Zastaprazan
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Hodoodo CAT#: H414730

CAS#: 2133852-18-1

Description: Zastaprazan, also known as JP-1366, is a proton pump inhibitor. JP-1366 mediates strong, selective, and dose-dependent inhibition of H+/K+-ATPase. JP-1366 significantly suppressed gastric acid secretion in histamine-treated pylorus-ligated rats in a dose-dependent manner. Additionally, JP-1366 inhibited histamine-stimulated gastric acid secretion in the HPD model. JP-1366 exhibited a more than 2-fold higher inhibitory effect on esophageal injury than TAK-438 in GERD lesions and had a more potent inhibitory effect in indomethacin- or aspirin-induced gastric ulcer rat models than TAK-438. Additionally, JP-1366 inhibited gastric ulcers.


Chemical Structure

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Zastaprazan
CAS# 2133852-18-1

Theoretical Analysis

Hodoodo Cat#: H414730
Name: Zastaprazan
CAS#: 2133852-18-1
Chemical Formula: C22H26N4O
Exact Mass: 362.21
Molecular Weight: 362.480
Elemental Analysis: C, 72.90; H, 7.23; N, 15.46; O, 4.41

Price and Availability

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5mg USD 750 2 Weeks
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Synonym: Zastaprazan; JP-1366; JP 1366; JP1366;

IUPAC/Chemical Name: (azetidin-1-yl)(8-{[(2,6-dimethylphenyl)methyl]amino}- 2,3-dimethylimidazo[1,2-a]pyridin-6-yl)methanone

InChi Key: FEQFUBYYZYQTOJ-UHFFFAOYSA-N

InChi Code: InChI=1S/C22H26N4O/c1-14-7-5-8-15(2)19(14)12-23-20-11-18(22(27)25-9-6-10-25)13-26-17(4)16(3)24-21(20)26/h5,7-8,11,13,23H,6,9-10,12H2,1-4H3

SMILES Code: O=C(N1CCC1)C2=CN3C(C(NCC4=C(C)C=CC=C4C)=C2)=NC(C)=C3C

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: To be determined

Shelf Life: >2 years if stored properly

Drug Formulation: To be determined

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info: The global prevalence of GERD is substantially increasing each year, and GERD is a chronic disease that reduces the quality of life of patients. The efficacy of conventional drugs is diverse, and most require long-term or lifetime administration; thus, the development of more effective therapeutic agents is needed.

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 362.48 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Ku JM, Cho JH, Kim K, Kim JY, Kim JY, Kim J, Cha H, Cheon B. JP-1366: A novel and potent potassium-competitive acid blocker that is effective in the treatment of acid-related diseases. Pharmacol Res Perspect. 2023 Jun;11(3):e01090. doi: 10.1002/prp2.1090. PMID: 37147903; PMCID: PMC10163344.


2: Hwang I, Ji SC, Oh J, Kim H, Cha H, Kim J, Lee CS, Yu KS, Lee S. Randomised clinical trial: Safety, tolerability, pharmacodynamics and pharmacokinetics of zastaprazan (JP-1366), a novel potassium-competitive acid blocker, in healthy subjects. Aliment Pharmacol Ther. 2023 Apr;57(7):763-772. doi: 10.1111/apt.17406. Epub 2023 Feb 2. PMID: 36732884.