LDN-214117
- Product Name
- LDN-214117
- CAS No.
- 1627503-67-6
- Chemical Name
- LDN-214117
- Synonyms
- CS-1539;LDN-214117;LDN-214117 ,S7627;LDN-214117;LDN214117;LDN-214117 USP/EP/BP;LDN-214117, 10 mM in DMSO;1-(4-(6-methyl-5-(3,4,5-trimethoxyphenyl)pyridin-3-yl)phenyl)piperazine;1-[4-[6-Methyl-5-(3,4,5-trimethoxyphenyl)-3-pyridinyl]phenyl]piperazine;Piperazine, 1-[4-[6-methyl-5-(3,4,5-trimethoxyphenyl)-3-pyridinyl]phenyl]-;LDN214117,LDN-214117,ALK2,BMP4,BMP2,Transforming growth factor beta receptors,LDN 214117,BMP6,TGF-β Receptor,diffuse intrinsic pontine glioma(DIPG),oral,ALK3,fibrodysplasia ossificans progressiva (FOP),ALK5,type I receptor kinases,ALK1,bone morphogenetic proteins (BMPs)
- CBNumber
- CB92729368
- Molecular Formula
- C25H29N3O3
- Formula Weight
- 419.52
- MOL File
- 1627503-67-6.mol
LDN-214117 Property
- Boiling point:
- 567.9±50.0 °C(Predicted)
- Density
- 1.134±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- DMF:30.0(Max Conc. mg/mL);71.51(Max Conc. mM)
DMF:PBS (pH 7.2) (1:1):0.5(Max Conc. mg/mL);1.19(Max Conc. mM)
DMSO:42.67(Max Conc. mg/mL);101.7(Max Conc. mM)
Ethanol:54.0(Max Conc. mg/mL);128.72(Max Conc. mM) - pka
- 8.86±0.10(Predicted)
- form
- Powder
- color
- Light yellow to yellow
N-Bromosuccinimide Price
- Product number
- SML1119
- Product name
- LDN-214117
- Purity
- ≥98% (HPLC)
- Packaging
- 5 mg
- Price
- $128.1
- Updated
- 2025/07/31
- Product number
- SML1119
- Product name
- LDN-214117
- Purity
- ≥98% (HPLC)
- Packaging
- 25 mg
- Price
- $611
- Updated
- 2025/07/31
- Product number
- 18006
- Product name
- LDN-214117
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $32
- Updated
- 2024/03/01
- Product number
- 18006
- Product name
- LDN-214117
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $109
- Updated
- 2024/03/01
- Product number
- 18006
- Product name
- LDN-214117
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $184
- Updated
- 2024/03/01
LDN-214117 Chemical Properties,Usage,Production
Uses
LDN 214117 is a highly selective ALK2 inhibitor.
Biological Activity
LDN-214117 is a selective inhibitor of the bone morphogenetic protein (BMP) type I receptor kinases with high selectivity for BMP versus TGF-β signaling, and low cytotoxicity. LDN-214117 inhibited ALK2 most, with a biochemical IC50 of 24 nM, followed by TNIK, RIPK2, and ABL1. LDN-214117 has a cell-based IC50 for BMP6 of approximately 100 nM and 164-fold selectivity for BMP6 versus TGF-β1. Fibrodysplasia ossificans progressiva (FOP) is a debilitating and progressive heterotopic ossification disease caused by activating mutations of ACVR1 encoding the BMP type I receptor kinase ALK2. LDN-214117 had nearly identical binding affinity for wild-type ALK2 and each of the FOP-causing mutants tested.
in vivo
LDN-214117 (p.o., 25 mg/kg, daily, for 14 days) has well-tolerated in mice[3].
| Animal Model: | NOD.SCID mice[3] |
| Dosage: | 25 mg/kg |
| Administration: | p.o., daily, for 14 days |
| Result: | Showed good-tolerated in mice. |
LDN-214117 Preparation Products And Raw materials
Raw materials
Preparation Products
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