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Triptoréline CAS:57773-63-4

Triptoréline CAS:57773-63-4

Triptoréline, un décapeptide,est un agoniste de l'hormone de libération des gonadotrophines (Agoniste de la GnRH) utilisé comme sels d'acétate ou de pamoate. En provoquant une stimulation constante de l'hypophyse, il diminue la sécrétion hypophysaire de gonadotrophines hormone lutéinisante (LH) et hormone folliculo-stimulante (FSH). Comme les autres agonistes de la GnRH, la triptoréline peut être utilisée dans le traitement des cancers hormono-sensibles tels que le cancer de la prostate ou le cancer du sein, puberté précoce, …

Fragment de HGH 176-191 CAS:221231-10-3

Fragment de HGH 176-191 CAS:221231-10-3

Fragment peptidique de l'hormone de croissance 176-191, également connu sous le nom de HGH Frag 176-191, est une forme modifiée d'acides aminés 176-191 du polypeptide GH. Des chercheurs de l'Université Monash ont découvert que les effets réducteurs de graisse de la GH semblent être contrôlés par une petite région près d'une extrémité de la molécule d'hormone de croissance.. Cette région, qui se compose d'acides aminés 176-191, est moins …

Pentadécapeptide BPC 157 CAS:137525-51-0

Pentadécapeptide BPC 157 CAS:137525-51-0

Pentadécapeptide BPC 157, composé de 15 acides aminés, est une séquence partielle de composé de protection corporelle (CPC) qui est découvert dans et isolé du suc gastrique humain. BPC-157 est considéré comme synthétique car cette séquence particulière n'existe pas dans la nature. Il est dérivé d'une protéine protectrice présente dans l'estomac. CPC 157 Application de peptides: 1) BPC 157’s anti-inflammatory properties

Ocytocine CAS:50-56-6

Ocytocine CAS:50-56-6

Usage : Pour le déclenchement du travail, ocytocine post-partum, et l'avortement dû à l'atonie utérine ou à la rétraction causée par le mauvais saignement de l'utérus; comprendre la réserve de fonction placentaire (test de provocation à l'ocytocine); les gouttes nasales peuvent favoriser l'éjection du lait. Ocytocine (Oxt) est une hormone neurohypophysaire de mammifère. Produit par l'hypothalamus et stocké et sécrété par l'hypophyse postérieure, oxytocin acts primarily as

Melanotan 2 CAS:121062-08-6

Melanotan 2 CAS:121062-08-6

Melanotan 2 (also referred to as Melanotan II) is a synthetically produced variant of a peptide hormone naturally produced in the body that stimulates melanogenesis,a process responsible for pigmentation of the skin. Melanotan II,a drug originally developed as a skin tanning agent,but subsequently investigated as a potential treatment for sexual dysfunction. As a result,Melanotan 2 has been shown in studies

Melanotan I CAS:75921-69-6

Melanotan I CAS:75921-69-6

1.MT-1 (or Melanotan I,or Afamelanotide,or CUV-1647) is a synthetic analog of peptides nature of endogenous melanocortine peptide alpha-melanocyte stimulating hormone.It has hormones nature as well as common proteins features.Metallothioneins(MTs) are cysteine-rich metal-binding proteins that are potentially involved in zinc homeostasis and free radical scavenging. The expression pattern of MT-1 and the binding activity of various MT-1 promoter elements were investigated

PT141CAS:189691-06-3

PT141CAS:189691-06-3

PT-141 Description PT-141 (Bremelanotide) is a highly potent synthetic peptide analogue of α-MSH that may elicit aphrodisiac effects through stimulation of melanocortin receptors. PT-141 (Bremelanotide) consists of seven amino acids and is a cyclic, shortened lactam variant of alpha-Melanocyte-stimulating hormone (α-MSH), a multifunctional peptide that regulates a broad array of physiological functions. In studies, bremelanotide was shown to induce lordosis

Trestolone Decanoate

Trestolone Decanoate

Trestolone Decanoate has the same function as Trestolone Acetate, the only difference is ester length, it’s obvious that Decanoate is long ester, so Trestolone Decanoate don’t need to be used everyday. Trestolone decanoate is a synthetic androgen taken to build muscle rapidly, and is a theoretical candidate drug for use in hormonal male contraceptive methods. In males, regular administration of

Trestolone Acetate CAS:6157-87-5

Trestolone Acetate CAS:6157-87-5

Trestolone acetate(MENT) is actually an alright looking drug. It doesn’t show much interaction with Sex Hormone Binding Globulin, which means that a good portion ought to stay unbound and active in the blood. Aussi, the drug is a potent binder to the androgen receptor, while showing minimal affinity for the progesterone and mineralocorticoid receptors respectively. Since it is not able

Trestolone CAS:3764-87-2

Trestolone CAS:3764-87-2

Trestolone is a synthetic androgen taken to build muscle rapidly, and is a theoretical candidate drug for use in hormonal male contraceptive methods. In males, regular administration of sufficient quantities of trestolone induces a state of temporary infertility Trestolone is an experimental contraceptive treatment and is not yet available commercially. It is currently being evaluated for safety and effectiveness in

Andarine CAS:401900-40-1

Andarine CAS:401900-40-1

Andarine S4 is a Selective Androgen Receptor Modulator (SARM) developed by GTx. Like all SARM’s S4 was developed in the treatment of muscle wasting diseases with benign prostatic hypertrophy treatment also being high on the list of possible treatment benefits. Andarine is not as strong as some of the other SARM’s in terms of an anabolic effect that leads to

Sunifiram CAS:314728-85-3

Sunifiram CAS:314728-85-3

Sunifiram (DM-235) is a synthetic derivative of Piracetam, although due to breaking the pyrrolidone backbone it is no longer in the Racetam class of drugs (yet by being derived from them, it is still commonly associated with this class). Sunifiram Applications: Sunifiram is one of the newest nootropics on the market to smart drugs family. It is considered to be

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