21

21 Publications Verification

Category:

Cardiovascular Disease Anti-aging Whitening Agent Research on Agricultural Breeding Food Research Agricultural Research Microorganisms Sunscreen Terpenoids Pigments Diterpenoids Cosmetic Research Disease Research Fields

Target:

PPAR Reactive Oxygen Species (ROS) STAT NF-κB Apoptosis

Astaxanthin, the red dietary carotenoid, is an orally effective and potent antioxidant. Astaxanthin inhibits NF-κB and down-regulates VEGF in blood glucose. Astaxanthin exerts anti-cancer cell proliferation, increases apoptosis, impairs migration and invasion by activating PPARγ and reducing the expression of STAT3. Astaxanthin also has neuroprotective and anti-inflammatory activity and can be used in studies of cancer, diabetic retinopathy, cardiovascular disease, and in the coloring of animal feed .

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14

Orexin A (human, rat, mouse)

14 Cited Publications

Cat. No.: HY-106224

CAS No.: 205640-90-0

Purity: 99.93%

Synonyms: Hypocretin-1 (human, rat, mouse)

Target:

Orexin Receptor (OX Receptor)

Research Areas:

Neurological Disease

Orexin A (human, rat, mouse) (Hypocretin-1 (human, rat, mouse)), a 33 amino acid excitatory neuropeptide, orchestrates diverse central and peripheral processes. Orexin A (human, rat, mouse) binds and activates two types of G protein-coupled receptors, the orexin-1 receptor (OX1R) and the orexin-2 receptor (OX2R). Orexin A (human, rat, mouse) has a role in the regulation of feeding behavior. Orexin A (human, rat, mouse) is an effective anti-nociceptive and anti-hyperalgesic agent in mice and rats .

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14

Orexin A (human, rat, mouse) TFA

14 Cited Publications

Cat. No.: HY-106224A

Purity: 97.13%

Synonyms: Hypocretin-1 (human, rat, mouse) TFA

Target:

Orexin Receptor (OX Receptor)

Research Areas:

Neurological Disease

Orexin A (human, rat, mouse) (Hypocretin-1 (human, rat, mouse)) TFA, a 33 amino acid excitatory neuropeptide, orchestrates diverse central and peripheral processes. Orexin A (human, rat, mouse) TFA binds and activates two types of G protein-coupled receptors, the orexin-1 receptor (OX1R) and the orexin-2 receptor (OX2R). Orexin A (human, rat, mouse) TFA has a role in the regulation of feeding behavior. Orexin A (human, rat, mouse) TFA is an effective anti-nociceptive and anti-hyperalgesic agent in mice and rats .

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11

Zearalenone

11 Cited Publications

Cat. No.: HY-103447

CAS No.: 17924-92-4

Purity: 98.22%

Synonyms: Mycotoxin F2; Toxin F2

Category:

Microorganisms Ketones, Aldehydes, Acids Other Diseases Phenols Polyphenols Disease Research Fields

Target:

Estrogen Receptor/ERR

Zearalenone is a mycotoxin produced mainly by fungi belonging to the genus Fusarium in foods and feeds. Possess oestrogenic activity in pigs, cattle and sheep, with low acute toxicity. Causes precocious development of mammae and other estrogenic effects in young gilts .

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8

Setmelanotide

8 Cited Publications

Cat. No.: HY-19870

CAS No.: 920014-72-8

Synonyms: RM-493; BIM-22493; IRC-022493

Target:

Melanocortin Receptor Calmodulin AMPK

Setmelanotide (RM-493) is a blood-brain barrier-permeable, selective MC4R agonist with a K_i value of 2.1 nM for hMC4R. Setmelanotide activates the CaMKK2/AMPK signaling pathway. Setmelanotide mediates body weight homeostasis, feeding regulation and energy expenditure modulation; it reduces food intake, induces weight loss, decreases obesity severity, increases daytime activity and energy expenditure, lowers levels of leptin, triglycerides, fasting insulin and diastolic blood pressure, improves insulin sensitivity, glucose tolerance and fatty liver condition, and reverses respiratory depression. Setmelanotide is applicable to research related to obesity, hyperinsulinemia, fatty liver and respiratory depression .

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8

Setmelanotide monoacetate

8 Cited Publications

Cat. No.: HY-19870C

CAS No.: 2759937-80-7

Synonyms: RM-493 monoacetate; BIM-22493 monoacetate; IRC-022493 monoacetate

Target:

Melanocortin Receptor Calmodulin AMPK

Research Areas:

Cardiovascular Disease Metabolic Disease Inflammation/Immunology

Setmelanotide monoacetate (RM-493 monoacetate) is a blood-brain barrier-permeable, selective MC4R agonist with a K_i value of 2.1 nM for hMC4R. Setmelanotide monoacetate activates the CaMKK2/AMPK signaling pathway. Setmelanotide monoacetate mediates body weight homeostasis, feeding regulation and energy expenditure modulation; it reduces food intake, induces weight loss, decreases obesity severity, increases daytime activity and energy expenditure, lowers levels of leptin, triglycerides, fasting insulin and diastolic blood pressure, improves insulin sensitivity, glucose tolerance and fatty liver condition, and reverses respiratory depression. Setmelanotide monoacetate is applicable to research related to obesity, hyperinsulinemia, fatty liver and respiratory depression .

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8

Clorgyline

8 Cited Publications

Cat. No.: HY-14197

CAS No.: 17780-72-2

Purity: 99.76%

Synonyms: M&B 9302

Target:

Monoamine Oxidase 5-HT Receptor Bcl-2 Family

Research Areas:

Neurological Disease Metabolic Disease Cancer

Clorgyline (M&B 9302) is a selective, irreversible monoamine oxidase A (MAO-A) inhibitor that can cross the blood-brain barrier and exhibits activity against the 5-HT Receptor at very high doses. Clorgyline regulates monoamine neurotransmitter levels, the release of dopamine and acetylcholine, the uptake and effects of Tyramine (HY-W007606), noradrenergic function, circadian locomotor activity rhythms, feeding behavior, and body weight. Clorgyline induces tumor-suppressive transcriptional programs, secretory differentiation, androgen signaling regulation, Bcl-2 expression, and radioprotective effects in non-malignant cells. Clorgyline is used in the research of high-grade prostate cancer, Huntington's disease, major affective disorder, radiation-induced normal tissue toxicity, and obesity .

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8

Clorgyline hydrochloride

8 Cited Publications

Cat. No.: HY-14197A

CAS No.: 17780-75-5

Purity: 99.92%

Synonyms: M&B 9302 hydrochloride

Target:

Monoamine Oxidase 5-HT Receptor Bcl-2 Family

Clorgyline hydrochloride (M&B 9302 hydrochloride) is a selective, irreversible monoamine oxidase A (MAO-A) inhibitor that can cross the blood-brain barrier and exhibits activity against the 5-HT Receptor at very high doses. Clorgyline hydrochloride regulates monoamine neurotransmitter levels, the release of dopamine and acetylcholine, the uptake and effects of Tyramine (HY-W007606), noradrenergic function, circadian locomotor activity rhythms, feeding behavior, and body weight. Clorgyline hydrochloride induces tumor-suppressive transcriptional programs, secretory differentiation, androgen signaling regulation, Bcl-2 expression, and radioprotective effects in non-malignant cells. Clorgyline hydrochloride is used in the research of high-grade prostate cancer, Huntington's disease, major affective disorder, radiation-induced normal tissue toxicity, and obesity .

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5

DO34

5 Cited Publications

Cat. No.: HY-117771

CAS No.: 1848233-58-8

Purity: 99.30%

Target:

DAGL

Research Areas:

Neurological Disease Metabolic Disease

DO34 is a selective DAGL inhibitor, with an IC₅₀ of 6 nM for DAGLα conversion of SAG to 2-AG. DO34 blocks de novo 2-AG synthesis, and suppresses tonic CB₁ receptor activation. DO34 blocks depolarization-induced suppression of excitation and inhibition in the cerebellum and hippocampus. DO34 regulates feeding behavior and locomotor activity in mice. DO34 abolishes AM251-mediated enhancement of parallel fiber-evoked excitatory postsynaptic currents in cerebellar slices from MAGL global knockout mice. DO34 can be used for the research of energy balance disorder and neuroinflammation .

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4

Lasalocid

4 Cited Publications

Cat. No.: HY-B1071

CAS No.: 25999-31-9

Synonyms: Lasalocid-A; Ionophore X-537A; Antibiotic X-537A

Category:

Microorganisms Monophenols Ketones, Aldehydes, Acids Phenols Disease Research Fields Cancer

Target:

Antibiotic Bacterial Autophagy Parasite Apoptosis

Lasalocid (Lasalocid-A) is an antibacterial and anticoccidial agent that can be used as feed additives. Lasalocid exhibits antitumor activity. Lasalocid is orally active .

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4

Lasalocid sodium

4 Cited Publications

Cat. No.: HY-B1071A

CAS No.: 25999-20-6

Synonyms: Lasalocid-A sodium; Ionophore X-537A sodium; Antibiotic X-537A sodium

Category:

Infection Microorganisms Monophenols Ketones, Aldehydes, Acids Phenols Disease Research Fields

Target:

Antibiotic Bacterial Autophagy Parasite Apoptosis

Lasalocid sodium (Lasalocid sodium-A) is an antibacterial and anticoccidial agent that can be used as feed additives. Lasalocid sodium exhibits antitumor activity. Lasalocid sodium is orally active .

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