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GPCR/G Protein

Chemical Structure Cat. No. Product Name CAS No.
L-368,899 hydrochloride Chemical Structure
BCP38590 L-368,899 hydrochloride 160312-62-9
L-368,899 hydrochloride is the hydrochloride salt of L-368,899, which is a non-peptide, orally active and potent oxytocin receptor antagonist with IC50 value of 8.9 nM.
Centanafadine hydrochloride Chemical Structure
BCP38626 Centanafadine hydrochloride 923981-14-0
Centanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter, with IC50s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.
Terbutaline Chemical Structure
BCP38566 Terbutaline 23031-25-6
Terbutaline is a β2 adrenergic receptor agonist, used as a "reliever" inhaler in the management of asthma symptoms and as a tocolytic (anti-contraction medication) to delay preterm labor for up to 48 hours. This time can then be used to administer steroid injections to the mother which help fetal lung maturity and reduce complications of prematurity. It should not be used to prevent preterm labor or delay labor more than 48–72 hours.
Cetrorelix diacetate Chemical Structure
BCP38364 Cetrorelix diacetate 130143-01-0
Cetrorelix diacetate is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM.
Seltorexant Chemical Structure
BCP38147 Seltorexant 1293281-49-8
Seltorexant, also known as JNJ-42847922 and MIN-202, is a selective orexin-2 receptor antagonist that has been shown to promote sleep in various species.
PSB-SB-487 Chemical Structure
BCP37990 PSB-SB-487 1399049-81-0
PSB-SB-487 is a potent, allosteric GPR55 antagonist
VU0155094 Chemical Structure
BCP38019 VU0155094 731006-86-3
VU0155094 is a potent, selective pan-Group III mGlu positive allosteric modulator with IC50 of 3.43/1.5/0.93 uM for mGlu8/7/4, respectively.
NPD8733 Chemical Structure
BCP38016 NPD8733 696655-62-6
NPD8733 is a small-molecule ligand of valosin-containing protein (VCP)/p97, binds to the D1 domain of VCP/p97.
VPC 23019 Chemical Structure
BCP37989 VPC 23019 449173-19-7
VPC 23019 is an aryl amide-containing S1P analog that acts as a competitive antagonist, inhibit S1P-induced migration of thyroid cancer cells, ovarian cancer cells, and neural stem cells.
OS-3-106 Chemical Structure
BCP37979 OS-3-106 1580000-17-4
OS-3-106 is a novel dopamine D3 receptor-selective partial agonist.
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