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SHIN1

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Catalog No. T12897LCas No. 2146095-85-2
Alias RZ-2994

SHIN1 (RZ-2994) is an inhibitor of human serine hydroxymethyltransferse 1(SHMT1) with IC50 of 5 nM and human serine hydroxymethyltransferse 2 (SHMT2) with an IC50 of 13 nM.

SHIN1

SHIN1

🥰Excellent
Purity: 98.18
Catalog No. T12897LAlias RZ-2994Cas No. 2146095-85-2
SHIN1 (RZ-2994) is an inhibitor of human serine hydroxymethyltransferse 1(SHMT1) with IC50 of 5 nM and human serine hydroxymethyltransferse 2 (SHMT2) with an IC50 of 13 nM.
Pack SizePriceAvailabilityQuantity
1 mg$71In Stock
5 mg$146In Stock
10 mg$218In Stock
25 mg$396In Stock
50 mg$616In Stock
100 mg$948In Stock
200 mg$1,300In Stock
1 mL x 10 mM (in DMSO)$159In Stock
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Purity:98.18
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Product Introduction

Bioactivity
Description
SHIN1 (RZ-2994) is an inhibitor of human serine hydroxymethyltransferse 1(SHMT1) with IC50 of 5 nM and human serine hydroxymethyltransferse 2 (SHMT2) with an IC50 of 13 nM.
Targets&IC50
SHMT1:5 nM, SHMT2:13 nM
In vitro
SHIN1 inhibits the growth of SHMT2 deletion HCT-116 cells (IC50: 10 nM). SHIN1 inhibits SHMT1/2 in HCT-116 cells. SHIN1 is particularly active against B-cell malignancies. SHIN1 blocks cell growth through a progressive depletion of purines, leading to loss of nucleotide triphosphates [1].
AliasRZ-2994
Chemical Properties
Molecular Weight400.47
FormulaC24H24N4O2
Cas No.2146095-85-2
SmilesCC(C)C1(c2c(C)n[nH]c2OC(N)=C1C#N)c1cc(CO)cc(c1)-c1ccccc1
Relative Density.1.32 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (124.85 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4971 mL12.4853 mL24.9707 mL124.8533 mL
5 mM0.4994 mL2.4971 mL4.9941 mL24.9707 mL
10 mM0.2497 mL1.2485 mL2.4971 mL12.4853 mL
20 mM0.1249 mL0.6243 mL1.2485 mL6.2427 mL
50 mM0.0499 mL0.2497 mL0.4994 mL2.4971 mL
100 mM0.0250 mL0.1249 mL0.2497 mL1.2485 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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