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C141

Sigma-Aldrich

CGS-21680 hydrochloride hydrate

solid

Synonym(e):

2-p-(2-Carboxyethyl)phenethylamino-5′-N-ethylcarboxamidoadenosine hydrochloride hydrate

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About This Item

Empirische Formel (Hill-System):
C23H29N7O6 · HCl · xH2O
CAS-Nummer:
124182-57-6
Molekulargewicht:
535.98 (anhydrous basis)
MDL-Nummer:
MFCD11045878
UNSPSC-Code:
12352200
PubChem Substanz-ID:
24277698
NACRES:
NA.77

Assay

≥98% (HPLC)

Qualitätsniveau

100

Form

solid

Lagerbedingungen

desiccated

Farbe

white

Löslichkeit

DMSO: >10 mg/mL
45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 20 mg/mL

Lagertemp.

−20°C

SMILES String

O.Cl.CCNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)nc(NCCc4ccc(CCC(O)=O)cc4)nc23

InChI

1S/C23H29N7O6.ClH.H2O/c1-2-25-21(35)18-16(33)17(34)22(36-18)30-11-27-15-19(24)28-23(29-20(15)30)26-10-9-13-5-3-12(4-6-13)7-8-14(31)32;;/h3-6,11,16-18,22,33-34H,2,7-10H2,1H3,(H,25,35)(H,31,32)(H3,24,26,28,29);1H;1H2/t16-,17+,18-,22+;;/m0../s1

InChIKey

VIRPCGAECNOLOO-VBQNEDDFSA-N

Angaben zum Gen

human ... ADORA2A(135) , ADORA2B(136)

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Verwandte Kategorien

Biochem./physiol. Wirkung

Adenosine receptor agonist, which possesses selectivity for A2 verses A1 receptors.

Vorsicht

Hygroscopic

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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PSB-603 ≥98% (HPLC)

Sigma-Aldrich

SML1983

PSB-603

Adenosin-A2A-Rezeptorantagonist I, ZM 241385 A highly potent, selective, non-xanthine adenosine A2A receptor antagonist (Ki = 800 pM for human adenosine A2AR stably expressed in HEK-293 cells).

Sigma-Aldrich

119149

Adenosin-A2A-Rezeptorantagonist I, ZM 241385

8-(3-Chlorostyryl)caffeine ≥98% (HPLC), solid

Sigma-Aldrich

C197

8-(3-Chlorostyryl)caffeine

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International journal of molecular sciences, 23(10) (2022-05-29)
The accumulation of specific metabolic intermediates is known to promote cancer progression. We analyzed the role of 4-pyridone-3-carboxamide-1-β-D-ribonucleoside (4PYR), a nucleotide metabolite that accumulates in the blood of cancer patients, using the 4T1 murine in vivo breast cancer model, and
Seema Gulyani et al.
Experimental neurology, 215(2), 236-242 (2008-11-18)
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Liu Yang et al.
Pediatric research (2022-02-28)
Reducing neuroinflammatory damage is an effective strategy for treating white-matter damage (WMD) in premature infants. Caffeine can ameliorate hypoxia-ischemia-induced brain WMD; however, its neuroprotective effect and mechanism against hypoxic-ischemic WMD remain unclear. We used 3-day-old Sprague-Dawley rats to establish a
J W Phillis
Brain research, 509(2), 328-330 (1990-02-19)
The A2 selective adenosine receptor agonist 2-p-(2-carboxyethyl)phenethylamino-5'-N-ethylcarboxamidoadenosine (CGS 21680) depressed the spontaneous, acetylcholine- and glutamate-evoked firing of rat cerebral sensorimotor cortical neurons. Iontophoretically applied CGS 21680 was equipotent with adenosine as a depressant and its actions were antagonized by 8-p-sulphophenyltheophylline
N Levens et al.
The Journal of pharmacology and experimental therapeutics, 257(3), 1005-1012 (1991-06-01)
This study compares the renal actions of the A2 selective adenosine agonist, CGS 21680A, with the A1 selective adenosine agonist, N6-cyclopentyladenosine (CPA), and the nonselective agonist, 5'-N-ethylcarboxamide adenosine (NECA), in the anesthetized dog. Initial receptor binding studies in dog brain
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