1 | www.apexbt.com Sorafenib Cat. No.: A3009 CAS No.: 284461-73-0 Formula: C21H16ClF3N4O3 M.Wt: 464.82 Synonyms: BAY-43-9006,Sorafenib,Nexavar,sorafenibum Target: Tyrosine Kinase Pathway: PDGFR Storage: Store at -20°C In Vitro ı23.25mg/mL in DMSO Preparing Stock Solutions Mass 1mg 5mg 10mg Solvent Concentration 1 mM 2.1514 mL 10.7569 mL 21.5137 mL 5 mM 0.4303 mL 2.1514 mL 4.3027 mL 10 mM 0.2151 mL 1.0757 mL 2.1514 mL Please refer to the solubility information to select the appropriate solvent. Shortsummary Raf kinases and tyrosine kinases inhibitor IC₅₀ & Target , 22 nM (B-Raf), 90 nM (VEGFR2), 57 nM (PDGFRβ) In Vitro Cell Viability Assay Cell Line: PLC/PRF/5 and HepG2 cells Preparation method˖ The solubility of this compound in DMSO is >10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while.Stock solution can be stored below -20°C for several months. Reacting conditions: IC50: 6.3 μM for PLC/PRF/5 cells 4.5 μM for HepG2 cells 72 hours Applications: The effect of sorafenib on cell proliferation was measured by CellTiter -Glo Product Name: Sorafenib Revision Date: //2020 Product Data Sheet Solvent & Solubility Biological Activity 1 | www.apexbt.com Sorafenib Cat. No.: A300 0 0 0 0 0 0 0 0 0 9 9 9 9 9 9 9 9 9 9 9 CAS No.: 28 28 8 8 28 8 8 8 28 28 28 28 28 2 28 28 8 28 2 2 2844 44 44 44 44 44 44 44 44 4461 61 61 61 61 61 61 61 61 1 61 1 - - - - 73 7 7 7 7 7 7 7 7 7 7 7 - 0 Formula: C C2 C2 C2 C2 C2 C2 C2 C2 C C2 C2 C C C 1H16ClF3N4O3 M.Wt: 464.82 Synonyms: BAY - Y Y 43 - 9006,Sorafenib,Nexa var,sorafenibum T arget: Tyrosine Kinase Pathway: PDGFR Storage: Store at - 20°C In Vitro ı ı ı ı ı ı ı ı ı ı ı ı ı 23.25mg/mL in DMSO Preparing Stock Solutions Mass 1mg 5mg 10mg Solvent Concentration 1 mM 2.1514 mL 10.7569 mL 21.5137 mL 5 mM 0.4303 mL 2.1514 mL 4.3027 mL 1 0 mM 0.2151 mL 1.07 7 7 7 7 7 7 7 757 57 57 57 57 57 57 57 5 57 57 m m m m m m m m m m mL L L L L L L L L L L 2.1514 mL Plea a a a a a a a a ase se se se s se s se se se e e e e e e r r r r r r r r r r ref ef ef ef ef ef ef ef f e e e e e ef e e e e e er er er er er er r er er er er t t t t t t t t t t t to o o o o o o o o o o t t th t t e solubility information to select the appropriate solvent nt nt t nt t t t t t. Shortsummary Raf kinases and tyrosine kinases inhibitor IC ₅₀ & Target , 22 nM (B - Raf), 90 nM (VEGFR2), 57 nM (PDGFRβ) In Vitro Cell Viability Assay Cell Line: e: e: e: e: e: e e e PLC/PRF/5 and HepG2 cells Pr Pr Pr Pr Pr r Pr Pr Pr P ep ep ep ep ep ep ep ep ep ep ep e ar ar a ar ar ar ar ar ar ar rat at a at at t t at at t t t t a at at t t ati i i i io io io i i io io io io o io io o io ion n n n n n n n n n n n n method ˖ The solubility of this compound in D D D D D D D D D D D DMS MS MS MS MS MS MS MS MS MS MS M MS MS M MS M O O O O O O O O O O O O O O O O O O is is is is s is is is is is s > > > > > > > > > > > >10 10 10 10 1 10 10 10 1 1 1 1 1 mM. General tips for obtaining a higher concentration: Please war ar ar ar r ar ar ar r r ar rm m m m m m m m m m m m m m th th th th th th th th th th th h h he tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while.Stock solution can be stored below - 20°C for several months. Reacting conditions: IC50: 6.3 μM for PLC/PRF/5 cells 4.5 μM for HepG2 cells 72 hours Applications: The effect of sorafenib on cell proliferation was measured by CellTiter - Glo Product Name: Sorafenib Revision Date: / /2 020 0 et Product Data Shee Solvent & Solu u u u u ub b b b bi i i i i il l l l l l l l li i i it t t t t t t ty y y y y y y y y Biologica a a al l l l l A A A A A Activity
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10 mM 0.2151 mL 1.0777777777575757575757575755757 mmmmmmmmmmmLLLLLLLLLLL 2.1514 mL
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Shortsummary Raf kinases and tyrosine kinases inhibitor
PrPrPrPrPrrPrPrPrP epepepepepepepepepepepe araraarararararararratataatatttatatttttaatatttatiiiiioioioiiioioioiooioiooioionn n nnnn nnnnnn method The solubility of this compound in DDDDDDDDDDDDMSMSMSMSMSMSMSMSMSMSMSMMSMSMMSM O OO OO O OOOOOOOOOOOOO isisisissisisisisiss >>>>>>>>>>>>10101010110101011111 mM. General tips for obtaining
a higher concentration: Please wararararrarararrrarrmmmmmmmmmmmmmm thththththththththththhhhe tube at 37 °C for 10 minutes and/or
shake it in the ultrasonic bath for a while.Stock solution can be stored below
-20°C for several months.
Reacting conditions: IC50: 6.3 μM for PLC/PRF/5 cells 4.5 μM for HepG2 cells 72 hours
Applications: The effect of sorafenib on cell proliferation was measured by CellTiter-Glo
2. Sieber J, Wieder N, et al. "GDC-0879, a BRAF(V600E) Inhibitor, Protects Kidney Podocytes fromDeath." Cell Chem Biol. 2017 Dec
6.PMID:29249695
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[1] Liu L, Cao Y, Chen C, et al. Sorafenib blocks the RAF/MEK/ERK pathway, inhibits tumor angiogenesis, and induces tumor cell
apoptosis in hepatocellular carcinoma model PLC/PRF/5. Cancer research, 2006, 66(24): 11851-11858.
FOR RESEARCH PURPOSES ONLY.NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.Specific storage and handling information for each product is indicated on the product datasheet. Most APExBIO products are stable
under the recommended conditions. Products are sometimes shipped at a temperature that differs from the recommended storage
temperature. Shortterm storage of many products are stable in the short-term at temperatures that differ from that required for
long-term storage. We ensure that the product is shipped under conditions that will maintain the quality of the reagents. Upon receipt
of the product, follow the storage recommendations on the product data sheet.
Product Citations
References
Caution
2 | www.apeexbt.commmmmmmmmmmmmm
assay. Sorafenib inhibited cell proliferation dose-dependently with an IC50 of
6.3 μmol/L in PLC/PRF/5 and 4.5 μmol/L in HepG2 cells.
In Vivo
Animal experiment
Animal models: Female CB17 SCID mice injected with PLC/PRF/5 cells
Dosage form: Oral administration; 10, 30, and 100 mg/kg body weighththththththththt;;;;;;;; onoooooooooo ce daily for 16 or 21
days
ApApApppppppppplplplplplplplpppliciciciciciciciciciccatatatatatatatataatatioioioioioioioioioonsnsnsnsnsnsnsnsnssns::::::::: Sorafenib tosylate produced dose-deeeeeeeepepepepepepepepeppepeendndndndndndndndndddenenenenenenenenennent ttttt tttt t tt t tt t t grgg owth inhibition of s.c.
implanted PLC/PRF/5 tumor xenogrgrgrgrgrgrgrgrgrrgrrrrrafafafafafafafafafafafafafafaftststststststststststststss iiiiiiiiiinnnnnnnnnn SCSCSCSCSCSCSCSCSCSCSCSCCID mice. Dose levels of 10 and 30
mg/kg produced significant and dddddddddososososososososososooooo eeeeeeeee-dependent TGIs of 49% and 78%,
respectively. Sorafenib tosylate produced durable partial tumor regressions in
50% of the mice at the 100 mg/kg dose level.
Other notes: Please test the solubility of all compounds indoor, and the actual solubility may
slightly differ with the theoretical value. This is caused by an experimental
system error and it is normal.
1. Cheriyan VT, AlAlAlAlAlAAAlAlAlAAlAlAAA sasasasasasasasasasasasasasas abaababababababbbbabbbabbaababab HHHHHH, et al. "A CARP-1 functional mimetic compound is synergistic wwwwwwwwwwwitititititititittitititittthhhhhhhhhhhhhh BRBRBRBRBRBRBRBRBRBRRRBRRBRBRRBRBRBRRAFAAAAAAAAAAA -targeting in non-small cell lung
2. Sieber J, Wieder N, et al. "GDC-0879, a BRAF(V600E) Inhibitor, Protects Kidney Podocytes fromDeath." Cell Chem Biol. 2017 Dec
6.PMID:29249695
See more customer validations on www.apexbt.com.
[1] Liu L, Cao Y, Chen C, et al. SSSSSSSSSSororororororororororrafafafafafafafafafaffenenenenenenenenenenene iiiibi blocks the RAF/MEK/ERK pathway, inhibits tumor annnnnnnnngigigigigigigigigiggiogogogogogogogogogogggeneeneneneneneneneenenenennneneeeeseseseseseseseeseseeeessesesisisisisississisisisiis, and induces tumor cell
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FOR RESEARCH PURPOSES ONLY.NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTTIC USE.Specific storage and handling information for each product is indicatted on the product datasheet. Most APEPEPEPEEPEPEEPEEExBxBxBxBxBxBxBxBBxBBEEEEEEEEEEEEEEEEE IOIOIOIOIOIOIOIOO ble products are stab
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