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来那度胺

沙利度胺类似物,TNF-α抑制剂
规格或纯度: ≥99%
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货号 (SKU) 包装规格 是否现货 价格 数量
L125046-50mg 50mg 现货 Stock Image
L125046-250mg 250mg 现货 Stock Image
L125046-1g 1g 现货 Stock Image
L125046-5g 5g 现货 Stock Image
L125046-10g 10g 期货 Stock Image
L125046-25g 25g 现货 Stock Image
L125046-100g 100g 现货 Stock Image
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cereblon

基本描述

规格或纯度 ≥99%
英文名称 Lenalidomide
别名 来那度胺;3-(4-氨基-1,3-二氢-1-氧代-2H-异吲哚-2-基)-2,6-哌啶二酮;3-(4-氨基-1-异吲哚啉-2-基)哌啶-2,6-二酮;3-(4-氨基-1-氧代异吲哚-2-基)哌啶-2,6-二酮;CC-5013;1-氧-4-氨基-2-(2,6-二氧哌啶-3-基)异吲哚
英文别名 1-Oxo-4-amino-2-(2,6-dioxopiperidin-3-yl)isoindole;3-(4-Amino-1,3-dihydro-1-oxo-2H-isoindol-2-yl)-2,6-piperidinedione;3-(4-Amino-1-oxoisoindolin-2-yl)piperidin-2,6-dione;3-(4-Amino-1-oxoisoindolin-2-yl)piperidine-2,6-dione; CC 5013
生化机理 Lenalidomide is a thalidomide analog known to inhibit TNF-α secretion and possess immunomodulatory properties.Thalidomide analog and TNF-α inhibitor. Potent antitumor and anti-inflammatory effects. Modulates and potentiates host immune responses against multiple myeloma. Active in vitro.
储存温度 -20°C储存,充氩
运输条件 超低温冰袋运输
备注 如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。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

Lenalidomide (CC-5013)是Thalidomide的衍生物,是一种TNF-α分泌抑制剂,IC50为13 nM。 A Thalidomide analog known to have immunomodulatory properties

Lenalidomide (CC-5013) is a TNF-α secretion inhibitor with IC50 of 13 nM.
A Thalidomide analog known to have immunomodulatory properties

名称和标识符

EC号 691-297-1
IUPAC Name 3-(7-amino-3-oxo-1H-isoindol-2-yl)piperidine-2,6-dione
INCHI InChI=1S/C13H13N3O3/c14-9-3-1-2-7-8(9)6-16(13(7)19)10-4-5-11(17)15-12(10)18/h1-3,10H,4-6,14H2,(H,15,17,18)
InChi Key GOTYRUGSSMKFNF-UHFFFAOYSA-N
Canonical SMILES C1CC(=O)NC(=O)C1N2CC3=C(C2=O)C=CC=C3N
分子式

C13H13N3O3

关联CAS 191732-72-6
NSC Number 747972
UNII F0P408N6V4
PubChem CID 216326
分子量 259.27

化学和物理性质

溶解性 Soluble in DMSO (≥52 mg/ml) at 25 °C, methanol and water (2: 1), buffered aqueous solvents, water (<1 mg/ml) at 25 °C, and ethanol (<1 mg/ml) at 25 °C.
敏感性 对热敏感

安全信息

象形图
ghs06

Toxic

ghs08

Health Hazard

ghs07

Harmful

信号词 Danger
危险声明 H301: Toxic if swallowed
H302: Harmful if swallowed
H312: Harmful in contact with skin
H332: Harmful if inhaled
H372: Causes damage to organs through prolonged or repeated exposure
H360: May damage fertility or the unborn child
预防措施声明 P261,P280,P302+P352,P321,P405,P501,P264,P260,P271,P270,P304+P340,P362+P364,P330,P203,P301+P316,P301+P317,P318,P317,P319

靶标

Target ID 3086
名称 cereblon
缩写名 SHP2
家族 E3 ubiquitin ligase components
别名 IRK2
基因和蛋白信息
Species Transmembrane Domains Amino Acids Chromosomal Location Gene Symbol Gene Name
Human 2 442 3p26.2 CRBN cereblon
Mouse 2 445 6 E1 Crbn cereblon
Rat 2 445 4q41 Crbn cereblon
Ensembl Gene ENSG00000113851 (Hs) , ENSMUSG00000005362 (Mm) , ENSRNOG00000006534 (Rn)
UniProtKB Q96SW2 (Hs) , Q8C7D2 (Mm) , Q56AP7 (Rn)
RefSeq Protein NP_057386 (Hs) , NP_780566 (Mm) , NP_001015003 (Rn)
Protein GI 39545580 (Hs) , 28202023 (Mm) , 62543497 (Rn)
RefSeq Nucleotide NM_016302 (Hs) , NM_175357 (Mm) , NM_001015003 (Rn)
OMIM 609262 (Hs)
Entrez Gene 51185 (Hs) , 58799 (Mm) , 297498 (Rn)
ChEMBL Target CHEMBL3763008 (Hs)

关联配体

Ligand ID 7331
名称 lenalidomide
别名 CC-5013
类别 Synthetic organic
学名 4-amino-2-(6-hydroxy-2-oxo-2,3,4,5-tetrahydropyridin-3-yl)-2,3-dihydro-1H-isoindol-1-one
生物活性评价 The sulfonamide class of antibacterial compounds are primarily bacteriostatic agents and have a broad spectrum of activity against both Gram-positive and Gram-negative species of bacteria (reviewed in ).
评价 Lenalidomide is a derivative of with anti-inflammatory and anti-cancer actions.
配体家族 PROTACs, molecular glues and other degraders

参考文献

1. Graubert TA, Payton MA, Shao J, Walgren RA, Monahan RS, Frater JL, Walshauser MA, Martin MG, Kasai Y, Walter MJ.  (2009)  Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis..  PLoS ONE,  (2):  (e4583).  [PMID:19240791]
2. Zhu YX, Braggio E, Shi CX, Bruins LA, Schmidt JE, Van Wier S, Chang XB, Bjorklund CC, Fonseca R, Bergsagel PL et al..  (2011)  Cereblon expression is required for the antimyeloma activity of lenalidomide and pomalidomide..  Blood,  118  (18):  (4771-9).  [PMID:21860026]
3. Petzold G, Fischer ES, Thom? NH.  (2016)  Structural basis of lenalidomide-induced CK1α degradation by the CRL4(CRBN) ubiquitin ligase..  Nature,  532  (7597):  (127-30).  [PMID:26909574]
4. Kr?nke J, Fink EC, Hollenbach PW, MacBeth KJ, Hurst SN, Udeshi ND, Chamberlain PP, Mani DR, Man HW, Gandhi AK et al..  (2015)  Lenalidomide induces ubiquitination and degradation of CK1α in del(5q) MDS..  Nature,  523  (7559):  (183-188).  [PMID:26131937]

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