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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
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A100625-50mg |
50mg |
现货 ![]() |
| |
A100625-250mg |
250mg |
现货 ![]() |
| |
A100625-1g |
1g |
现货 ![]() |
| |
A100625-5g |
5g |
现货 ![]() |
| |
A100625-25g |
25g |
现货 ![]() |
|
别名 | 5-氮杂胞嘧啶核苷;4-氨基-1-(β-D-呋喃核糖基)-1,3,5-三嗪-2(1H)-酮; 阿扎胞苷;5-阿扎胞苷 |
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英文别名 | 4-Amino-1-(β-D-ribofuranosyl)-1,3,5-triazin-2(1H)-one; Ladakamycin |
规格或纯度 | 98% |
英文名称 | 5-Azacytidine |
生化机理 | 强大的DNA甲基转移酶1(DNMT1)抑制剂(IC 50 = 0.2μM)。掺入DNA中,抑制DNMT1活性以诱导DNA低甲基化。干扰蛋白质合成。在体外显示抗代谢和抗癌活性。体内具有活性 |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
备注 | 不稳定 重新制作解决方案并立即使用。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。 |
产品介绍 |
溶于甲醇。 一种潜在的生长抑制因子和细胞毒素载体;抑制DNA甲基化转移酶,该酶是一种重要的调控基因表达、基因激活和基因关闭的机关。 该因子引起DNA去甲基化或半去甲基化,允许转录因子结合到DNA上,重新激活肿瘤抑制基因。 |
PubChem SID | 488180979 |
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EC号 | 206-280-2 |
IUPAC Name | 4-amino-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3,5-triazin-2-one |
INCHI | InChI=1S/C8H12N4O5/c9-7-10-2-12(8(16)11-7)6-5(15)4(14)3(1-13)17-6/h2-6,13-15H,1H2,(H2,9,11,16)/t3-,4-,5-,6-/m1/s1 |
InChi Key | NMUSYJAQQFHJEW-KVTDHHQDSA-N |
Canonical SMILES | C1=NC(=NC(=O)N1C2C(C(C(O2)CO)O)O)N |
WGK Germany | 3 |
RTECS | XZ3017500 |
PubChem CID | 9444 |
分子量 | 244.2 |
Beilstein号 | 620461 |
Reaxy-Rn | 620461 |
DrugBank Ligand | DB00928 |
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PubChem CID | 9444 |
CAS Registry No. | 320-67-2 |
ChEMBL Ligand | CHEMBL1489 |
Wikipedia | Azacitidine |
ChEBI | CHEBI:2038 |
RCSB PDB Ligand | 5AE |
DrugCentral Ligand | 25 |
PubChem SID | 488180979 |
溶解性 | 可溶于水 |
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密度 | 2.08 |
敏感性 | 对光线、热敏感 |
熔点 | 228-230°C |
象形图 |
![]() Health Hazard ![]() Harmful |
---|---|
信号词 | Danger |
危险声明 |
H302: Harmful if swallowed H340: May cause genetic defects H350: May cause cancer |
预防措施声明 | P280,P405,P501,P264,P201,P308+P313,P281,P403,P270,P202,P330,P301+P312,P203,P318 |
WGK Germany | 3 |
RTECS | XZ3017500 |
Reaxy-Rn | 620461 |
Merck Index | 887 |
个人防护装备 | Eyeshields,full-face particle respirator type N100 (US),Gloves,respirator cartridge type N100 (US),type P1 (EN143) respirator filter,type P3 (EN 143) respirator cartridges |
输入批号以搜索COA:
1. Stresemann C, Lyko F. (2008) Modes of action of the DNA methyltransferase inhibitors azacytidine and decitabine.. Int J Cancer, 123 (1): (8-13). [PMID:18425818] |
2. Chen MY, Liao WS, Lu Z, Bornmann WG, Hennessey V, Washington MN, Rosner GL, Yu Y, Ahmed AA, Bast Jr RC. (2011) Decitabine and suberoylanilide hydroxamic acid (SAHA) inhibit growth of ovarian cancer cell lines and xenografts while inducing expression of imprinted tumor suppressor genes, apoptosis, G2/M arrest, and autophagy.. Cancer, 117 (19): (4424-38). [PMID:21491416] |
3. Dear AE. (2016) Epigenetic Modulators and the New Immunotherapies.. N Engl J Med, 374 (7): (684-6). [PMID:26886527] |
4. Jones PA, Taylor SM. (1980) Cellular differentiation, cytidine analogs and DNA methylation.. Cell, 20 (1): (85-93). [PMID:6156004] |
5. Chen J et al.. (2019) 5-Aza-CdR Regulates RASSF1A By Inhibiting DNMT1 To Affect Colon Cancer Cell Proliferation, Migration And Apoptosis.. Cancer Manag Res, 11 (): (9517-9528). [PMID:31807076] |
6. Schwenzer H et al.. (2021) LARP1 isoform expression in human cancer cell lines.. RNA Biol, 18 (2): (237-247). [PMID:32286153] |
7. Fort RS et al.. (2018) Nc886 is epigenetically repressed in prostate cancer and acts as a tumor suppressor through the inhibition of cell growth.. BMC Cancer, 18 (): (127). [PMID:29394925] |
8. Nam H et al.. (2022) Presenilin 2 N141I mutation induces hyperactive immune response through the epigenetic repression of REV-ERBα.. Nat Commun, 13 (): (1972). [PMID:35418126] |
9. Alarcón MA et al.. (2020) The Reprimo-Like Gene Is an Epigenetic-Mediated Tumor Suppressor and a Candidate Biomarker for the Non-Invasive Detection of Gastric Cancer.. Int J Mol Sci, 21 (24): (). [PMID:33322837] |
10. Jacobs AH. (1977) The skin in childhood.. Hosp Pract, 12 (8): (91-112). [PMID:142744] |