Adamax

Adamax is a synthetic heptapeptide derived from semax; the specific amino acid sequence being Ac-MEHFPG-AG-NH₂

 

 

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پنهنجو پيار ورهايو

Adamax is a synthetic heptapeptide derived from نه ٻڌو; the specific amino acid sequence being Ac-MEHFPG-AG-NH₂.

Semax itself, a fragment of adrenocorticotropic hormone (ACTH), possesses potent neurotrophic and cognitive-enhancing properties.

Structural limitations within semax lead to significant limitations to its half-life and efficiency of crossing the blood-brain barrier.

To alleviate these limitations scientists introduced a bulky adamantylacetate group through covalent تعلق at the carboxyl terminus.

This modification significantly improved the pharmacokinetic properties of the peptide molecule.

Introduction of this moiety provides near complete resistance to subsequent enzymatic degradation; retention time of the active form of adamax within the body is greatly prolonged.

More excitingly, the previously mentioned ‘ingenious’ design promotes an increase in efficiency with which the peptide crosses said barrier, and enhanced specificity and selectivity is achieved.

Compromising no biological activity, all known effects of semax are either maintained or enhanced.

تسلسل

Ac-MEHFPGP-Adam-NH2

CAS نمبر

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ماليڪيولر فارمولا

C50H68N10O12S

ماليڪيولر وزن

1033.212

Research Of Adamax:

1.Therapeutic Efficacy and Clinical Potential

Clinical trials have shown Adamax to outperform Semax in promoting the growth and protection of دماغ مان نڪتل neurotrophic عنصر (بي ڊي اين ايف) ۽ هڪ نقطي تائين nerve growth factor (NGF).

Replacing Semax as a therapeutic agent, particularly for psychiatric disorders or social cognition enhancement, is a very real possibility.

2.Cognitive Enhancement (Intelligence being a subset)

Direct stimulation of BDNF upregulation is Adamax’s primary function.

Neuronal cell activity, new neuron generation/differentiation and all associated synaptic improvements are what the research is currently focused on.

Hippocampal and prefrontal cortex activity is also increased.

Long term experimental groups have and will continue to show, quantifiably, superior memory and learning abilities.

3.Neuroprotective اثرات

Adamax’s cognitive enhancement and intelligence-boosting functions originate not only from its direct promotion of neural cell growth, but also from demonstrable neuroprotective properties.

Effective reduction of cerebral infarction areas in stroke patients has been demonstrated; stimulation and subsequent recovery of various necrotic cells is another key aspect of this neuroprotection.

گھٽائڻ excitotoxicity and providing near-constant antioxidant effects are additional, well-documented activities.

Positioning itself within this realm, Adamax holds much promise as a true therapeutic agent for neurodegenerative disorders – Alzheimer’s being the prime example, Parkinson’s following closely behind.

4.Stress and Anxiety Relief

Adamax enhances the human ability to adapt to environmental changes; the brain itself must rapidly adjust to, and resist, a variety of physiological stressors resulting from these quick environmental shifts.

Maintaining some form of homeostasis is the end goal.

Modulation of the hypothalamic-pituitary-adrenal (ايڇ پي اي) محور is central to this process, increasing or decreasing the appropriate release of neurotransmitters, all lesser ‘stress responses’ being suppressed.

Anxiolytic effects are a primary benefit – drowsiness and cognitive impairment (the near universal side effects of traditional anxiolytics) are completely avoided.

Enhancing cognitive function during any form of anxiety relief is what makes Adamax particularly alluring to researchers and patients alike.

COA

HPLC

ايم ايس

(1)لاڳت, ن. وي.; سوڪولوف, او. يو.; گابيوا, ايم. وي.; Grivennikov, اي. اي.; اينڊريوا, ايل. اي.; Myasoedov, ن. ايف.; Zozulya, اي. اي. Semax and Selank Inhibit the Enkephalin-Degrading Enzymes of Human Serum. Russian Journal of Bioorganic Chemistry 2001, 27(3), 156-159. DOI: 10.1023/هڪ:1011373002885.

(2)ولاسوا, اي. ايم.; Buravtcov, ڊي. اي.; سالٽسڪي, اي. ايم. دماغي اسڪيميا ۾ دوا "سيمڪس" جي نيوروپروٽيڪٽو پراپرٽيز جي مطالعي ۾ رت جي اجزاء جو لومينسنس تجزيو. اپلائيڊ اسپيڪٽروڪوپي جو جرنل 2009, 76(1), 121-126. DOI: 10.1007/s10812-009-9141-y.

(3)Abraham, ايم. ايڇ.; Acree, ڊبليو. اي.; ليو, ايڪس. Descriptors for adamantane and some of its derivatives. Journal of Molecular Liquids 2021, 325. DOI: 10.1016/j.molliq.2020.114894.

(4)Dane, سي.; Montgomery, اي. پي.; Kassiou, ايم. The adamantane scaffold: Beyond a lipophilic moiety. European Journal of Medicinal Chemistry 2025, 291. DOI: 10.1016/j.ejmech.2025.117592.

(5)دمتريوا, وي. جي.; پووارووا, او. وي.; Skvortsova, وي. اي.; لمبورسڪا, ايس. اي.; Myasoedov, ن. ايف.; درگونووا, ايل. وي. سيمڪس ۽ پرو-گلي-پرو دماغي اسڪيميا کان پوءِ نيوروٽروفينز ۽ انهن جي ريڪٽر جينز جي ٽرانسپشن کي چالو ڪن ٿا. سيلولر ۽ ماليڪيولر نيروبيولوجي 2009, 30(1), 71-79. DOI: 10.1007/s10571-009-9432-0.

(6)اريمين, ڪي. او.; ڪُدرين, وي. ايس.; سارنسري, پي.; پيداوار, ايس. ايس.; Grivennikov, اي. اي.; Myasoedov, ن. ايف.; Rayevsky, ڪي. ايس. نه ٻڌو, هڪ ACTH(4-10) Nootropic Properties سان اينالاگ, Rodents ۾ Dopaminergic ۽ Serotoninergic دماغي سسٽم کي چالو ڪري ٿو. نيورو ڪيميڪل ريسرچ 2005, 30(12), 1493-1500. DOI: 10.1007/s11064-005-8826-8.

(7)گلزووا, ن. يو.; منچنڪو, ڊي. ايم.; وولودينا, ايم. اي.; مرچيوا, ايس. اي.; اينڊريوا, ايل. اي.; ڪُدرين, وي. ايس.; Myasoedov, ن. ايف.; Levitskaya, ن. جي. نه ٻڌو, مصنوعي ACTH(4-10) اينالاگ, سفيد چوتن ۾ شروعاتي زندگي جي فلووڪسامين جي نمائش جي پٺيان رويي ۽ نيورو ڪيميڪل تبديلين کي گھٽائي ٿو. Neuropeptides 2021, 86. DOI: 10.1016/j.npep.2020.102114.

(8)ميدوديوا, اي. وي.; دمتريوا, وي. جي.; لمبورسڪا, ايس. اي.; Myasoedov, ن. ايف.; درگونووا, ايل. وي. نه ٻڌو, ACTH جو هڪ اينالاگ(4-7), چوڪن ۾ اسڪيمڪ دماغ جي زخم دوران مدافعتي ردعمل جين جي اظهار کي منظم ڪري ٿو. ماليڪيولر جينياتي ۽ جينومڪس 2017, 292(3), 635-653. DOI: 10.1007/s00438-017-1297-1.

(9)پائي, C.-U. ڊپريشن لاء "سيمڪس" جي علاج جو امڪان. CNS اسپيڪٽرم 2014, 13(1), 20-21. DOI: 10.1017/s1092852900016102.

تسلسل:

Ac-MEHFPGP-Adam-NH2

CAS:

N/A

M.W:

1033.21جي/مول

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