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51

抑制剂 & 化合物

6

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T38218	1-Stearoyl-2-docosahexaenoyl-sn-glycero-3-PC
	1-Stearoyl-2-docosahexaenoyl-sn-glycero-3-PC 是一种在生物膜中的磷脂，在 sn-1 和 sn-2 位置分别含有硬脂酸和二十二碳六烯酸。它已被用于研究脂膜的组织和动力学。在超氧化物歧化酶 1 突变体转基因小鼠肌萎缩性脊髓侧索硬化症（ALS）模型中1-Stearoyl-2-docosahexaenoyl-sn-glycero-3-PC 的水平在疾病晚期会在 L5 前角下降。1-Stearoyl-2-docosahexaenoyl-sn-glycero-3-PC 可用于研究生物膜。
T37486	1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PC
	1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PC is a phospholipid that contains stearic acid at the sn-1 position and 15(S)-HpETE at the sn-2 position. It is produced via oxidation of 1-stearoyl-2-arachidonoyl-sn-glycero-3-PC by 15-lipoxygenase (15-LO). 1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PC is toxic to human umbilical vein endothelial cells (HUVECs) when used at a concentration of 100 μM.
T37485	1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PC
	1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PC is a phospholipid that contains stearic acid at the sn-1 position and 15(S)-HETE at the sn-2 position. It is produced via oxidation of 1-stearoyl-2-arachidonoyl-sn-glycero-3-PC by 15-lipoxygenase (15-LO).
T16961	Supinoxin RX-5902	Apoptosis; DNA/RNA Synthesis	Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Supinoxin (RX-5902) 是磷酸化 p68 RNA 解旋酶的强效口服活性抑制剂，是一种抗肿瘤试剂。它与 Y593 磷酸化的 p68 相互作用并减弱 β-catenin 的核穿梭性。它诱导细胞凋亡并抑制 TNBC 癌细胞系的生长，IC50的范围为 10 nM 至 20 nM。
T16996	TAS6417	Apoptosis; EGFR	Angiogenesis; Apoptosis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	TAS6417 是一种高效的、具有口服活性的 EGFR 突变型抑制剂，可独特的结合到 EGFR 铰链区的 ATP 结合位点，其 IC50值为 1.1-8.0 nM。
T2490	Osimertinib AZD-9291,Mereletinib,奥希替尼	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Osimertinib (AZD-9291) 是一种 EGFR 三代抑制剂，抑制二代 EGFR 抑制剂产生的 T790M 耐药突变，具有不可逆性和口服活性。Osimertinib 具有抗肿瘤活性，用于治疗 EGFR 突变的非小细胞肺癌。
T3634	Osimertinib mesylate 甲磺酸奥希替尼,Mereletinib mesylate,奥希替尼甲磺酸盐,AZD-9291 mesylate	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Osimertinib mesylate (Mereletinib mesylate) 是一种不可逆的突变选择性 EGFR 抑制剂，对EGFRL858R 和EGFRL858R/T790M 的IC50值分别为 12 和 1 nM。
T64546	1-Stearoyl-2-myristoyl-sn-glycero-3-PC
	1-Stearoyl-2-myristoyl-sn-glycero-3-PC 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T64546，CAS号为 20664-02-2。
T130784	6-(1-Hydroxypentyl)-4-methoxy-2H-pyran-2-one. PC
	6-(1-Hydroxypentyl)-4-methoxy-2H-pyran-2-one. PC 是一种有用的有机化合物，可用于生命科学领域的相关研究，其产品编号为 T130784。
T60812	Cathepsin X-IN-1	Cysteine Protease	Proteases/Proteasome
	Cathepsin X-IN-1 (compound 25) 降低人前列腺癌细胞 PC-3 的迁移且具有较低的细胞毒性，它是组织蛋白酶 X 的有效抑制剂 (IC50 = 7.13 μM)。
T77526	Pim-1 kinase inhibitor 4	Apoptosis; Pim	Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling
	Pim-1 kinase inhibitor 4 是一种高效的 Pim-1 激酶抑制剂，IC50 值为 17.01 nM。Pim-1 kinase inhibitor 4 还具有抗氧化活性和潜在的抗癌活性，对 DPPH 有抑制作用。Pim-1 kinase inhibitor 4 促进 PC-3 细胞凋亡 (apoptosis)，对 PC-3 细胞生长有抑制作用，IC50 为 16 nM。Pim-1 kinase inhibitor 4 可用于研究前列腺癌。
T4306	CCG-203971 CCG203971	Rho; Ras	Cell Cycle/Checkpoint; GPCR/G Protein; MAPK
	CCG-203971 是一种Rho/MRTF/SRF 通路抑制剂，具有潜在的抗转移作用。它有效靶向 RhoA/C 激活的 SRE 荧光素酶，IC50为 6.4 μM。它抑制 PC-3 细胞迁移，IC50为 4.2 μM。
T60341	Pyruvate Carboxylase-IN-1
	Pyruvate Carboxylase-IN-1 (compound 37) 是一种有效的丙酮酸羧化酶(PC) 抑制剂，对于基于细胞裂解物和基于细胞的 PC 活性，IC50s 分别为 0.204 和 0.104 μM。Pyruvate Carboxylase-IN-1 是毛兰素的天然类似物。Pyruvate Carboxylase-IN-1 抑制 PC 的酶活性，介导人肝细胞癌 (HCC) 的抗癌作用。
T18517	PC Azido-PEG11-NHS carbonate ester	Others	Others
	PC Azido-PEG11-NHS carbonate ester is a PEG-based PROTAC linker utilized in PROTAC synthesis[1].
T18525	PC SPDP-NHS carbonate ester	Others	Others
	PC SPDP-NHS carbonate ester is a cleavable linker compound utilized in the synthesis of antibody-drug conjugates (ADCs)[1].
T18520	PC-Biotin-PEG4-PEG3-azide	Others	Others
	PC-Biotin-PEG4-PEG3-azide is a cleavable 7-unit polyethylene glycol (PEG) antibody-drug conjugate (ADC) linker employed for the synthesis of ADCs [1].
T18519	PC-Biotin-PEG4-NHS carbonate	Others	Others
	PC-Biotin-PEG4-NHS carbonate is a polyethylene glycol (PEG) derived linker employed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
T81477	Phytochelatin 4 PC 4
	Phytochelatin 4 (PC 4)为植物体内富含Cys的小分子短肽，其结构特征为含有γ-Glu-Cys基序。
T81479	Phytochelatin 3 PC 3
	Phytochelatin 3 (PC 3)是一种具有金属螯合能力的小型肽，主要用途为螯合重金属离子。
T81476	Phytochelatin 4 TFA PC 4 TFA
	Phytochelatin 4 (PC 4) TFA，一种在植物中发现的短肽，富含 Cys，且具有 γ-Glu-Cys 基序。
T18523	PC Methyltetrazine-PEG4-NHS carbonate ester	Others	Others
	PC Methyltetrazine-PEG4-NHS carbonate ester is a polyethylene glycol (PEG) derived linker specifically designed for the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].
T16438	PC Biotin-PEG3-azide	Others	Others
	PC Biotin-PEG3-azide is a cleavable three-unit polyethylene glycol (PEG) antibody-drug conjugate (ADC) linker, employed in the synthesis of ADCs[1].
T37123	1,2-Dioctanoyl PC
	Phosphatidylcholine (PC) species are a common class of phospholipids that comprise the mammalian cell membrane. 1,2-Dioctanoyl PC is a synthetic analog of natural phosphatidylcholine species containing saturated C8:O fatty acids in the sn-1 and sn-2 positions of the glycerol backbone. It exhibits a critical micelle concentration (CMC) value of 0.25 mM at 27°C. 1,2-Dioctanoyl PC serves as an efficient substrate for phospholipase D (PLD) as well as sPLA2 isozymes from bovine pancreas and bee venom...
T83476	1,2-Diheptadecanoyl-sn-glycero-3-phosphorylcholine DHPC
	1,2-Diheptadecanoyl-sn-glycero-3-phosphorylcholine (DHPC) 是生物活性磷脂化合物，属于磷脂酰胆碱 (PC) 的衍生物。
T18518	PC Biotin-PEG3-NHS ester	Others	Others
	PC Biotin-PEG3-NHS ester is a cleavable ADC linker comprising three PEG units. This linker is specifically designed for use in the synthesis of antibody-drug conjugates (ADCs)[1].
T18516	PC Alkyne-PEG4-NHS ester	Others	Others
	PC Alkyne-PEG4-NHS ester is a cleavable 4-unit PEG linker employed for the synthesis of antibody-drug conjugates (ADCs)[1].
T17586	Biotin-PEG4-PC-PEG4-alkyne	Others	Others
	Biotin-PEG4-PC-PEG4-alkyne is a polyethylene glycol (PEG)-based proteolysis targeting chimera (PROTAC) linker utilized in the synthesis of PROTACs[1].
T81478	Phytochelatin 3 TFA PC 3 TFA
	Phytochelatin 3 (PC 3) TFA，一小分子螯合肽，专用于重金属离子螯合。
T35580	POV-PC
	Oxidized low-density lipoprotien (oxLDL) particles contain low molecular weight species which are cytotoxic and pro-atherogenic. Many of these substances were recently isolated and purified from oxLDL, and identified as phosphatidylcholine species containing a fragmented, oxidized short-chain fatty acid remnant at the sn-2 position. 1-(Palmitoyl)-2-(5-oxovaleroyl)-phosphatidylcholine, or POV-PC, is one of the oxLDL species derived from 2-arachidonoyl or eicosapentanoyl phospholipids. POV-PC conf...
T78306	Ulenistamab PBP1510
	Ulenistamab (PBP1510)为首创人源化IgG1单克隆抗体，专一靶向胰腺癌上调因子(PAUF)，适用于胰腺癌(PC)的研究。
T75000	Mal-Pc	Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB
	Mal-Pc为基于酞菁和马来酰亚胺设计的多功能分子光敏剂。它能在癌细胞内与GSH反应，耗减GSH并抑制其聚集，进而增强ROS介导的PDT效果。
T37623	1,2-Dierucoyl-sn-glycero-3-PC
	1,2-Dierucoyl-sn-glycero-3-PC is a phospholipid containing erucic acid at the sn-1 and sn-2 positions. It has been used in the study of lipid membranes and to determine the effect of long-chain phospholipids on the secondary structure of human islet amyloid polypeptide (hIAPP).
T36172	KOdiA-PC
	Oxidized low-density lipoprotien (oxLDL) particles contain low molecular weight species which are cytotoxic and pro-atherogenic. Many of these substances were recently isolated and purified from oxLDL, and identified as phosphatidylcholine species containing a fragmented, oxidized short-chain fatty acid remnant at the sn-2 position. 1-(Palmitoyl)-2-(5-keto-6-octene-dioyl) phosphatidylcholine, or KOdiA-PC, is one of the most potent CD36 ligands among the oxLDL species. KOdiA-PC confers CD36 scave...
T79495	VEGFR-2-IN-32	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	VEGFR-2-IN-32（Comp 3a）作为一种VEGFR-2的抑制剂，其IC50值为8.93 nM。该化合物对PC-3细胞表现出细胞毒性，IC50为1.22 μM，适用于前列腺癌研究。
T18521	PC DBCO-PEG3-biotin	Others	Others
	PC DBCO-PEG3-biotin is a trimeric polyethylene glycol (PEG) linker, specifically designed for antibody-drug conjugate (ADC) synthesis, with a cleavable moiety consisting of a dibenzocyclooctyne (DBCO) group and a biotin molecule. This linker provides a platform for the efficient attachment of drugs to antibodies, facilitating the targeted delivery and controlled release of therapeutic agents in ADCs[1].
T60727	B-Raf IN 8
	B-Raf IN 8 (compound 7g) 是 B-Raf 的有效抑制剂 (IC50 = 70.65 nM)。B-Raf IN 8 显示出抗肿瘤活性，其对肝细胞癌 (HEPG-2)、结肠癌 (HCT-116)，乳腺癌 (MCF-7) 和人前列腺癌 (PC-3) 细胞的 IC50值分别为9.78、13.78、18.52 和 29.85 μM。
T38356	1,2-Dipalmitoyl-13C-sn-glycero-3-PC
	1,2-Dipalmitoyl-13C-sn-glycero-3-PC is intended for use as an internal standard for the quantification of 1,2-dipalmitoyl-sn-glycero-3-PC by GC- or LC-MS. 1,2-Dipalmitoyl-sn-glycero-3-PC (DPPC) is a zwitterionic glycerophospholipid commonly used in the formation of lipid monolayers, bilayers, and liposomes for use in a variety of applications.1,2,3,4 It has been used in the formation of proteoliposomes for implantation of γ-glutamyl transpeptidase into human erythrocyte membranes.3 Incorporation...
T74557	α1A-AR Degrader 9c	PROTACs	PROTAC
	α1A-AR Degrader 9c（化合物 9c）是一种高效、选择性且可逆的α1A-AR PROTAC降解剂，DC50值为2.86 μM。它通过蛋白酶体途径诱导α1A-AR的降解，并且在抑制PC-3细胞增殖方面表现出活性，IC50为6.12 μM。此外，α1A-AR Degrader 9c展现出在前列腺癌研究中的抗肿瘤潜力。
T79558	fac-[Re(CO)3(L3)(H2O)][NO3]
	fac-[Re(CO)3(L3)(H2O)][NO3]（简称compound 3），是一种与线粒体功能障碍相关的抗前列腺癌剂。这种铼(I)三羰基水配合物对前列腺癌细胞系(PC-3)表现出显著的细胞毒性，其IC50值为0.32 μM。研究表明，fac-[Re(CO)3(L3)(H2O)][NO3]主要在线粒体中积聚，能够降低PC-3细胞的ATP生成，进而触发细胞副凋亡(paraptosis)机制，而不通过引发坏死、凋亡或自噬途径作用。
T80173	BDS-I	Potassium Channel	Membrane transporter/Ion channel
	BDS-I，又名降血物质，源自苏卡达银莲花的海洋毒素。它作为钾通道特异性抑制剂，针对Kv3.4。BDS-I能够抑制由Aβ1-42诱导的Kv3.4活性增强，减少caspase-3的激活，阻止NGF诱导的PC-12细胞分化以及异常核形态的出现，并可逆转Aβ肽引发的细胞死亡。
T79152	PROTAC EGFR degrader 8	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	PROTACEGFRdegrader 8 (T-184) 是一种能够定向降解EGFR的PROTACEGFR降解剂，其在HCC827细胞中的DC50为15.56 nM。该化合物有效抑制多种肺癌细胞系，包括H1975、PC-9和HCC827，其IC50分别为7.72 nM、121.9 nM和14.21 nM。PROTACEGFRdegrader 8 主要用于研究非小细胞肺癌（NSCLC）。
T18522	PC Mal-NHS carbonate ester	Others	Others
	PC Mal-NHS carbonate ester is a cleavable linker specifically designed for the synthesis of antibody-drug conjugates (ADCs)[1]. This chemical compound plays a crucial role in facilitating the conjugation of drugs to antibodies, enabling targeted delivery and enhanced efficacy of therapeutic agents. Its unique carbonate ester structure allows for efficient cleavage in the targeted environment, ensuring the controlled release of the drug payload. Its application in ADC synthesis highlights its imp...
T82493	EGFR/HER2/DHFR-IN-2	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	EGFR/HER2/DHFR-IN-2 (Compound 4b) 是针对EGFR、HER2和DHFR的三重抑制剂，IC50分别为0.248、0.156、0.138 μM。该化合物对包括Hep G2, HeLa, HEp-2, HCT 116, PC-3, MCF7在内的多种癌细胞系展现出显著的抗癌活性(IC50分别为9.14、7.33、14.18、24.87、20.07、6.16 μM)，并能有效减缓乳腺癌肿瘤的生长。
T60933	B-Raf IN 7
	B-Raf IN 7 (compound 6a) 是 B-Raf 的有效抑制剂，IC50值为 110.23 nM。B-Raf IN 7 对结肠癌细胞(HCT-116)、乳腺癌细胞 (MCF-7)、肝癌细胞 (HEPG-2)、人宫颈癌细胞 (Hela) 和人前列腺癌细胞 (PC-3) 具有抗肿瘤活性。其 IC50值分别为 7.50、9.87、10.57、11.63 和 12.83 μM。
T68861	MS-0022
	MS-0022 is a SMO antagonist. MS-0022 showed effective Hh signaling pathway inhibition at the level of SMO in the low nM range, and Hh pathway inhibition downstream of Suppressor of fused (SUFU) in the low µM range. MS-0022 reduced growth in the tumor cell lines PANC-1, SUIT-2, PC-3 and FEMX in vitro. MS-0022 is a treatment led to a transient delay of tumor growth that correlated with a reduction of stromal Gli1 levels in SUIT-2 xenografts in vivo.
T79557	fac-[Re(CO)3(L6)(H2O)][NO3]	Apoptosis	Apoptosis
	fac-[Re(CO)3(L6)(H2O)][NO3]（compound 6）是一种具有针对线粒体功能失调的抗癌活性的铼(I)三羰基水配合物。该化合物对前列腺癌细胞展现出显著的细胞毒性，具有50 nM的IC50值（PC-3细胞）。fac-[Re(CO)3(L6)(H2O)][NO3]能够主要集中在细胞核，抑制PC3细胞的ATP生成并诱导细胞凋亡，而不触发坏死、焦亡或自噬过程。
T78810	BWA-522	Androgen Receptor	Endocrinology/Hormones
	BWA-522是一种口服有效的小分子PROTACs，针对AR-FL和AR-V7显示出显著的降解活性。该化合物通过对Androgen Receptor的AR-NTD进行拮抗，诱发PC细胞的apoptosis。在LNCaP异种移植模型中，BWA-522以每日60 mg/kg的剂量口服给药，实现了76%的肿瘤生长抑制(TGI=76%)。在VCaP和LNCaP细胞系中对AR-V7和AR-FL的降解效率分别达到77.3%(1 μM)和72.0%(5 μM)。
T81469	PI3Kα-IN-14	PI3K	PI3K/Akt/mTOR signaling
	PI3Kα-IN-14（复合物F8）是一款高度选择性的PI3Kα抑制剂，其IC50值为0.14 nM 。此化合物能显著降低线粒体膜的完整性，并在U87-MG细胞中引起G1期细胞周期的停滞以及凋亡现象。此外，PI3Kα-IN-14在不同来源的肿瘤细胞系中均展现出明显的抗增殖能力，其中PC-3的IC50为0.28 μM，HCT-116的IC50为0.57 μM，以及U87-MG的IC50为1.37 μM。
T78811	PROTAC AR-NTD degrader 1	Androgen Receptor	Endocrinology/Hormones
	PROTACAR-NTD antagonist 1 (compound 18) 是一款针对雄激素受体AR-V7变体的PROTACs，它特异性地拮抗AR的N末端结构域 (AR-NTD)，能有效诱导前列腺癌细胞凋亡，并在VCaP细胞中以1 μM 和 5 μM的浓度分别实现了62.2%和71.1%的AR-V7蛋白降解率。
T35897	ASK120067
	ASK120067 is a potent and orally active inhibitor of EGFRT790M (IC50:0.3 nM) with selectivity over EGFRWT (IC50:6.0 nM). ASK120067 is a third-generation EGFR-TKI for the research of non-small cell lung cancer (NSCLC)[1]. In the in vitro kinase assay ASK120067 potently inhibits the EGFR L858R/T790M and EGFR T790M resistant mutants with IC50 values of 0.3 nM and 0.5 nM, respectively, as well as the EGFRexon19del sensitizing mutant (IC50= 0.5 nM). The 50 of ASK120067 against wild-type EGFR (EGFRWT...

化合物

1-Stearoyl-2-docosahexaenoyl-sn-glycero-3-PC

Cat.No: T38218

1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PC

Cat.No: T37486

1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PC

Cat.No: T37485

Cat.No: T16961

Synonym: RX-5902

Target: Apoptosis, DNA/RNA Synthesis

Cat.No: T16996

Target: Apoptosis, EGFR

Cat.No: T2490

Synonym: AZD-9291,Mereletinib,奥希替尼

Target: EGFR

Osimertinib mesylate

Cat.No: T3634

Synonym: 甲磺酸奥希替尼,Mereletinib mesylate,奥希替尼甲磺酸盐,AZD-9291 mesylate

Target: EGFR

1-Stearoyl-2-myristoyl-sn-glycero-3-PC

Cat.No: T64546

6-(1-Hydroxypentyl)-4-methoxy-2H-pyran-2-one. PC

Cat.No: T130784

Cathepsin X-IN-1

Cat.No: T60812

Target: Cysteine Protease

Pim-1 kinase inhibitor 4

Cat.No: T77526

Target: Apoptosis, Pim

Cat.No: T4306

Synonym: CCG203971

Target: Rho, Ras

Pyruvate Carboxylase-IN-1

Cat.No: T60341

PC Azido-PEG11-NHS carbonate ester

Cat.No: T18517

Target: Others

PC SPDP-NHS carbonate ester

Cat.No: T18525

Target: Others

PC-Biotin-PEG4-PEG3-azide

Cat.No: T18520

Target: Others

PC-Biotin-PEG4-NHS carbonate

Cat.No: T18519

Target: Others

Phytochelatin 4

Cat.No: T81477

Synonym: PC 4

Phytochelatin 3

Cat.No: T81479

Synonym: PC 3

Phytochelatin 4 TFA

Cat.No: T81476

Synonym: PC 4 TFA

PC Methyltetrazine-PEG4-NHS carbonate ester

Cat.No: T18523

Target: Others

PC Biotin-PEG3-azide

Cat.No: T16438

Target: Others

1,2-Dioctanoyl PC

Cat.No: T37123

1,2-Diheptadecanoyl-sn-glycero-3-phosphorylcholine

Cat.No: T83476

Synonym: DHPC

PC Biotin-PEG3-NHS ester

Cat.No: T18518

Target: Others

PC Alkyne-PEG4-NHS ester

Cat.No: T18516

Target: Others

Biotin-PEG4-PC-PEG4-alkyne

Cat.No: T17586

Target: Others

Phytochelatin 3 TFA

Cat.No: T81478

Synonym: PC 3 TFA

Cat.No: T35580

Cat.No: T78306

Synonym: PBP1510

Cat.No: T75000

Target: Reactive Oxygen Species

1,2-Dierucoyl-sn-glycero-3-PC

Cat.No: T37623

Cat.No: T36172

Cat.No: T79495

Target: VEGFR

PC DBCO-PEG3-biotin

Cat.No: T18521

Target: Others

Cat.No: T60727

1,2-Dipalmitoyl-13C-sn-glycero-3-PC

Cat.No: T38356

α1A-AR Degrader 9c

Cat.No: T74557

Target: PROTACs

fac-[Re(CO)3(L3)(H2O)][NO3]

Cat.No: T79558

Cat.No: T80173

Target: Potassium Channel

PROTAC EGFR degrader 8

Cat.No: T79152

Target: EGFR

PC Mal-NHS carbonate ester

Cat.No: T18522

Target: Others

EGFR/HER2/DHFR-IN-2

Cat.No: T82493

Target: EGFR

Cat.No: T60933

Cat.No: T68861

fac-[Re(CO)3(L6)(H2O)][NO3]

Cat.No: T79557

Target: Apoptosis

Cat.No: T78810

Target: Androgen Receptor

Cat.No: T81469

Target: PI3K

PROTAC AR-NTD degrader 1

Cat.No: T78811

Target: Androgen Receptor

Cat.No: T35897

Cat. No.	Product Name	Target	Signaling Pathways
T19085	1-Palmitoyl-2-oleoyl-sn-glycero-3-PC POPC,2-油酰-1-棕榈锡甘油-3-磷酸胆碱,1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine,Palmitoyloleoylphosphatidylcholine	Others	Others
	1-Palmitoyl-2-oleoyl-sn-glycero-3-PC (Palmitoyloleoylphosphatidylcholine) 是生物膜的主要成分，是一种磷脂。它用于脂质体的制备以及脂质双层的特性的研究。
T74236	1-Oleoyl-2-palmitoyl-sn-glycero-3-PC
	1-Oleoyl-2-palmitoyl-sn-glycero-3-PC，由油酸衍生，用于脂质体合成。
T4S2126	Ginkgetin 银杏双黄酮,银杏素	Apoptosis; Wnt/beta-catenin; COX; STAT; Autophagy	Apoptosis; Autophagy; Cytoskeletal Signaling; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Stem Cells
	Ginkgetin 是从银杏叶中分离得到的一种双黄酮，具有抗肿瘤、抗炎、神经保护、抗真菌的作用。它也是 Wnt 信号抑制剂，IC50值为 5.92 μM。
T81529	Peganumine A
	Peganumine A，一种天然产物，源自Peganum harmala，具备对HL-60、MCF-7、PC-3、HepG2细胞线显示出细胞毒性作用，其IC50值依次为5.8、38.5、40.2、55.4 µM[1]< /sup>。
T83471	10-Deacetyl-13-oxobaccatin III
	10-Deacetyl-13-oxobaccatin III是一款从Taxus sumatrana分离的紫杉烷。在30 μg/mL的浓度下，对A498、NCI-H226、A549、PC-3细胞系展现细胞毒性作用，其抑制率分别达到29.7%、49.2%、43.9%、65.3%。
T36791	Lysophosphatidylcholine 18:2
	1-Linoleoyl-2-hydroxy-sn-glycero-3-PC (LGPC) is a lysophospholipid containing linoleic acid at thesn-1 position that has been found in mouse heart, lung, liver, spleen, kidney, plasma, and serum.1Serum levels of LGPC decrease with increasing insulin resistance and dysglycemia in humans.2 1.Okudaira, M., Inoue, A., Shuto, A., et al.Separation and quantification of 2-acyl-1-lysophospholipids and 1-acyl-2-lysophospholipids in biological samples by LC-MS/MSJ. Lipid Res.55(10)2178-2192(2014) 2.Gall, ...

天然产物

1-Palmitoyl-2-oleoyl-sn-glycero-3-PC

Cat.No: T19085

Synonym: POPC,2-油酰-1-棕榈锡甘油-3-磷酸胆碱,1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine,Palmitoyloleoylphosphatidylcholine

Target: Others

1-Oleoyl-2-palmitoyl-sn-glycero-3-PC

Cat.No: T74236

Cat.No: T4S2126

Synonym: 银杏双黄酮,银杏素

Target: Apoptosis, Wnt/beta-catenin, COX, STAT, Autophagy

Cat.No: T81529

10-Deacetyl-13-oxobaccatin III

Cat.No: T83471

Lysophosphatidylcholine 18:2

Cat.No: T36791

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