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RB-005

  Cat. No.:  DC11161  
Chemical Structure
1425049-20-2
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More than 5000 active chemicals with high quality for research!
Field of application
RB-005 (RB-005) is a potent, selective inhibitor of sphingosine kinase SphK1 (SK1) with IC50 of 3.6 uM, displays 15-fold selectivity over SphK2..
Chemicals PropertiesBiological activity COA & MSDSRelated productsDatasheet
Cas No.: 1425049-20-2
Chemical Name: 1-(4-octylphenethyl)piperidin-4-ol
Synonyms: RB005
SMILES: N(CCC1=CC=C(CCCCCCCC)C=C1)1CCC(O)CC1
Formula: C21H35NO
M.Wt: 317.517
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: RB-005 (RB-005) is a potent, selective inhibitor of sphingosine kinase SphK1 (SK1) with IC50 of 3.6 uM, displays 15-fold selectivity over SphK2.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC44002 SK1-I SK1-I (BML-258), an analog of sphingosine, is an isozyme-specific competitive SPHK1 inhibitor with a Ki value of 10 µM. SK1-I (BML-258) has good water solubility. SK1-I (BML-258) shows no activity at SPHK1 PKCα, PKCδ, PKA, AKT1, ERK1, EGFR, CDK2, IKKβ or
DC44001 SK1-​I hydrochloride SK1-I hydrochloride (BML-258 hydrochloride), an analog of sphingosine, is an isozyme-specific competitive SPHK1 inhibitor with a Ki value of 10 µM. SK1-I hydrochloride (BML-258 hydrochloride) has good water solubility. SK1-I hydrochloride (BML-258 hydroch
DC11161 RB-005 RB-005 (RB-005) is a potent, selective inhibitor of sphingosine kinase SphK1 (SK1) with IC50 of 3.6 uM, displays 15-fold selectivity over SphK2..
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