammation/Immunology

STING agonist-12 (Compound 53) is a potent, orally active human STING activator with an EC50 of 185 nM .
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4
4 Cited Publications
Cat. No.: HY-N0892
CAS No.: 67416-61-9
Synonyms: Acetyl-11-keto-β-boswellic acid
AKBA (Acetyl-11-keto-β-boswellic acid) is an active triterpenoid compound from the extract of Boswellia serrate and a novel Nrf2 activator.
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4
4 Cited Publications
Cat. No.: HY-N2584A
CAS No.: 521-48-2
Isoxanthohumol is an orally active flavonoid compound. Isoxanthohumol has biological activities such as anti-tumor, anti-inflammatory, antioxidant, antiviral, antifungal, and inhibition of adipogenesis. Isoxanthohumol can induce apoptosis, autophagy, and migration of tumor cells. Isoxanthohumol is active against viruses such as HSV, BVDV, CMV, and Rhino. Isoxanthohumol can be used for the research of tumors, metabolic, and inflammatory diseases .
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4
4 Cited Publications
Cat. No.: HY-161015
CAS No.: 2778330-90-6
Target:  

JAK

Research Areas:  

Inflammation/Immunology

JAK1-IN-13 (compound 36b) is an orally active, potent and highly selective inhibitor of JAK1 with an IC50 of 0.044 nM. JAK1-IN-13 significantly decreases STAT3 phosphorylation .
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4
4 Cited Publications
Cat. No.: HY-N0883
CAS No.: 465-11-2
Synonyms: Gamabufagin
Gamabufotalin (Gamabufagin), a main active compound isolated from Chinese medicine Chansu, has been shown to strongly inhibit cancer cell growth and inflammatory response. Gamabufotalin could inhibite angiogenesis by inhibiting the activation of VEGFR-2 signaling pathways.
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4
4 Cited Publications
Cat. No.: HY-12820
CAS No.: 1616113-45-1
Purity:  99.70%
Synonyms: Antibiotic-202
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Sibofimloc (Antibiotic-202) is a first-in-class, gut-restricted, orally active FimH adhesion inhibitor extracted from patent WO2014100158A1, Compound Example 202. Sibofimloc has anti-bacterial infective activity. Sibofimloc is developed for inflammatory bowel disease (IBD) .
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4
4 Cited Publications
Cat. No.: HY-130254
CAS No.: 2380027-49-4
Purity:  98.04%
Target:  

Src

Research Areas:  

Inflammation/Immunology Cancer

CSK-IN-1 (compound 13) is a potent, orally active c-terminal Src kinase (CSK) with IC50 values below 3 nM and 4 nM in CSK HTRF and Caliper assay, respectively. CSK-IN-1 shows the ability to increase T cell proliferation induced by T cell receptor signaling .
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4
4 Cited Publications
Cat. No.: HY-133017
CAS No.: 2114339-57-8
Purity:  99.79%
Synonyms: SAR439859
Target:  

Estrogen Receptor/ERR

Research Areas:  

Cancer

SAR439859 (compound 43d) is an orally active, non-steroidal, and selective estrogen receptor degrader (SERD). SAR439859 is an effective ER antagonist with ER degradation activity, an EC50 of 0.2 nM. SAR439859 can show potent anti-tumor effects and limited cross-resistance in ER + breast cancer.
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4
4 Cited Publications
Cat. No.: HY-10322
CAS No.: 196612-93-8
Purity:  99.41%
Synonyms: BIBX 1382
Target:  

EGFR

Research Areas:  

Cancer

Falnidamol (BIBX 1382) is an orally active, selective EGFR tyrosine kinase inhibitor with an IC50 of 3 nM. Falnidamol displays > 1000-fold lower potency against ErbB2 (IC50=3.4 μM) and a range of other related tyrosine kinases (IC50>10 μM). Falnidamol is a pyrimido-pyrimidine compound and has anti-cancer activity .
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4
4 Cited Publications
Cat. No.: HY-151427
CAS No.: 2348795-14-0
Purity:  99.47%
Target:  

TGF-β Receptor

Research Areas:  

Inflammation/Immunology

TGFβ1-IN-1 (compound 42) is a potent, orally active TGF-β1 inhibitor. TGFβ1-IN-1 inhibits the upregulation of TGF-β1-induced fibrosis markers (α-SMA and fibronectin) and can be used in liver fibrosis disease studies .
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4
4 Cited Publications
Cat. No.: HY-N0126
CAS No.: 90-47-1
Xanthone is a monoamine oxidase A (MAO-A) inhibitor with an IC50 of 0.84 µM. Xanthon inhibits Norepinephrine (HY-13715) and high-K +-induced vasoconstriction with IC50 values of 60.26 μM and 82.9 μM, respectively. Xanthon increases intracellular cyclic adenosine 3′,5′-monophosphate (cAMP) content and blocks Ca 2+ channels. Xanthone is the scaffold of several pharmacologically active compounds .
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3
3 Cited Publications
Cat. No.: HY-N0661
CAS No.: 556-27-4
Alliin, an orally active sulfoxide compound that can be isolated from garlic, exhibits hypoglycemic, antioxidant, anti-inflammatory and antitumor activities .
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3
3 Cited Publications
Cat. No.: HY-N8253
CAS No.: 20229-56-5
Synonyms: Quercetin 4′-O-glucoside
Spiraeoside, an orally active natural compound, exerts antioxidant activity, inhibits reactive oxygen species (ROS) and malondialdehyde production. Spiraeoside possesses antiallergic, anti-inflammatory and antitumor activities .
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3
3 Cited Publications
Cat. No.: HY-101509
CAS No.: 2095156-13-9
Purity:  99.65%
Target:  

Lipase

Research Areas:  

Metabolic Disease

HSL-IN-1 (compound 24b) is a potent and orally active hormone sensitive lipase (HSL) inhibitor (IC50=2 nM) with a significantly reduced reactive metabolite liability .
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3
3 Cited Publications
Cat. No.: HY-112185
CAS No.: 2212020-52-3
Purity:  99.80%
Synonyms: LY3502970; GLP-1 receptor agonist 1
Target:  

GCGR

Orforglipron (LY3502970) (Compound 67) is an orally active agonist for Glucagon-like peptide-1 receptor (GLP-1R), which exhibits potency in ameliorates the type 2 diabete .
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3
3 Cited Publications
Cat. No.: HY-133122
CAS No.: 1515888-53-5
Purity:  98.38%
Target:  

TNF Receptor

Research Areas:  

Inflammation/Immunology Cancer

UCB-9260, an orally active compound, inhibits TNF signaling by stabilising an asymmetric form of the trimer. UCB-9260 is selective for TNF over other superfamily members, and binds TNF with a similar Kd of 13 nM .
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3
3 Cited Publications
Cat. No.: HY-111278
CAS No.: 85-66-5
Purity:  99.23%
Synonyms: Pyocyanine; Sanazin; Sanasin
Pyocyanin (Pyocyanine) is a toxic, quorum sensing (QS) controlled metabolite produced by Pseudomonas aeruginosa. Pyocyanin is a REDOX active compound that promotes the production of reactive oxygen species (ROS). Pyocyanin has antibacterial and anti-inflammatory activity .
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