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P1784

Sigma-Aldrich

Pentoxifylline

solid

Sinónimos:

3,7-Dimethyl-1-(5-oxohexyl)xanthine, Trental

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About This Item

Fórmula empírica (notación de Hill):
C13H18N4O3
Número de CAS:
6493-05-6
Peso molecular:
278.31
Número CE:
229-374-5
Número MDL:
MFCD00063379
Código UNSPSC:
41106305
ID de la sustancia en PubChem:
24278190
NACRES:
NA.77

Formulario

solid

Nivel de calidad

100

color

white

solubilidad

H2O: ≥43 mg/mL, colorless to almost colorless

emisor

Sanofi Aventis

cadena SMILES

CN1C=NC2C1C(=O)N(CCCCC(C)=O)C(=O)N2C

InChI

1S/C13H20N4O3/c1-9(18)6-4-5-7-17-12(19)10-11(14-8-15(10)2)16(3)13(17)20/h8,10-11H,4-7H2,1-3H3

Clave InChI

MQGNNJQTNFHNHK-UHFFFAOYSA-N

Información sobre el gen

human ... ADORA2B(136) , LITAF(9516) , PDE4B(5142) , TNF(7124)
rat ... Tnf(24835)

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Aplicación

Pentoxifylline has been used:
  • used in the combinatorial treatment with itraconazole for paracoccidioidomycosis (PCM)
  • to treat harvested sperms to check the effect of ′pentoxifylline exposed sperms′ in the contribution of embryonic growth
  • to intrathecally inject female and male mice to investigate whether astrocytes and microglia could be causally involved in the maintenance of pain-like behaviour

Acciones bioquímicas o fisiológicas

Pentoxifylline (PTX) is considered as a nonspecific phosphodiesterase inhibitor. It possesses rheologic properties. Pentoxifylline is used to treat peripheral vascular disease. It has the ability to block the phosphorylation of I kappa B-alpha (IĸBα) in serines 32 and 36.
Phosphodiesterase inhibitor; inhibits synthesis of tumor necrosis factor α (TNF-α).

Características y beneficios

This compound is a featured product for Cyclic Nucleotide research. Click here to discover more featured Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Histamine Synthesis and Metabolism and Phosphodiesterases pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Sanofi Aventis. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Pictogramas

Exclamation mark
GHS07

Palabra de señalización

Warning

Frases de peligro

H302,H362

Clasificaciones de peligro

Acute Tox. 4 Oral - Lact.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Equipo de protección personal

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCM2481
BCCJ8061
BCCJ7939
BCCK3414
BCBQ0515

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B K Reuter et al.
The American journal of physiology, 277(4 Pt 1), G847-G854 (1999-10-12)
Although the ability of nonsteriodal anti-inflammatory drugs (NSAIDs) to injure the small intestine has been well established in humans and animals, the mechanism involved in this type of injury has yet to be elucidated. The cytokine tumor necrosis factor-alpha (TNF-alpha)
Maria Del Mar Castro et al.
Pathogens (Basel, Switzerland), 11(3) (2022-03-27)
Addition of the immunomodulator pentoxifylline (PTX) to antimonial treatment of mucosal leishmaniasis has shown increased efficacy. This randomized, double-blind, placebo-controlled trial evaluated whether addition of pentoxifylline to meglumine antimoniate (MA) treatment improves therapeutic response in cutaneous leishmaniasis (CL) patients. Seventy-three
PP-023-Effect of ICSI with `pentoxifylline exposed sperms? on subsequent embryo development
Mangoli V S, et al.
Reproductive Biomedicine Online, 32, S11-S11 (2016)
Exploring the transcriptome of resident spinal microglia after collagen antibody-induced arthritis
Fernandez-Zafra T, et al.
Pain, 160(1), 224-224 (2019)
Combined itraconazole-pentoxifylline treatment promptly reduces lung fibrosis induced by chronic pulmonary paracoccidioidomycosis in mice
Naranjo T W, et al.
Pulmonary Pharmacology & Therapeutics, 24(1), 81-91 (2011)
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