12 Results for "

hypogonadism

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "hypogonadism" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-118861
CAS No.: 15690-57-0
Synonyms: (E)-Clomiphene; trans-Clomiphene; Enclomifene
Target:  

Estrogen Receptor/ERR

Research Areas:  

Metabolic Disease Endocrinology

Enclomiphene ((E)-Clomiphene) is a potent and orally active non-steroidal estrogen receptor antagonist, with antioestrogenic property. Enclomiphene can be used for the research of ovarian dysfunction, testosterone deficiency, male hypogonadism and type 2 diabetes .
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1
1 Cited Publications
Cat. No.: HY-118861A
CAS No.: 7599-79-3
Purity:  99.96%
Synonyms: (E)-Clomiphene citrate; trans-Clomiphene citrate; Enclomifene citrate
Target:  

Estrogen Receptor/ERR

Research Areas:  

Metabolic Disease Endocrinology

Enclomiphene ((E)-Clomiphene) citrate is a potent and orally active non-steroidal estrogen receptor antagonist, with antioestrogenic property. Enclomiphene citrate can be used for the research of ovarian dysfunction, testosterone deficiency, male hypogonadism and type 2 diabetes .
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1
1 Cited Publications
Cat. No.: HY-P4157
CAS No.: 2460055-10-9
Target:  

MDM-2/p53 Apoptosis

Research Areas:  

Metabolic Disease

FOXO4-DRI is a cell-permeable peptide antagonist that blocks the interaction of FOXO4 and p53. FOXO4-DRI is a senolytic peptide that induces apoptosis of senescent cells .
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Cat. No.: HY-P0242
CAS No.: 86933-75-7
Neurokinin B is a tachykinin family peptide that preferentially binds to and activates NK3R over other tachykinin receptors. Neurokinin B preferentially binds to the substance P receptor (SP-N receptor) and mediates acetylcholine release from cholinergic neurons. Neurokinin B regulates the pulsatile release of Kisspeptin and GnRH, stimulates or inhibits the secretion of luteinizing hormone (HY-P2293), regulates reproductive function via metabolic signals, and drives the onset of puberty. Neurokinin B exerts vasoactive effects and induces contraction of isolated guinea pig ileum. Neurokinin B can be used in studies related to hypogonadotropic hypogonadism .
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Cat. No.: HY-P0242A
CAS No.: 101536-55-4
Neurokinin B TFA is a tachykinin family peptide that preferentially binds to and activates NK3R over other tachykinin receptors. Neurokinin B TFA preferentially binds to the substance P receptor (SP-N receptor) and mediates acetylcholine release from cholinergic neurons. Neurokinin B TFA regulates the pulsatile release of Kisspeptin and GnRH, stimulates or inhibits the secretion of luteinizing hormone (HY-P2293), regulates reproductive function via metabolic signals, and drives the onset of puberty. Neurokinin B TFA exerts vasoactive effects and induces contraction of isolated guinea pig ileum. Neurokinin B TFA can be used in studies related to hypogonadotropic hypogonadism .
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Cat. No.: HY-118861B
CAS No.: 14158-65-7
Synonyms: (E)-Clomiphene hydrochloride; trans-Clomiphene hydrochloride; Enclomifene hydrochloride
Target:  

Estrogen Receptor/ERR

Research Areas:  

Metabolic Disease Endocrinology

Enclomiphene ((E)-Clomiphene) hydrochloride is a potent and orally active non-steroidal estrogen receptor antagonist, with antioestrogenic property. Enclomiphene hydrochloride can be used for the research of ovarian dysfunction, testosterone deficiency, male hypogonadism and type 2 diabetes .
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Cat. No.: HY-P4157A
Target:  

MDM-2/p53 Apoptosis

Research Areas:  

Metabolic Disease

FOXO4-DRI acetate is a cell-permeable peptide antagonist that blocks the interaction of FOXO4 and p53. FOXO4-DRI acetate is a senolytic peptide that induces apoptosis of senescent cells .
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Cat. No.: HY-111309
CAS No.: 847235-85-2
Target:  

Androgen Receptor

Research Areas:  

Endocrinology

LGD-2941 is an orally active, potent and selective androgen receptor modulator. LGD-2941 shows excellent anabolic activity in muscle with reduced effect on the prostate in a rat model of hypogonadism. LGD-2941 also improves bone strength in a rat model of post-menopausal osteoporosis .
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Cat. No.: HY-143656
CAS No.: 2338793-00-1
Target:  

Autophagy

Research Areas:  

Endocrinology

SH379 is the derivative of 2-methylpyrimidine-fused tricyclic diterpene. SH379 is a potent and orally active anti-late-onset hypogonadism agent. SH379 significantly promotes the expression of the key testosterone synthesis-related enzymes StAR and 3β-HSD. SH379 stimulates autophagy through regulating AMPK/mTOR signaling pathway .
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Cat. No.: HY-N13215
Research Areas:  

Metabolic Disease

Tongkat Ali Extract is the extract of Tongkat Ali, a testosterone modulator. Tongkat Ali Extract activates CYP17 enzyme to enhance conversion of pregnenolone and progesterone to dehydroepiandrosterone, androstenedione, and testosterone. Tongkat Ali Extract demonstrates antimalarial, antimicrobial, anticancer, and antidiabetic activity. Tongkat Ali Extract can be used for the research of diabetic and male infertility .
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Cat. No.: HY-P705680
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: LHCGR; Hypergonadotropic hypogonadism; Prev. HHG; LH/CG-R; LCGR; LHRHR; LGR2; LSH-R; LHR; Lutropin/Choriogonadotropin Receptor; Lutropin-Choriogonadotropic Hormone Receptor; Uncharacterized Protein LHCGR; ULG5; LH/CGR; Luteinizing Hormone/Choriogonadotrop
Species:  
Rat
Source:  
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Cat. No.: HY-P992149
CAS No.: 152923-57-4

Target:  

GnRH Receptor

Research Areas:  

Endocrinology

Lutropin alfa (FLAG, His Tag) is a recombinant human luteinizing hormone (LH). Lutropin alfa (FLAG, His Tag) consists of non-covalently linked α and β subunits, and its activity is similar to that of natural luteinizing hormone. Lutropin alfa (FLAG, His Tag) is used to stimulate follicular development in infertility .
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