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Grapiprant

Grapiprant Struktur
415903-37-6
CAS-Nr.
415903-37-6
Englisch Name:
Grapiprant
Synonyma:
N-((4-(2-ethyl-4,6-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl)phenethyl)carbamoyl)-4-methylbenzenesulfonamide;RQ 7;MR 10A7;AAT 007;CS-1556;Grprant;CJ-023423;Grapiprant;RQ 00000007;CAS#415903-37-6
CBNumber:
CB03054518
Summenformel:
C26H29N5O3S
Molgewicht:
491.61
MOL-Datei:
415903-37-6.mol

Grapiprant Eigenschaften

Schmelzpunkt:
>151°C (dec.)
Dichte
1.29±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Store in freezer, under -20°C
L?slichkeit
Soluble in DMSO (up to at least 10 mg/ml)
pka
5.19±0.10(Predicted)
Aggregatzustand
solid
Farbe
Off-white
Stabilit?t:
Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChIKey
HZVLFTCYCLXTGV-UHFFFAOYSA-N
SMILES
C1(S(NC(NCCC2=CC=C(N3C4C=C(C)N=C(C)C=4N=C3CC)C=C2)=O)(=O)=O)=CC=C(C)C=C1

Sicherheit

Grapiprant Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Prostaglandin E2 (PGE2) activates four E prostanoid (EP) receptors, EP1-4. EP4 is a Gs protein-coupled receptor that, by elevating the second messenger cAMP, plays important roles in bone formation and resorption, cancer, and atherosclerosis. CJ-023423 is a potent and selective antagonist of the EP4 receptor (Ki = 13 and 20 nM for human and rat EP4, respectively). It inhibits PGE2-evoked elevation in intracellular cAMP in cells and, in vivo, reduces thermal hyperalgesia induced by intraplantar injection of PGE2. CJ-023423 reduces acute and chronic inflammatory pain in different mouse models.

Verwenden

CJ-023423 is a potent and selective antagonist of E prostanoid 4 (EP4) receptor.

Biologische Funktion

Grapiprant (CJ-023423) is an orally available, a potent and selective EP4 receptor antagonist that exhibits significant inhibitory effects on paw swelling, inflammatory biomarkers, synovial inflammation and bone destruction in AIA rats. Grapiprant is highly selective for the human EP4 receptor over other human prostanoid receptor subtypes. It also inhibits PGE2-evoked elevation in intracellular cAMP at the human and rat EP4 receptors with pA2 of 8.3 and 8.2 nM, respectively. In vivo, oral administration of grapiprant significantly reduces thermal hyperalgesia induced by intraplantar injection of PGE2 (ED50 = 12.8 mg/kg). It is also effective in models of acute and chronic inflammatory pain. Grapiprant significantly reduces mechanical hyperalgesia in the carrageenan model. Furthermore, it significantly reverses complete Freund′s adjuvant-induced chronic inflammatory pain response. It produces antihyperalgesic effects in animal models of inflammatory pain. Grapiprant is approved and widely used for treatment of osteoarthritis related pain in dogs. Grapiprant is classify as a non-cyclooxygenase inhibiting non-steroidal anti-inflammatory drug (NSAID).

Nebenwirkungen

Possible side effects of Grapiprant include: vomiting, drowsiness, diarrhoea, loss of appetite, blood or mucus in the stool, and reduced blood protein levels. The degree of reaction can vary from mild to severe, but if your dog experiences a loss of appetite or abnormal faeces, you should contact your veterinarian promptly.

Grapiprant Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Grapiprant Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 108)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hpets Biotech Company (Chongqing) Co.,ltd
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info@hanpets.com China 26 58
Hangzhou ICH Biofarm Co., Ltd
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sales@ichemie.com China 1001 58
ATK CHEMICAL COMPANY LIMITED
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ivan@atkchemical.com China 32957 60
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TopScience Biochemical
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eric@witopchemical.com China 23541 58
Guangzhou TongYi biochemistry technology Co.,LTD
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mack@tongyon.com China 2994 58
InvivoChem
+1-708-310-1919 +1-13798911105
sales@invivochem.cn United States 6391 58
Nanjing Doge Biomedical Technology Co., Ltd
+86-25-58227606 +86-15305155328
sales@dogechemical.com China 4128 58
LEAP CHEM CO., LTD.
+86-852-30606658
market18@leapchem.com China 24727 58

  • CJ-023423
  • Grapiprant
  • 2-Ethyl-4,6-dimethyl-1-[4-[2-[[[[(4-methylphenyl)sulfonyl]amino]carbonyl]amino]ethyl]phenyl]-1H-imidazo[4,5-c]pyridine
  • AAT 007
  • MR 10A7
  • RQ 00000007
  • RQ 7
  • Grapiprant (CJ-023423)
  • 1-[2-[4-(2-ethyl-4,6-dimethylimidazo[4,5-c]pyridin-1-yl)phenyl]ethyl]-3-(4-methylphenyl)sulfonylurea
  • CAS#415903-37-6
  • CJ-023423; CJ 023423; CJ023423; CAS#415903-37-6; RQ-00000007; RQ 00000007; RQ00000007; AAT-007; AAT007; AAT 007; GRAPIPRANT
  • CS-1556
  • GRAPIPRANT;RQ-00000007;AAT-007
  • Grprant
  • N-((4-(2-ethyl-4,6-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl)phenethyl)carbamoyl)-4-methylbenzenesulfonamide
  • N-[[2,4-(2-ethyl-4,6-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl)phenylethylamino]carbonyl]-4-methyl-benzenesulfonamide
  • RQ 00000007,Inhibitor,Grapiprant,CJ 023423,RQ00000007,Prostaglandin Receptor,AAT 007,inhibit,AAT007,CJ023423
  • Grapiprant, CJ-023423, AAT-007
  • 415903-37-6
  • API
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