K 02288
K 02288 物理性質(zhì)
- 融點 :
- 201-203°C
- 沸點 :
- 522.2±50.0 °C(Predicted)
- 比重(密度) :
- 1.232±0.06 g/cm3(Predicted)
- 貯蔵溫度 :
- 2-8°C
- 溶解性:
- DMSO(微量)、メタノール(微量)
- 酸解離定數(shù)(Pka):
- 9.33±0.10(Predicted)
- 外見 :
- 粉
- 色:
- 白からベージュ
- InChI:
- 1S/C20H20N2O4/c1-24-17-9-13(10-18(25-2)19(17)26-3)16-8-14(11-22-20(16)21)12-5-4-6-15(23)7-12/h4-11,23H,1-3H3,(H2,21,22)
- InChIKey:
- CJLMANFTWLNAKC-UHFFFAOYSA-N
- SMILES:
- NC1=C(C2=CC(OC)=C(OC)C(OC)=C2)C=C(C3=CC=CC(O)=C3)C=N1
| メーカー |
製品番號 |
製品説明 |
CAS番號 |
包裝 |
価格 |
更新時間 |
購入 |
|
富士フイルム和光純薬株式會社(wako)
|
W01TOC4986 |
K 02288 |
1431985-92-0 |
10mg |
¥87000 |
2024-03-01 |
購入 |
|
富士フイルム和光純薬株式會社(wako)
|
W01COBQM-5350 |
3-[6-Amino-5-(3,4,5-trimethoxyphenyl)pyridin-3-yl]phenol |
1431985-92-0 |
100mg |
¥400000 |
2024-03-01 |
購入 |
|
東京化成工業(yè)
|
K0065 |
K 02288 >98.0%(HPLC)
K 02288
>98.0%(HPLC) |
1431985-92-0 |
10mg |
¥11100 |
2024-03-01 |
購入 |
|
東京化成工業(yè)
|
K0065 |
K 02288 >98.0%(HPLC)
K 02288
>98.0%(HPLC) |
1431985-92-0 |
50mg |
¥38500 |
2024-03-01 |
購入 |
|
Sigma-Aldrich Japan
|
SML1307 |
>98% (HPLC)
K02288 >98% (HPLC) |
1431985-92-0 |
5mg |
¥31200 |
2024-03-01 |
購入 |
K 02288 化學(xué)特性,用途語,生産方法
外観
白色~ほとんど白色粉末~結(jié)晶
説明
Activation of bone morphogenetic protein (BMP) type I receptors, also known as activin receptor-like kinases (ALK1-7), leads to the assembly of SMAD complexes, which translocate to the nucleus to induce transcriptional activation important for normal development and tissue repair. K02288 is a 2-aminopyridine-based inhibitor of ALK1 and ALK2 with IC
50 values of 1.8 and 1.1 nM, respectively. It is less selective for ALK3, 4, 5, and 6 subtypes and the type II BMP receptor ActRIIA, demonstrating IC
50 values of 34.4, 302, 321, 6.4, and 220 nM, respectively. K02288 can prevent BMP4-induced SMAD1/5/8 pathway activation
in vitro (IC
50 = 100 nM) without affecting TGF-β signaling. Furthermore, at 8-10 μM, K02288 has been used to induce the dorsalization of zebrafish embryos. Through specific inhibition of BMP signaling, this compound can be used to research stem cell biology and disease models of musculoskeletal dysplasia and cancer.
使用
K02288 is a potent and selective type 1 BMP (bone morphogenetic protein) receptor inhibitor with in vitro activity against ALK-2 (activin receptor-like kinase-2) at low nanomolar concentrations. K02288 also inhibits the BMP-induced Smad pathway without affecting TGF-β signaling and induces dorsalization of zebrafish embryos.
一般的な説明
K02288 is a 2-aminopyridine compound.
K 02288 上流と下流の製品情報
原材料
準(zhǔn)備製品
K 02288 生産企業(yè)
Global( 132)Suppliers
1431985-92-0(K 02288)キーワード:
- 1431985-92-0
- LM-3151
K02288
- K 02288
- 3-[(6-Amino-5-(3,4,5-trimethoxyphenyl)-3-pyridinyl]phenol
- K 02288 Phenol, 3-[6-amino-5-(3,4,5-trimethoxyphenyl)-3-pyridinyl]-
- K02288 3-[(6-Amino-5-(3,4,5-trimethoxyphenyl)-3-pyridinyl]phenol
- K 02288(K 02288a)
- K 02288a
- K 02288 USP/EP/BP
- 3-[6-Amino-5-(3,4,5-trimethoxyphenyl)pyridin-3-yl]phenol
- Phenol, 3-[6-amino-5-(3,4,5-trimethoxyphenyl)-3-pyridinyl]-
- CS-1877
- K02288;K 02288;K-02288
- K02288, 10 mM in DMSO
- K02288 (K 02288
- K 02288
- K02288
- 3-[5-(3,4,5-トリメトキシフェニル)-6-アミノ-3-ピリジニル]フェノール
- 3-[6-アミノ-5-(3,4,5-トリメトキシフェニル)ピリジン-3-イル]フェノール