45150
双羟萘酸
≥97.0% (T)
别名:
1,1′-亚甲基-双(2-羟基-3-萘甲酸), 4,4′-亚甲基双(3-羟基-2-萘甲酸), 帕莫酸
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关于此项目
经验公式（希尔记法）:
C23H16O6
化学文摘社编号:
分子量:
388.37
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-998-0
Beilstein/REAXYS Number:
901319
MDL number:
产品名称
双羟萘酸, ≥97.0% (T)
InChI key
WLJNZVDCPSBLRP-UHFFFAOYSA-N
InChI
1S/C23H16O6/c24-20-16(14-7-3-1-5-12(14)9-18(20)22(26)27)11-17-15-8-4-2-6-13(15)10-19(21(17)25)23(28)29/h1-10,24-25H,11H2,(H,26,27)(H,28,29)
SMILES string
OC(=O)c1cc2ccccc2c(Cc3c(O)c(cc4ccccc34)C(O)=O)c1O
assay
≥97.0% (T)
mp
≥300 °C (dec.)
functional group
carboxylic acid
Quality Level
Gene Information
human ... PTPN1(5770), PTPRF(5792)
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Pamoic acid determined from powder diffraction data.
Haynes DA, et al.
Acta Crystallographica Section E, Structure Reports Online, 62(3), o1170-o1172 (2006)
Multi-component hydrogen-bonding assembly of a pharmaceutical agent pamoic acid with piperazine or 4, 4'-bipyridyl: A channel hydrated salt with multiple-helical motifs vs a bimolecular cocrystal.
Du M, et al.
Crystal Growth & Design, 9(4), 1655-1657 (2009)
R W Roos et al.
Journal of chromatography, 370(3), 403-418 (1986-12-24)
Triethylamine (TEA) was evaluated as a competing base for the retention control and peak shape improvement in the reversed-phase high-performance liquid chromatographic (RP-HPLC) analysis of selected acidic, basic, and neutral drugs. The effects of this amine on the capacity factor
A series of four-connected entangled metal-organic frameworks assembled from pamoic acid and pyridine-containing ligands: interpenetrating, self-penetrating, and supramolecular isomerism.
MLA Wang S, et al.
Crystal Growth & Design, 12(1), 79-92 (2011)
Chad Deisenroth et al.
Molecular and cellular biology, 30(16), 3981-3993 (2010-06-16)
The ever-expanding knowledge of the role of p53 in cellular metabolism, apoptosis, and cell cycle control has led to increasing interest in defining the stress response pathways that regulate Mdm2. In an effort to identify novel Mdm2 binding partners, we
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