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Merck
CN

45150

Pamoic acid

≥97.0% (T)

Synonym(s):

1,1′-Methylene-bis(2-hydroxy-3-naphthoic acid), 4,4′-Methylenebis(3-hydroxy-2-naphthoic acid), Embonic acid

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About This Item

Empirical Formula (Hill Notation):
C23H16O6
CAS Number:
Molecular Weight:
388.37
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-998-0
Beilstein/REAXYS Number:
901319
MDL number:
Assay:
≥97.0% (T)
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Quality Level

assay

≥97.0% (T)

mp

≥300 °C (dec.)

functional group

carboxylic acid

SMILES string

OC(=O)c1cc2ccccc2c(Cc3c(O)c(cc4ccccc34)C(O)=O)c1O

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

Gene Information



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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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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)
Pamoic acid determined from powder diffraction data.
Haynes DA, et al.
Acta Crystallographica Section E, Structure Reports Online, 62(3), o1170-o1172 (2006)
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



Global Trade Item Number

SKUGTIN
45150-100G-F04061832324203