SML1225
吲哚美辛
≥98% (HPLC), carbonic anhydrase inibitor, powder
别名:
N 1 -（3-氯-1 H -吲哚-7-基）-1,4-苯二磺酰胺, N -（3-氯-1H-吲哚-7-基）-4-氨磺酰基苯磺酰胺
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关于此项目
经验公式（希尔记法）:
C14H12ClN3O4S2
化学文摘社编号:
分子量:
385.85
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
产品名称
吲哚美辛, ≥98% (HPLC)
SMILES string
ClC1=CNC2=C1C=CC=C2NS(C3=CC=C(S(=O)(N)=O)C=C3)(=O)=O
InChI
1S/C14H12ClN3O4S2/c15-12-8-17-14-11(12)2-1-3-13(14)18-24(21,22)10-6-4-9(5-7-10)23(16,19)20/h1-8,17-18H,(H2,16,19,20)
InChI key
SETFNECMODOHTO-UHFFFAOYSA-N
assay
≥98% (HPLC)
form
powder
color
white to pink
solubility
DMSO: 20 mg/mL, clear
storage temp.
−20°C
Quality Level
Biochem/physiol Actions
Indisulam 是一种碳酸酐酶抑制剂和抗肿瘤 CDK 抑制剂。
Indisulam 是一种碳酸酐酶抑制剂和抗肿瘤 CDK 抑制剂。Indisulam 通过耗竭细胞周期蛋白 E 来靶向细胞周期的 G1 期。诱导 p53 和 p21，并抑制 CDK2，导致 G1/S 转换受阻。
靛磺兰是合成的磺胺化合物。 体外 和 体内 研究指出，靛玉红可阻止视网膜母细胞瘤蛋白磷酸化。也抑制细胞周期蛋白 A 和 B1 的活性。已知吲哚美辛可促进细胞凋亡。吲哚美辛是一种强效的细胞脱氢酶抑制剂，因此，可能干扰代谢途径，如苹果酸-天冬氨酸穿梭、糖酵解和糖异生。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Semi-physiological model describing the hematological toxicity of the anti-cancer agent indisulam.
van Kesteren C, et al.
Investigational New Drugs, 23(3), 225-234 (2005)
Sung Ah Kim et al.
Molecules and cells, 43(11), 935-944 (2020-11-11)
Aryl hydrocarbon receptor nuclear translocator (ARNT) plays an essential role in maintaining cellular homeostasis in response to environmental stress. Under conditions of hypoxia or xenobiotic exposure, ARNT regulates the subset of genes involved in adaptive responses, by forming heterodimers with
Cristina Mayor-Ruiz et al.
Nature chemical biology, 16(11), 1199-1207 (2020-08-05)
Targeted protein degradation is a new therapeutic modality based on drugs that destabilize proteins by inducing their proximity to E3 ubiquitin ligases. Of particular interest are molecular glues that can degrade otherwise unligandable proteins by orchestrating direct interactions between target
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