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产品目录

编号化学名称Cas号纯度化学结构
26A018AD-80071497439-74-3≧98.0%
AD-8007是一种选择性且可穿透血脑屏障的乙酰辅酶A合成酶2(ACSS2)
26A019AD-55842306525-79-9≧98.0%
AD-5584是一种新型脑渗透性ACSS2抑制剂。
26A004Atumelnant ( CRN-04894 )2392970-97-5≧98.0%
Atumelnant是第一种每日一次的口服黑皮质素2型受体(MC2R)拮抗剂,
26B0015-氮杂螺[4.5]癸-5-溴化鎓16431-36-0≧98.0%
25211AXKO-00463103525-82-9≧98.0%
AXKO-0046是一种小分子LDHB选择性抑制剂。
25205AF710BN/A≧98.0% ; EE≧98.0%
AF710B 是一种高效、选择性变构 M1 毒蕈碱和 σ1 受体激动剂。 AF710
25176AG-2702201056-66-6≧98.0%
MAT2A 抑制剂 AG-270 是一种口服的蛋氨酸腺苷转移酶 II α (MAT2A) 小分
25173Anatibant (同义词: LF 16-0687; XY-2405)209733-45-9≧98.0%
25172Amcasertib (同义词: BBI503)1129403-56-0≧98.0%
25171Alnodesertib ( 同义词: ART0380 )2267316-76-5≧98.0%
25159APS6-452188236-41-998% Min.
APS6-45 is a tumor calibrated inhibitor, showing unique polypharmacology. APS6-45 sho
25156ARN144941037837-27-6≧98.0%
ARN14494 是一种选择性丝氨酸棕榈酰转移酶 (SPT) 抑制剂,它是鞘脂
25157ALT-0072035010-37-6≧98.0%
ALT-007 是一种口服生物可利用的 SPT 抑制剂,比多球菌素更有效,
25148Atebimetinib2669009-92-9≧98.0%
Atebimetinib(IMM-1-104)是一种口服的小分子MEK1和MEK2激酶变构抑制剂
25145Atuzabrutinib1581714-49-998% Min.
Atuzabrutinib, also known as PRN 473, is a Bruton's tyrosine kinase inhibitor.
25144Andamertinib2254145-43-098% Min.
Andamertinib is an epidermal growth factor receptor tyrosine kinase inhibitor. It is
25136AC-0032258671-03-198% Min.
25134AZD-97503056515-10-498% Min.
25133ARV-3932851885-95-398% Min.
ARV-393 is an orally active PROTAC that utilizes the ubiquitin-proteasome system to t
25120Alixorexton2648347-56-098% Min.
Alixorexton, also known as TAK-994 or firazorexton, is a potent, orally bioavailable,
25112Ajulemic acid137945-48-398% Min.
25111Afuresertib1047644-62-198% Min.
Afuresertib, also known as GSK-2110183 or GSK-2110183C, is an orally bioavailable inh
25110Aficamten2364554-48-198% Min.
Aficamten, also known as CK-3773274 and CK-274, is a Next-Generation Cardiac Myosin I
25109Admilparant2170126-74-498% Min.
Admilparant, also known as BMS-986278, is a potent lysophosphatidic acid receptor 1 (
25108Avasopasem manganese435327-40-598% Min.
Avasopasem manganese, also known as GC-4419; M 40419 and SC-72325A, is a superoxide d
25071AT-0072170729-29-898% Min.
AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
25033Azeliragon603148-36-3≧98.0%
Azeliragon (TTP488) 是一种口服生物可利用的 AGE (RAGE) 受体小分子抑制
24152AKOS0376522562171065-77-198% Min.
AKOS037652256 can be used as a TRPML modulator for the treatment of diseases associat
24135AF-615122510-61-698% Min.
AF-615 is a novel Inhibitor of CDT1/Geminin Protein Complex, promoting DNA Damage and
24134AkaLumine HCl2558205-28-898% Min.
AkaLumine is a luciferin analogue. The bioluminescence produced by AkaLumine in react