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Chemical Structure| 1801747-42-1 Chemical Structure| 1801747-42-1

Structure of SHP099
CAS No.: 1801747-42-1

Chemical Structure| 1801747-42-1

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SHP099 is a potent, selective, and orally available SHP2 inhibitor with an IC50 of 70 nM.

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Product Details of SHP099

CAS No. :1801747-42-1
Formula : C16H19Cl2N5
M.W : 352.26
SMILES Code : NC1=NC(N2CCC(C)(N)CC2)=CN=C1C3=CC=CC(Cl)=C3Cl
MDL No. :MFCD29059453
InChI Key :YGUFCDOEKKVKJK-UHFFFAOYSA-N
Pubchem ID :118238298

Safety of SHP099

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Mouse spleen T cells 3, 10, or 30 µM 1 hour To measure the intracellular phosphatase activity of SHP2, results showed that SHP2 activity increased by approximately 40% after treatment with 30 mmol/L oleanolic acid. PMC11143531
HB11;19 5 μM 1 hour To study the effect of SHP099 on HB11;19 cells, results showed that the cells developed resistance to SHP099 PMC9177641
MGH049-1A 5 μM 14 days To evaluate the effect of SHP099 in combination with ceritinib on cell proliferation, results showed that the combination significantly inhibited cell proliferation. PMC6343825
MGH073-2B 5 μM 14 days To evaluate the effect of SHP099 in combination with ceritinib on cell proliferation, results showed that the combination significantly inhibited cell proliferation. PMC6343825
MGH065-1B 5 μM 14 days To evaluate the effect of SHP099 in combination with ceritinib on cell proliferation, results showed that the combination significantly inhibited cell proliferation. PMC6343825
MGH045-2A 5 μM 14 days To evaluate the effect of SHP099 in combination with ceritinib on cell proliferation, results showed that the combination significantly inhibited cell proliferation. PMC6343825
THP-1-derived macrophages 30 µM 2, 4, 6 hours To investigate the effect of SHP099 on type I interferon signaling in THP-1-derived macrophages, results showed that SHP099 significantly increased the mRNA levels of CXCL10, IFIT1, IFIT2, ISG15 and the expression of IFN-β. PMC8802865
BMDMs 500 mg/mL 2, 4, 6 hours To investigate the effect of SHP2 deletion on type I interferon signaling in BMDMs, results showed that SHP2 deletion significantly increased the mRNA levels of Cxcl10, I?t1, I?t2, Isg15 and the expression of IFN-β. PMC8802865
RAW264.7 cells 20 μM 24 hours SHP099 inhibited LPS-induced M1 macrophage polarization, decreased the proportion of CD80+ cells, downregulated M1 macrophage-related inflammatory genes, and reduced the secretion of inflammatory cytokines TNF-α and IL-6. PMC9293663
Bone marrow-derived macrophages (BMDMs) 20 μM 24 hours SHP099 inhibited LPS-induced M1 macrophage polarization, decreased the proportion of CD80+ cells, downregulated M1 macrophage-related inflammatory genes, and reduced the secretion of inflammatory cytokines TNF-α and IL-6. PMC9293663
Murine splenic CD8+ T cells 10 μM 24 hours To evaluate the effect of SHP099 on the activation of CD8+ T cells, results showed that SHP099 significantly enhanced the production of GZMB and PRF in CD8+ T cells at a concentration of 10 μmol/L. PMC6437555
Human peripheral blood mononuclear cells (PBMCs) 10 μM 24 hours To evaluate the effect of SHP099 on human PBMCs, results showed that SHP099 significantly upregulated the mRNA levels of IFN-γ, GZMB, and PRF. PMC6437555
HUVECs 5 μM 24 hours To investigate the inhibitory effect of SHP099 on HUVECs, the results showed that SHP099 reversed the pro-proliferative effect of E2-treated endothelial cells on endometrial organoids. PMC11538683
KRAS amplified gastric cancer cells 3, 5 or 10 µM 5 days To evaluate the anti-proliferative effect of SHP099 in combination with GSK1120212 on KRAS amplified gastric cancer cells, results showed significant inhibition of cell proliferation PMC6039276
H358 NSCLC cells 10 μM 7 days To evaluate the effect of SHP099 in combination with MEK inhibitors on colony formation, results showed that cells expressing SHP099-resistant mutants did not respond to the combination treatment PMC6170706
PDAC cell lines 10 μM 7 or 10 days To evaluate the effect of SHP099 in combination with MEK inhibitors on cell proliferation and colony formation, results showed that the combination significantly inhibited cell proliferation and colony formation PMC6170706
Kmt2d KO LUSC cells 0.559 μM, 0.310 μM, 1.165 μM (IC50) 72 hours Evaluate the effect of SHP099 on the viability of Kmt2d KO LUSC cells, showing that these cells are highly sensitive to SHP099. PMC10388706
KP cells 10 μM 72 hours SHP099 significantly inhibited the MEK/ERK signaling pathway in KP cells and induced CXCL1 and CXCL5 expression. PMC8758507
H1975 cells 10 μM 72 hours SHP099 significantly inhibited the MEK/ERK signaling pathway in H1975 cells and induced GRO family gene expression. PMC8758507
Neural progenitor cells (NPCs) 0.1 to 100 μM 72 hours To evaluate the effects of SHP099 on the survival of neural progenitor cells, it was found that SHP099 significantly inhibited the survival of neural progenitor cells. PMC6827835
GBM cell lines 0.1 to 100 μM 72 hours To evaluate the effects of SHP099 on the survival of GBM cell lines, it was found that SHP099 significantly inhibited the survival of GBM cell lines. PMC6827835
Patient-derived glioma stem-like cells (GSCs) 0.1 to 100 μM 72 hours To evaluate the effects of SHP099 on the survival of patient-derived glioma stem-like cells, it was found that SHP099 significantly inhibited the survival of these cells. PMC6827835
MV-4-11 2.5 μM 72 hours To study the inhibitory effect of SHP099 on MV-4-11 cells, results showed that the cells developed resistance to SHP099 PMC9177641
MOLM-13 10 μM 72 hours To study the inhibitory effect of SHP099 on MOLM-13 cells, results showed that the cells developed resistance to SHP099 PMC9177641
Alveolar macrophages 10-50 μM Not used To evaluate the effect of SHP099 on TBET ubiquitination in alveolar macrophages, results showed that 50 μM SHP099 significantly enhanced TBET ubiquitination levels. PMC11126869
CT-26 cells 0.3 – 10 μM To evaluate the effect of SHP099 on the viability of CT-26 cells, results showed that SHP099 did not significantly inhibit the viability of CT-26 cells at concentrations ranging from 0.3 – 10 μmol/L. PMC6437555
Lin-negative bone marrow cells 0.1 μM 36~48 hours SHP099 treatment of Tet2-KO Lin-negative bone marrow cells inhibits IL-6 induced cell survival PMC6317370

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
129Sv/Ev mice Anti-PD-1 resistant 344SQ NSCLC adenocarcinoma model Oral 100 mg/kg Starting from day 5, continued for 5 days on and 2 days off, until death To evaluate the effect of SHP099 combined with radiotherapy and anti-PD-L1, results showed that the combination therapy significantly enhanced local and abscopal tumor control, reduced lung metastases, and improved mouse survival. PMC10173258
NOD-SCID mice KRAS amplified gastric cancer xenograft model Oral 50 mg/kg daily for 5 weeks To evaluate the anti-tumor effect of SHP099 in combination with GSK1120212 on KRAS amplified gastric cancer xenograft models, results showed significant inhibition of tumor growth PMC6039276
Mice Kmt2d KO LUSC model Oral SHP099 75mpk, afatinib 10mpk once daily, 5 days/week Evaluate the effect of SHP099 and afatinib on the growth of Kmt2d KO LUSC tumors, showing that the combination therapy significantly inhibits tumor growth and prolongs survival. PMC10388706
Mice Capan-2, MIAPaCa-2 and H358 xenograft models Oral SHP099 75 mg/kg, trametinib 0.25 mg/kg SHP099 daily, trametinib daily, for 37, 19, or 21 days To evaluate the effect of SHP099 in combination with MEK inhibitors on tumor growth, results showed that the combination significantly inhibited tumor growth and reduced tumor cellularity and vascularity PMC6170706
Mice KP NSCLC allograft model Oral gavage 75 mg/kg once daily for 4 weeks SHP099 significantly inhibited KP tumor growth, increased T-cell infiltration, but also increased granulocytic myeloid-derived suppressor cell (gMDSC) infiltration. PMC8758507
Nu/Nu mice Subcutaneous xenograft model Oral 75 mg/kg SHP099, 25 mg/kg ceritinib Daily, continuous treatment To evaluate the effect of SHP099 in combination with ceritinib on tumor growth, results showed that the combination significantly inhibited tumor growth. PMC6343825
C57BL/6J mice orthotopic xenograft models Oral gavage 100 mg/kg Single dose, observed for 24 hours To evaluate the pharmacokinetics of SHP099 in vivo and its antitumor effects on orthotopic xenograft models of glioblastoma, it was found that SHP099 reached effective concentrations in brain tissues and significantly inhibited tumor growth. PMC6827835
C57BL/6 mice MC38 colon cancer xenograft model Oral 5 mg/kg Once daily for 14 days To evaluate the anti-tumor effect of SHP099 in the MC38 colon cancer xenograft model, results showed that SHP099 significantly reduced tumor volume and weight, and enhanced anti-tumor immune responses in the tumor microenvironment. PMC8802865
Mice TNBS-induced colitis model Oral or intraperitoneal injection 5 mg/kg Daily administration for 4 days To verify whether the improvement of TNBS-induced colitis by oleanolic acid was dependent on SHP2, results showed that SHP099 eliminated the ameliorative effect of oleanolic acid. PMC11143531
Mouse inv(16)/ KitD816Y AML model 100 nmol/L 10 days To study the effect of RMC-4550 on the inv(16)/ KitD816Y AML mouse model, results showed that combined treatment with RMC-4550 and BLU-285 significantly reduced AML clonogenic potential PMC9177641
C57BL/6 mice Destabilization of medial meniscus (DMM)-induced osteoarthritis model Intra-articular injection 20 µmol/L Twice a week for two weeks SHP099 significantly attenuated DMM-induced osteoarthritis progression by inhibiting M1 macrophage polarization, including joint synovitis and cartilage damage. PMC9293663
BALB/c mice CT-26 colon cancer xenograft model Intraperitoneal injection 5 mg/kg Once daily, until the end of the experiment To evaluate the effect of SHP099 on tumor growth in the CT-26 colon cancer xenograft model, results showed that SHP099 significantly reduced tumor volume and weight without affecting the overall health of the mice. PMC6437555
Mice Endometrial hyperplasia model Subcutaneous injection 10 mg/kg Once daily for 21 days To investigate the inhibitory effect of SHP099 on endometrial hyperplasia in mice, the results showed that SHP099 significantly alleviated E2-induced endometrial hyperplasia. PMC11538683

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.84mL

0.57mL

0.28mL

14.19mL

2.84mL

1.42mL

28.39mL

5.68mL

2.84mL

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