• TAK-653

TAK-653 powder

95.00

TAK-653 – pure powder

SKU: tak-653-powder

ACTIVE INGREDIENT: TAK-653

ADDITIONAL INGREDIENTS:

OTHER NAMES: 9-[4-(cyclohexyloxy)phenyl]-7-methyl-3,4-dihydropyrazino[2,1-c][1,2,4]thiadiazine 2,2-dioxide

CAS NUMBER: 1358751-06-0

ATC CODE:

FORMULA: C19H23N3O3S

MOLAR MASS: 373.47 g·mol−1

ITEM TYPE: Powder

QUANTITY PER PACK: 0.100 gram

SERVINGS PER PACK:

SUGGESTED USE:

STORAGE: Store in a cool and dry place. Keep away from direct sunlight and heat.

WARNING: Keep out of reach of children. Do not take this or any other supplement if under the age of 18, pregnant or nursing a baby, or if you have any known or suspected medical conditions, and/or taking prescription drugs or over the counter medications.

DISCLAIMER: Always consult with a qualified health physician before taking any new dietary supplement. This product is not intended to diagnose, treat, cure, or prevent any diseases.

SCOOPS: This product includes a measuring scoop (red) = 3 mg

The product is not intended for human use. For laboratory use only.

TAK-653 is an experimental drug being investigated as a treatment for treatment-resistant depression. It is being developed by Takeda Pharmaceuticals (Millennium Pharmaceuticals, Inc.)

TAK-653 is a selective positive allosteric modulator (PAM) of the AMPA receptor. TAK-653 and other AMPA PAMs potentiate the effects of agonists at the main site of the AMPA receptor by slowing the rate of desensitization and internalization of the receptor

There is evidence suggesting that activation of the AMPA receptor, downstream activation of mTOR, and upregulation of BDNF are central to the antidepressant effects of certain NMDA receptor antagonists such as ketamine. Blockage of the AMPA receptor nullifies the anti-depressant action of ketamine. By potentiating the effect of endogenous glutamate at the AMPA receptor, TAK-653 more directly influences AMPA receptor-mediated transcription.

The potential use of TAK-653 as a non-psychotomimetic antidepressant is cited as reason for its investigation. Initial research found that TAK-653, unlike ketamine, did not induce hyperlocomoter responses in rats. However, a later human trial investigating the CNS stimulatory properties and tolerability of TAK-653 reported that although the CNS stimulatory properties of the drug were less pronounced than other psychostimulants, TAK-653 did appear to possess at least some stimulant-like effects. No severe adverse effects were noted in the trial.

AMPA receptor agonists are likely not viable for clinical applications as they present a risk of inducing seizures and overexcitation-induced neurotoxicity at doses close to their therapeutic window. TAK-653 possesses minimal direct AMPA agonist properties. TAK-653 provides a 419 fold safety margin against convulsions relative to therapeutic doses in rats.

Source: Wikipedia