11 Results for "

hypogonadism

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 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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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-164032
CAS No.: 366472-45-9
Synonyms: 7α,11β-Dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate
Target:  

Androgen Receptor

Research Areas:  

Endocrinology

Dimethandrolone undecanoate (7α,11β-Dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate) is an orally active androgen . Dimethandrolone undecanoate is cleaved to the active Dimethandrolone, which then mediates androgenic and progestational effects, stimulating ventral prostate and levator ani muscle weight. Dimethandrolone undecanoate suppresses serum LH. Dimethandrolone undecanoate can be used in research on hypogonadism .
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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-133676S
CAS No.: 679789-44-7
Synonyms: MEOHP-d4; 5-oxo-MEHP-d4
Mono(2-ethyl-5-oxohexyl) phthalate-d4 (MEOHP-d4; 5-oxo-MEHP-d4) is the deuterated-labeled Mono(2-ethyl-5-oxohexyl) phthalate (HY-133676). Mono (2-ethyl-5-oxohexyl) phthalate (MEOHP; 5-oxo-MEHP) is a secondary metabolite produced by cytochrome P450 enzyme-mediated oxidation of di(2-ethylhexyl) phthalate. Exposure levels of Mono (2-ethyl-5-oxohexyl) phthalate are associated with late-onset hypogonadism. Mono (2-ethyl-5-oxohexyl) phthalate can be used for research on mechanisms related to male reproductive endocrine disorders .
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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:  
E. coli
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Cat. No.: HY-133676
CAS No.: 40321-98-0
Synonyms: MEOHP; 5-oxo-MEHP
Research Areas:  

Endocrinology

Mono (2-ethyl-5-oxohexyl) phthalate (MEOHP; 5-oxo-MEHP) is a secondary metabolite produced by cytochrome P450 enzyme-mediated oxidation of di(2-ethylhexyl) phthalate. Exposure levels of Mono (2-ethyl-5-oxohexyl) phthalate are associated with late-onset hypogonadism. Mono (2-ethyl-5-oxohexyl) phthalate can be used for research on mechanisms related to male reproductive endocrine disorders .
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