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297

抑制剂 & 化合物

8

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T19609	HP-β-CD 羟丙基-β-环糊精,羟丙基-BETA-环糊精,Hydroxypropyl-β-cyclodextrin,Hydroxypropyl betadex	Others	Others
	HP-β-CD (HP-β-CD) 是一种药物递送载体，可提高稳定性和利用度。
T19967	Fendosal 芬度柳,HP 129,P 71-0129,P71-0129,P-71-0129,HP129,HP-129	Immunology/Inflammation related	Immunology/Inflammation
	Fendosal (HP-129) 是一种非甾体抗炎药。在预防性和治疗性辅助诱导的慢性炎症多关节炎模型中，它的活性是阿司匹林的 6.9 至 9.5 倍。
T25507	HP 228 HP-228,Ac-Nle-gln-his-D-phe-arg-D-trp-gly-NH2,HP228
	HP 228 is a heptapeptide by inhibits the induction of nitric oxide synthase.
T26778	Besipirdine HP 749 free base,P-867493,P867493,HP 749,HP749,P 867493	Sodium Channel; Adrenergic Receptor	GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
	Besipirdine (HP 749 free base)是一种非受体依赖性拟胆碱化合物，具有α-肾上腺素能活性和心血管活性。Besipirdine 抑制电压依赖性钠钾通道，抑制生物胺的摄取。Besipirdine 可减少大鼠的时间表诱导的烦渴，增强中枢神经系统中的胆碱能和肾上腺素能神经传递。
T1539	Iloperidone 伊潘立酮,HP 873	Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Iloperidone (HP 873) 是一种D2/5-HT2受体拮抗剂，是非典型抗精神病药，可治疗精神分裂症。
T21556	Hydroxytacrine maleate Velnacrine maleate,HP 029 maleate	AChE	Neuroscience
	Hydroxytacrine maleate (Velnacrine maleate) 是一种胆碱酯酶(cholinesterase) 抑制剂，可增强啮齿动物的记忆力，可用于研究阿尔茨海默型老年性痴呆（SDAT）。
T19333	Gadoteridol ProHance,SQ-32692,钆特醇,Gd-HP-DO3A	Others	Others
	Gadoteridol (Gd-HP-DO3A) 是含钆基的 MRI 造影剂，可用于中枢神经系统成像。
T26778L	Besipirdine hydrochloride HP 749 hydrochloride,Besipirdine hydrochloride（119257-34-0 Free base)	Adrenergic Receptor	GPCR/G Protein; Neuroscience
	Besipirdine hydrochloride 是一种非受体依赖性拟胆碱化合物，具有α-肾上腺素能活性和心血管活性。Besipirdine hydrochloride 抑制电压依赖性钠钾通道，抑制生物胺的摄取。Besipirdine hydrochloride 可减少大鼠的时间表诱导的烦渴，增强中枢神经系统中的胆碱能和肾上腺素能神经传递。
T32125	Hyperphyllin HP
	Hyperphyllin specifically mimics the branch defects of AMP1, including plastid reduction and expansion and proliferation of the branch meristem.
T30590	Brocrinat HP 522
	Brocrinat (HP 522) is an active diuretic with at least one site of action in the medulla oblongata branch of the Henle loop.
T28160	Nerispirdine HCl HP-184,HP 184,Nerispirdine hydrochloride,HP184
	Nerispirdine is a acetylcholine release enhancer, sodium channel blocker and K(V) 2.1 channel blocker. Nerispirdine inhibits voltage-dependent Na(+) channel currents recorded from human SH-SY5Y cells with an IC(50) of 11.9 micromol/L when measured from a
TP1939L1	RVD-Hpα acetate(1193362-76-3 free base)	Cannabinoid Receptor	GPCR/G Protein
	RVD-Hpα acetate(1193362-76-3 free base) 是人血加压素的 N 末端延伸形式，可作为选择性 CB1 受体激动剂。增加体外表达 CB1 受体的细胞中的细胞内 Ca2+ 水平。也是高亲和力 CB2 正变构调节剂 (Ki = 50 nM)。
T27563	Hydroxypropyl-beta-cyclodextrin HP-beta-CyD,VTS-270,HP-beta-CD,Hydroxypropyl-beta-cyclodextri,THPB,HPbCD
	Hydroxypropyl-beta-cyclodextrin, also known as Hydroxypropyl-beta-cyclodextrin; THPB; HP-beta-CD; HPbCD; HP-beta-CyD; VTS-270; HPbetaCD; HPbetaCyD, is a drug candidate potentially for the treatment of Niemann-Pick type C diseases. In April 2009, hydroxypr
T34223	Quilostigmine HP 290,NXX 066,NXX-066
	Quilostigmine is a cholinergic.
T32018	Guanoxyfen sulfate CI-515,C.I. 515,HP 1598,CN-34,799-5A,CI 515
	Guanoxyfen sulfate is a bio-active chemical.
T34031	Phosphazide AZT-5'-Phosphonate,AZT-5'-H2PO3,Nicavir,AZT-HP
	Phosphazide is a zidovudine prodrug.
T27635	Isoxepac 伊索克酸,Olopatadine USP Related Compound C	Others	Others
	Isoxepac (Olopatadine USP Related Compound C) 是非甾体抗炎剂，显示出抗炎、镇痛和解热活性，已在多种动物模型中进行了相关研究。
TP2340	Hemoregulatory peptide 5b hp 5B,Pglu-glu-asp-cys-lys-OH,Peedck,Glp-glu-asp-cys-lys-OH,SP1 Pentapeptide
	Hemoregulatory peptide 5b is a synthetic analog of granulocyte chalone which initially identified in extracts of rodent bone marrow and human leukocytes. Monomer inhibits both formations of GM-CFC colonies and cytotoxic drug-induced recruitment of murine
T75936	RVD-Hpα TFA
	RVD-Hpα TFA is the N-terminally extended form of human hemopressin that acts as a selectiveCB1receptoragonist. RVD-Hpα TFA increases intracellular Ca2+levels in cells expressingCB1receptors in vitro. RVD-Hpα TFA also high affinityCB2positive allosteric modulator (Ki=50 nM).
T61329	HP1142
	HP1142 is a highly effective and specific inhibitor targeting the FLT3 receptor tyrosine kinase, with a particular affinity for its mutant variant FLT3/ITD. It exhibits a benzoimidazole scaffold-based structure, making it a promising compound for investigating and studying the FLT3/ITD mutation in the context of leukemia research [1].
T78073	HP210	Glucocorticoid Receptor	Endocrinology/Hormones
	HP210是一种选择性糖皮质激素受体调节剂(SGRM)，可以抑制IL-1β和IL-6的mRNA表达，有望用于研究炎症相关疾病。
T83865	HP661
	HP661是一种针对线粒体复合物I（也称为NADH脱氢酶）的抑制剂，对复合物I具有选择性，以1 µM的浓度抑制其77.6%，而对复合物III抑制率为28.1%，对复合物II和IV则无抑制作用。HP661特异性降低具有高水平氧化磷酸化作用的人类肺癌细胞H460、NCI H441及对trametinib耐药的A549细胞的生存能力（IC50分别为10.6、29.7和15.1 nM），相较于氧化磷酸化水平低的NCI H358人类肺癌细胞（IC50 >10,000 nM）以及非癌性人类胰腺正常上皮细胞（HPNE）和MRC-5人类胎肺成纤维细胞（两者的IC50均>10,000 nM）。当以每天两次，每次30 mg/kg的剂量给药时，HP661在H460小鼠异种移植模型中减少肿瘤体积，并对trametinib引导的肿瘤生长减少产生加成效应。
T64182	HP590
	HP590 是一种新型的、强效的、口服具有活力的 STAT3 抑制剂 (STAT3 荧光素酶活性:IC50=27.8 nM; ATP 抑制:IC50=24.7 nM)。HP590 具有抗胃癌细胞增殖的作用，能够诱导细胞凋亡。
T61758	HP1328
	HP1328 is a highly effective inhibitor of FLT3 receptor tyrosine kinase with a specific focus on FLT3/ITD mutation. It belongs to the benzoimidazole scaffold-based compound family. Significantly reducing the leukemia burden, HP1328 effectively extends the survival of mice afflicted with FLT3/ITD leukemia [1].
T62253	S-HP210
	S-HP210 是一种选择性的、有效的糖皮质激素受体 (GR) 调节剂，能够抑制 NF-κB 转录 (IC50: 1.92 μM)。S-HP210 对于 LPS 诱导的多种促炎基因（如 IL-1β、IL-6 和 COX-2）的转录具有抑制作用。S-HP210 在有效剂量下对小鼠成纤维细胞 3T3 没有毒性。
T62252	R-HP210
	R-HP210 能够抑制 LPS 诱导的多种促炎基因（IL-1β、IL-6 和 COX-2）的转录。R-HP210 对 NF-κB 介导的栓系反式抑制功能的 IC50 值为 3.80 μM。R-HP210 不诱导糖皮质激素 (GCs) 的反式激活功能。
T71279	BPR1K653
	BPR1K653 is a potent Aurora kinase inhibitor with potential anticancder activity. BPR1K653 specifically inhibited the activity of Aurora-A and Aurora-B kinase at low nano-molar concentrations in vitro. BPR1K653 was potent in targeting a variety of cancer cell lines regardless of the tissue origin, p53 status, or expression of MDR1. At the cellular level, BPR1K653 induced endo-replication and subsequent apoptosis in both MDR1-negative and MDR1-positive cancer cells. Importantly, it showed potent ...
T22021	ACHP IKK-2 Inhibitor VIII	IκB/IKK	NF-κB
	ACHP(IKK-2 Inhibitor VIII) 是一种新型具有选择性和高效性的 IKK 抑制剂，对IKK-α和IKK-β 具有抑制作用。ACHP 具有抗 HIV-1 活性，通过抑制 NF-κB 激活来抑制 HIV-1 长末端重复序列（LTR）驱动的基因表达，抑制 TNF-α 诱导的 NF-κB （p65）募集到 HIV-1 LTR。
T17909	(S,R,S)-AHPC-PEG3-N3 VHL Ligand-Linker Conjugates 8,VH032-PEG3-N3,E3 ligase Ligand-Linker Conjugates 12	Others; E3 Ligase Ligand-Linker Conjugate; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-PEG3-N3 (VHL Ligand-Linker Conjugates 8) 包含基于 (S,R,S)-AHPC 的 VHL 配体和 3 个单元 PEG linker，是一种合成的 E3 连接酶配体-linker 偶联物。
T17924	(S,R,S)-AHPC-PEG2-NH2 hydrochloride VH032-PEG2-NH2 hydrochloride,VHL Ligand-Linker Conjugates 3 hydrochloride,E3 ligase Ligand-Linker Conjugates 6	Others; E3 Ligase Ligand-Linker Conjugate	Others; PROTAC
	(S,R,S)-AHPC-PEG2-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 6) 包含基于 (S,R,S)-AHPC 的 VHL 配体和 2 个单元 PEG linker，是一种合成的 E3 连接酶配体-linker 偶联物，可用于 PROTAC 的合成分子。
T10809L	CHPG hydrochloride CHPG hydrochloride(170846-74-9 Free base)	ERK; NF-κB; GluR	MAPK; Neuroscience; NF-κB
	CHPG hydrochloride 是 mGluR5 的选择性激动剂。
T28410	PHPS1 PHPS-1,PHPS 1	Phosphatase	Metabolism
	PHPS1 是 Shp2的选择性抑制剂，对 Shp2，Shp2-R362K，Shp1，PTP1B 和 PTP1B-Q 的 Ki 分别为 0.73，5.8，10.7，5.8 和 0.47 μM。
T18675	(S,R,S)-AHPC-PEG2-NH2 dihydrochloride VH032 amide-PEG2-amine,VH032-PEG2-NH2 dihydrochloride,(S,R,S)-AHPC-PEG2-NH2二盐酸盐,VH032-linker 12	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-PEG2-NH2 dihydrochloride (VH032-linker 12) 包含基于 (S,R,S)-AHPC 的 VHL 配体和 2 个单元 PEG linker，是一种合成的 E3 连接酶配体-linker 偶联物，可用于 PROTAC 分子的合成。
T1804	HPGDS inhibitor 1 HPGDS-inhibitor-1	PGE Synthase	Immunology/Inflammation
	HPGDS inhibitor 1 是口服具有活性的HPGDS 选择性抑制剂，在酶和细胞分析中的IC50值分别为 0.6 nM 和 32 nM，但对 L-PGDS、mPGES、COX-1、COX-2 、5-LOX 无抑制作用。
T8412	(S,R,S)-AHPC VH032-NH2,MDK7526,VHL ligand 1	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC (VH032-NH2) 是一种 VH032-based VHL ligand，可用于募集 von Hippel-Lindau (VHL)蛋白。它能够利用 linker 与靶蛋白配体连接，得到 PROTAC 分子。
T18640	(S,R,S)-AHPC-C4-NH2 hydrochloride VH032-C4-NH2 hydrochloride,E3 ligase Ligand-Linker Conjugates 28,VHL Ligand-Linker Conjugates 13	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-C4-NH2 hydrochloride (E3 ligase Ligand-Linker Conjugates 28) 是一种合成的 E3 连接酶配体- linker 偶联物，包含基于 (S,R,S)-AHPC 的 VHL 配体和 linker。
T9777	THP104c	Mitochondrial Metabolism	Metabolism
	THP104c 是有效的线粒体分裂抑制剂。
T77668	hPL-IN-1	Others	Others
	hPL-IN-1 是一种有效的可逆胰脂肪酶 (PL) 抑制剂 (IC50=1.86 μM)，可用于研究与肥胖相关的疾病。
T17920	(S,R,S)-AHPC-PEG1-N3 VHL Ligand-Linker Conjugates 9,VH032-PEG1-N3,E3 ligase Ligand-Linker Conjugates 3	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-PEG1-N3 (E3 ligase Ligand-Linker Conjugates 3) 是 E3 连接酶配体和linker 连接得到的偶联物，包含基于 (S,R,S)-AHPC 的 VHL 配体和 1 个单元 PEG linker。
T19955	Biotin-HPDP Pyridyldisulfide-biotin,Pyridyldithiol-biotin	Others	Others
	Biotin-HPDP (Pyridyldithiol-biotin) 是一种巯基反应性生物素化试剂。
T17921	(S,R,S)-AHPC-PEG4-N3 VH032-PEG4-N3,VHL Ligand-Linker Conjugates 5,E3 ligase Ligand-Linker Conjugates 4	Others; PROTAC Linker	Others; PROTAC
	(S,R,S)-AHPC-PEG4-N3 (VHL Ligand-Linker Conjugates 5) is a synthesized conjugate that functions as a ligand-linker in E3 ligase-based systems. It is composed of the (S,R,S)-AHPC VHL ligand and a 4-unit PEG linker, both commonly employed in PROTAC technology.
T18912	ADHP 10-乙酰基-3,7-二羟基吩嗪,10-Acetyl-3,7-dihydroxyphenoxazine	Others	Others
	ADHP (10-Acetyl-3,7-dihydroxyphenoxazine) 是荧光过氧化物酶底物，其λex=530 nm，λem=590 nm。
T10237	ACHP Hydrochloride IKK-2 Inhibitor VIII	IκB/IKK	NF-κB
	ACHP Hydrochloride (IKK-2 Inhibitor VIII) 是选择性的IKK-β抑制剂 (IC50=5.8 nM)。
T2430	HPOB	Apoptosis; HDAC	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair
	HPOB 是一种高选择性HDAC6抑制剂，IC50为 56 nM，其选择性是其他 HDAC 的 30 倍以上。它提高 DNA 损伤抗癌药物在转化细胞中的有效性。
T4658	MHP Methyl caprooyl tyrosinate	S1P Receptor	GPCR/G Protein
	MHP (Methyl caprooyl tyrosinate) 是一种鞘氨醇激酶 (SPHK1) 激活剂，可显著增加 CAMP mRNA 和蛋白水平，还可增强抗微生物防御能力和先天免疫力。
T2681	hPGDS-IN-1	PGE Synthase	Immunology/Inflammation
	hPGDS-IN-1是 hPGDS 抑制剂，使用荧光偏振检测或通过 EIA 法测得的 IC50值为12 nM。
T38948	MS-PEG4-THP	PROTAC Linker	PROTAC
	MS-PEG4-THP 是PEG 类PROTAC linker，可用于合成 PROTAC 分子。
T40028	(S,R,S)-AHPC	Ligand for E3 Ligase	PROTAC
	(S,R,S)-AHPC 是一种 VHL 配体，用于募集 VHL 蛋白。
T13671	(S,R,S)-AHPC-Me hydrochloride VHL ligand 2 hydrochloride,E3 ligase Ligand 1	Others; Ligand for E3 Ligase	Others; PROTAC
	(S,R,S)-AHPC-Me hydrochloride (VHL ligand 2 hydrochloride) is a chemical compound utilized in the synthesis of ARV-771, an exceptionally potent BET protein degrader. This compound selectively degrades BET protein in cells resistant to castration, exhibiting a remarkable DC50 <1 nM. Recognized as VHL ligand 2 hydrochloride, (S,R,S)-AHPC-Me hydrochloride serves as the VHL ligand derived from (S,R,S)-AHPC for the recruitment of von Hippel-Lindau (VHL) protein.
T6967	RHPS4 RHPS 4 methosulfate,NSC714187	Apoptosis; Telomerase	Apoptosis; DNA Damage/DNA Repair
	RHPS4 (RHPS 4 methosulfate) 是 DNA 损伤诱导剂，是一种有效的亚微摩尔端粒酶抑制剂，IC50为0.33 μM。

化合物

Cat.No: T19609

Synonym: 羟丙基-β-环糊精,羟丙基-BETA-环糊精,Hydroxypropyl-β-cyclodextrin,Hydroxypropyl betadex

Target: Others

Cat.No: T19967

Synonym: 芬度柳,HP 129,P 71-0129,P71-0129,P-71-0129,HP129,HP-129

Target: Immunology/Inflammation related

Cat.No: T25507

Synonym: HP-228,Ac-Nle-gln-his-D-phe-arg-D-trp-gly-NH2,HP228

Cat.No: T26778

Synonym: HP 749 free base,P-867493,P867493,HP 749,HP749,P 867493

Target: Sodium Channel, Adrenergic Receptor

Cat.No: T1539

Synonym: 伊潘立酮,HP 873

Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor

Hydroxytacrine maleate

Cat.No: T21556

Synonym: Velnacrine maleate,HP 029 maleate

Target: AChE

Cat.No: T19333

Synonym: ProHance,SQ-32692,钆特醇,Gd-HP-DO3A

Target: Others

Besipirdine hydrochloride

Cat.No: T26778L

Synonym: HP 749 hydrochloride,Besipirdine hydrochloride（119257-34-0 Free base)

Target: Adrenergic Receptor

Cat.No: T32125

Synonym: HP

Cat.No: T30590

Synonym: HP 522

Nerispirdine HCl

Cat.No: T28160

Synonym: HP-184,HP 184,Nerispirdine hydrochloride,HP184

RVD-Hpα acetate(1193362-76-3 free base)

Cat.No: TP1939L1

Target: Cannabinoid Receptor

Hydroxypropyl-beta-cyclodextrin

Cat.No: T27563

Synonym: HP-beta-CyD,VTS-270,HP-beta-CD,Hydroxypropyl-beta-cyclodextri,THPB,HPbCD

Cat.No: T34223

Synonym: HP 290,NXX 066,NXX-066

Guanoxyfen sulfate

Cat.No: T32018

Synonym: CI-515,C.I. 515,HP 1598,CN-34,799-5A,CI 515

Cat.No: T34031

Synonym: AZT-5'-Phosphonate,AZT-5'-H2PO3,Nicavir,AZT-HP

Cat.No: T27635

Synonym: 伊索克酸,Olopatadine USP Related Compound C

Target: Others

Hemoregulatory peptide 5b

Cat.No: TP2340

Synonym: hp 5B,Pglu-glu-asp-cys-lys-OH,Peedck,Glp-glu-asp-cys-lys-OH,SP1 Pentapeptide

Cat.No: T75936

Cat.No: T61329

Cat.No: T78073

Target: Glucocorticoid Receptor

Cat.No: T83865

Cat.No: T64182

Cat.No: T61758

Cat.No: T62253

Cat.No: T62252

Cat.No: T71279

Cat.No: T22021

Synonym: IKK-2 Inhibitor VIII

Target: IκB/IKK

(S,R,S)-AHPC-PEG3-N3

Cat.No: T17909

Synonym: VHL Ligand-Linker Conjugates 8,VH032-PEG3-N3,E3 ligase Ligand-Linker Conjugates 12

Target: Others, E3 Ligase Ligand-Linker Conjugate, Ligand for E3 Ligase

(S,R,S)-AHPC-PEG2-NH2 hydrochloride

Cat.No: T17924

Synonym: VH032-PEG2-NH2 hydrochloride,VHL Ligand-Linker Conjugates 3 hydrochloride,E3 ligase Ligand-Linker Conjugates 6

Target: Others, E3 Ligase Ligand-Linker Conjugate

CHPG hydrochloride

Cat.No: T10809L

Synonym: CHPG hydrochloride(170846-74-9 Free base)

Target: ERK, NF-κB, GluR

Cat.No: T28410

Synonym: PHPS-1,PHPS 1

Target: Phosphatase

(S,R,S)-AHPC-PEG2-NH2 dihydrochloride

Cat.No: T18675

Synonym: VH032 amide-PEG2-amine,VH032-PEG2-NH2 dihydrochloride,(S,R,S)-AHPC-PEG2-NH2二盐酸盐,VH032-linker 12

Target: Others, Ligand for E3 Ligase

HPGDS inhibitor 1

Cat.No: T1804

Synonym: HPGDS-inhibitor-1

Target: PGE Synthase

Cat.No: T8412

Synonym: VH032-NH2,MDK7526,VHL ligand 1

Target: Others, Ligand for E3 Ligase

(S,R,S)-AHPC-C4-NH2 hydrochloride

Cat.No: T18640

Synonym: VH032-C4-NH2 hydrochloride,E3 ligase Ligand-Linker Conjugates 28,VHL Ligand-Linker Conjugates 13

Target: Others, Ligand for E3 Ligase

Cat.No: T9777

Target: Mitochondrial Metabolism

Cat.No: T77668

Target: Others

(S,R,S)-AHPC-PEG1-N3

Cat.No: T17920

Synonym: VHL Ligand-Linker Conjugates 9,VH032-PEG1-N3,E3 ligase Ligand-Linker Conjugates 3

Target: Others, Ligand for E3 Ligase

Cat.No: T19955

Synonym: Pyridyldisulfide-biotin,Pyridyldithiol-biotin

Target: Others

(S,R,S)-AHPC-PEG4-N3

Cat.No: T17921

Synonym: VH032-PEG4-N3,VHL Ligand-Linker Conjugates 5,E3 ligase Ligand-Linker Conjugates 4

Target: Others, PROTAC Linker

Cat.No: T18912

Synonym: 10-乙酰基-3,7-二羟基吩嗪,10-Acetyl-3,7-dihydroxyphenoxazine

Target: Others

ACHP Hydrochloride

Cat.No: T10237

Synonym: IKK-2 Inhibitor VIII

Target: IκB/IKK

Cat.No: T2430

Target: Apoptosis, HDAC

Cat.No: T4658

Synonym: Methyl caprooyl tyrosinate

Target: S1P Receptor

Cat.No: T2681

Target: PGE Synthase

Cat.No: T38948

Target: PROTAC Linker

Cat.No: T40028

Target: Ligand for E3 Ligase

(S,R,S)-AHPC-Me hydrochloride

Cat.No: T13671

Synonym: VHL ligand 2 hydrochloride,E3 ligase Ligand 1

Target: Others, Ligand for E3 Ligase

Cat.No: T6967

Synonym: RHPS 4 methosulfate,NSC714187

Target: Apoptosis, Telomerase

Cat. No.	Product Name	Target	Signaling Pathways
T4797	DEHP Bis(2-ethylhexyl) phthalate,邻苯二甲酸二(2-乙基己)酯	Others; Endogenous Metabolite	Metabolism; Others
	DEHP (Bis(2-ethylhexyl) phthalate) 是内源性代谢产物的一种。
TN6684	Cyclo(Tyr-Hpro)
	Cyclo(Tyr-Hpro) 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN6684，CAS号为 813461-21-1。
T36560	(±)9-HpODE
	(±)9-HpODE is a racemic mixture of the fatty acid hydroperoxide product (9(S)-HpODE) formed from lipoxygenase action on linoleic acid. It shows antimicrobial activity against various fungal and bacterial pathogens and thus may play a role in plant defense. In mammalian species, monocyte-induced oxidization of LDL generates significant amounts of esterified 9-HpODE, which is rapidly reduced to 9-HODE.
TN3118	5-Hydroxy-7-(4'-hydroxy-3'-methoxyphenyl)-1-phenyl-3-heptanone (DHPA)	Others	Others
	5-Hydroxy-7-(4'-hydroxy-3'-methoxyphenyl)-1-phenyl-3-heptanone (DHPA) is a pancreatic lipase inhibitor, it shows antihyperlipidemic activity.
TN7019	DNHP
	DNHP is a natural product.
TN6429	Cyclo(Phe-Hpro)
	Cyclo(Phe-Hpro) 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN6429，CAS号为 1016899-94-7。
TN6680	Cyclo(Hpro-Leu)
	Cyclo(Hpro-Leu) 是一种天然产物，可用于生命科学领域的相关研究。其产品编号为 TN6680，CAS号为 1016899-93-6。
T74193	(R)-IDHP
	(R)-IDHP为IDHP异构体，属于丹参代谢物。该化合物能通过抑制血管平滑肌细胞电压依赖性钙通道与受体操作钙通道的Ca2+释放和Ca2+内流，发挥血管松弛作用，适用于心脑血管疾病研究。

天然产物

Cat.No: T4797

Synonym: Bis(2-ethylhexyl) phthalate,邻苯二甲酸二(2-乙基己)酯

Target: Others, Endogenous Metabolite

Cyclo(Tyr-Hpro)

Cat.No: TN6684

Cat.No: T36560

5-Hydroxy-7-(4'-hydroxy-3'-methoxyphenyl)-1-phenyl-3-heptanone (DHPA)

Cat.No: TN3118

Target: Others

Cat.No: TN7019

Cyclo(Phe-Hpro)

Cat.No: TN6429

Cyclo(Hpro-Leu)

Cat.No: TN6680

Cat.No: T74193

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