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33

抑制剂 & 化合物

5

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T12268	NTP42	Prostaglandin Receptor; PPAR	DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Metabolism
	NTP42 是血栓素 A2 (TXA2) 受体的拮抗剂，IC50为 3.278 nM，可用于肺动脉高压的相关研究。
T8900	Seralutinib GB002	PDGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	Seralutinib (GB002) 是可吸入的PDGFRα 和 PDGFRβ激酶抑制剂，可用于研究肺动脉高压。
T14782	Brilaroxazine RP5063	Dopamine Receptor; 5-HT Receptor	GPCR/G Protein; Neuroscience
	Brilaroxazine (RP5063) 是一种有效的多模式多巴胺/5-HT 调节剂。 Brilaroxazine 是多巴胺 D2、D3 和 D4 受体、5-HT1A (Ki = 1.5 nM) 和 5-HT2A (Ki = 2.5 nM) 的部分激动剂，具有拮抗活性 5-HT2B 和 5-HT7 受体，Ki 分别为 0.19 nM 和 2.7 nM。 Brilaroxazine 可用于研究神经精神和神经系统疾病的认知障碍。
T8840	PF-543 hydrochloride PF-543	Apoptosis; S1P Receptor; Autophagy; LPL Receptor	Apoptosis; Autophagy; GPCR/G Protein
	PF-543 hydrochloride (PF-543) 是一种选择性可逆和鞘氨醇竞争性SPHK1抑制剂，对SPHK1的选择性是 SPHK2 的 100 倍以上。它还是全血中 1-磷酸鞘氨醇形成的有效抑制剂，诱导细胞凋亡、坏死和自噬。
T6085	PF-543 Sphingosine Kinase 1 Inhibitor II,PF 543	Apoptosis; S1P Receptor; Autophagy; LPL Receptor	Apoptosis; Autophagy; GPCR/G Protein
	PF-543 (Sphingosine Kinase 1 Inhibitor II) 是一种选择性可逆和鞘氨醇竞争性 SPHK1抑制剂，可诱导细胞凋亡、坏死和自噬。它对 SPHK1的选择性是 SPHK2 的 100 倍以上。它还抑制全血中 1-磷酸鞘氨醇形成，IC50为 26.7 nM。
T35447	10(S)-PAHSA
	10(S)-PAHSA is a stereoisomer of 10-PAHSA , an endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs).
T34746	Sulfo-SANPAH Crosslinker Sulfo-SANPAH Cross-linker,Sulfo-SANPAH Cross linker,6-[(4-叠氮-2-硝基苯基)氨基]己酸磺酸基琥珀酰亚胺酯	Others	Others
	Sulfo-SANPAH Crosslinker (Sulfo-SANPAH Cross linker) 是一种水溶性同双功能蛋白质交联剂。
T23178	PPAHV	Others	Others
	vanilloid TRPV1 (VR1) receptor agonist
T36588	9(R)-PAHSA
	9(R)-PAHSA is a stereoisomer of 9-PAHSA , an endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs).
T36586	12-PAHSA
	Branched fatty acid esters of hydroxy fatty acids (FAHFAs) are newly identified endogenous lipids regulated by fasting and high-fat feeding and associated with insulin sensitivity. Structurally, these esters are comprised of a C-16 or C-18 fatty acid (e.g., palmitoleic, palmitic, oleic, or stearic acid) linked to either a C-16 or C-18 hydroxy substituent. 12-PAHSA is a FAHFA in which palmitic acid is esterified at the 12th carbon of hydroxy stearic acid. Among the FAHFA family members, PAHSAs ar...
T35446	10(R)-PAHSA
	10(R)-PAHSA is a stereoisomer of 10-PAHSA , an endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs).
T36142	10-PAHSA
	10-PAHSA is a newly identified endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs). It is a FAHFA in which palmitic acid is esterified to 10-hydroxy stearic acid. Among the FAHFA family members, PAHSAs are the most abundant in the adipose tissue of glucose tolerant AG4OX mice, which overexpress the Glut4 glucose transporter specifically in adipose tissue. As other FAHFAs improve glucose tolerance, stimulate insulin secretion, and have anti-...
T36590	9-PAHSA
	Branched fatty acid esters of hydroxy fatty acids (FAHFAs) are newly identified endogenous lipids regulated by fasting and high-fat feeding and associated with insulin sensitivity. Structurally, these esters are comprised of a C-16 or C-18 fatty acid (e.g., palmitoleic, palmitic, oleic, or stearic acid) linked to a hydroxylated C-16 or C-18 lipid. 9-PAHSA is a FAHFA in which palmitic acid is esterified to 9-hydroxy stearic acid. PAHSAs are the most abundant forms of FAHFA in serum as well as whi...
T73841	9-PAHPA
	9-PAHPA，一种羟基脂肪酸的脂肪酸酯 (FAHFA)，属于一类新的内源性脂质家族，显示出抗糖尿病和抗炎特性。
T126416	Homopahutoxin
	Homopahutoxin 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 T126416。
T125133	Pahutoxin
	Pahutoxin 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 T125133。
T2561	Macitentan 马西替坦,ACT-064992	Apoptosis; Endothelin Receptor	Apoptosis; GPCR/G Protein
	Macitentan (ACT-064992) 是一种内皮素受体拮抗剂，用于治疗肺动脉高压。
T0352	Dibenzothiophene 二苯并噻吩,Imino semicarbazide,Diphenylene sulfide	Others	Others
	Dibenzothiophene (Imino semicarbazide) 是有机合成过程的中间体，是由两个苯环稠合到一个中心的噻吩环。
T3216	Selexipag NS-304,ACT-293987,赛乐西帕,Uptravi	Others; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Others
	Selexipag (ACT-293987) 是前列环素受体激动剂，可引起肺血管舒张，用于治疗肺动脉高压。
T78835	Phosphatase-IN-1	Antifungal	Microbiology/Virology
	Phosphatase-IN-1（compound II-8）是Propranolol的衍生物，充当磷脂酸磷酸酶（Pah）的抑制剂。Phosphatase-IN-1能够与 MoPah1结合，展现出19.8 μM的亲和常数。Phosphatase-IN-1能够抑制植物病原体的生长，并显示出抗真菌特性，同时对稻苗和麦穗表现出无毒性。
T13193	TPN171	PDE	Metabolism
	TPN171是一种有效的 PDE5抑制剂，对 PDE5具有亚纳摩尔效价，对 PDE5比对 PDE6具有良好的选择性，具有治疗肺动脉高压(PAH)的潜力。在动物模型中，TPN171被证明具有比西地那非更持久的作用，为临床使用每日一次口服提供了基础。
T1655	Ambrisentan BSF-208075,BSF 208075,安倍生坦,LU 208075	Endothelin Receptor	GPCR/G Protein
	Ambrisentan (BSF 208075) 是 ET A 型受体选择性拮抗剂。
TP1016L	Aviptadil Acetate 醋酸阿肽地尔,阿肽地尔,Vasoactive Intestinal Peptide acetate salt	RAAS; SARS-CoV	Endocrinology/Hormones; Microbiology/Virology
	Aviptadil Acetate (Vasoactive Intestinal Peptide acetate salt) 是模拟血管活性肠多肽类似物，具有血管舒张效应。它可诱导肺血管舒张并抑制血管 SMC 的增殖和血小板聚集。它可用于研究 SARS-CoV-2 引起的肺纤维化、肺动脉高压和呼吸衰竭。
T36696	DMBA
	7,12-Dimethylbenz[a]anthracene (DMBA) is a polycyclic aromatic hydrocarbon (PAH) that has been found in tobacco smoke and diesel exhaust and has carcinogenic activity.1,2It undergoes metabolic activation by numerous enzymes, including the cytochrome P450 (CYP450) isoform CYP1B1, as well as microsomal epoxide hydrolase (mEH), producing a variety of reactive metabolites that form DNA adductsin vivo, and it has been commonly used to induce tumor formation in various rodent models.2,3,1DMBA increase...
T79575	ET receptor antagonist 3	Estrogen Receptor/ERR	Endocrinology/Hormones
	ET receptor antagonist 3 (compound 17d)为ET受体拮抗剂，其IC50值为0.26 nM，主要用于肺动脉高压(PAH)的研究应用。在大鼠模型中，该化合物能有效减轻由野百合碱诱导的PAH症状。
T79573	ET receptor antagonist 1	Estrogen Receptor/ERR	Endocrinology/Hormones
	ET receptor antagonist 1 (compound 16h)，作为ET受体拮抗剂（IC50=0.18 nM），主要用于肺动脉高压(PAH)的研究。该化合物能缓解大鼠模型中由野百合碱引发的PAH症状。
T71847	Terguride
	Terguride is 5-HT receptor antagonist. Terguride is a drug used to treat hyperprolactinemia that antagonizes 5-HT2A and 5-HT2B and activates dopamine receptors. It has also been extensively studied for the treatment of PAH.
T16779	Rodatristat ethyl RVT-014,KAR5585,RVT-1201	5-HT Receptor; Hydroxylase	GPCR/G Protein; Metabolism; Neuroscience
	Rodatristat ethyl (KAR5585) 是一种首新型具有口服活性和有效性的 tryptophan hydroxylase 1 (TPH1) 抑制剂，低浓度下可显著降低 5-hydroxytryptamine (5-HT) 的水平并降低肺动脉高压 (PAH)，
T79574	ET receptor antagonist 2	Estrogen Receptor/ERR	Endocrinology/Hormones
	ET receptor antagonist 2 (compound 16j) 作为一种ET受体拮抗剂，具有0.22 nM的IC50，主要应用于肺动脉高压(PAH)的研究。在大鼠模型中，它能够有效减缓野百合碱诱导的PAH症状。
T78076	PBR28	Others	Others
	PBR28是一种TSPO调节剂，适用于肺动脉高压(PAH)预防研究。通过增加放射性标记的PBR28能够示踪18KDa转运蛋白(TSPO)，在脑正电子发射断层扫描(PET)成像中具有关键作用。
T11935	Macitentan (n-butyl analogue)	Others	Others
	Macitentan n-butyl analogue, a derivative of Macitentan, functions as an orally active dual antagonist targeting both endothelin ETA and ETB receptors. This compound shows promise for treating idiopathic pulmonary fibrosis (IPF) and pulmonary arterial hypertension (PAH), leveraging its non-peptide structure for potential therapeutic applications.
TP2096	ELA-21 (human)
	High affinity apelin receptor agonist. Binds apelin receptors in left ventricle from normal and pulmonary arterial hypertensive (PAH) hearts (pKi values are 9.31 and 9.46, respectively). Bioactive fragment of ELA-32. Inhibits forskolin-induced cAMP produc
T65598	Cefminox sodium
	Cefminox (Sodium) is a new cephamycin antibiotic possessing a D-amino acid moiety derived from D-cysteine at the C-7B side chain. Cefminox is active against a wide range of bacteria, especially Gram-negative and anaerobic bacteria. Cefminox shows excellent in vivo efficacy (ED50) which is higher than would be expected from its in vitro activity (MIC). Moreover, cefminox possesses more potent activity in suppression of bacterial regrowth than other cephems[1]. Cefminox (Sodium) was the most activ...

化合物

Cat.No: T12268

Target: Prostaglandin Receptor, PPAR

Cat.No: T8900

Synonym: GB002

Target: PDGFR

Cat.No: T14782

Synonym: RP5063

Target: Dopamine Receptor, 5-HT Receptor

PF-543 hydrochloride

Cat.No: T8840

Synonym: PF-543

Target: Apoptosis, S1P Receptor, Autophagy, LPL Receptor

Cat.No: T6085

Synonym: Sphingosine Kinase 1 Inhibitor II,PF 543

Target: Apoptosis, S1P Receptor, Autophagy, LPL Receptor

Cat.No: T35447

Sulfo-SANPAH Crosslinker

Cat.No: T34746

Synonym: Sulfo-SANPAH Cross-linker,Sulfo-SANPAH Cross linker,6-[(4-叠氮-2-硝基苯基)氨基]己酸磺酸基琥珀酰亚胺酯

Target: Others

Cat.No: T23178

Target: Others

Cat.No: T36588

Cat.No: T36586

Cat.No: T35446

Cat.No: T36142

Cat.No: T36590

Cat.No: T73841

Cat.No: T126416

Cat.No: T125133

Cat.No: T2561

Synonym: 马西替坦,ACT-064992

Target: Apoptosis, Endothelin Receptor

Dibenzothiophene

Cat.No: T0352

Synonym: 二苯并噻吩,Imino semicarbazide,Diphenylene sulfide

Target: Others

Cat.No: T3216

Synonym: NS-304,ACT-293987,赛乐西帕,Uptravi

Target: Others, Prostaglandin Receptor

Phosphatase-IN-1

Cat.No: T78835

Target: Antifungal

Cat.No: T13193

Target: PDE

Cat.No: T1655

Synonym: BSF-208075,BSF 208075,安倍生坦,LU 208075

Target: Endothelin Receptor

Aviptadil Acetate

Cat.No: TP1016L

Synonym: 醋酸阿肽地尔,阿肽地尔,Vasoactive Intestinal Peptide acetate salt

Target: RAAS, SARS-CoV

Cat.No: T36696

ET receptor antagonist 3

Cat.No: T79575

Target: Estrogen Receptor/ERR

ET receptor antagonist 1

Cat.No: T79573

Target: Estrogen Receptor/ERR

Cat.No: T71847

Rodatristat ethyl

Cat.No: T16779

Synonym: RVT-014,KAR5585,RVT-1201

Target: 5-HT Receptor, Hydroxylase

ET receptor antagonist 2

Cat.No: T79574

Target: Estrogen Receptor/ERR

Cat.No: T78076

Target: Others

Macitentan (n-butyl analogue)

Cat.No: T11935

Target: Others

Cat.No: TP2096

Cefminox sodium

Cat.No: T65598

Cat. No.	Product Name	Target	Signaling Pathways
TN5358	Eupahualin C
	Eupahualin C shows significant activities against cell lines of human chronic myelogenous leukemia (K562) and human bone cancer (U2OS).
T14961	Chrysene 䓛,屈	Others	Others
	Chrysene 是高分子量 (HMW) 多环芳烃，有极强的顽固性和致癌性。
T7914	Acenaphthylene	Others	Others
	Acenaphthylene 是多环芳烃。其中多环芳烃是自然衍生于煤和焦油沉积物中，并由有机质的不完全燃烧得到。
T5290	(S)-2-Hydroxy-3-phenylpropanoic acid L-(−)-3-Phenyllactic acid,L-3-苯乳酸	Others; Endogenous Metabolite	Metabolism; Others
	(S)-2-Hydroxy-3-phenylpropanoic acid (L-(−)-3-Phenyllactic acid) 是苯丙氨酸的代谢产物。苯丙酮尿症患者体液中苯丙氨酸的水平升高。
T82897	Benzo[e]pyrene
	Benzo[e]pyrene为化石燃料中检出的多环芳烃(PAHs)类剧毒成员。

天然产物

Cat.No: TN5358

Cat.No: T14961

Synonym: 䓛,屈

Target: Others

Cat.No: T7914

Target: Others

(S)-2-Hydroxy-3-phenylpropanoic acid

Cat.No: T5290

Synonym: L-(−)-3-Phenyllactic acid,L-3-苯乳酸

Target: Others, Endogenous Metabolite

Cat.No: T82897

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