Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN320927 Cenicriviroc Mesylate 497223-28-6
Cenicriviroc Mesylate (TAK-652 Mesylate) is a dual CCR2/CCR5 antagonist, also inhibits both HIV-1 and HIV-2, and displays potent anti-inflammatory and antiinfective activity.
YN480459 TR antagonist 1 500794-88-7
TR antagonist 1 is a high-affinitythyroid hormone receptor (TR)antagonist with IC50s of 36 and 22nM for TRα and TRβ, respectively.
YN320846 Vilanterol 503068-34-6
Vilanterol (GW642444) is a long-actingβ2-adrenoceptor(β2-AR) agonist with 24 h activity. ThepEC50s for β2-AR,β1-AR and β3-AR is 10.37±0.05, 6.98±0.03 and 7.36±0.03, respectively.
YN320847 Vilanterol trifenatate 503070-58-4
Vilanterol trifenatate is a novel inhaled long-acting beta2 adrenoceptor agonist with inherent 24-hour activity for once daily treatment of COPD and asthma.
YN321273 CCR2-RA-[R] 512177-83-2
CCR2-RA-[R] is an allosteric antagonist of theC-C chemokine receptor type 2 (CCR2)with an IC50 of 103nM.
YN320315 JNJ-10229570 524923-88-4
JNJ-10229570 is an antagonist ofmelanocortin receptor 1 (MC1R) and melanocortin receptor 5 (MC5R), which inhibits sebaceous gl and differentiation and the production of sebum-specific lipids. JNJ-10229570 inhibits the binding...
YN321580 Fexofenadine D6 548783-71-7
Fexofenadine D6 (MDL-16455 D6) is deuterium labeled is Fexofenadine, which is an antihistamine pharmaceutical agent.
YN320904 Rolapitant 552292-08-7
Rolapitant is a potent, selective and orally active neurokinin NK1 receptor antagonist.
YN320832 Macitentan (n-butyl analogue) 556797-16-1
Macitentan n-butyl analogue is a n-butyl analogue of Macitentan. Macitentan is an orally active, non-peptide dual endothelinETA and ETB receptorantagonist for the potential treatment of idiopathic pulmonary fibrosis (IPF) and ...
YN321274 Mavorixafor 558447-26-0
Mavorixafor (AMD-070) is a potent, selective and orally availableCXCR4antagonist, with an IC50 value of 13nM against CXCR4125I-SDF binding, and also inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in M...
AZD2098 is a potent and bioavailable CCR4 receptor antagonist with pIC50 of 7.8.
YN321278 Laropiprant 571170-77-9
Laropiprant is a potent, selectiveDP receptorantagonist with Ki values of 0.57nM and 2.95nM for DP receptor and TP Receptor, respectively.
YN321125 Vicriviroc maleate 599179-03-0
Vicriviroc maleate (SCH-417690 maleate; SCH-D maleate) is a potent, selective, oral bioavailable and CNS penetrated antagonist ofCCR5, with a Ki of 2.5nM, and also inhibits HIV-1 in PBMC cells, withIC90s of 3.3n...
MK-0773 is aselective and rogen receptor modulators (SARMs)that binds to AR with an IC50 of 6.6nM.
YN322021 SUN 1334H 607736-84-5
SUN 1334H is a potent, orally active, highly selectiveH1 receptorantagonist, with Kiof 9.7nM.
YN320915 Tasimelteon 609799-22-6
Tasimelteon is a melatonin MT1 and MT2 receptor agonist.
YN321086 Tradipitant 622370-35-8
Tradipitant (VLY-686) is aneurokinin-1(NK-1) antagonist.
YN480732 BMS-564929 627530-84-1
BMS-564929 is an and rogen receptor(AR) agonist, binds to and rogen receptor (AR) with a Ki of 2.11±0.16nM.
AGL-2263 is aninsulin receptor and insulin-like growth factor (IGF) receptorinhibitor.
YN371335 Homo Sildenafil 642928-07-2
Homo Sildenafil, an analog of Sildenafil, acts as aphosphodiesteraseinhibitor.
TELL : +86-020-82000279
Add:Room 519, Block F, Guangzhou International Business Incubator, No.3 Lanyue Road, Science Town, Huangpu District, Guangzhou, China.