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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T21936 | M50054 | Caspase | |
Apoptosis Inhibitor was a novel inhibitor of programmed cell death associate with caspase-3 inhibition. | |||
T0488 | Finasteride | MK-906 | Reductase |
Finasteride (MK-906) is an oral inhibitor of active testosterone 5-alpha-reductase and Ki value is 10 nM. | |||
T21444 | Diphenylcyclopropenone | DPCP,Diphencyprone | Others |
Diphenylcyclopropenone (DPCP) is a topical drug used to treat alopecia areata, alopecia totalis, and refractory warts. Diphencyprone acts as a local stimulator that triggers an immune response against the action of autor... | |||
T10889 | CRTh2 antagonist 2 | GPR | |
CRTh2 antagonist 2 is a selective and potent CRTH2 antagonist, IC50≤10 nM. CRTh2 antagonist 2 can be used to study the direction of androgenic alopecia. | |||
T3378 | Alpha-Estradiol | Alfatradiol,17α-Estradiol,Epiestrol,Epiestradiol | Estrogen/progestogen Receptor , Reductase , Endogenous Metabolite |
Alpha-Estradiol (Epiestradiol) is an estrogen that inhibits 5alpha-reductase and has potential in the study of androgenetic alopecia. | |||
T27798 | Lapisteride | CS891B,CS-891,CS-891B,CS891 | Others |
Lapisteride (CS-891) a steroidal 5α-reductase inhibitor is used to treat benign prostatic hyperplasia (BPH) and androgenetic alopecia and may be effective in preventing or treating AGA . | |||
T17256 | Wnt pathway activator 1 | Wnt/beta-catenin | |
Wnt pathway activator 1 is a potent Wnt activator with an IC50 of 28-29 nM. Wnt pathway activator 1 is a potent Wnt activator for the treatment of androgenetic alopecia (AGA). | |||
T10636 | 5α-reductase-IN-1 | Others | |
5α-reductase-IN-1 is a potent inhibitor of the enzyme 5α-reductase. This compound is primarily employed in research studies to investigate its potential efficacy in treating patterned alopecia. It is commonly used in com... | |||
T28358 | PF 00277343 | PF-00277343,PF00277343 | |
PF 00277343, a thyroid receptor agonist, is used for the treatment of androgenetic alopecia. | |||
T82202 | H-Gly-Leu-Phe-OH | ||
GLF (H-Gly-Leu-Phe-OH), a tripeptide isolated from α-lactalbumin with immunostimulatory properties, prevents alopecia, epidermal thickening, and adipocyte layer thinning induced by the anticancer agent Etoposide [1]. | |||
T38467 | (Rac)-PF-998425 | ||
(Rac)-PF-998425 is a potent, selective, nonsteroidal antagonist of the androgen receptor (AR), with IC50 values of 26 nM and 90 nM in AR binding and cellular assays, respectively. This compound shows promise for investig... | |||
T27519 | GW 9578 | GW9578,GW-9578 | PPAR |
GW 9578 is a selective and potent PPARα agonist with potent lipid-lowering activity for the study of psoriasis, arthritis, alopecia, asthma and type I diabetes. | |||
T61029 | TP0427736 hydrochloride | ||
TP0427736 hydrochloride can be used in the androgenic alopecia (AGA) research. TP0427736 hydrochloride inhibits the phosphorylation of Smad2/3 in A549 cells induced by TGF-β1 with an IC50 value of 8.68 nM. TP0427736 hydr... | |||
T21668 | Finasteride acetate | ||
Finasteride (MK-906) acetate is a potent and competitive 5α-reductase inhibitor, with an IC 50 of 4.2 nM for type II 5α-reductase. The affinity of Finasteride acetate for type II 5α-reductase enzyme was approximately 100... |