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Merck
CN

SML4036

AN3661

≥98% (HPLC)

Synonym(s):

1,3-Dihydro-1-hydroxy-2,1-benzoxaborole-7-propanoic acid, 3-(1-Hydroxy-1,3-dihydro-2,1-benzoxaborol-7-yl)propanoic acid; 3-(1-Hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-7-yl)propanoicacid

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About This Item

Empirical Formula (Hill Notation):
C10H11BO4
CAS Number:
Molecular Weight:
206.00
MDL number:
NACRES:
NA.21
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
Technical Service
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InChI

1S/C10H11BO4/c12-9(13)5-4-7-2-1-3-8-6-15-11(14)10(7)8/h1-3,14H,4-6H2,(H,12,13)

InChI key

CEVOKIPNIZQANN-UHFFFAOYSA-N

SMILES string

OC(CCC1=CC=CC2=C1B(OC2)O)=O

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

Quality Level

Biochem/physiol Actions

Boron containing antimalarial agent that targets Plasmodium falciparum CPSF3 (cleavage and polyadenylation specific factor 3).
AN3661 is a boron containing antimalarial agent that targets Plasmodium falciparum CPSF3 (cleavage and polyadenylation specific factor 3). AN3661potently inhibits Plasmodium falciparum laboratory-adapted strains (mean IC50=32 nM). Also, AN3661 inhibits T. gondii growth in human cells at low micromolar concentrations.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Saiqi Hao et al.
Plant physiology, 193(1), 537-554 (2023-06-19)
Cleavage and polyadenylation specificity factor (CPSF) is a protein complex that plays an essential biochemical role in mRNA 3'-end formation, including poly(A) signal recognition and cleavage at the poly(A) site. However, its biological functions at the organismal level are mostly
Transcriptional dynamics in the protozoan parasite Sarcocystis neurona and mammalian host cells after treatment with a specific inhibitor of apicomplexan mRNA polyadenylation
PLoS ONE, 16(10) (2021)
Andrés Palencia et al.
EMBO molecular medicine, 9(3), 385-394 (2017-02-06)
Toxoplasma gondii is an important food and waterborne pathogen causing toxoplasmosis, a potentially severe disease in immunocompromised or congenitally infected humans. Available therapeutic agents are limited by suboptimal efficacy and frequent side effects that can lead to treatment discontinuation. Here

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