
Turosteride
CAS No. 137099-09-3
Turosteride( —— )
Catalog No. M36376 CAS No. 137099-09-3
Turosteride is a small molecule steroidal 5α-reductase (5α-reductase) inhibitor.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 198 | Get Quote |
![]() ![]() |
5MG | 304 | Get Quote |
![]() ![]() |
10MG | 456 | Get Quote |
![]() ![]() |
25MG | 723 | Get Quote |
![]() ![]() |
50MG | 994 | Get Quote |
![]() ![]() |
100MG | 1332 | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameTurosteride
-
NoteResearch use only, not for human use.
-
Brief DescriptionTurosteride is a small molecule steroidal 5α-reductase (5α-reductase) inhibitor.
-
DescriptionTurosteride is a small molecule steroidal 5α-reductase (5α-reductase) inhibitor.Turosteride has antitumor activity for the treatment of oncologic diseases and genitourinary disorders, and may be used in the study of prostate cancer.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayEndocrinology/Hormones
-
TargetReductase
-
RecptorReductase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number137099-09-3
-
Formula Weight459.66
-
Molecular FormulaC27H45N3O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESC[C@@]12[C@]([C@]3([C@@]([C@]4(C)[C@@](CC3)(N(C)C(=O)CC4)[H])(CC1)[H])[H])(CC[C@@H]2C(N(C(NC(C)C)=O)C(C)C)=O)[H]
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog



related products
-
(R)-Viloxazine Hydro...
(R)-Viloxazine Hydrochloride is the R-isomer of Viloxazine, a selective norepinephrine reuptake inhibitor (NRI) used as an antidepressant.
-
beta-Glucogallin
beta-Glucogallin (beta-Glucogallin) is a selective aldose reductase (AKR1B1) inhibitor with antioxidant, anti-glycation, and anti-inflammatory properties.
-
Ganoderic acid C2
Ganoderic acid C2 has anti-inflammatory,and anti-tumor-promoting activities. Ganoderic acid C2 can inhibit histamine release, it also has inhibitory effects on the induction of Epstein-Barr Virus early antigen.