214 Results for "

mouse fibroblast

" in MedChemExpress (MCE) Product Catalog:
Products (214)

214 Results for "mouse fibroblast" in MCE Product Catalog:

14
14 Publications Verification
Cat. No.: HY-P7066
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF2; BFGF; Prev. FGFB; Basic fibroblast Growth Factor; fibroblast Growth Factor 2 (Basic); fibroblast Growth Factor; Heparin-Binding Growth Factor 2; Prostatropin; HBGF-2; FGF2A; FGF-2; FGF; fibroblast Growth Factor 2; Basic fibroblast Growth Factor BFGF
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10
10 Cited Publications
Cat. No.: HY-P73130
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: IFNB1; IFF; Prev. IFNB; fibroblast Interferon; IFB; IFN-Beta; Interferon Beta; Interferon-Beta; Interferon Beta 1; Interferon, Beta 1, fibroblast
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6
6 Cited Publications
Cat. No.: HY-18601
CAS No.: 1416258-16-6
Target:  

HIV HIV Integrase

Research Areas:  

Infection

(±)-BI-D is a potent ALLINI (allosteric integrase inhibitor). (±)-BI-D binds integrase at the LEDGF/p75 binding site. (±)-BI-D inhibits HIV-Luc infection in cells (IC50: 0.16 μM in Psip1 knockout E9 mouse embryonic fibroblasts, 2.9 μM in wild-type E9 mouse embryonic fibroblasts) .
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5
5 Cited Publications
Cat. No.: HY-P7170
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF10; Produced By fibroblasts Of Urinary Bladder Lamina Propria; fibroblast Growth Factor 10; fibroblast Growth Factor; Keratinocyte Growth Factor 2; LADD3; FGF-10; FGF
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5
5 Cited Publications
Cat. No.: HY-P1290
CAS No.: 121932-06-7
Synonyms: PKI-(6-22)-amide
Target:  

PKA

Research Areas:  

Neurological Disease

PKA Inhibitor Fragment (6-22) amide is a highly potent and specific competitive inhibitor of PKA, with Ki values of 1.7 nM and 1.6 nM against human and bovine PKA catalytic subunits, respectively. The IC50 of PKA Inhibitor Fragment (6-22) amide targeting bovine PKA is 8.6 nM. PKA Inhibitor Fragment (6-22) amide effectively abolishes PKA activity in mouse brain and spinal cord, and exerts in vivo efficacy via intracerebroventricular administration. PKA Inhibitor Fragment (6-22) amide significantly reverses low-dose morphine analgesic tolerance in mice and blocks photoaffinity labeling of cAMP-dependent protein kinase. PKA Inhibitor Fragment (6-22) amide can be applied to research in fields related to the mechanism of morphine analgesic tolerance and skin wound healing .
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4
4 Cited Publications
Cat. No.: HY-P7173
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF21; FGF-21; fibroblast Growth Factor 21; FGF; fibroblast Growth Factor
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3
3 Cited Publications
Cat. No.: HY-107588
CAS No.: 916734-43-5
Purity:  99.94%
Target:  

Integrin

Research Areas:  

Cardiovascular Disease

TC-I 15 (TC-I-15) is a type of allosteric collagen-binding integrin α2β1 inhibitor, and it also inhibits α1β1 and α11β1. TC-I 15 inhibits platelet adhesion to collagen and thrombus deposition. TC-I 15 prevents the formation of a pre-metastatic microenvironment by inhibiting the uptake of cancer-associated fibroblast (CAF) extracellular vesicles (EVs) by lung fibroblasts, which reduces the metastasis of salivary gland adenocystic carcinoma (SACC) to the lungs in mouse models, .
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3
3 Cited Publications
Cat. No.: HY-P72651
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF21; FGF-21; fibroblast Growth Factor 21; FGF; fibroblast Growth Factor
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3
3 Cited Publications
Cat. No.: HY-P73052
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF2; BFGF; Prev. FGFB; Basic fibroblast Growth Factor; fibroblast Growth Factor 2 (Basic); fibroblast Growth Factor; Heparin-Binding Growth Factor 2; Prostatropin; HBGF-2; FGF2A; FGF-2; FGF; fibroblast Growth Factor 2; Basic fibroblast Growth Factor BFGF
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3
3 Cited Publications
Cat. No.: HY-P70533
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF8; HBGF-8; fibroblast Growth Factor 8; FGF-8; AIGF; fibroblast Growth Factor; Androgen-Induced Growth Factor; KAL6; fibroblast Growth Factor 8 (Androgen-Induced); HH6; Heparin-Binding Growth Factor 8; FGF
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2
2 Cited Publications
Cat. No.: HY-P991218
Synonyms: EnX203
Anti-IL11 Antibody (X203) (EnX203) is a human-derived IgG1, κ type antibody inhibitor, targeting to human IL-11 . Recommend Isotype Controls: Human IgG1 kappa, Isotype Control (HY-P99001).
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2
2 Cited Publications
Cat. No.: HY-P71084
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: S100A4; fibroblast-Specific Protein-1; Prev. CAPL; Murine Placental Homolog; Prev. MTS1; Protein S100-A4; PEL98; Metastasin 1; P9KA; Protein Mts1; 18A2; Calvasculin; FSP1; Leukemia Multidrug Resistance Associated Protein; 42A; Malignant Transformation Sup
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1
1 Cited Publications
Cat. No.: HY-148764
CAS No.: 890808-56-7
Purity:  99.90%
Research Areas:  

Cancer

M47 is a molecular glue that selectively destabilizes Cryptochrome 1 (CRY1) and increases degradation of the CRY1 in the nucleus. M47 enhances apoptosis in Ras-transformed P53-deficient mouse skin fibroblast lines and enhances life span in p53 knockout mice. M47 can be used in research of cancer .
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1
1 Cited Publications
Cat. No.: HY-128895
CAS No.: 1800405-30-4
Purity:  99.94%
KL1333, a derivative of β-lapachone, is an orally available NAD+ modulator. KL1333 reacts with NAD(P)H:quinone oxidoreductase 1 (NQO1) as a substrate, resulting in increases in intracellular NAD+ levels via NADH oxidation. KL1333 improves energy metabolism and mitochondrial dysfunction in MELAS fibroblasts. KL1333 protects against Cisplatin-induced ototoxicity in mouse cochlear cultures .
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1
1 Cited Publications
Cat. No.: HY-16160
CAS No.: 851636-83-4
Target:  

Autophagy ICMT

Research Areas:  

Neurological Disease Cancer

Cysmethynil is an Icmt inhibitor(IC50 = 2.4 μM). Cysmethynil inhibites RAS membrane binding and EGF signal transduction. Cysmethynil prevents the cells in the G1 phase and induces autophagy. Cysmethynil inhibits PC3 cells proliferation, has synergistic effect with Paclitaxel (HY-B0015) and Doxorubicin (HY-15142A). Cysmethynil has anti-tumor effects and can be used for solid tumor (such as prostate cancer et al.) research .
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1
1 Cited Publications
Cat. No.: HY-N0008
CAS No.: 21082-33-7
Orcinol glucoside is an orally active, blood-brain barrier permeable osteoblast proliferation promoter that targets the Nrf2/Keap1, mTOR and p38 signaling pathways. Orcinol glucoside promotes Nrf2 nuclear translocation, upregulates antioxidant enzyme levels, enhances the phosphorylation of mTOR and p70S6K, and inhibits the enzymatic activity of HAS2 as well as the nuclear translocation of GR. Orcinol glucoside also alleviates oxidative stress, inhibits autophagic flux, osteoclastogenesis and TGF-β1-induced M2 polarization, while reducing collagen deposition and effectively promoting the proliferation, differentiation and mineralization of osteoblasts. Orcinol glucoside also exhibits anti-pulmonary fibrosis, anxiolytic and antidepressant activities. Orcinol glucoside can be used in the research of senile and glucocorticoid-induced osteoporosis, idiopathic pulmonary fibrosis (IPF), anxiety and other related diseases .
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1
1 Cited Publications
Cat. No.: HY-136093B
CAS No.: 1422365-93-2
Synonyms: IM156 free base; HL156A free base; HL271 free base
Lixumistat (IM156 free base) is a potent and orally active AMPK activator and OXPHOS inhibitor. Lixumistat strongly activates AMPK, while it lacks the systemic metabolic regulatory effects of classic metformin, such as hypoglycemic and weight-lowering activities. Lixumistat exhibits significant therapeutic effects on cognitive decline associated with brain aging and pulmonary fibrosis .
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1
1 Cited Publications
Cat. No.: HY-101317
CAS No.: 1217628-73-3
Purity:  99.20%
Synonyms: SB-205607 dihydrobromide
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

TAN-67 (SB-205607) dihydrobromide is a potent and selective nonpeptidic δ-opioid receptor agonist with a Ki value of 0.647 nM. TAN-67 dihydrobromide has neuroprotective effect. TAN-67 dihydrobromide can be used in research of ischemic stroke .
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1
1 Cited Publications
Cat. No.: HY-P71526
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: fibroblast growth factor 15; FGF-15; Fgf15; FGF15_mouse; FGF19
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1
1 Cited Publications
Cat. No.: HY-P7176
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: FGF7; HBGF-7; fibroblast Growth Factor 7; FGF-7; KGF; fibroblast Growth Factor 7 (Keratinocyte Growth Factor); Keratinocyte Growth Factor; fibroblast Growth Factor; Heparin-Binding Growth Factor 7; FGF
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