MedKoo Cat#: 526985 | Name: ZD-9379
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

ZD-9379 is a NMDA receptor antagonist potentially for the treatment of pain and stroke. ZD9379 is also a glycine site antagonist, ZD9379 which reduces number of spreading depressions and infarct size in rats with permanent middle cerebral artery occlusion. ZD9379 reduces number of spreading depressions and infarct size in rats with permanent middle cerebral artery occlusion.

Chemical Structure

ZD-9379
ZD-9379
CAS# 170142-20-8

Theoretical Analysis

MedKoo Cat#: 526985

Name: ZD-9379

CAS#: 170142-20-8

Chemical Formula: C19H14ClN3O4

Exact Mass: 383.0673

Molecular Weight: 383.79

Elemental Analysis: C, 59.46; H, 3.68; Cl, 9.24; N, 10.95; O, 16.67

Price and Availability

Size Price Availability Quantity
10mg USD 450.00
20mg USD 750.00
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Related CAS #
No Data
Synonym
ZD-9379; ZD 9379; ZD9379.
IUPAC/Chemical Name
7-Chloro-2,3-dihydro-2-(4-methoxy-2-methylphenyl)pyridazino [4,5-b] quinoline-1,4,10(5H)trione
InChi Key
PSTDMIAVUUYOOQ-UHFFFAOYSA-N
InChi Code
InChI=1S/C19H14ClN3O4/c1-9-7-11(27-2)4-6-14(9)23-19(26)15-16(18(25)22-23)21-13-8-10(20)3-5-12(13)17(15)24/h3-8H,1-2H3,(H,21,24)(H,22,25)
SMILES Code
O=C1N(C2=CC=C(OC)C=C2C)NC(C(NC3=C4C=CC(Cl)=C3)=C1C4=O)=O
Appearance
White to off-white crystalline 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
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
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
Related CAS# CAS No. 170142-20-8 (ZD-9379 Free) 170142-29-7 (ZD-9379 sodium)

Preparing Stock Solutions

The following data is based on the product molecular weight 383.79 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
1: Danysz W, Parsons CG. Neuroprotective potential of ionotropic glutamate receptor antagonists. Neurotox Res. 2002 Mar;4(2):119-26. doi: 10.1080/10298420290015872. PMID: 12829411. 2: Tatlisumak T, Takano K, Meiler MR, Fisher M. A glycine site antagonist ZD9379 reduces number of spreading depressions and infarct size in rats with permanent middle cerebral artery occlusion. Acta Neurochir Suppl. 2000;76:331-3. doi: 10.1007/978-3-7091-6346-7_68. PMID: 11450037. 3: ZD 9379. Drugs R D. 1999 Jan;1(1):44-5. doi: 10.2165/00126839-199901010-00018. PMID: 10565985. 4: Tatlisumak T, Takano K, Meiler MR, Fisher M. A glycine site antagonist, ZD9379, reduces number of spreading depressions and infarct size in rats with permanent middle cerebral artery occlusion. Stroke. 1998 Jan;29(1):190-5. doi: 10.1161/01.str.29.1.190. PMID: 9445350. 5: Qiu H, Hedlund LW, Gewalt SL, Benveniste H, Bare TM, Johnson GA. Progression of a focal ischemic lesion in rat brain during treatment with a novel glycine/NMDA antagonist: an in vivo three-dimensional diffusion-weighted MR microscopy study. J Magn Reson Imaging. 1997 Jul-Aug;7(4):739-44. doi: 10.1002/jmri.1880070421. PMID: 9243396. 6: Takano K, Tatlisumak T, Formato JE, Carano RA, Bergmann AG, Pullan LM, Bare TM, Sotak CH, Fisher M. Glycine site antagonist attenuates infarct size in experimental focal ischemia. Postmortem and diffusion mapping studies. Stroke. 1997 Jun;28(6):1255-62; discussion 1263. doi: 10.1161/01.str.28.6.1255. PMID: 9183359.