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Sigma-Aldrich

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:
130-85-8
Molecular Weight:
388.37
Beilstein:
901319
EC Number:
204-998-0
MDL number:
MFCD00004079
UNSPSC Code:
12352100
PubChem Substance ID:
57650260
NACRES:
NA.22

Assay

≥97.0% (T)

mp

≥300 °C (dec.)

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

human ... PTPN1(5770) , PTPRF(5792)

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Pamoic acid determined from powder diffraction data.
Haynes DA, et al.
Acta Crystallographica Section E, Structure Reports Online, 62(3), o1170-o1172 (2006)
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
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)
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)
Ju-Yi Hsieh et al.
Oncotarget, 6(24), 20084-20098 (2015-05-27)
Here, we found a natural compound, embonic acid (EA), that can specifically inhibit the enzymatic activity of mitochondrial NAD(P)+-dependent malic enzyme (m-NAD(P)-ME, ME2) either in vitro or in vivo. The in vitro IC50 value of EA for m-NAD(P)-ME was 1.4
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