126 Results for "

bone morphogenetic protein

" in MedChemExpress (MCE) Product Catalog:
Products (126)

126 Results for "bone morphogenetic protein" in MCE Product Catalog:

93
93 Publications Verification
Cat. No.: HY-12071
CAS No.: 1062368-24-4
Purity:  99.41%
Synonyms: DM-3189
Research Areas:  

Cancer

LDN193189 (DM-3189) is a potent selective BMP type I receptor (BMP I) inhibitor. LDN193189 efficiently inhibits transcriptional activity of the BMP type I receptors ALK2 and ALK3 with IC50 values of 5 nM and 30 nM, respectively. LDN193189 can be used for the research of bone morphogenetic protein signalling, such as fibrodysplasia ossificans progressiva .
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93
93 Publications Verification
Cat. No.: HY-12071B
CAS No.: 1435934-00-1
Purity:  99.75%
Synonyms: DM-3189 dihydrochloride
Research Areas:  

Cancer

LDN193189 (DM-3189) dihydrochloride is a potent selective BMP type I receptor (BMP I) inhibitor. LDN193189 efficiently inhibits transcriptional activity of the BMP type I receptors ALK2 and ALK3 with IC50 values of 5 nM and 30 nM, respectively. LDN193189 can be used for the research of bone morphogenetic protein signalling, such as fibrodysplasia ossificans progressiva .
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93
93 Publications Verification
Cat. No.: HY-12071A
CAS No.: 2310134-98-4
Purity:  99.79%
Synonyms: DM-3189 Tetrahydrochloride
Research Areas:  

Cancer

LDN193189 (DM-3189) Tetrahydrochloride is a potent selective BMP type I receptor (BMP I) inhibitor. LDN193189 efficiently inhibits transcriptional activity of the BMP type I receptors ALK2 and ALK3 with IC50 values of 5 nM and 30 nM, respectively. LDN193189 can be used for the research of bone morphogenetic protein signalling, such as fibrodysplasia ossificans progressiva .
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81
81 Cited Publications
Cat. No.: HY-12071C
CAS No.: 1062368-62-0
Synonyms: DM-3189 hydrochloride
LDN193189 (DM-3189) hydrochloride is a potent selective BMP type I receptor (BMP I) inhibitor. LDN193189 efficiently inhibits transcriptional activity of the BMP type I receptors ALK2 and ALK3 with IC50 values of 5 nM and 30 nM, respectively. LDN193189 can be used for the research of bone morphogenetic protein signalling, such as fibrodysplasia ossificans progressiva .
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22
22 Cited Publications
Cat. No.: HY-P7007
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BMP4; MCOPS6; Prev. BMP2B; OFC11; bone morphogenetic protein 2B; BMP-4; bone morphogenetic protein 4 Preproprotein; ZYME; Alternative protein BMP4; DVR4; BMP2B1; bone morphogenetic protein 4; BMP-2B
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21
21 Cited Publications
Cat. No.: HY-P7006
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BMP2; SSFSC1; Prev. BMP2A; SSFSC; bone morphogenetic protein 2A; BMP-2; BMP2 protein; BDA2; bone morphogenetic protein 2; BMP-2A
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8
8 Cited Publications
Cat. No.: HY-124697
CAS No.: 100874-08-6
Purity:  99.98%
Target:  

TGF-β Receptor

Research Areas:  

Cancer

BMP signaling agonist sb4 is a potent benzoxazole bone morphogenetic protein 4 (BMP4) signaling agonist with a EC50 value of 74 nM, activates BMP signaling by stabilizing intracellular p-SMAD-1/5/9. BMP signaling agonist sb4 activates BMP4 target genes (inhibitors of DNA binding,?Id1?and?Id3) canonical BMP signaling .
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5
5 Cited Publications
Cat. No.: HY-P7008
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BMP7; Eptotermin Alfa; bone morphogenetic protein 7; BMP-7; Osteogenic protein 1; OP1; OP-1
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4
4 Cited Publications
Cat. No.: HY-12278
CAS No.: 1431985-92-0
Purity:  99.65%
Target:  

TGF-β Receptor

Research Areas:  

Others

K02288 is a potent bone morphogenetic protein (BMP) type I receptor inhibitor with IC50s of 1.8, 1.1, 6.4 nM for ALK1, ALK2 and ALK6, respectively. K02288 shows slightly weaker inhibition against ALK3 and ALK6 with IC50s of of 5-34 nM.
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4
4 Cited Publications
Cat. No.: HY-P74379
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: BMP4; MCOPS6; Prev. BMP2B; OFC11; bone morphogenetic protein 2B; BMP-4; bone morphogenetic protein 4 Preproprotein; ZYME; Alternative protein BMP4; DVR4; BMP2B1; bone morphogenetic protein 4; BMP-2B
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3
3 Cited Publications
Cat. No.: HY-N0316
CAS No.: 55481-88-4
Mollugin is an orally active and potent NF-κB inhibitor. Mollugin induces S-phase arrest of HepG2 cells, and increased intracellular reactive oxygen species (ROS) levels. Mollugin induces DNA damage in HepG2 cells, as well as an increase in the expression of p-H2AX. Mollugin shows anti-cancer effect by inhibiting TNF-α-induced NF-κB activation. Mollugin enhances the osteogenic action of BMP-2 (bone morphogenetic protein 2) via the p38-Smad signaling pathway .
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3
3 Cited Publications
Cat. No.: HY-112331
CAS No.: 425613-09-8
Purity:  99.66%
Target:  

TGF-β Receptor

Research Areas:  

Cancer

SJ000291942 is an activator of the canonical bone morphogenetic proteins (BMP) signaling pathway. BMPs are members of the transforming growth factor beta (TGFβ) family of secreted signaling molecules.
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3
3 Cited Publications
Cat. No.: HY-P77945
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: GDF15; Placental bone morphogenetic protein; Growth Differentiation Factor 15; Macrophage Inhibitory Cytokine 1; MIC-1; NSAID-Activated Gene 1 protein; NAG-1; NSAID-Regulated Gene 1 protein; PTGFB; Placental TGF-Beta; PLAB; GDF-15; MIC1; NRG-1; PDF; NSAID
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2
2 Cited Publications
Cat. No.: HY-16712
CAS No.: 1627503-67-6
Target:  

TGF-β Receptor

Research Areas:  

Cancer

LDN-214117 is an orally active ALK2 inhibitor with well-tolerated and good brain penetration. LDN-214117 has a high selectivity and low cytotoxicity for ALK2 with an IC50 value of 24 nM. LDN-214117 also is a specific bone morphogenetic proteins (BMPs) signaling inhibitor and has relatively selective inhibition for BMP6 with an IC50 value of 100 nM. LDN-214117 can be used for the research of fibrodysplasia ossificans progressiva (FOP), diffuse intrinsic pontine glioma (DIPG) .
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2
2 Cited Publications
Cat. No.: HY-15897
CAS No.: 1432597-26-6
Purity:  99.70%
Target:  

TGF-β Receptor

Research Areas:  

Cancer

LDN-212854 is a bone morphogenetic protein (BMP) inhibitor that potently inhibits ALK2 (IC50: 1.3 nM). LDN-212854 also inhibits ALK1 (IC50: 2.40 nM). LDN-212854 can be used in the research of fibrodysplasia ossificans progressive and cancers, such as hepatocellular carcinoma (HCC) .
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2
2 Cited Publications
Cat. No.: HY-P72854
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BMP2; SSFSC1; Prev. BMP2A; SSFSC; bone morphogenetic protein 2A; BMP-2; BMP2 protein; BDA2; bone morphogenetic protein 2; BMP-2A
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2
2 Cited Publications
Cat. No.: HY-P7332
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: GDF10; bone-Inducing protein; Growth Differentiation Factor 10; BMP3B; BMP-3b; BIP; Growth/Differentiation Factor 10; BMP-3B; bone morphogenetic protein 3B; GDF-10
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2
2 Cited Publications
Cat. No.: HY-P72633
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: GDF5; LAP-4; Growth Differentiation Factor 5; Cartilage-Derived morphogenetic protein 1; CDMP1; GDF5 protein; BMP14; DUPANS; Growth/Differentiation Factor 5; CDMP-1; bone morphogenetic protein 14; BDA1C; Cartilage-Derived morphogenetic protein-1; SYM1B; Lipopolysaccharide-Associated protein 4; SYNS2; LPS-Associated protein 4; GDF-5; Radotermin; LAP4; BMP-14; OS5
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2
2 Cited Publications
Cat. No.: HY-P700530
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: GDF2; Growth/Differentiation Factor 2; Growth Differentiation Factor 2; bone morphogenetic protein 9; BMP-9; GDF-2; BMP9; HHT5
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2
2 Cited Publications
Cat. No.: HY-76520
CAS No.: 184036-34-8
Synonyms: IPI 1040; TBC-11251
Sitaxsentan (IPI 1040 sodium; TBC11251 sodium) is a potent, selective and orally active endothelin A receptor (ETA) antagonist with an IC50 of 1.4 nM and a Ki of 0.43 nM. Sitaxsentan exhibits an IC50 for the ETB receptor of as high as 9800 nM. Sitaxsentan is metabolized by CYP2C9 and CYP3A4, normalizes shunt-induced endothelial abnormalities, restores BMPR signaling, and suppresses pulmonary vascular remodeling and hemodynamic deterioration. Sitaxsentan can be applied in the research of pulmonary arterial hypertension and portopulmonary hypertension .
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