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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
25149Safusidenib1898206-17-1≧98.0%
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl
25117Sepiapterin17094-01-898% Min.
Sepiapterin is a tetrahydrobiopterin (BH4) precursor.
25107Sovleplenib1415792-84-598% Min.
Sovleplenib is a tyrosine kinase inhibitor. It is also an antineoplastic agent.
25087SUVN-G3031 HCl1394808-20-898% Min.
SUVN-G3031 is a Histamine H3 receptor antagonist, which is potentially useful for tre
25079Sevabertinib ( BAY-2927088 )2521285-05-0 ≧98.0%
Sevabertinib ( BAY-2927088 ) is a oral, non-covalent, tyrosine kinase receptor inhibi
25066SPB linker858128-57-198% Min.
SPB is a agent-linker conjugate for ADC with potent anti-inflammatory activity by usi
25063Seladelpar sodium salt3026272-26-1≧98.0%
Seladelpar is a PPAR-delta agonist.
25059SDU-0713036109-10-898% Min.
SDU-071 is a potent and orally active inhibitor of BRD4-p53 inhibitor. SDU-071 suppre
25053SABA1690681-65-398% Min.
SABA1 is an antibacterial agent against Pseudomonas aeruginosa and Escherichia coli.
25043Survodutide2805997-46-898% Min.
24153SR-11302160162-42-598% Min.
SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor.
24142Stafib-22097938-74-298% Min.
Stafib-2 is a potent and selctive inhibitor of the transcription factor STAT5b, with
24137SR 165841150153-86-898% Min.
SR 16584 is an antagonist of the α3β4 nAChR subtype (IC50 = 10.2 μM).
24119Sepetaprost1262873-06-298% Min.
Sepetaprost is a prodrug of ONO-AG-367. It has been used in trials studying the treat
24106SB-202190152121-30-798% Min.
SB-202190 is a highly selective, potent and cell-permeable inhibitor of p38 MAP kinas
24100Saruparib2589531-76-898% Min.
Saruparib, also known as AZD5305 is a potent, selective and oral active PARP inhibito
24090SMU-L113029695-07-398% Min.
24082SX-6821648843-04-298% Min.
SX-682 is a potent and selective Cxcr1/2 inhibitor potentially useful for castration-
24065SPG-3022274723-90-798% Min.
Phenylbenzothiazole-PEG4-OH (compound 1) can treat spinal cord injury and promote spi
24049(S)-Colchicine64-86-898% Min.
(S)-Colchicine is a medication most commonly used to treat gout. Colchicine inhibits
24048Sebetralstat free base1933514-13-698% Min.
Sebetralstat (KVD-900), an oral plasma kallikrein inhibitor.
24042SPG-601 ( VSN-16R )863713-78-4≧98.0%
SPG-601 (formerly VSN-16R) is an orally available cannabinoid receptor agonist.
24016SY-008 Acetate1878218-66-6≧98.0%
SY-008 is a sodium glucose transporter 1 (SGLT1) inhibitor.
24021SY-0081480443-32-0≧98.0%
SY-008 is a sodium glucose transporter 1 (SGLT1) inhibitor.
24019(S)-3-amino-3-(4-chlorophenyl)propan-1-ol886061-26-3≧98.0%
20671Soquelitinib ( CPI-818 )2226636-04-898.0%
Soquelitinib is an oral interleukin-2-inducible T cell kinase (ITK) inhibitor‌.
20663Sotuletinib HCl2222138-31-8 (HCl)98% Min.
Sotuletinib, also known as BLZ945, is a potent and selective CSF-1R kinase inhibitor.
20662SKF-91488 HCl68941-21-998% Min.
SKF 91488 dihydrochloride is a homolog of dimaprit.
20650Sonrotoclax (BGB-11417)2383086-06-2≧98.0%
Sonrotoclax is an antineoplastic.
20639SOP1812 (QN-302)2546091-70-5≧98.0%
QN-302 is a G-quadruplex (G4)-selective transcription inhibitor.