analogue Search Results


94
MedChemExpress price 1 ido in 7
Price 1 Ido In 7, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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KCAS Bioanalytical and Biomarker Services electrodes
Electrodes, supplied by KCAS Bioanalytical and Biomarker Services, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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91
Novus Biologicals recombinant human proinsulin c peptide
Recombinant Human Proinsulin C Peptide, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Toronto Research Chemicals dehydro nifedipine
Figure 3. Matrix effect: postcolumn infusion (T-Joint) method for <t>nifedipine</t> and nifedipine–d4 (RT 2.88) to demonstrate absence of any ion suppression/enhancement.
Dehydro Nifedipine, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Selleck Chemicals nucleoside analogues
Surface structure of lead FDA approved drug, <t>nucleoside</t> inhibitor and natural substrate at SARS-CoV-2 A1pp domain active site. (A) Surface structure of lactobionic acid at ADP-ribose-1″-phosphatase active site. (B) Surface structure of NA 1 at ADP-ribose-1″-phosphatase active site. (C) Surface structure of adenosine-5-diphosphoribose at ADP-ribose-1″-phosphatase active site. (D) 2D structure of lactobionic acid. (E) 2D structure of NA 1 . (F) 2D structure of adenosine-5-diphosphoribose.
Nucleoside Analogues, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
National Research Council Canada mussel tissue certified reference material
Surface structure of lead FDA approved drug, <t>nucleoside</t> inhibitor and natural substrate at SARS-CoV-2 A1pp domain active site. (A) Surface structure of lactobionic acid at ADP-ribose-1″-phosphatase active site. (B) Surface structure of NA 1 at ADP-ribose-1″-phosphatase active site. (C) Surface structure of adenosine-5-diphosphoribose at ADP-ribose-1″-phosphatase active site. (D) 2D structure of lactobionic acid. (E) 2D structure of NA 1 . (F) 2D structure of adenosine-5-diphosphoribose.
Mussel Tissue Certified Reference Material, supplied by National Research Council Canada, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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97
MedChemExpress pi3k inhibitor
Surface structure of lead FDA approved drug, <t>nucleoside</t> inhibitor and natural substrate at SARS-CoV-2 A1pp domain active site. (A) Surface structure of lactobionic acid at ADP-ribose-1″-phosphatase active site. (B) Surface structure of NA 1 at ADP-ribose-1″-phosphatase active site. (C) Surface structure of adenosine-5-diphosphoribose at ADP-ribose-1″-phosphatase active site. (D) 2D structure of lactobionic acid. (E) 2D structure of NA 1 . (F) 2D structure of adenosine-5-diphosphoribose.
Pi3k Inhibitor, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
TargetMol vps34
EFNB1-induced autophagy is independent of MTOR inhibition. (A) Ls174t cells were treated as indicated, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (B-D) Ls174t cells were pretreated with SBI-0206965 (10 μM) (B), 3-MA (5 mM) (C) or wortmannin (100 nM) (D) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitors for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (E) Ls174t cells were pretreated with DMSO, 3-MA (5 mM) or wortmannin (100 nM) for 1 h, followed by plate-coated Fc or ephrin-B1-Fc (10 μg/ml) for 2 h in presence of the inhibitors and followed by confocal microscopy analysis of MAP1LC3B puncta. Quantification of cells with puncta of MAP1LC3B-II was shown in the bottom panel. Scale bar: 5 μm. (F) Ls174t cells were pretreated with <t>VPS34-IN1</t> (2 μM) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitor for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification was shown in the right panel. (G) Control-gRNA or ATG5-gRNA infected Ls174t cells were treated with 10 μg/ml plate-coated Fc (0 time point) or ephrin-B1-Fc, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. WT: wild type; KO: knockout; 3-MA: 3-methyladenine. All error bars represent SEM of technical replicates. *: P < 0.05, **: P < 0.01, ***: P < 0.001, ****: P < 0.0001 based on two-sided unpaired T test (A-G). Densitometry quantification of A-D and F-G were based on three independent experiments. Data are representative of three independent experiments
Vps34, supplied by TargetMol, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
KCAS Bioanalytical and Biomarker Services liquid chromatography
EFNB1-induced autophagy is independent of MTOR inhibition. (A) Ls174t cells were treated as indicated, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (B-D) Ls174t cells were pretreated with SBI-0206965 (10 μM) (B), 3-MA (5 mM) (C) or wortmannin (100 nM) (D) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitors for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (E) Ls174t cells were pretreated with DMSO, 3-MA (5 mM) or wortmannin (100 nM) for 1 h, followed by plate-coated Fc or ephrin-B1-Fc (10 μg/ml) for 2 h in presence of the inhibitors and followed by confocal microscopy analysis of MAP1LC3B puncta. Quantification of cells with puncta of MAP1LC3B-II was shown in the bottom panel. Scale bar: 5 μm. (F) Ls174t cells were pretreated with <t>VPS34-IN1</t> (2 μM) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitor for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification was shown in the right panel. (G) Control-gRNA or ATG5-gRNA infected Ls174t cells were treated with 10 μg/ml plate-coated Fc (0 time point) or ephrin-B1-Fc, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. WT: wild type; KO: knockout; 3-MA: 3-methyladenine. All error bars represent SEM of technical replicates. *: P < 0.05, **: P < 0.01, ***: P < 0.001, ****: P < 0.0001 based on two-sided unpaired T test (A-G). Densitometry quantification of A-D and F-G were based on three independent experiments. Data are representative of three independent experiments
Liquid Chromatography, supplied by KCAS Bioanalytical and Biomarker Services, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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91
Selleck Chemicals tic10 analogue
EFNB1-induced autophagy is independent of MTOR inhibition. (A) Ls174t cells were treated as indicated, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (B-D) Ls174t cells were pretreated with SBI-0206965 (10 μM) (B), 3-MA (5 mM) (C) or wortmannin (100 nM) (D) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitors for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (E) Ls174t cells were pretreated with DMSO, 3-MA (5 mM) or wortmannin (100 nM) for 1 h, followed by plate-coated Fc or ephrin-B1-Fc (10 μg/ml) for 2 h in presence of the inhibitors and followed by confocal microscopy analysis of MAP1LC3B puncta. Quantification of cells with puncta of MAP1LC3B-II was shown in the bottom panel. Scale bar: 5 μm. (F) Ls174t cells were pretreated with <t>VPS34-IN1</t> (2 μM) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitor for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification was shown in the right panel. (G) Control-gRNA or ATG5-gRNA infected Ls174t cells were treated with 10 μg/ml plate-coated Fc (0 time point) or ephrin-B1-Fc, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. WT: wild type; KO: knockout; 3-MA: 3-methyladenine. All error bars represent SEM of technical replicates. *: P < 0.05, **: P < 0.01, ***: P < 0.001, ****: P < 0.0001 based on two-sided unpaired T test (A-G). Densitometry quantification of A-D and F-G were based on three independent experiments. Data are representative of three independent experiments
Tic10 Analogue, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Selleck Chemicals glpg0634
KEY RESOURCES TABLE
Glpg0634, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Santa Cruz Biotechnology gleevec
A) The percentage of inhibition of MCF-7-S cells treated with increasing concentrations of TAM and <t>Gleevec.</t> The shade of red represents the amount of inhibition in cells. B) Observed synergism scores that correspond to the percent inhibition values of TAM and Gleevec treatment using ZIP synergy from SynergyFinder 2.0.
Gleevec, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Figure 3. Matrix effect: postcolumn infusion (T-Joint) method for nifedipine and nifedipine–d4 (RT 2.88) to demonstrate absence of any ion suppression/enhancement.

Journal: International Journal of Pharmacokinetics

Article Title: Method development challenges and regulatory expectation in nifedipine

doi: 10.4155/ipk-2016-0004

Figure Lengend Snippet: Figure 3. Matrix effect: postcolumn infusion (T-Joint) method for nifedipine and nifedipine–d4 (RT 2.88) to demonstrate absence of any ion suppression/enhancement.

Article Snippet: Dehydro nifedipine (purity: 98%) and hydroxydehydro nifedipine carboxylate (purity: 97%) were procured from Toronto Research Chemicals (Ontario, Canada).

Techniques:

Surface structure of lead FDA approved drug, nucleoside inhibitor and natural substrate at SARS-CoV-2 A1pp domain active site. (A) Surface structure of lactobionic acid at ADP-ribose-1″-phosphatase active site. (B) Surface structure of NA 1 at ADP-ribose-1″-phosphatase active site. (C) Surface structure of adenosine-5-diphosphoribose at ADP-ribose-1″-phosphatase active site. (D) 2D structure of lactobionic acid. (E) 2D structure of NA 1 . (F) 2D structure of adenosine-5-diphosphoribose.

Journal: Computers in Biology and Medicine

Article Title: Identification of FDA approved drugs and nucleoside analogues as potential SARS-CoV-2 A1pp domain inhibitor: An in silico study

doi: 10.1016/j.compbiomed.2020.104185

Figure Lengend Snippet: Surface structure of lead FDA approved drug, nucleoside inhibitor and natural substrate at SARS-CoV-2 A1pp domain active site. (A) Surface structure of lactobionic acid at ADP-ribose-1″-phosphatase active site. (B) Surface structure of NA 1 at ADP-ribose-1″-phosphatase active site. (C) Surface structure of adenosine-5-diphosphoribose at ADP-ribose-1″-phosphatase active site. (D) 2D structure of lactobionic acid. (E) 2D structure of NA 1 . (F) 2D structure of adenosine-5-diphosphoribose.

Article Snippet: The structures of FDA approved drugs and nucleoside analogues were downloaded from selleckchem ( https://www.selleckchem.com/ ) in. sdf format and converted to different formats using Open Babel software.

Techniques:

EFNB1-induced autophagy is independent of MTOR inhibition. (A) Ls174t cells were treated as indicated, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (B-D) Ls174t cells were pretreated with SBI-0206965 (10 μM) (B), 3-MA (5 mM) (C) or wortmannin (100 nM) (D) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitors for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (E) Ls174t cells were pretreated with DMSO, 3-MA (5 mM) or wortmannin (100 nM) for 1 h, followed by plate-coated Fc or ephrin-B1-Fc (10 μg/ml) for 2 h in presence of the inhibitors and followed by confocal microscopy analysis of MAP1LC3B puncta. Quantification of cells with puncta of MAP1LC3B-II was shown in the bottom panel. Scale bar: 5 μm. (F) Ls174t cells were pretreated with VPS34-IN1 (2 μM) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitor for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification was shown in the right panel. (G) Control-gRNA or ATG5-gRNA infected Ls174t cells were treated with 10 μg/ml plate-coated Fc (0 time point) or ephrin-B1-Fc, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. WT: wild type; KO: knockout; 3-MA: 3-methyladenine. All error bars represent SEM of technical replicates. *: P < 0.05, **: P < 0.01, ***: P < 0.001, ****: P < 0.0001 based on two-sided unpaired T test (A-G). Densitometry quantification of A-D and F-G were based on three independent experiments. Data are representative of three independent experiments

Journal: Autophagy

Article Title: RNF186 regulates EFNB1 (ephrin B1)-EPHB2-induced autophagy in the colonic epithelial cells for the maintenance of intestinal homeostasis

doi: 10.1080/15548627.2020.1851496

Figure Lengend Snippet: EFNB1-induced autophagy is independent of MTOR inhibition. (A) Ls174t cells were treated as indicated, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (B-D) Ls174t cells were pretreated with SBI-0206965 (10 μM) (B), 3-MA (5 mM) (C) or wortmannin (100 nM) (D) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitors for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. (E) Ls174t cells were pretreated with DMSO, 3-MA (5 mM) or wortmannin (100 nM) for 1 h, followed by plate-coated Fc or ephrin-B1-Fc (10 μg/ml) for 2 h in presence of the inhibitors and followed by confocal microscopy analysis of MAP1LC3B puncta. Quantification of cells with puncta of MAP1LC3B-II was shown in the bottom panel. Scale bar: 5 μm. (F) Ls174t cells were pretreated with VPS34-IN1 (2 μM) for 1 h, followed by the treatment of plate-coated Fc or ephrin-B1-Fc (10 ug/ml) in presence of the inhibitor for the indicated time. Cell lysates were analyzed by western blot for the indicated proteins. Densitometry quantification was shown in the right panel. (G) Control-gRNA or ATG5-gRNA infected Ls174t cells were treated with 10 μg/ml plate-coated Fc (0 time point) or ephrin-B1-Fc, followed by western blot analysis of the indicated proteins. Densitometry quantification from three independent experiments was shown in the right panel. WT: wild type; KO: knockout; 3-MA: 3-methyladenine. All error bars represent SEM of technical replicates. *: P < 0.05, **: P < 0.01, ***: P < 0.001, ****: P < 0.0001 based on two-sided unpaired T test (A-G). Densitometry quantification of A-D and F-G were based on three independent experiments. Data are representative of three independent experiments

Article Snippet: ULK inhibitor SBI-0206965 (T2128), PtdIns3K inhibitor 3-MA (T1879), wortmannin (T6283) and Vps34-IN-1 (T7015) were bought from TargetMol.

Techniques: Inhibition, Western Blot, Confocal Microscopy, Infection, Knock-Out

KEY RESOURCES TABLE

Journal: Cell stem cell

Article Title: Jak1 Integrates Cytokine Sensing to Regulate Hematopoietic Stem Cell Function and Stress Hematopoiesis

doi: 10.1016/j.stem.2017.08.011

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: To test the effect of pharmacological Jak1 or Cdk6 inhibition, whole BM cells from wt mice were plated with varying concentrations of GLPG0634 or PD332991 (Selleckchem).

Techniques: Recombinant, Microscopy, Software

A) The percentage of inhibition of MCF-7-S cells treated with increasing concentrations of TAM and Gleevec. The shade of red represents the amount of inhibition in cells. B) Observed synergism scores that correspond to the percent inhibition values of TAM and Gleevec treatment using ZIP synergy from SynergyFinder 2.0.

Journal: bioRxiv

Article Title: CRISPRa screen identifies a role for c-KIT signaling in tamoxifen resistance, potentially through upregulation of ABC transporters

doi: 10.1101/2022.08.22.504845

Figure Lengend Snippet: A) The percentage of inhibition of MCF-7-S cells treated with increasing concentrations of TAM and Gleevec. The shade of red represents the amount of inhibition in cells. B) Observed synergism scores that correspond to the percent inhibition values of TAM and Gleevec treatment using ZIP synergy from SynergyFinder 2.0.

Article Snippet: The following cell culture media supplements and concentrations were used throughout this study unless indicated otherwise: Doxycycline hyclate (2ug/ml, Sigma, cat# D9891-5G), tamoxifen as (Z)-4-Hydroxytamoxifen (1uM, 4-OHT; Sigma-Aldrich; Cat# H7904), and Gleevec (Imatinib mesylate; Santa Cruz; cat # CAS 220127-57-1).

Techniques: Inhibition