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产品目录

编号化学名称Cas号纯度化学结构
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.
20650 Sonrotoclax2383086-06-298% Min.
Sonrotoclax is an antineoplastic.
20639SOP1812 (QN-302)2546091-70-5≧98.0%
QN-302 是一种 G4选择性转录抑制剂。
20633STX-4782883540-92-7≧98.0%
STX-478 is an allosteric PI3Kα inhibitor that selectively targets prevalent PI3Kα h
20604SEW2871256414-75-298% Min.
SEW2871 is a S1P1 agonist (sphingosine-1-phosphate type 1 receptor agonist). SEW2871
20576STX-7212765525-82-2≧98.0%
STX-721 is a next-generation, orally delivered therapy, designed with potential best-
20549STC-152648257-56-9≧98.0%
STC-15 is a first-in-class inhibitor of RNA modification and is the first ever RNA me
20541(S)-1-BOC-2-甲基-[1,4]二氮杂环庚烷194032-32-198% Min.
20522(S)-5-fluoro-3-methylbenzo[c][1,2]oxaborol-1(3H)-ol2921961-53-598% Min.
20516(S)-3-氨基-3-(4-氯苯基)-丙酸131690-60-398% Min.
20454Samidorphan852626-89-298% Min.
Samidorphan, also known as ALKS-33 and RDC-0313, is an opioid modulator with μ-antag
20412Spiro[cyclohexane-1,9'(6'H)-pyrazino[1',2':1,5]pyrrolo[2,3-d]pyrimidine]-7'(8'H)-carboxylic acid, 2'-(methylthio)-6'-oxo-5'-[[(trifluoromethyl)sulfonyl]oxy]-, 1,1-dimethylethyl ester2170746-98-098% Min.
20396(S)-1-(6-(4-氟-1H-吡唑-1-甲基)吡啶-3-甲基)乙胺1980023-96-898% Min.
G20378SB-4 agonist100874-08-698% Min.
SB 4 is a potent BMP4 agonist.
822222SEP-363856 盐酸盐 1310422-41-3 (HCl)≧98.0%
SEP-363856 是一种新型微量胺受体 1 (TAAR1) 激动剂,具有血清素 5-HT1
1711224SRI-37330 free base2322245-42-9 (free base)98% Min.
SRI-37330 is a novel inhibitor of TXNIP expression, decreasing glucagon secretion and
20369Sunvozertinib ( DZD 9008 )2370013-12-8≧98.0%
Sunvozertinib,也称为 DZD9008,是一种口服、强效、不可逆和选择性
20368SHMT-IN-2 抑制剂2102681-49-0≧98.0%
SHMT-IN-2 是一种丝氨酸羟甲基转移酶 (SHMT) 抑制剂,可有效抑制人
L20355SRI-0113811629138-41-598% Min.
SRI-011381 is an agonist of the TGF-beta signaling pathway for treatment of Alzheimer
L20353 SJ-172550431979-47-498% Min.
SJ-172550, also known as MDMX Inhibitor II, is an inhibitor of MDMX that disrupts MDM
20344SMN-C3 抑制剂1449597-34-5≧98.0%
SMN-C3 是一种口服活性 SMN2 剪接调节剂。可用于脊椎肌肉萎缩 (SMA)
L20338Stafia-1 2582757-90-098% Min.
20321STM24572499663-01-198% Min.
STM2457 is a highly potent and selective first-in-class catalytic inhibitor of METTL3
20306SRI-37330 HCl2322245-49-6≧98.0%
SRI-37330 hydrochloride 是一种新型 TXNIP 表达抑制剂,呈剂量依赖性抑
21252 SM-1022089251-47-6≧98.0%
SM-102 is an ionizable amino lipid that has been used in combination with other lipid
21238Seralutinib1619931-27-998% Min.
Seralutinib,也称为 PK-10571 和 GB002,是一种新型吸入性 Pdgfr 激酶抑
21232Sonidegib (LDE-225)956697-53-398% Min.
Sonidegib, also known as, erismodegib, LDE225, NVP-LDE225, is an orally bioavailable
21230SB-366791472981-92-398% Min.
SB-366791 is a potent and selective TRPV1 antagonist. SB-366791 inhibits glutamatergi
21229Scriptaid287383-59-998% Min.
Scriptaid, also known as GCK 1026, is a HDAC inhibitor. Scriptaid protects against tr