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Merck

F3055

Sigma-Aldrich

夫拉平度 盐酸盐

≥98% (HPLC), powder

别名:

(−)-2-(2-氯苯基)-5,7-二羟基-8-[(3 S ,4 R )-3-羟基-1-甲基-4-哌啶基]-4 H -1-苯并吡喃-4-酮 盐酸盐, L-86-8276, NSC-649890

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About This Item

经验公式(希尔记法):
C21H20ClNO5 ·HCl · xH2O
分子量:
438.30 (anhydrous basis)
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

儲存條件

desiccated

顏色

white to light brown

溶解度

H2O: ~2 mg/mL
DMSO: >5 mg/mL

儲存溫度

2-8°C

SMILES 字串

OC1=C(C(C=C(C2=C(Cl)C=CC=C2)O3)=O)C3=C([C@H]4CCN(C)C[C@H]4O)C(O)=C1.Cl

InChI

1S/C21H20ClNO5.ClH/c1-23-7-6-12(17(27)10-23)19-14(24)8-15(25)20-16(26)9-18(28-21(19)20)11-4-2-3-5-13(11)22;/h2-5,8-9,12,17,24-25,27H,6-7,10H2,1H3;1H/t12-,17+;/m0./s1

InChI 密鑰

LGMSNQNWOCSPIK-LWHGMNCYSA-N

應用

夫拉平度盐酸盐已:
  • 用作周期蛋白依赖性激酶9 (CDK9)抑制剂,以研究其对猪胚胎成纤维细胞组蛋白H3赖氨酸36位点甲基化(H3K36)和转录失活的影响
  • 用作RNA聚合酶抑制剂,以研究其对肝细胞的影响
  • 用作RNA转录抑制剂,以研究其对斑马鱼胚胎常染色质粗化的影响

生化/生理作用

黄烷醇是一种从双花叶姜中提取的半合成黄酮类化合物,作为抗肿瘤剂可对抗几种癌症。它还显示出抗癌特性,因此,它已被研究用于治疗急性髓系白血病(AML)。
盐酸 Flavopiridol 是一种强效的 CDK(细胞周期蛋白依赖性激酶)和 CDC25 磷酸酶家族抑制剂。

特點和優勢

《受体分类和信号转导》手册的 CDK 页面有该化合物的介绍。想要浏览手册的其他页面, 请单击此处

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Saowaluk Saisomboon et al.
Heliyon, 5(5), e01675-e01675 (2019-06-14)
Flavopiridol, a pan-cyclin-dependent kinase (CDK) inhibitor, was recently identified as an effective antitumor agent for several cancers. We investigated the antitumor effect of flavopiridol on cholangiocarcinoma (CCA), in vitro and in vivo. A methylthiotetrazole assay revealed that the proliferation of
Elisa Barbieri et al.
Cell reports, 33(6), 108373-108373 (2020-11-12)
Genome-wide profiling of nascent RNA has become a fundamental tool to study transcription regulation. Unlike steady-state RNA-sequencing (RNA-seq), nascent RNA profiling mirrors real-time activity of RNA polymerases and provides an accurate readout of transcriptome-wide variations. Some species of nuclear RNAs
Anne Pumfery et al.
Current pharmaceutical design, 12(16), 1949-1961 (2006-06-22)
Cyclin-dependent kinases (CDKs) are key regulators of the cell cycle and RNA polymerase II transcription. Several pharmacological CDK inhibitors (PCIs) are currently in clinical trials as potential cancer therapeutics since CDK hyperactivation is detected in the majority of neoplasias. Within
Nicole Pinto et al.
PloS one, 15(9), e0239315-e0239315 (2020-09-25)
Anaplastic thyroid cancer (ATC) is a rare, but nearly uniformly fatal disease that is typically resistant to chemotherapy and radiation. Alternative strategies to target this cancer at a molecular level are necessary in order to improve dismal outcomes for ATC
Nazia Abbasi et al.
Life science alliance, 3(10) (2020-08-21)
Tumorigenesis in different segments of the intestinal tract involves tissue-specific oncogenic drivers. In the colon, complement component 3 (C3) activation is a major contributor to inflammation and malignancies. By contrast, tumorigenesis in the small intestine involves fatty acid-binding protein 1

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