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| あなたへ/カタログ番号 | 在庫状況 | 単価 |
|---|---|---|
5 mg | カートの在庫状況を確認する | ¥54,900 |
25 mg | カートの在庫状況を確認する | ¥168,000 |
この商品について
実験式(ヒル表記法):
C24H29N7O
CAS番号:
分子量:
431.53
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥95% (HPLC)
Form:
powder
Quality Segment
assay
≥95% (HPLC)
form
powder
color
off-white
solubility
DMSO: ≥10 mg/mL
storage temp.
2-8°C
SMILES string
CC[C@H](CO)Nc1nc(NCc2ccc(cc2)-c3ccccn3)c4ncn(C(C)C)c4n1
InChI
1S/C24H29N7O/c1-4-19(14-32)28-24-29-22(21-23(30-24)31(15-27-21)16(2)3)26-13-17-8-10-18(11-9-17)20-7-5-6-12-25-20/h5-12,15-16,19,32H,4,13-14H2,1-3H3,(H2,26,28,29,30)/t19-/m1/s1
InChI key
HOCBJBNQIQQQGT-LJQANCHMSA-N
Biochem/physiol Actions
CR8はCDK1, CDK2, CDK5, CDK7, CDK9の強力な阻害剤です。
CR8 is a potent and selective inhibitor of cyclin dependent kinase (CDK1, 2, 5, 7, and 9). CR8 is a more potent pyridyl analogue of roscovitine (Cat. No. R7772). In comparison to roscovirtine, the compound gains in potency toward CK1, which is involved in amyloid-β formation. The R-CR8 enantiomer is slightly more potent than S. CR8 is around 30 times more potent at cellular assay then roscovitine. Acts as a molecular glue to induce cyclin K degradation.
Features and Benefits
This compound is featured on the CDKs page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
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当該品目 | |||
|---|---|---|---|
| form powder | form powder | form powder | form powder |
| assay ≥95% (HPLC) | assay ≥98% (TLC) | assay ≥96% (HPLC) | assay ≥98% (HPLC) |
| Quality Level 100 | Quality Level 200 | Quality Level 100 | Quality Level 100 |
| storage temp. 2-8°C | storage temp. −20°C | storage temp. 2-8°C | storage temp. 2-8°C |
| solubility DMSO: ≥10 mg/mL | solubility chloroform: 50 mg/mL, clear, colorless to light yellow | solubility DMSO: 20 mg/mL, clear | solubility DMSO: 2 mg/mL, clear |
| color off-white | color - | color white to beige | color white to beige |
保管分類
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable



