14 Results for "

Androgenic alopecia

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "Androgenic alopecia" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-13635
CAS No.: 98319-26-7
Purity:  99.97%
Synonyms: MK-906
Research Areas:  

Cancer

Finasteride (MK-906) is an orally active and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
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2
2 Cited Publications
Cat. No.: HY-118528A
CAS No.: 2459963-17-6
Purity:  99.22%
Target:  

TGF-β Receptor

Research Areas:  

Endocrinology

TP0427736 hydrochloride is a potent inhibitor of ALK5 kinase activity with an IC50 of 2.72 nM and this effect is 300-fold higher than the inhibitory effect on ALK3 (IC50=836 nM). TP0427736 hydrochloride also inhibits Smad2/3 phosphorylation in A549 cells induced by TGF-β1 with an IC50 value of 8.68 nM. TP0427736 hydrochloride can be used for the research of androgenic alopecia (AGA) .
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1
1 Cited Publications
Cat. No.: HY-B0141A
CAS No.: 57-91-0
Synonyms: Alfatradiol; Epiestradiol; Epiestrol
Alpha-Estradiol is a weak estrogen and a 5α-reductase inhibitor which is used as a topical medication in the treatment of androgenic alopecia.
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Cat. No.: HY-B0141AR
CAS No.: 57-91-0
Synonyms: Alfatradiol(Standard); Epiestradiol(Standard); Epiestrol (Standard)
Alpha-Estradiol (Standard) is the analytical standard of Alpha-Estradiol. This product is intended for research and analytical applications. Alpha-Estradiol is a weak estrogen and a 5α-reductase inhibitor which is used as a topical medication in the treatment of androgenic alopecia.
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Cat. No.: HY-152094
CAS No.: 2279077-93-7
Purity:  99.82%
Target:  

5 alpha Reductase

Research Areas:  

Endocrinology

SRD5A1-IN-1 (Compound 4) is a competitive and covalent steroid 5α-reductase type 1 (SRD5A1) inhibitor with an IC50 of 1.44 µM. SRD5A1-IN-1 modulates SRD5A1 function, leading to a lower level of dihydrotestosterone (DHT) production and SRD5A1 protein suppression .
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Cat. No.: HY-13635A
CAS No.: 222989-99-3
Synonyms: MK-906 acetate
Target:  

5 alpha Reductase

Research Areas:  

Cancer

Finasteride (MK-906) acetate is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride acetate has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride acetate can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
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Cat. No.: HY-B0141AS1
CAS No.: 81586-94-9
Synonyms: Alfatradiol-d2; Epiestradiol-d2; Epiestrol-d2
Alpha-Estradiol-d2 is the deuterium labeled Alpha-Estradiol. Alpha-Estradiol is a weak estrogen and a 5α-reductase inhibitor which is used as a topical medication in the treatment of androgenic alopecia .
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Cat. No.: HY-106174
CAS No.: 142139-60-4
Purity:  ≥99.0%
Synonyms: CS 891
Target:  

5 alpha Reductase

Research Areas:  

Endocrinology

Lapisteride (CS 891) is an orally active 5α-reductase inhibitor. Lapisteride can inhibit 5α-reductaseactivity in the hair follicles (HF). Lapisteride can be used in prostatic hyperplasia and androgenic alopecia research .
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Cat. No.: HY-13635R
CAS No.: 98319-26-7
Synonyms: MK-906 (Standard)
Research Areas:  

Cancer

Finasteride (Standard) is the analytical standard of Finasteride. This product is intended for research and analytical applications. Finasteride (MK-906) is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
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Cat. No.: HY-125970
CAS No.: 780763-95-3
Purity:  99.78%
Research Areas:  

Endocrinology

CRTh2 antagonist 2 is selective and potent CRTH2 antagonist extracted from patent US20140148470A1, compound Example 1, has an IC50 of ≤10 nM. CRTh2 antagonist 2 can be used in research of androgenic alopecia .
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Cat. No.: HY-118528
CAS No.: 864374-00-5
Target:  

TGF-β Receptor

Research Areas:  

Cancer

TP0427736 is a selective inhibitor of ALK5 with an IC50 of 2.72 nM. TP0427736 inhibits Smad2/3 phosphorylation in A549 cells. TP0427736 decreases the growth inhibition of human outer root sheath cells .
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Cat. No.: HY-B0141AS
Synonyms: Alfatradiol-d3; Epiestradiol-d3; Epiestrol-d3
Alpha-Estradiol-d3 is the deuterium labeled Alpha-Estradiol. Alpha-Estradiol is a weak estrogen and a 5α-reductase inhibitor which is used as a topical medication in the treatment of androgenic alopecia.
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Cat. No.: HY-170450
AR ligand-38 is the ligand for androgen receptor, that can be used for synthesis of PROTAC AR Degrader-9 (HY-170448) .
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Cat. No.: HY-13635S
CAS No.: 1131342-85-2
Purity:  99.13%
Synonyms: MK-906-d9
Finasteride-d9 is deuterium labeled Finasteride. Finasteride (MK-906) is a potent and competitive 5α-reductase inhibitor, with an IC50 of 4.2 nM for type II 5α-reductase. Finasteride has approximately a 100-fold greater affinity for type II 5α-reductase enzyme than for the type I enzyme. Finasteride can be used for the research of benign prostatic hyperplasia (BPH) and androgenic alopecia .
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