TFM-4AS-1 is a dual
selective androgen receptor modulator
Selective androgen receptor modulators (SARMs) are a class of drugs that tissue selectivity, selectively activate the androgen receptor in specific tissue (biology), tissues, promoting muscle and bone growth while having less effect on male re ...
(SARM) and
5α-reductase inhibitor.
It is a potent and
selective partial agonist
In pharmacology, partial agonists are drugs that bind to and activate a given Receptor (biochemistry), receptor, but have only partial Intrinsic activity, efficacy at the receptor relative to a full agonist. They may also be considered Ligand (bio ...
(
Emax = 55%) of the
androgen receptor
The androgen receptor (AR), also known as NR3C4 (nuclear receptor subfamily 3, group C, member 4), is a type of nuclear receptor that is activated by binding any of the androgenic hormones, including testosterone and dihydrotestosterone, in th ...
(
IC50 = 30nM) and
inhibitor
Inhibitor or inhibition may refer to:
Biology
* Enzyme inhibitor, a substance that binds to an enzyme and decreases the enzyme's activity
* Reuptake inhibitor, a substance that increases neurotransmission by blocking the reuptake of a neurotransmi ...
of
5α-reductase types I and
II (IC
50 = 2 and 3 nM, respectively).
TFM-4AS-1 shows
tissue-selective
Tissue selectivity is a topic in distribution (pharmacology) and property of some drugs. It refers to when a drug occurs in disproportionate concentrations and/or has disproportionate effects in specific tissues relative to other tissues. An examp ...
androgen
An androgen (from Greek ''andr-'', the stem of the word meaning ) is any natural or synthetic steroid hormone that regulates the development and maintenance of male characteristics in vertebrates by binding to androgen receptors. This includes ...
ic effects; it promotes the accumulation of
bone
A bone is a rigid organ that constitutes part of the skeleton in most vertebrate animals. Bones protect the various other organs of the body, produce red and white blood cells, store minerals, provide structure and support for the body, ...
and
muscle
Muscle is a soft tissue, one of the four basic types of animal tissue. There are three types of muscle tissue in vertebrates: skeletal muscle, cardiac muscle, and smooth muscle. Muscle tissue gives skeletal muscles the ability to muscle contra ...
mass and has reduced effects in
reproductive
The reproductive system of an organism, also known as the genital system, is the biological system made up of all the anatomical organs involved in sexual reproduction. Many non-living substances such as fluids, hormones, and pheromones are al ...
tissues and
sebaceous gland
A sebaceous gland or oil gland is a microscopic exocrine gland in the skin that opens into a hair follicle to secrete an oily or waxy matter, called sebum, which lubricates the hair and skin of mammals. In humans, sebaceous glands occur in ...
s.
In an animal study, TFM-4AS-1 stimulated sebaceous gland formation only 31% as much as
dihydrotestosterone
Dihydrotestosterone (DHT, 5α-dihydrotestosterone, 5α-DHT, androstanolone or stanolone) is an endogenous androgen sex steroid and hormone primarily involved in the growth and repair of the prostate and the penis, as well as the production o ...
(DHT) at doses that were as anabolic or more so than DHT.
In addition, TFM-4AS-1 only weakly promoted growth of the prostate gland and it
partially antagonized the actions of DHT in the seminal vesicles and endogenous androgens in the prostate gland.
Structurally, TFM-4AS-1 is a
4-azasteroid.
A structurally related and more advanced version of TFM-4AS-1,
MK-0773, was developed and pursued for potential pharmaceutical use.
See also
*
Cl-4AS-1
*
MK-0773
*
MK-4541
MK-4541 is a dual selective androgen receptor modulator (SARM) and 5α-reductase inhibitor (5α-RI) which has been of interest for the potential treatment of prostate cancer but has not been marketed at this time. It is intended for use by mout ...
*
YK-11
References
5α-Reductase inhibitors
Abandoned drugs
Androstanes
Carboxamides
Ketones
Selective androgen receptor modulators
Trifluoromethyl compounds
{{Genito-urinary-drug-stub