Minoxidil 5mg 100pcs Oral steroids tablets
Original price was: $100.00.$50.00Current price is: $50.00.K-ATP channel opener for hair growth and vasodilation research. Study follicular stimulation mechanisms.
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K-ATP channel opener for hair growth and vasodilation research. Study follicular stimulation mechanisms.
KPV (Lys-Pro-Val) is a C-terminal tripeptide fragment of alpha-MSH that modulates NF-kB signaling to suppress pro-inflammatory cytokine cascades. An oral formulation for investigating targeted anti-inflammatory pathways and mucosal tissue homeostasis.
Ivermectin is a macrocyclic lactone that potently agonizes glutamate-gated chloride channels in invertebrate nerve and muscle cells, inducing hyperpolarization and neuromuscular paralysis. An essential research tool for investigating antiparasitic mechanisms with an 18-hour half-life.
Type II 5-AR inhibitor for DHT suppression research. Study androgenetic alopecia and BPH pathways.
Dutasteride is a dual Type I and Type II 5-alpha-reductase inhibitor that reduces systemic DHT levels by over 90%, surpassing Finasteride’s single-isoenzyme selectivity. A thorough research tool for investigating maximal androgen blockade in DHT-sensitive tissues.
Enclomiphene (Androxal) is the purified trans-isomer of clomiphene that acts as a pure estrogen receptor antagonist at the pituitary, potently stimulating endogenous LH and FSH secretion without the mixed agonist properties of zuclomiphene. A go-to HPTA restoration research tool.
5-Amino-1MQ is a potent NNMT inhibitor that prevents nicotinamide methylation, diverting it into the NAD+ salvage pathway to elevate intracellular NAD+ and activate SIRT1. An oral formulation for investigating metabolic remodeling and adipose tissue reduction.
Ripex-225 is a complementary triple-blend injectable combining Testosterone Propionate, Trenbolone Acetate, and Drostanolone Propionate at 225mg/ml. It simultaneously activates androgen receptors, inhibits aromatase, and maintains physiological androgen levels for extensive anabolic signaling.
Estradiol Cypionate is an injectable estrogen receptor agonist that provides sustained 17-beta-estradiol release through gradual cypionate ester cleavage. It activates nuclear ER-alpha and ER-beta receptors for investigating estrogen-mediated gene transcription.
Vitamin B12 (Methylcobalamin) Injection 1mg/ml is an essential methyl-donor cofactor that catalyzes homocysteine-to-methionine conversion and supports myelin sheath integrity. The injectable delivery bypasses gastrointestinal absorption for superior bioavailability.
Prednisone is a glucocorticoid prodrug that undergoes hepatic conversion to active prednisolone, which binds cytosolic glucocorticoid receptors to translocate into the nucleus and repress NF-kB-driven pro-inflammatory gene transcription.
M1T (17a-Methyl-1-testosterone) is a highly potent C17-alpha-alkylated DHT derivative that delivers exceptional anabolic signaling through direct androgen receptor activation. A primary research compound for studying extreme nitrogen retention and rapid muscle hypertrophy.
Salbutamol is a selective Beta-2 adrenergic receptor agonist that activates adenylate cyclase to increase cAMP levels, driving both bronchodilation and lipolysis. A research tool for investigating adrenergic signaling in respiratory and metabolic models.
Halotestin (Fluoxymesterone) is an extremely potent C17-alkylated androgen featuring 9-alpha-fluoro and 11-beta-hydroxy modifications that maximize androgen receptor binding while preventing aromatization. A trusted compound for investigating central nervous system androgenic signaling.
Letrozole (Femara) is a non-steroidal Type II aromatase inhibitor that competitively coordinates with the CYP19A1 heme iron, reversibly blocking androgen-to-estrogen conversion. A high-potency research tool for achieving strong estrogen suppression.
Flibanserin is a multifunctional serotonin ligand that acts as a 5-HT1A agonist and 5-HT2A antagonist, shifting the neurochemical balance to increase dopamine and norepinephrine while reducing serotonin inhibition. A targeted tool for female libido and neurotransmitter research.
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