Leelamine hydrochloride
CAS No. 16496-99-4
Leelamine hydrochloride( Dehydroabietylamine )
Catalog No. M12521 CAS No. 16496-99-4
Leelamine hydrochloride (Dehydroabietylamine) is a novel inhibitor of androgen receptor (AR).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameLeelamine hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionLeelamine hydrochloride (Dehydroabietylamine) is a novel inhibitor of androgen receptor (AR).
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DescriptionLeelamine hydrochloride (Dehydroabietylamine) is a novel inhibitor of androgen receptor (AR), inhibits castration-resistant prostate cancer cells; causes apoptosis and suppresses 22Rv1 xenograft growth in vivo; Leelamine mediates cancer cell death through inhibition of intracellular cholesterol transport.
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In Vitro——
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In Vivo——
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SynonymsDehydroabietylamine
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PathwayEndocrinology/Hormones
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TargetAndrogen Receptor (AR)
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RecptorAndrogen Receptor (AR)
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Research Area——
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Indication——
Chemical Information
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CAS Number16496-99-4
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Formula Weight321.933
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Molecular FormulaC20H32ClN
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 25 mg/mL (77.66 mM)
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SMILESCC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CN)C.Cl
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Chemical Name1R,2,3,4,4aS,9,10,10aR-octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-phenanthrenemethanamine, monohydrochloride
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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ORM-15341
The active main metabolite of ODM-201, a potent wt/mutant androgen receptor (AR) inhibitor.
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Ralaniten triacetate
Ralaniten triacetate (EPI-506), a precursor of Ralaniten, is a first-of-its-kind, orally active androgen receptor N-terminal structural domain (AR-NTD) inhibitor with anticancer activity and can be used to study prostate and breast cancer.
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UT-34
UT-34 is a selective and orally active antagonist of second-generation pan-androgen receptor (AR) and degrader(IC50s of 211.7 nM, 262.4 nM and 215.7 nM for wild-type, F876L and W741L AR, respectively), and has anti-prostate cancer efficacy. In LNCaP cells, UT-34 (3-10 μM; 24 hours) treatment inhibits the expression of PSA and FKBP5 and growth of LNCaP cells starting from 100 nM with maximum effect observed at 10 μM.
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