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RCGD423 (Cat No.:I019699) is a compound that acts as a Glycoprotein130 (gp130) signal modulator. It has shown potential in preclinical studies for regulating cartilage growth and differentiation. In vitro research indicates RCGD423 prevents articular cartilage
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Tocris
rcgd423 ![]() Rcgd423, supplied by Tocris, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/rcgd+423/pmc08615769-51-25-26?v=Tocris Average 91 stars, based on 1 article reviews
rcgd423 - by Bioz Stars,
2026-08
91/100 stars
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Mebiol Inc
rcgd 423 ![]() Rcgd 423, supplied by Mebiol Inc, 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/product/rcgd+423/pmc08444286-85-180-148?v=Mebiol+Inc Average 90 stars, based on 1 article reviews
rcgd 423 - by Bioz Stars,
2026-08
90/100 stars
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MolPort Inc
rcgd 423 n-(4-bromophenyl)-4-phenyl-1,3-thiazol-2-amine ![]() Rcgd 423 N (4 Bromophenyl) 4 Phenyl 1,3 Thiazol 2 Amine, supplied by MolPort Inc, 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/product/rcgd+423/us11247974-1401-0-8?v=MolPort+Inc Average 90 stars, based on 1 article reviews
rcgd 423 n-(4-bromophenyl)-4-phenyl-1,3-thiazol-2-amine - by Bioz Stars,
2026-08
90/100 stars
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RCGD 423 is a modulator of gp130 It increases levels of phosphorylated STAT3 and Myc in isolated pig articular chondrocytes ECs 4 5 7 2 µM effects that can be reversed by the gp130 inhibitor
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Image Search Results
Journal: Cancers
Article Title: Conversion of Osteoclasts into Bone-Protective, Tumor-Suppressing Cells
doi: 10.3390/cancers13225593
Figure Lengend Snippet: Conversion of RAW264.7 pre-osteoclasts into iTS cells by the treatment with BML284. CN = control, CM = conditioned medium, RAW = RAW264.7 osteoclasts, MC3T3 = MC3T3 osteoblasts, MSC = mesenchymal stem cells, A5 = MLO-A5 osteocytes, 231 = MDA-MB-231 breast cancer cells, EO = EO771 mammary tumor cells, and 4T1.2 = 4T1.2 mammary tumor cells. ** p < 0.01 vs. CN, while ## p < 0.01 vs. A5 CM. ( A – D ) MTT-based viability of EO771 mammary tumor cells in response to a chemically treated conditioned medium, derived from MLO-A5 osteocytes, MSCs, MC3T3 osteoblasts, and RAW264.7 osteoclasts, respectively. NS = NSC228155 (EGF activator), RC = RCGD423 (JAK/STAT activator), m3 = m-3M3FBS (phospholipase C activator), CW = CW008 (PKA activator), OA = OAC2 (Oct4 activator), YS = YS49 (PI3K activator), and BM = BML284 (Wnt activator). ( E , F ) Tumor selectivity of the inhibitory action of RAW CM, examined tumor selectivity of the inhibitory action using 3 tumor cell lines (MDA-MB-231 breast cancer cell line using 3 tumor cell lines (MDA-MB-231 breast cancer cell line, EO771 mammary tumor cell line, and 4T1.2 mammary tumor cell line), and KTB6 human breast epithelial cells. ( G ) Reduction in PTHrP in BM CM.
Article Snippet: RAW264.7 pre-osteoclast cells, MC3T3 osteoblasts, MSCs, and MLO-A5 osteocyte-like cells were treated with 0.5 μM of NSC228155 (Cayman, Ann Arbor, MI, USA), 20 μM of
Techniques: Control, Derivative Assay