Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN320434 ALB-127158(a) 1173154-32-9
ALB-127158(a) is a potent and selective melanin concentrating hormone 1 (MCH1) receptor antagonist.
AM211 is a potent, selective and orally bioavailableprostagl and in D2 (PGD2) receptor type 2 (DP2)antagonist, with IC50s of 4.9nM, 7.8nM, 4.9nM, 10.4nM for human, mouse, guinea pig, and rat DP2, respectively.
RAD140 is a potent, orally bioavailable, nonsteroidal selective androgen receptor modulator with Ki value of 7 nM as well as good selectivity over other steroid hormone nuclear receptors.
YN321608 Cinnarizine D8 1185242-27-6
Cinnarizine D8 is a deuterium labeled Cinnarizine. Cinnarizine is an antihistamine and a calcium channel blocker.
ML-109 is a potent and full thyroid stimulating hormone receptor (TSHR) agonist, with an EC50of 40nM.
YN321171 Omidenepag 1187451-41-7
Omidenepag,a pharmacologically active form of Omidenepag Isopropyl, is a selective, non-prostanoidEP2receptor agonist, with an EC50 of 1.1nM. Omidenepag shows binding affinities (IC50) 10nM for h-EP2.
YN321089 Ralinepag 1187856-49-0
Ralinepag is a potent, orally bioavailable and non-prostanoidprostacyclin (IP) receptoragonist, with EC50s of 8.5nM, 530nM and 850nM for human and rat IP receptor and human DP1 ...
YN321532 Hydroxyzine D8 1189480-47-4
Hydroxyzine D8 is deuterium labeled Hydroxyzine. Hydroxyzine is ahistamine H1-receptorantagonist.
YN321226 (±)-Methotrimeprazine (D6) 1189805-51-3
(±)-Methotrimeprazine (D6) is the deuterium labeled Methotrimeprazine, which is a D3 dopamine and Histamine H1 receptor antagonist.
YN320151 GSK1059865 1191044-58-2
GSK1059865 is a potentorexin 1 receptorantagonist.
YN321252 Burixafor hydrobromide 1191450-19-7
Burixafor hydrobromide (TG-0054 hydrobromide) is an orally bioavailable and potent antagonist ofCXCR4 and a well water soluble anti-angiogenic drug that is of potential value in treating choroid neovascularization. Burixafor hydr...
YN320749 ADRA1D receptor agonist 1 1191908-14-1
ADRA1D receptor agonist 1 (compound (R)-9S) is a potent, selective and orally activeα1Dadrenoceptorantagonist, with a Ki of 1.6nM.
AZD7594 is a potent selective nonsteroidalglucocorticoid receptormodulator, with an IC50 of 0.9nM.
YN360605 Esomeprazole magnesium salt 1198768-91-0
Esomeprazole magnesium salt ((S)-Omeprazole magnesium salt) is a potent and orally active proton pump inhibitor and reduces acid secretion through inhibition of theH+, K+-ATPasein gastric parietal cells. Esomeprazole magnesium ...
INT-777 is a potentTGR5agonist with an EC50 of 0.82μM.
YN320545 BI-167107 1202235-68-4
BI-167107 is a high affinity, full agonist that binds to the β2 adrenergic receptor (β2AR) with a dissociation constantKdof 84 pM.
SRT3109 is an antagonist ofCXCR2, with apIC50 of 8.2, and used in the research of chemokine mediated diseases.
SRT3190 is an antagonist ofCXCR2, used in the research of chemokine mediated diseases.
MK1064 is a selective orexin 2 receptor antagonist (2-SORA) with an IC50 of 18 nM.
KAG-308 is a potent selective and orally active agonist ofEP4 receptor(a prostagl and in E2 receptor subtype), suppresses colitis and promotes histological mucosal healing, potently inhibits TNF-α production. KAG-308 shows ...
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