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Methyl-1-testosterone (M1T; developmental code name SC-11195), also known as 17α-methyl-4,5α-dihydro-δ 1-testosterone (17α-methyl-δ 1-DHT) or 17α-methyl-5α-androst-1-en-17β-ol-3-one, as well as methyldihydroboldenone, is a synthetic and orally active anabolic–androgenic steroid (AAS) [1] which was never marketed for medical use.
Methyltestosterone, also known as 17α-methyltestosterone or as 17α-methylandrost-4-en-17β-ol-3-one, is a synthetic, 17α-alkylated androstane steroid and a derivative of testosterone differing from it only in the presence of a methyl group at the C17α position. [1] [2] [4] Close synthetic relatives of methyltestosterone include metandienone ...
These locks are often compromised through power analysis attacks. [12] [13] Several tools exist that can automatically retrieve or reset the combination of an electronic lock; notably, the Little Black Box [14] and Phoenix. Tools like these are often connected to wires in the lock that can be accessed without causing damage to the lock or ...
Mesterolone, also known as 1α-methyl-4,5α-dihydrotestosterone (1α-methyl-DHT) or as 1α-methyl-5α-androstan-17β-ol-3-one, is a synthetic androstane steroid and derivative of DHT. [ 19 ] [ 20 ] [ 2 ] It is specifically DHT with a methyl group at the C1α position.
A typical lineman's handset integrates an earpiece, a mouthpiece, a dialing interface, and a set of test leads for connecting to the telephone circuit. Originally, lineman's handsets featured a rotary dial , but modern sets use some variant of the standard 12-button DTMF keypad and also employ an amplifier for speaker use.
In computer architecture, the test-and-set CPU instruction (or instruction sequence) is designed to implement mutual exclusion in multiprocessor environments. Although a correct lock can be implemented with test-and-set, the test and test-and-set optimization lowers resource contention caused by bus locking, especially cache coherency protocol overhead on contended locks.
Trestolone, also known as 7α-methyl-19-nortestosterone (MENT), is an experimental androgen/anabolic steroid (AAS) and progestogen medication which has been under development for potential use as a form of hormonal birth control for men and in androgen replacement therapy for low testosterone levels in men but has never been marketed for medical use.
GML-1 is selective for TSPO versus the central benzodiazepine receptor (CBR, GABAA receptor). The compound GML-1 was the most active of a series of 1-arylpyrrolo[1,2-a]pyrazine-3-carboxamides, and its anxiolytic effects were examined using the open field test (OFT) and the elevated plus maze (EPM) test. The EPM test is a general anxiety test ...