Nastorazepide hemicalcium
Based on 1 publication(s) in Google Scholar
Nastorazepide (Z-360) hemicalcium is an orally active 1,5-benzodiazepine derivative and gastrin/CCK-2 receptor antagonist. Nastorazepide hemicalcium inhibits the specific binding of [3H]CCK-8 to the human CCK-2 receptor with a Ki value of 0.47 nM. Nastorazepide hemicalcium inhibits IL-1β, ephrin B1, VEGF, and HIF-1alpha, reduces Akt and NR2B phosphorylation. Nastorazepide hemicalcium has antitumor activity against pancreatic cancer. Nastorazepide hemicalcium inhibits colorectal cancer liver metastasis and relieves pain.
For research use only. We do not sell to patients.
- CAS No.: 343326-69-2
- Formula: C29H36N4O5.1/2Ca
- Molecular Weight:540.66
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
-
Biological Activity
-
Chemical Information
- Purity & Documentation
- References
-
Help & FAQs
Publications Citing Use of MedChemExpress (MCE) Nastorazepide hemicalcium
MoreAll VEGFR Isoforms
More
Biological Activity
Nastorazepide (0.1 μM; 24 h) hemicalcium suppresses Gemcitabine (HY-17026)-induced expression of HIF-1alpha genes in PANC-1 cells[1].
Nastorazepide hemicalcium potently inhibits specific binding of [3H]CCK-8 to the human CCK-2 receptor, with a Ki value of 0.47 nM[2].
Nastorazepide (10 nM-1 μM) hemicalcium reduces basal Akt phosphorylation and antagonises the effect of G17 on Akt phosphorylation in OE33 cells[3].
Nastorazepide (1, 10, 100 nM) hemicalcium dose-dependently inhibits the increase in total cell number induced by 1 nM Gastrin-17 or 1 nM Gastrin-34 in MIA PaCa-2/hCCK2R cells[4].
Nastorazepide (100 nM; 24 h) hemicalcium suppresses Gemcitabine-induced VEGFA gene expression and protein levels in PANC-1 cells[7].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Nastorazepide (3-100 mg/kg; p.o.; once daily) hemicalcium inhibits colorectal cancer liver metastasis in the C170HM2 mouse model, increases survival in the MGLVA1 ascites mouse model, and inhibits pancreatic tumor growth when combined with Gemcitabine in the PAN-1 orthotopic mouse model[3].
Nastorazepide (100 mg/kg; p.o.; once daily; 3 weeks) hemicalcium suppresses tumor growth in MIA PaCa-2-bearing mice via inhibition of Gastrin-induced anti-apoptotic effects[4].
Nastorazepide (30-300 mg/kg; p.o.; starting from day 7 and continuing until day 21 in the cancer pain model) hemicalcium can inhibit the late-phase nociceptive responses in the Formalin-induced pain model, produce an anti-allodynic effect in the cancer pain model[5].
Nastorazepide (100 mg/kg; p.o.; once daily; from day 7 to day 14) hemicalcium prevents up-regulation of ephrin B1 gene expression and phosphorylation of NR2B via suppression of IL-1β production in a cancer-induced pain model in mice[6].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:BALB/c-nu/nuSlc nude mice (female, 7-week-old) with subcutaneous xenograft of MiaPaCa2 cells[2]
-
Dosage:10 mg/kg, 30 mg/kg, 100 mg/kg
-
Administration:Oral administration, once daily, for 21 days
-
Result:Significantly inhibited tumor growth of MiaPaCa2 subcutaneous xenografts in a dose-dependent manner.
Resulted in final tumor weight inhibition of 16.5%, 39.6%, and 41.7% at 10, 30, and 100 mg/kg, respectively.
-
Animal Model:Nude mice with PAN-1 orthotopic pancreatic model[3]
-
Dosage:30 mg/kg, 100 mg/kg
-
Administration:Oral gavage (p.o.), once daily
-
Result:Did not suppress basal tumor area or weight at all doses when used as monotherapy.
Inhibited both tumor area and weight when used in combination with Gemcitabine.
Chemical Information
-
CAS No. 343326-69-2
-
Molecular Weight 540.66
-
Formula C29H36N4O5.1/2Ca
-
SMILES
O=C([O-])C1=CC=CC(NC(N[C@H]2C(N(CC(C(C)(C)C)=O)C3=CC=CC=C3N(C4CCCCC4)C2)=O)=O)=C1.[0.5].[Ca+2]
-
Synonyms
Z-360 hemicalcium
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (1)
-
Journal Impact Factor
-
Most Recent
Purity & Documentation
References
[1]. Kato H, et al. CCK-2/gastrin receptor signaling pathway is significant for gemcitabine-induced gene expression of VEGF in pancreatic carcinoma cells. Life Sci. 2011 Oct 24;89(17-18):603-8. [Content Brief]
[2]. Kawasaki D, et al. Effect of Z-360, a novel orally active CCK-2/gastrin receptor antagonist on tumor growth in human pancreatic adenocarcinoma cell lines in vivo and mode of action determinations in vitro. Cancer Chemother Pharmacol. 2008 Apr;61(5):883-92. [Content Brief]
[3]. Grabowska AM, et al. Pre-clinical evaluation of a new orally-active CCK-2R antagonist, Z-360, in gastrointestinal cancer models. Regul Pept. 2008 Feb 7;146(1-3):46-57. [Content Brief]
[4]. Shiomi Y, et al. Z-360 Suppresses Tumor Growth in MIA PaCa-2-bearing Mice via Inhibition of Gastrin-induced Anti-Apoptotic Effects. Anticancer Res. 2017 Aug;37(8):4127-4137. [Content Brief]
[5]. Yoshinaga K, et al. Pharmacological evaluation of analgesic effects of the cholecystokinin2 receptor antagonist Z-360 in mouse models of formalin- and cancer-induced pain. Biol Pharm Bull. 2010;33(2):244-8. [Content Brief]
[6]. Orikawa Y, et al. Z-360, a novel therapeutic agent for pancreatic cancer, prevents up-regulation of ephrin B1 gene expression and phosphorylation of NR2B via suppression of interleukin-1 β production in a cancer-induced pain model in mice. Mol Pain. 2010 Oct 28;6:72. [Content Brief]
[7]. Kobayashi N, et al. Z-360, a novel cholecystokinin-2/gastrin receptor antagonist, inhibits gemcitabine-induced expression of the vascular endothelial growth factor gene in human pancreatic cancer cells. Biol Pharm Bull. 2010;33(2):216-22. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Powered by Bioz