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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
60634Ulodesine548486- 59-598% Min.
20629Usnoflast2455519-86-398% Min.
Usnoflast is a non-steroidal anti-inflammatory (NSAID).
20573URAT1 inhibitor 71632002-28-898% Min.
URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor.
171456Urea, N-[5-chloro-6-(2H-1,2,3-triazol-2-yl)-3-pyridinyl]-N'-[8-[(1S)-1-methoxyethyl]imidazo[1,2-b]pyridazin-7-yl]-2577171-33-498% Min.
21249UAMC-11101448440-52-598% Min.
UAMC-1110, also known as SP-13786, is a novel potent and selective inhibitor of fibro
20110401U-18666A3039-71-298% Min.
U-18666A is an inhibitor of cholesterol synthesis. It acts by inhibiting desmosterol
2071516UCB96082244989-34-098% Min.
UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
2071515UCB96081616413-96-798% Min.
UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
112591U-73343142878-12-498% Min.
U-73343 is a negative control (or inactive analogue) of U73122, which is a putative p
6111901UNC25411612782-86-198% Min.
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
193251UPGL000041890169-95-5>98%
UPGL00004 is a potent inhibitor of glutaminase C (GAC).
193223Umibecestat free base1387560-01-1>98%
Umibecestat, also known as CNP-520, is a beta-secretase inhibitor and is a drug candi
19343UVI3003847239-17-2>98%
UVI3003 is a RXR antagonist. It displays high RXR binding affinity. UVI3003 does not
192142Upacicalcet1333218-50-0≧98.0%
Upacicalcet (formerly SK-1403/AJT240) is a novel non-peptide calcimimetic agent that
1812292UC-1728948304-40-3≧98.0%
UC-1728, also known as t-TUCB, is a Soluble epoxide hydrolase inhibitor.
1810252URMC-0991229582-33-5>98%
URMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibi
186282UM-164903564-48-7>98%
UM-164 is a anticancer inhibitor.CAS 903564-48-7.
18584UNC-926 free base1184136-10-4>98%
UNC-926 is a L3MBTL1 domain inhibitor. UNC-926 binds to the MBT domain of the L3MBTL1
184105Upadacitinib1310726-60-3>98%
Upadacitinib, also known as ABT-494, is a potent and selective JAK inhibitors in deve
1791520UPF-10691048371-03-498.0%
UPF-1069 is a selective and potent PARP2 inhibitor. UPF-1069 induces apoptosis. UPF-1
179153Ulixertinib HCl1956366-10-198.0%
Ulixertinib, also known as BVD-523 and VRT752271, is an inhibitors of ERK protein kin
1791114UK-371804256477-09-598.0%
UK-371804 is a potent and selective uPA inhibitor with excellent enzyme potency (Ki 1
178312UNC-669314241-44-598.0%
UNC-669 is a L3MBTL domain inhibitor. UNC669 specifically targets lethal 3 malignant
17031008UK-371804 HCl256476-36-598% 
UK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibi
17030711URB602565460-15-398% 
URB602 is a selective inhibitor of monoglycerol lipase (MGL), exhibiting an IC50 of 2
17030602Ubenimex58970-76-698% 
Ubenimex, also known as NK 421 and Bestatin, is a CD13 inhibitor. Ubenimex attenuates
17011102UNC38661872382-47-298% 
UNC3866 is a potent antagonist of the methyllysine (Kme) reading function of the Poly
16122843Ulipristal acetate126784-99-498% 
Ulipristal acetate, also known as CDB-2914, is a selective progesterone receptor modu
16122842UF-010537672-41-698% 
UF-010 is a Class I HDAC inhibitor (IC50 values are 0.06, 0.1, 0.5 and 1.5 M for HDAC
16122841U-93631152273-12-698% 
U-93631 is a GABAA receptor antagonist. U-93631 causes rapid decay of gamma-aminobuty