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MedChemExpress
compounds sitagliptin ![]() Compounds Sitagliptin, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/compounds sitagliptin/product/MedChemExpress Average 93 stars, based on 1 article reviews
compounds sitagliptin - by Bioz Stars,
2026-02
93/100 stars
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Boehringer Ingelheim
sitagliptin ![]() Sitagliptin, supplied by Boehringer Ingelheim, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/sitagliptin/product/Boehringer Ingelheim Average 90 stars, based on 1 article reviews
sitagliptin - by Bioz Stars,
2026-02
90/100 stars
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Cayman Chemical
auda ![]() Auda, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/auda/product/Cayman Chemical Average 90 stars, based on 1 article reviews
auda - by Bioz Stars,
2026-02
90/100 stars
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Novartis
vildagliptin ![]() Vildagliptin, supplied by Novartis, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/vildagliptin/product/Novartis Average 90 stars, based on 1 article reviews
vildagliptin - by Bioz Stars,
2026-02
90/100 stars
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Sitagliptin Related Compound 1 is an impurity of Sitagliptin Sitagliptin is a dipeptidyl peptidase 4 DPP 4 inhibitor for treatment of diabetes mellitus type 2
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Sitagliptin Related Compound
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Sitagliptin phosphate monohydrate (MK-0431 phosphate monohydrate) is a potent inhibitor of DPP4 with an IC50 of 19 nM in Caco-2 cell extracts.
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Sitagliptin-d4 (phosphate) is the deuterium labeled Sitagliptin phosphate. Sitagliptin phosphate (MK-0431 phosphate) is a potent inhibitor of DPP4 with an IC50 of 19 nM in Caco-2 cell extracts.
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Sitagliptin 100 µg mL in Acetonitrile
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(S)-Sitagliptin is the S-isomer of Sitagliptin Phosphate, as an impurity.
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Sitagliptin is an oral dipeptidyl peptidase-4 (DPP-4) inhibitor used for the management of type 2 diabetes mellitus.
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Image Search Results
Journal: BMC Pharmacology & Toxicology
Article Title: Repurposing DPP-4 inhibitors as anticancer agents in KRAS-mutated pancreatic ductal adenocarcinoma
doi: 10.1186/s40360-025-01020-z
Figure Lengend Snippet: IC 50 plots of Sitagliptin (A) and Linagliptin (C) in MIA PaCa-2 and PANC-1 cells and 2D structures Sitagliptin (B) and Linagliptin (D) were depicted. The viability percentage was normalized to the control. All the experiments were performed in double triplicates ( n = 6) and the data were shown as mean ± SD respectively
Article Snippet: The
Techniques: Control
Journal: BMC Pharmacology & Toxicology
Article Title: Repurposing DPP-4 inhibitors as anticancer agents in KRAS-mutated pancreatic ductal adenocarcinoma
doi: 10.1186/s40360-025-01020-z
Figure Lengend Snippet: Wound healing of Sitagliptin and Linagliptin in MIA PaCa-2 (A & C) and PANC-1 (B & D) cells. The wound closure was measured at 0, 24, and 48 h. All the experiments were performed in triplicates ( n = 3) and the data were shown as mean ± SD respectively
Article Snippet: The
Techniques:
Journal: BMC Pharmacology & Toxicology
Article Title: Repurposing DPP-4 inhibitors as anticancer agents in KRAS-mutated pancreatic ductal adenocarcinoma
doi: 10.1186/s40360-025-01020-z
Figure Lengend Snippet: Colony formation of Sitagliptin and Linagliptin in MIA PaCa-2 (A) and PANC-1 (B) cells. All the experiments were performed in triplicates ( n = 3) and the data were shown as mean ± SD respectively
Article Snippet: The
Techniques:
Journal: BMC Pharmacology & Toxicology
Article Title: Repurposing DPP-4 inhibitors as anticancer agents in KRAS-mutated pancreatic ductal adenocarcinoma
doi: 10.1186/s40360-025-01020-z
Figure Lengend Snippet: Intracellular ROS production (DCFH-DA) and DNA fragmentation (DAPI) of Sitagliptin and Linagliptin in MIA PaCa-2 (A & B) and PANC-1 (C & D) cells respectively. All the experiments were performed in triplicates ( n = 3) and the data were shown as mean ± SD respectively
Article Snippet: The
Techniques:
Journal: BMC Pharmacology & Toxicology
Article Title: Repurposing DPP-4 inhibitors as anticancer agents in KRAS-mutated pancreatic ductal adenocarcinoma
doi: 10.1186/s40360-025-01020-z
Figure Lengend Snippet: Apoptosis induction potential of Sitagliptin and Linagliptin in MIA PaCa-2 (A) and PANC-1 cells (B) . The apoptosis induced cells in the control and treated groups were determined by employing FITC detection in x-axis and PI detection in y-axis respectively. In the plot, LL, LR, UR, & UL represents the amount of cells in the normal, early apoptotic, late apoptotic, and necrosis states respectively. All the experiments were performed in triplicates ( n = 3) and the data were shown as mean ± SD respectively
Article Snippet: The
Techniques: Control
Journal: BMC Pharmacology & Toxicology
Article Title: Repurposing DPP-4 inhibitors as anticancer agents in KRAS-mutated pancreatic ductal adenocarcinoma
doi: 10.1186/s40360-025-01020-z
Figure Lengend Snippet: mRNA expression analysis of Sitagliptin and Linagliptin in MIA PaCa-2 (A) and PANC-1 cells (B) . All the mRNA expression levels were normalized with GAPDH, and the normalized expression levels of BAX, BCL-2, CASP3, PARP, KRAS, BRAF, MEK, and ERK were calculated by 2-ΔΔCT method. All the experiments were performed in triplicates ( n = 3) and the data were shown as mean ± SD respectively
Article Snippet: The
Techniques: Expressing
Journal: BMC Pharmacology & Toxicology
Article Title: Repurposing DPP-4 inhibitors as anticancer agents in KRAS-mutated pancreatic ductal adenocarcinoma
doi: 10.1186/s40360-025-01020-z
Figure Lengend Snippet: Commonly shared targets of pancreatic ductal adenocarcinoma (PDAC) with Sitagliptin (A1) and Linagliptin (A2) were showed in Venn diagram. The protein-protein interaction (PPI) network of 63 commonly shared targets of Sitagliptin (B1) and 75 commonly shared targets of Linagliptin (B2) were showed. Then the hub genes were identified by using parametes like MCC, degree, betweenness, & closeness for Sitagliptin (C1) and Linagliptin (C2) and showed in Venn diagram. The PPI interaction network of TOP hub genes were shown, for Sitagliptin (D1) and Linagliptin (D2) respectively
Article Snippet: The
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