123 Results for "

LH

" in MedChemExpress (MCE) Product Catalog:
Products (123)

123 Results for "LH" in MCE Product Catalog:

12
12 Publications Verification
Cat. No.: HY-110258
CAS No.: 1432500-66-7
Purity:  ≥99.0%
Synonyms: LH601A
Research Areas:  

Cancer

ML334 is a potent, cell permeable activator of NRF2 by inhibition of Keap1-NRF2 protein-protein interaction. ML334 binds to Keap1 Kelch domain with a Kd of 1 μM. ML334 stimulates NRF2 expression and nuclear translocation and induces antioxidant response elements (ARE) activity .
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4
4 Cited Publications
Cat. No.: HY-P2161B
Target:  

Kisspeptin Receptor

Research Areas:  

Cancer

TAK-683 acetate is a potent full KISS1 receptor (KISS1R) agonist (IC50=170 pM) with improved metabolic stability. TAK-683 acetate is a nonapeptide metastin analog, exhibits agonistic activities to KISS1R with EC50 values of 0.96 nM and 1.6 nM for human and rat, respectively . TAK-683 acetate depletes GnRH in the hypothalamus and reduces plasma FSH, LH, and testosterone levels in vivo, it has the potential for the study of hormone-dependent prostate cancer .
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3
3 Cited Publications
Cat. No.: HY-P2293
CAS No.: 39341-83-8
Target:  

Endogenous Metabolite

Research Areas:  

Endocrinology

Luteinizing hormone (human), a heterodimeric glycoprotein hormone produced by the pituitary gland (LH), plays key roles in human reproduction .
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3
3 Cited Publications
Cat. No.: HY-P1022
CAS No.: 374683-24-6
Synonyms: Metastin(human)
Target:  

GnRH Receptor

Research Areas:  

Endocrinology Cancer

Kisspeptin-54(human) (Metastin(human)) is an endogenous ligand for kisspeptin receptor (KISS1, GPR54). Kisspeptin-54(human) binds to rat and human GPR54 receptors with Ki values of 1.81 nM and 1.45 nM, respectively. Kisspeptin-54(human) inhibits tumor metastasis and stimulates the secretion of gonadotropin (LH) and testosterone .
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2
2 Cited Publications
Cat. No.: HY-15704
CAS No.: 639052-78-1
Purity:  98.18%
Target:  

Casein Kinase

Research Areas:  

Cancer

LH846 is a selective inhibitor of CKIδ, with an IC50 of 290 nM, and less potently inhibits CKIα and CKIε, with IC50s of 2.5 μM and 1.3 μM, respectively.
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1
1 Cited Publications
Cat. No.: HY-18572
CAS No.: 94-75-7
Synonyms: 2,4-Dichlorophenoxyacetic acid
2,4-D (2, 4-dichlorophenoxyacetic acid) is a selective herbicide that can be used for the control of broad-leaved weeds. 2,4-D can induce apoptosis. 2,4-D inhibits DNA and protein synthesis, thereby preventing normal plant growth and development .
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1
1 Cited Publications
Cat. No.: HY-16474
CAS No.: 737789-87-6
Synonyms: TAK-385
Target:  

GnRH Receptor

Research Areas:  

Endocrinology Cancer

Relugolix (TAK-385)?is a potent, orally active, nonpeptidic gonadotropin-releasing hormone (GnRH) antagonist. Relugolix possesses high affinity and potent antagonistic activity for human receptor (binding IC50=0.33 nM) and monkey receptor (IC50=0.32 nM) compared with TAK-013 (HY-100209) . Relugolix is used for the study of sex-hormone-dependent diseases, such as including endometriosis, uterine fibroids and prostate cancer et al .
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1
1 Cited Publications
Cat. No.: HY-130248
CAS No.: 2471967-92-5
Purity:  99.93%
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

BAY-899, a chemical probe, is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 185 nM and 46nM for hLH (human LH) and rLH (rat LH), respectively. BAY-899 can reduce sex hormone levels .
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1
1 Cited Publications
Cat. No.: HY-P9939
CAS No.: 1610833-03-8
Synonyms: KRN23; N5KG1_C10_LH; UX-023

Target:  

Inhibitory Antibodies

Research Areas:  

Metabolic Disease Cancer

Burosumab (KRN23) is a humanized FGF23-neutralizing antibody. By neutralizing FGF23, Burosumab blocks its inhibitory effect on renal phosphate reabsorption, thereby increasing serum phosphate levels and improving abnormal bone mineralization. Burosumab can be used in the research of diseases such as X-linked hypophosphatemia (XLH) and osteomalacia .
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1
1 Cited Publications
Cat. No.: HY-18572A
CAS No.: 2702-72-9
Synonyms: 2,4-Dichlorophenoxyacetic acid sodium
2,4-D (2,4-Dichlorophenoxyacetate) sodium is a selective herbicide that can be used for the control of broad-leaved weeds. 2,4-D sodium salt can induce apoptosis. 2,4-D sodium salt inhibits DNA and protein synthesis, thereby preventing normal plant growth and development .
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1
1 Cited Publications
Cat. No.: HY-121827
CAS No.: 611207-11-5
Purity:  99.83%
Target:  

Cannabinoid Receptor

Research Areas:  

Metabolic Disease

LH-21 is a potent in vivo neutral cannabinoid CB1 receptor antagonist. LH-21 reduces food intake and body weight gain in obese Zucker rats. , and displays efficacy as a feeding inhibitor .
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1
1 Cited Publications
Cat. No.: HY-N2787
CAS No.: 53846-50-7
8-Prenylnaringenin is an orally active prenyl flavonoid. 8-Prenylnaringenin can be isolated from the hop spike Humulus lupulus. 8-Prenylnaringenin activates the PI3K/Akt pathway and the AMPK pathway, upregulates OXPHOS complexes (II, III, and V) and Sirt1, and reduces ROS production and SOD activity. 8-Prenylnaringenin improves muscle atrophy and obesity and inhibits angiogenesis. 8-Prenylnaringenin exhibits anticancer activity against glioblastoma and colon cancer. 8-Prenylnaringenin also has LH/FSH regulatory activity. 8-prenylnaringenin may be used in bone health research .
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Cat. No.: HY-W011100
CAS No.: 2624-43-3
Cyclofenil is a selective estrogen receptor modulator and an ovulation-inducing agent. Cyclofenil shows an inhibitory effect on dengue virus replication in Vero cells with an EC50 of 1.62 μM. Cyclofenil has anti-dengue-virus activity .
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Cat. No.: HY-P3668
CAS No.: 52671-12-2
Target:  

GnRH Receptor

Research Areas:  

Endocrinology Cancer

[D-Lys6]-LH-RH is a Luteinizing-hormone-releasing hormone (LHRH) analogue. [D-Lys6]-LH-RH acts as a GnRH receptor agonist .
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Cat. No.: HY-P0243
CAS No.: 86073-88-3
Synonyms: Salmon GnRH; Salmon gonadotropin-releasing hormone; sGnRH
Target:  

GnRH Receptor

Research Areas:  

Metabolic Disease

Luteinizing Hormone Releasing Hormone (LH-RH), salmon (Salmon GnRH) is the hypophysiotropic decapeptide synthesized in the hypothalamus that plays a crucial role in the control of reproductive functions.
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Cat. No.: HY-P1628
CAS No.: 124904-93-4
Target:  

GnRH Receptor

Research Areas:  

Metabolic Disease

Ganirelix is a competitive and selective gonadotropin releasing hormone (GnRH) antagonist. Ganirelix prevents endogenous GnRH from inducing luteinising hormone (LH) and follicle stimulating hormone relea .
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Cat. No.: HY-130249
CAS No.: 2471978-97-7
Purity:  99.96%
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

BAY-298 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC50s of 96 nM, 23 nM and 78 nM for hLH (human LH) and rLH (rat LH) and cLH (cynomolgus monkey LH), respectively. BAY-298 can reduce sex hormone levels .
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Cat. No.: HY-19464
CAS No.: 501444-88-8
Research Areas:  

Endocrinology

Org 43553 is an orally active and low molecular weight (LMW) luteinizing hormone receptor (LH-R) agonist. Org 43553 shows agonistic activity to human LH and FSH receptors with EC50 values of 3.7 and 110 nM, respectively. Org 43553 can be used for the research of endocrine .
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Cat. No.: HY-P0053
CAS No.: 38234-21-8
Target:  

GnRH Receptor

Research Areas:  

Endocrinology

Fertirelin is a GnRH and LH-RH analogue. Fertirelin can be used of the study for reversing cow follicular cysts .
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Cat. No.: HY-100812
CAS No.: 117354-64-0
Purity:  ≥98.0%
Target:  

GABA Receptor

Research Areas:  

Neurological Disease Endocrinology

2-Hydroxysaclofen is a potent γ-amino-butyric-acid-B (GABAB) receptor antagonist. 2-Hydroxysaclofen can abolish nicotine-induced hypolocomotor effects and increases the antinociceptive effects. 2-Hydroxysaclofen can stimulate luteinizing hormone (LH) secretion in female rats .
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