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BiohacksAI

Evidence-Based Biohacking

Patent Pending

Assembly and cell surface presentation of NMDA receptors

REACTOME PATHWAY
Reactome: R-HSA-960973624 genes36 compounds

The Assembly and cell surface presentation of NMDA receptors pathway (Reactome ID: R-HSA-9609736) involves 24 genes and is affected by 36 compounds in the BiohacksAI evidence corpus. Compound-pathway associations are derived from target overlap: a compound is linked to this pathway if it targets ≥2 genes within the pathway.

Genes in this Pathway

CAMK2BCAMK2DCASKGRIN1GRIN2AGRIN2BGRIN2CTUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBA8TUBAL3TUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TUBB8B

Compounds Affecting Assembly and cell surface presentation of NMDA receptors

#CompoundTargets HitStudies
1Colchicine300
2Nocodazole Nocodazole is215
3Vincristine299
4Noscapine300
5Podophyllotoxin14
6Demecolcine246
7Maytansine300
8vinblastine sulfate81
9Vorinostat299
10Glutamic Acid297
11Glutamic Acid300
12Glycine300
13pentamidine299
14Dextromethorphan Methyl analog of DEXTRORPHAN that shows high affinity binding to several regions of296
15Dextrorphan Dextro form of levorphanol. It acts as300
16Levorphanol297
17cycloserine298
18Aspartic Acid300
19D-Aspartic Acid29
20Ethidium300
21Dextrothyroxine134
22Dizocilpine Maleate300
23Ibotenic Acid300
24Spermine300
25eliprodil33
26Memantine AMANTADINE derivative that has some dopaminergic effects. It has been proposed as34
27KN 92 [Supplementary Concept] KN 93 isomer;26
28sp600125117
29Kynurenic Acid300
30Phenformin300
31Carvedilol296
32Ibogaine300
33Quercetin300
34Sorafenib300
35alsterpaullone12
36Crizotinib298

About the Assembly and cell surface presentation of NMDA receptors Pathway

The Assembly and cell surface presentation of NMDA receptors pathway is catalogued in Reactome (ID: R-HSA-9609736) and involves 24 genes. In the BiohacksAI corpus, 36 compounds have documented interactions with at least 2 genes in this pathway, establishing mechanistic relevance. Key pathway genes include CAMK2B, CAMK2D, CASK, GRIN1, GRIN2A.