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Merck

T1633

Theophylline

≥99% (HPLC), powder, phosphodiesterase inhibitor

Synonim(y):

1,3-Dimethylxanthine, 2,6-Dihydroxy-1,3-dimethylpurine, 3,7-Dihydro-1,3-dimethyl-1H-purine-2,6-dione

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Wybierz wielkość

50 G

203,00 zł

100 G

354,00 zł

250 G

660,00 zł

1 KG

1270,00 zł

203,00 zł


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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C7H8N4O2
Numer CAS:
Masa cząsteczkowa:
180.16
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
200-385-7
MDL number:
Beilstein/REAXYS Number:
13463
Assay:
≥99%
Form:
powder
Quality level:

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Nazwa produktu

Theophylline, anhydrous, ≥99%, powder

InChI key

ZFXYFBGIUFBOJW-UHFFFAOYSA-N

InChI

1S/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9)

SMILES string

CN1C(=O)N(C)c2[nH]cnc2C1=O

grade

anhydrous

assay

≥99%

form

powder

color

white

solubility

H2O: slightly soluble 8.3 mg/ml, NH4OH: 50 mg/ml, clear, colorless, alcohol: 12.5 mg/ml, chloroform: soluble 9.1 mg/ml, 0.1 M HCl: soluble, 0.1 M NaOH: soluble, ammonium hydroxide: soluble, aqueous base: soluble, diethyl ether: slightly soluble, dilute HCl: soluble, dilute nitric acid: soluble, ethanol: moderately soluble

originator

Forest Labs

Quality Level

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Ta pozycja
PHR10231653117D0633
form

powder

form

-

form

-

form

powder

assay

≥99%

assay

-

assay

-

assay

-

Quality Level

200

Quality Level

300

Quality Level

-

Quality Level

200

solubility

H2O: slightly soluble 8.3 mg/ml, alcohol: 12.5 mg/ml, 0.1 M HCl: soluble, ammonium hydroxide: soluble, diethyl ether: slightly soluble, dilute nitric acid: soluble, NH4OH: 50 mg/ml, clear, colorless, 0.1 M NaOH: soluble, dilute HCl: soluble, chloroform: soluble 9.1 mg/ml, ethanol: moderately soluble, aqueous base: soluble

solubility

-

solubility

-

solubility

-

color

white

color

-

color

-

color

-

originator

Forest Labs

originator

-

originator

-

originator

-

Application

Theophylline has been used to study its effects on rat gene expression in the ubiquitin-proteasome pathway that regulates spermatogenesis and epididymal sperm quality[1]. Theophylline has also been used as an internal standard for the measurement of plasma paracetamol levels in humans[2].

Biochem/physiol Actions

Phosphodiesterase inhibitor; diuretic; cardiac stimulant; muscle relaxant; asthma medication.
Theophylline is a tea alkaloid that functions as a nonselective PDE4 inhibitor. It can induce smooth muscle relaxation in the bronchiolae of asthma patients. At increased concentrations, theophylline can function as a reprotoxic agent and can cause infertility by incapacitating Sertoli cells. This subsequently causes the premature release of late differentiating spermatogenic cells[1].

Features and Benefits

This compound is a featured product for ADME Tox and Cyclic Nucleotide research. Discover more featured ADME Tox and 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 Adenosine Receptors and Phosphodiesterases pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Forest Labs. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Preparation Note

Theophylline dissolves in 1 M NH4OH at 50 mg/ml to yield a clear, colorless solution. It is soluble in 0.1 M HCl, 0.1 M NaOH and is slightly soluble(8.3 mg/ml) in water. It is also moderately soluble in ethanol. Furthermore, it is soluble in alcohol (12.5 mg/ml), and chloroform (9.1 mg/ml), alkali hydroxides, ammonia, dilute hydrochloric or nitric acid, but is sparingly soluble in ether.

The solubility of the methylxanthines is low, but can be enhanced by the formation of complexes (usually 1:1) with a wide variety of compounds such as ethylenediamine (to form aminophylline). The formation of complex double salts (caffeine and sodium benzoate) or true salts (like choline theophyllinate, and oxtriphylline) also improves aqueous solubility. These salts or complexes dissociate to yield the parent methylxanthines when dissolved in biological fluids and should not be confused with covalently modified derivatives such asdyphylline (1,3-dimethyl-7-(2,3-dihydroxypropyl)-xanthine).
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pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Repr. 1B

Klasa składowania

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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58-55-9

CAS No.

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Matthew T Eddy et al.
Structure (London, England : 1993), 29(2), 170-176 (2020-11-26)
In drug design, G protein-coupled receptor (GPCR) partial agonists enable one to fine-tune receptor output between basal and maximal signaling levels. Here, we add to the structural basis for rationalizing and monitoring partial agonism. NMR spectroscopy of partial agonist complexes
Nagi Reddy Dumpa et al.
Pharmaceutics, 12(1) (2020-01-16)
This study was performed to develop novel core-shell gastroretentive floating pulsatile drug delivery systems using a hot-melt extrusion-paired fused deposition modeling (FDM) 3D printing and direct compression method. Hydroxypropyl cellulose (HPC) and ethyl cellulose (EC)-based filaments were fabricated using hot-melt
F J Sevilla-Tirado et al.
Methods and findings in experimental and clinical pharmacology, 25(7), 531-535 (2003-10-23)
The aim of this study was to compare the main pharmacokinetic characteristics of two new paracetamol formulations, powder sachet and tablet, with that of three commercially available paracetamol formulations: two conventional solid tablets and one effervescent tablet. Twelve healthy volunteers
Mohammed Al-Sharabi et al.
International journal of pharmaceutics, 584, 119380-119380 (2020-05-15)
Fast disintegrating tablets have commonly been used for fast oral drug delivery to patients with swallowing difficulties. The different characteristics of the pore structure of such formulations influence the liquid transport through the tablet and hence affect the disintegration time
Matthew R Wilson et al.
The Journal of pharmacy and pharmacology, 69(1), 32-42 (2016-10-18)
This research examined the application of hot melt extrusion (HME) in the preparation of matrix formulations containing hydroxypropyl cellulose (HPC) as a base polymer in combination with methyl cellulose (MC) and hydroxypropyl methylcellulose (HPMC). The limit to which formulations could

Produkty

Discover Bioactive Small Molecules for ADME/Tox

Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.

Questions

  1. Buenos días, ¿Cuáles son las condiciones de conservación de la Teofilina? (T1633). Muchas gracias

    1 answer
    1. This product should be stored in ambient temperature.

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