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Safety Information

P94

Sigma-Aldrich

Embonic acid

98%

Synonym(s):

4,4′-Methylenebis(3-hydroxy-2-naphthoic acid), 4,4′-Methylenebis(3-hydroxy-2-naphthoicacid), Pamoic acid

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About This Item

Empirical Formula (Hill Notation):
C23H16O6
CAS Number:
Molecular Weight:
388.37
Beilstein:
901319
UNSPSC Code:
12352100
PubChem Substance ID:

Quality Level

Assay

98%

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)

InChI key

WLJNZVDCPSBLRP-UHFFFAOYSA-N

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O Gavrilova-Ruch et al.
The Journal of membrane biology, 188(2), 137-149 (2002-08-13)
Human IGR1 cells are a model for malignant melanoma. Since progression through the cell cycle is accompanied by transient cell hyperpolarization, we studied the properties of potassium and chloride ion channels and their impact on cell growth. The major potassium
S Handali et al.
The Southeast Asian journal of tropical medicine and public health, 28 Suppl 1, 22-25 (1997-01-01)
A community survey was conducted in Gran Dani Valley, Jayawijaya District, Irian Jaya Province, Indonesia. A total of 537 adults were asked whether they experienced epilepsy, and were physically examined for cysticercosis cysts. Forty-eight percent experienced at least one attack
Richard R Neubig
Molecular pharmacology, 78(4), 558-559 (2010-07-24)
Many pharmacological agents include "inactive" constituents that are used to alter the solubility, stability, or pharmaceutical properties of a drug. These "salts" are often ignored, and the "active ingredient" gets all of the attention. Pamoic acid (4-[(3-carboxy-2-hydroxynaphthalen-1-yl)methyl]-3-hydroxynaphthalene-2-carboxylic acid) has been
Quantitative high-performance liquid chromatographic determination of ampicillin embonate and amoxycillin embonate.
T Saesmaa
Journal of chromatography, 455, 415-419 (1988-11-25)
Corinne Hazan et al.
BMC structural biology, 8, 22-22 (2008-04-18)
DNA polymerase beta (pol beta), the error-prone DNA polymerase of single-stranded DNA break repair as well as base excision repair pathways, is overexpressed in several tumors and takes part in chemotherapeutic agent resistance, like that of cisplatin, through translesion synthesis.

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