(-)-MK 801 maleate - 10mM in DMSO , CAS No.121917-57-5

CAS: 121917-57-5 Cat. No.: M408999 Molecular Weight: 337.37
AVAILABLE TO ORDER
GRADE & PURITY 10mM in DMSO
Synonyms
C13737 | 5H-Dibenzo[a,d]cyclohepten-5,10-imine, 10,11-dihydro-5-methyl-, (5R,10S)-, (2Z)-2-butenedioate (1:1)
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
M408999-1ml
2

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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

(-)-MK-801 (Dizocilpine, C13737) is a potentN-methyl-D-aspartate (NMDA)receptor antagonist withKiof 30.5 nM.
In vitro

Neurophysiological studies in vitro, using a rat cortical-slice preparation, demonstrates a potent, selective, and noncompetitive antagonistic action of dizocilpine on depolarizing responses to N-Me-D-Asp but not to kainate or quisqualate. The potencies of phencyclidine, ketamine, SKF 10047, and the enantiomers of dizocilpine as N-Me-D-Asp antagonists correlate closely (r = 0.99) with their potencies as inhibitors of [3H] dizocilpine binding. This suggests that the dizocilpine binding sites are associated with N-Me-D-Asp receptors and provides an explanation for the mechanism of action of dizocilpine as an anticonvulsant.

In vivo

All the control rats have severe permanent neurological deficits after ischemic spinal cord injury (ISCI), whereas the dizocilpine–treated rats have statistically (P < .05) better neurological outcome and good recovery. Histopathology reveals severe neuronal necrosis in the lumbar gray matter of control rats, whereas dizocilpine–treated rats show mild injury. These results demonstrate that a single dose of dizocilpine given before ISCI provides significant neuroprotection.
Cell Data

cell lines:Caco-2, wild-type, and P-gp-overexpressing LLC-PK1

Concentrations:10 μM

Incubation Time:30 minutes

Powder Purity:≥99%

Specifications

Synonyms
C13737 | 5H-Dibenzo[a, d]cyclohepten-5, 10-imine, 10, 11-dihydro-5-methyl-, (5R, 10S)-, (2Z)-2-butenedioate (1:1)
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
(-)-MK-801 (Dizocilpine, C13737) is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30.5 nM.
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Isomeric SMILES C[C@]12C3=CC=CC=C3C[C@H](N1)C4=CC=CC=C24.C(=C\C(=O)O)\C(=O)O
Molecular Weight 337.37
Reaxy-Rn 34955296
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=34955296&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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1 results found

Lot NumberCertificate TypeDateItem
G2401114Certificate of AnalysisMay 13, 2026 M408999
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 58 mg/mL (200.43 mM); Ethanol: 58 mg/mL (200.43 mM); Water: Insoluble;
Solution Calculators
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