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www.sigmaaldrich.com, Drugs acting on the genito-urinary system, Androgens and anabolic steroids, Norepinephrine releasing agents

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METHAMPHETAMINE (51-57-0, 537-46-2)  
Desoxyn  ·  Methylamphetamine  ·  Methamphetamine Hydrochloride
Methamphetamine (contracted from N-methylamphetamine) is a strong central nervous system (CNS) stimulant that is mainly used as a recreational drug and less commonly as a second-line treatment for attention deficit hyperactivity disorder and obesity. Methamphetamine was discovered in 1893 and exists as two enantiomers: levo-methamphetamine and dextro-methamphetamine. Methamphetamine properly refers to a specific chemical, the racemic free base, which is an equal mixture of levomethamphetamine and dextromethamphetamine in their pure amine forms.
Levmetamfetamine (33817-09-3)  
Levomethamphetamine is the levorotary (L-enantiomer) form of methamphetamine. Levomethamphetamine is a sympathomimetic vasoconstrictor which is the active ingredient in some over-the-counter (OTC) nasal decongestant inhalers in the United States.

Related Results:
Dirigestran (33515-09-2, 6918-09-8, 9002-67-9, 9034-40-6)  
GnRH  ·  LHRH  ·  Gonadotropin Releasing Hormone
Gonadorelin, also known as gonadotropin-releasing hormone (GnRH) and sold under the brand names Factrel, HRF, Kryptocur, Lutrelef, Lutrepulse, and Relefact among others, is a GnRH agonist which is used in fertility medicine and to treat amenorrhea and hypogonadism. It is also used in veterinary medicine. The drug is a pharmaceutical form of endogenous GnRH and is identical to it in chemical structure.
GONADORELIN (71447-49-9, 33515-09-2, 9034-40-6)  
GnRH  ·  LHRH  ·  Gonadotropin Releasing Hormone
Gonadorelin, also known as gonadotropin-releasing hormone (GnRH) and sold under the brand names Factrel, HRF, Kryptocur, Lutrelef, Lutrepulse, and Relefact among others, is a GnRH agonist which is used in fertility medicine and to treat amenorrhea and hypogonadism. It is also used in veterinary medicine. The drug is a pharmaceutical form of endogenous GnRH and is identical to it in chemical structure.
Testosterone phenylpropionate (1255-49-8)  
testosterone 17-phenylpropionate  ·  Retandrol
SOMATOSTATIN (51110-01-1, 61950-59-2, 38916-34-6)  
Somatostatin 14  ·  Cyclic Somatostatin  ·  Somatotropin Release Inhibiting Factor
stanozolol (10418-03-8, 302-96-5)  
Winstrol  ·  Stanazolol  ·  Stromba
Stanozolol, sold under many brand names, is an androgen and anabolic steroid (AAS) medication which was derived from dihydrotestosterone (DHT). It was developed by American pharmaceutical company Winthrop Laboratories (Sterling Drug) in 1962, and has been approved by the Food and Drug Administration for human use, though it is no longer marketed in this country. It is also used in veterinary medicine.
Estradiol mustard (22966-79-6)  
Estradiol mustard (developmental code name NSC-112259), also known as chlorphenacyl estradiol diester, as well as estradiol 3,17β-bis(4-(bis(2-chloroethyl)amino)phenyl)acetate, is a synthetic, steroidal estrogen and alkylating antineoplastic agent and a chlorphenacyl nitrogen mustard-coupled estrogen ester that was never marketed. It is selectively distributed into estrogen receptor (ER)-positive tissues such as ER-expressing tumors like those seen in breast and prostate cancers. For this reason, estradiol mustard and other cytostatic-linked estrogens like estramustine phosphate have reduced toxicity relative to non-linked nitrogen mustard alkylating antineoplastic agents.
testosterone (58-22-0)  
Testim  ·  Testoderm  ·  AndroGel
Testosterone is the primary male sex hormone and an anabolic steroid. In male humans, testosterone plays a key role in the development of male reproductive tissues such as testes and prostate, as well as promoting secondary sexual characteristics such as increased muscle and bone mass, and the growth of body hair. In addition, testosterone is involved in health and well-being, and the prevention of osteoporosis.
testosterone enanthate (315-37-7)  
Delatestryl  ·  Andropository  ·  Durathate
Testosterone enanthate, sold under the brand name Delatestryl among others, is an androgen and anabolic steroid (AAS) medication which is used mainly in the treatment of low testosterone levels in men. It is also used in hormone therapy for transgender men. It is given by injection into muscle usually once every two to four weeks.
ESTRADIOL UNDECYLATE (3571-53-7)  
estradiol 17-undecanoate
Estradiol undecylate, or estradiol undecanoate, sold under the brand name Progynon Depot 100 among others, is a medication which has been used in the treatment of prostate cancer in men. It has also been used as a part of hormone therapy for transgender women. Although estradiol undecylate has been used in the past, it has mostly or fully been discontinued and hence is now mostly or fully no longer available.
Dehydroepiandrosterone (53-43-0)  
DHEA  ·  Dehydroisoandrosterone  ·  Androstenolone
Prasterone, also known as dehydroepiandrosterone (DHEA), is a naturally occurring steroid which is used as a supplement and medication. It is an androstane derivative and a precursor of steroid hormones like testosterone and estradiol. Prasterone has weak androgenic activity, weak estrogenic activity, and neurosteroid activity, and acts as a prohormone of androgens and estrogens depending on its dosage and route of administration.
TESTOSTERONE CYPIONATE (58-20-8)  
Duratest  ·  Andronate  ·  testosterone 17 beta-cyclopentylpropionate
Testosterone cypionate, sold under the brand name Depo-Testosterone among others, is an androgen and anabolic steroid (AAS) medication which is used mainly in the treatment of low testosterone levels in men. It is also used in hormone therapy for transgender men. It is given by injection into muscle usually once every two to four weeks.
estradiol (50-28-2, 73459-61-7)  
Oestradiol  ·  Estrace  ·  Vivelle
Estradiol (E2), also spelled oestradiol, is an estrogen steroid hormone and the major female sex hormone. It is involved in the regulation of the estrous and menstrual female reproductive cycles. Estradiol is responsible for the development of female secondary sexual characteristics such as the breasts, widening of the hips, and a feminine pattern of fat distribution in women and is important in the development and maintenance of female reproductive tissues such as the mammary glands, uterus, and vagina during puberty, adulthood, and pregnancy.
ethisterone (434-03-7)  
Pregneninolone  ·  Anhydrohydroxyprogesterone  ·  17 alpha Ethynyltestosterone
Ethisterone (brand names Proluton C, Pranone among others), also known as ethinyltestosterone, pregneninolone, or anhydrohydroxyprogesterone, is a progestin with androgenic activity which was derived from testosterone and was introduced for medical use in 1939. It was the second progestogen to be marketed (intramuscular progesterone was introduced as Proluton in 1934) and was both the first orally active progestogen and the first progestin (synthetic progestogen) to be introduced. Although ethisterone has largely been superseded by newer drugs and is now little used, it reportedly continues to be available in some countries.
estradiol cypionate (313-06-4)  
Depo-estradiol  ·  estradiol 17 beta-cyclopentylpropionate  ·  estradiol 17 beta-cypionate
Estradiol cypionate, sold under the brand name Depo-Estradiol among others, is a medication which is used in hormone therapy such as for menopausal symptoms and in hormonal birth control. It is given by injection into muscle. Side effects of estradiol cypionate include breast tenderness, breast enlargement, nausea, headache, and fluid retention.
androstenone (18339-16-7)  
AEON steroid  ·  androst-16-en-3-one  ·  androst-16-en-3-one, (5beta)-isomer
Androstenone (5α-androst-16-en-3-one) is a steroidal pheromone. It is found in boar's saliva, celery cytoplasm, and truffle fungus. Androstenone was the first mammalian pheromone to be identified.
formestane (566-48-3)  
Formestane, sold under the brand name Lentaron among others, is a steroidal, selective aromatase inhibitor which is used in the treatment of estrogen receptor-positive breast cancer in postmenopausal women. The drug is not active orally, and is instead available only as an intramuscular depot injection. Because of this, it is no longer popular as many orally active aromatase inhibitors have been identified and introduced.
53-00-9 (53-00-9)  
7α-Hydroxydehydroepiandrosterone (7α-hydroxy-DHEA; 7α-OH-DHEA), also known as 3β,7α-dihydroxyandrost-4-ene-17-one, is an endogenous, naturally occurring steroid and a major metabolite of dehydroepiandrosterone (DHEA) that is formed by CYP7B1 (steroid 7α-hydroxylase) in tissues such as the prostate gland and by CYP3A4 in the liver. The major metabolic pathway of DHEA outside the liver is via 7-hydroxylation into 7α-OH-DHEA and 7β-OH-DHEA. 7α-OH-DHEA has weak estrogenic activity, selectively activating the estrogen receptor ERβ.
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