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Merck
CN

SML3372

Glutipyran

≥98% (HPLC)

Synonym(s):

rel-N-(3,4-Dimethoxybenzyl)-N-((R)-3-((S)-2,2-dimethyltetrahydro-2H-pyran-4-yl)-3-phenylpropyl)furan-2-carboxamide

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About This Item

Empirical Formula (Hill Notation):
C30H37NO5
Molecular Weight:
491.62
UNSPSC Code:
12352200
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
Storage condition:
desiccated
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assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

white to beige

solubility

DMSO: 2 mg/mL, clear

shipped in

dry ice

storage temp.

-10 to -25°C

Quality Level

Biochem/physiol Actions

Broad-spectrum potent and selective glucose transporter (GLUT) inhibitor
Glutipyran is a broad-spectrum potent and selective glucose transporter (GLUT) inhibitor that targets both GLUT1 and GLUT3. Glutipyran inhibits glycolytic activity and cell growth in PANC-1 cells (IC50 = 1.9 µM). It exhibits antitumor activity (12.5 mg/kg, i.v.) once daily in MIA PaCa-2 xenograft mouse model.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Makoto Kawatani et al.
ACS chemical biology, 16(8), 1576-1586 (2021-07-24)
Cancer cells reprogram their metabolism to survive and grow. Small-molecule inhibitors targeting cancer are useful for studying its metabolic pathways and functions and for developing anticancer drugs. Here, we discovered that glutipyran and its derivatives inhibit glycolytic activity and cell

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