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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
18672Takinib1111556-37-6>98%
Takinib is a selective TAK1 inhibitor that induces apoptosis following TNF-α stimula
185254TMP2691314890-29-3>98%
TMP269 is a highly potent, selective and cell-permeable class IIa HDAC inhibitor with
185235Trilaciclib (G1T28)1374743-00-6>98%
TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A
185181TAPI-1171235-71-5>98%
TAPI-1 is and inhibitor of TACE. It inhibits the cleavage of TNF-a, TNFRI (p60), and
185175TG100572 HCl867331-64-4>98%
TG-100572 is a potent and selective VEGFR2/Src kinase inhibitor.
18594TLN-232158899-10-6>98%
TLN-232, also known as CAP-232, is a synthetic cyclic heptapeptide with potential ant
18593TRC051384867164-40-7>98%
TRC051384 is a inducer of heat shock protein Hsp70.
18592Triptorelin Acetate140194-24-7>98%
Triptorelin is a gonadotropin-releasing hormone agonist (GnRH agonist) used as the ac
18591Tropifexor1383816-29-2>98%
Tropifexor, also known as LJN452, is a farnesoid X receptor agonist for the Treatment
184172THZ5311702809-17-3>98%
THZ531 is a covalent CDK12 and CDK13 covalent inhibitor. Cyclin-dependent kinases 12
184311Tofogliflozin903565-83-3>98%
Tofogliflozin, also known as CSG 452, is a potent and high selective SGLT2 inhibitor
18423TPX-0005 1802220-02-5>98%
TPX-0005 is a Src/FAK/Janus kinase 2 (JAK2) inhibitor. TPX-0005 plus EGFR TKI suppres
183214tert-butyl ((1H-benzo[d][1,2,3]triazol-1-yl)methyl)carbamate305860-41-7>96%
tert-butyl (1H-benzo[d][1,2,3]triazol-1-yl)methylcarbamate是一种药物中间体。
1712152Timapiprant851723-84-7>98%
Timapiprant,又名OC000459,是一种强效、选择性和口服的CRTH2拮抗剂。
1791519TUG-7701402601-82-498.0%
TUG-770 is a Highly Potent Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonist for Treatm
179157TH-212081686-22-898.0%
TH-2120, also known as Sodium ionophore III, is a ionophore. Ionophore is suitable fo
1791113Thiomyristoyl1429749-41-698.0%
Thiomyristoyl is a potent and specific SIRT2 inhibitor with an IC50 of 28 nM. IC50 &
179828TC-O9311444932-31-498.0%
TC-O9311 is a potent GPR139 agonist (EC50 = 39 nM in CHO-K1 cells expressing human GP
179811Trelagliptin succinate1029877-94-898.0%
Trelagliptin, also known as SYR-472, is a long acting dipeptidyl peptidase-4 (DPP-4)
1783014TUG-8911374516-07-098.0%
TUG-891 is a potent and selective agonist of the free fatty acid receptor 4 (FFA4/GPR
178303TP-36541361951-15-698.0%
TP-3654 is a Pim-1 and Pim-3 kinase inhibitor potentially for the treatment of prosta
1791412TAK1 INHIBITOR1326712-16-6>98%
TAK1 inhibitor is discontinued.
17031308TPCA-1507475-17-498% 
TPCA-1 is a potent IKK-2 inhibitor. TPCA-1 is also an effective inhibitor of STAT3 ph
17031306Trichostatin A58880-19-698% 
Trichostatin A, also known as TSA, is a HDAC inhibitor. TSA inhibits the eukaryotic c
17031304Thiotepa52-24-498% 
Thiotepa is a polyfunctional, organophosphorus alkylating agent and a stable derivati
17031303Tirabrutinib free base ( ONO-4059 )1351636-18-4≧98.0%
Tirabrutinib, also known as ONO-4059 is a potent and orally active Bruton agammaglobu
17031302TCS-OX2-29 HCl1610882-30-898% 
TCS-OX2-29 or TCS OX2 29 , also known as TCSOX229 and TCS-OX229, is a selective OX2 r
17030713TX1-85-11603845-32-498% 
TX1-85-1 is ErbB3 inhibitor. TX2-121-1 may exert Her3-dependent pharmacology through
17030710Tipiracil HCl183204-72-098% 
Tipiralacil, also known as TPI, is a thymidine phosphorylase inhibitor (TPI). Tipirac
17030707Turofexorate isopropyl629664-81-998% 
Turofexorate isopropyl, also known as WAY-362450 and XL335, is a highly potent, selec