Fig. 1 · Structure

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Salirasib

Cat. No. A11572 CAS 162520-00-5

PPMTase inhibitor

Salirasib is an inhibitor of prenylated protein methyltransferase (PPMTase) with Ki value of 2.6 uM.

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Biological Activity

Target & Activity

Target Activity Value
PPMTase Ki 2.6 μM

Cellular Effect

Cell Line Activity Value Description Reference
Bel-7402 IC50 76.13 μM Cytotoxicity against human Bel7402 cells after 48 hrs by MTT based ELISA [PMID: 21504204]
BXPC-3 EC50 > 20 μM Cytotoxicity against human BxPC3 cells after 48 hrs by fluorescence assay [PMID: 24852279]
EJ IC50 47.6 μM Cytotoxicity against human EJ cells after 48 hrs by MTT assay [PMID: 24300920]
EJ IC50 48.6 μM Cytotoxicity against human EJ cells assessed as inhibition of cell growth by MTT assay [PMID: 32791404]
HEK293 EC50 0.8 μM Agonist activity at human TRPA1 expressed in HEK293 cells assessed as increase in calcium influx by Fluo-4-AM dye based fluorescence assay [PMID: 30878828]
HEK293 EC50 7 μM Agonist activity at human TRPA1 expressed in HEK293 cells assessed as increase in calcium influx by Fluo-3/acetoxymethyl ester dye based FLIPR analysis [PMID: 30878828]
Hep 3B2 IC50 63.75 μM Cytotoxicity against human Hep3B cells after 48 hrs by MTT based ELISA [PMID: 21504204]
HepG2 IC50 107.51 μM Cytotoxicity against human HepG2 cells after 48 hrs by MTT based ELISA [PMID: 21504204]
HepG2 IC50 48.6 μM Cytotoxicity against human HepG2 cells assessed as inhibition of cell growth by MTT assay [PMID: 32791404]
MCF7 IC50 46.75 μM Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay [PMID: 20435479]
MCF7 IC50 48.6 μM Cytotoxicity against human MCF7 cells assessed as inhibition of cell growth by MTT assay [PMID: 32791404]
MCF7 IC50 49.1 μM Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay [PMID: 24300920]
MDA-MB-231 IC50 51.22 μM Cytotoxicity against human MDA-MB-231 cells after 48 hrs by MTT assay [PMID: 20435479]
MEF IC50 14.3 μM Cytotoxicity against icmt-double mutant MEF cells after 5 days by MTT assay [PMID: 22754607]
MEF IC50 15.3 μM Cytotoxicity against icmt-positive MEF cells after 5 days by MTT assay [PMID: 22754607]
MIA PaCa-2 EC50 > 20 μM Cytotoxicity against human MIAPaCa2 cells harboring K-Ras mutant oncogene after 48 hrs by fluorescence assay [PMID: 24852279]
NCI-H460 IC50 48.6 μM Cytotoxicity against human NCI-H460 cells assessed as inhibition of cell growth by MTT assay [PMID: 32791404]
NCI-H460 IC50 49.2 μM Cytotoxicity against human H460 cells after 48 hrs by MTT assay [PMID: 24300920]
PANC-1 IC50 35 μM Cytotoxicity against human PANC1 cells after 5 to 7 days [PMID: 19072665]
PANC-1 IC50 53.6 μM Cytotoxicity against human PANC1 cells after 48 hrs by MTT assay [PMID: 24300920]

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Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 162520-00-5
Applications PPMTase inhibitor
Formula C22H30O2S
Molecular Weight 358.54
Synonyms S-Farnesylthiosalicylic acid; Farnesyl Thiosalicylic Acid; FTS
SMILES
CC(=CCCC(=CCCC(=CCSC1=CC=CC=C1C(=O)O)C)C)C

Storage & Solubility

In Vitro Solubility

Reported Solubility

No reported solubility data are available for this product.

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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