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Chemical Structure Cat. No. Product Name CAS No.
Enalapril Maleate Chemical Structure
 BCP21378 Enalapril Maleate 76095-16-4
Enalapril Maleate is the maleate salt form of enalapril, a dicarbocyl-containing peptide and angiotensin-converting enzyme (ACE) inhibitor with antihypertensive activity.
BMS-564929 Chemical Structure
 BCP21121 BMS-564929 627530-84-1
BMS-564929 is an androgen receptor (AR) agonist, binds to androgen receptor (AR) with a Ki of 2.11±0.16 nM.
JDTic dihydrochloride Chemical Structure
 BCP21083 JDTic dihydrochloride 785835-79-2
JDTic (dihydrochloride) is a potent antagonist of kappa-opioid receptors (KOR), blocking the κ-agonist U50, 488-induced antinociception.
U69593 Chemical Structure
 BCP23063 U69593 96744-75-1
U69593 is a selective kappa opioid receptor agonist.
Trap101 HCl Chemical Structure
 BCP23061 Trap101 HCl 873567-76-1
Trap 101 is a potent and selective nociceptin/orphanin FQ (NOP) receptor antagonist (pA2 = 7.75).
SNC162 Chemical Structure
 BCP23060 SNC162 178803-51-5
SNC 162 is a potent and selective non-peptide δ-opioid receptor agonist (Ki = 0.63 nM), displaying > 8000-fold selectivity over μ-opioid receptors.
Stanolone Chemical Structure
 BCP22808 Stanolone 521-18-6
Androstanolone is a potent androgenic metabolite of testosterone. Dihydrotestosterone (DHT) is generated by a 5-alpha reduction of testosterone. Unlike testosterone, DHT cannot be aromatized to estradiol therefore DHT is considered a pure androgenic steroid.
Idoxifene Chemical Structure
 BCP22721 Idoxifene 116057-75-1
Idoxifene is a novel tissue-specific selective estrogen receptor modulator (SERM).
Algestone acetophenide Chemical Structure
 BCP22648 Algestone acetophenide 24356-94-3
Algestone acetophenide is a progesterone that has been used in ESTRUS SYNCHRONIZATION and has been evaluated as an injectable contraceptive in combination with estradiol enanthate.
PCO371 Chemical Structure
 BCP31012 PCO371 1613373-33-3
PCO371 is an orally active full agonist of parathyroid hormone receptor 1 (PTHR1), with no effect on PTH type 2 receptor.
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