首页工具

登录

搜索结果

Search Results for " synthase "

514

抑制剂 & 化合物

100

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T10404	ATP synthase inhibitor 1	ATPase	Membrane transporter/Ion channel
	ATP synthase inhibitor 1 是 F1/FO-ATP 合酶复合物 c 亚基的有效抑制剂，抑制线粒体通透性转换孔的开放。
T4380	Ac-CoA Synthase Inhibitor1 ACSS2 inhibitor	RSV; Fatty Acid Synthase	Metabolism; Microbiology/Virology
	Ac-CoA Synthase Inhibitor1 (ACSS2 inhibitor) 是一种可逆的醋酸盐依赖性乙酰辅酶 A 合成酶 2 抑制剂，IC50为 0.6 µM，可抑制呼吸道合胞病毒。
T27066	Prostaglandin G/H synthase 1 inhibitor CP74006,CP 74006,2-Amino-N-(4-chlorophenyl)benzamide	Others	Others
	Prostaglandin G/H synthase 1 inhibitor (CP 74006) 是一种选择性D5D 抑制剂，IC(50)值为20nM。
T61147	Chitin synthase inhibitor 4	Antibiotic	Microbiology/Virology
	Chitin synthase inhibitor 4 是一种具有抗菌活性的几丁质合成酶（CHS）抑制剂。Chitin synthase inhibitor 4 是一种基于CHS 的化合物，是一种候选的杀菌剂。
T39883	Polyketide synthase 13-IN-1
	Polyketide synthase 13-IN-1 (compound 32) is a polyketide synthase 13 inhibitor.
T39693	Polyketide synthase 13-IN-3
	Polyketide synthase 13-IN-3 (compound 41) is a potent inhibitor of polyketide synthase 13, demonstrating a minimum inhibitory concentration (MIC) range of 0.0625-0.125 μg/mL against the M. tuberculosis strain H37Rv.
T40945	Phospho-Glycogen Synthase Peptide-2(substrate)
	Phospho-Glycogen Synthase Peptide-2, a substrate for glycogen synthase kinase-3 (GSK-3), serves as a peptide substrate effective in the affinity purification of protein-serine kinases.
T38168	S.pombe lumazine synthase-IN-1
	S.pombe lumazine synthase-IN-1 is an inhibitor of lumazine synthases with Ki values of 243 μM and 9.6 μM for Schizosaccharomyces pombe and Mycobacterium tuberculosis lumazine synthases, respectively[1]. [1]. Arindam Talukdar, et al. Discovery and Development of a Small Molecule Library With Lumazine Synthase Inhibitory Activity. J Org Chem. 2009 Aug 7;74(15):5123-34.
T75397	Hyaluronan synthase (PmHAS)
	Hyaluronan synthase (PmHAS)为膜蛋白，依赖Mg+2及两种糖-UDP底物（GlcUA-UDP与GlcNAc-UDP）合成HA链。该酶负责透明质酸(HA)的生物合成。
T62475	Chitin synthase inhibitor 7
	Chitin synthase inhibitor 7 (compound 9c) 是一种 chitin synthase (CHS) 的有效抑制剂 (IC50: 0.37 nM)。Chitin synthase inhibitor 7 对耐药真菌具有广谱抗真菌作用。Chitin synthase inhibitor 7 能够用于研究真菌感染。
T79481	Chitin synthase inhibitor 13
	Chitin synthase inhibitor 13 (compound 12g) 为非竞争性几丁质合酶抑制剂，其IC50为106.7 μM，展现出广谱抗真菌活性。
T61649	ATP synthase inhibitor 2
	ATP synthase inhibitor2 是一个铜绿假单胞菌 (PA)ATP synthase 抑制剂 (IC50=10 μg/mL)，在 128 μg/mL 时可完全抑制铜绿假单胞菌 (PA) 的 ATP 合成活性。
T61398	Chitin synthase inhibitor 3
	Chitin synthase inhibitor 3 (compound 2d) 是一种高效的chitin synthase抑制剂，具有0.16 mM的IC50值，并对candida albicans显示出1 μg/mL的MIC，表现出抗真菌活性。
T62701	Dihydropteroate synthase-IN-1
	Dihydropteroate synthase-IN-1 (compound 5g) 是一种dihydropteroate synthase (DHPS) 的有效抑制剂，对细胞色素 P450 具有抑制作用。Dihydropteroate synthase-IN-1 具有抗微生物活性和抗真菌作用。Dihydropteroate synthase-IN-1 能够用作放射诊断影像材料。
T62738	Chitin synthase inhibitor 6
	Chitin synthase inhibitor 6 (compound 9b) 是一种 chitin synthase (CHS) 的有效抑制剂 (IC50: 0.21 mM)。Chitin synthase inhibitor 6 对耐药真菌表现出广谱抗真菌效果，能够用于研究真菌感染。
T62246	Chitin synthase inhibitor 8
	Chitin synthase inhibitor 8 是一种 chitin synthase (CHS) 抑制剂，具有广谱抗真菌作用，能够用于真菌感染相关研究。
T62664	Glucosylceramide synthase-IN-2
	Glucosylceramide synthase-IN-2 (compound T-690) 是一种有效的、具有血脑屏障通透性的、口服具有活力的 glucosylceramide synthase (GCS) 抑制剂，作用于人 GCS (IC50: 15 nM) 和小鼠 GCS (IC50: 190 nM)。Glucosylceramide synthase-IN-2 能够非竞争性抑制 C8 神经酰胺和 UDP 葡萄糖。Glucosylceramide synthase-IN-2 能够用于研究戈谢病。
T63353	Chitin synthase inhibitor 11
	Chitin synthase inhibitor 11 是一种高效的几丁质合酶 (CHS) 抑制剂，能够明显抑制 CHS 的活性 (IC50: 0.10 mM)，具有广谱体外抑菌作用。Chitin synthase inhibitor 11 能够用于研究侵袭性真菌感染 (IFIs)。
T81109	Squalene synthase-IN-1
	Squalene synthase-IN-1（compound 1）是一种通过抑制Squalene Synthase来发挥降血脂作用的有效药物。该化合物也展现了卓越的抗氧化和抗炎特性，能显著降低葡萄糖水平和氧化应激，且不引起毒性。
T62068	Chitin synthase inhibitor 1
	Chitin synthase inhibitor 1 是有效的、选择性的几丁质合酶 (CHS) 抑制剂，IC50值为0.12 mM。Chitin synthase inhibitor 1 强效抑制耐药真菌变体。
T63392	Chitin synthase inhibitor 5
	Chitin synthase inhibitor 5 是一种几丁质合成酶的抑制剂 (IC50: 0.14 mM)。Chitin synthase inhibitor 5 表现出广谱的真菌抗活性，能够较好的抑制白色念珠菌、黄曲霉、烟毒念珠菌和新生念珠菌，能够用于研究真菌。
T1866	AT-56	Others; PGE Synthase	Immunology/Inflammation; Others
	AT56 是口服有活性的脂钙蛋白型前列腺素 D 合酶 (L-PGDS) 选择性抑制剂，其IC50=95 μM，Ki=75 μM。它能够特异性地抑制L-PGDS 催化的 PGD2介导的嗜睡或疼痛反应。
TP2195	Nitric Oxide Synthase (599-613) Blocking Peptide, Bovine Endothelial Cell	Others	Others
	Nitric Oxide Synthase (599-613) Blocking Peptide, Bovine Endothelial Cell (Ac-Pro-Tyr-Asn-Ser-Ser-Pro-Arg-Pro-Glu-Gln-His-Lys-Ser-Tyr-Lys-Cys) is a peptide that inhibits the function of NOSs as a result it blocks the production of NO. Because of the invol
T63077	Chitin synthase inhibitor 12
	Chitin synthase inhibitor 12 是一种几丁质合酶 (CHS) 抑制剂，具有优异的 CHS 抑制作用 (IC50: 0.16 mM)。Chitin synthase inhibitor 12 也是一种广谱抗真菌剂，对耐药真菌变体（如 C. albicans、C. neoformans）具有抗性。Chitin synthase inhibitor 12 能够用于研究侵袭性真菌感染 (IFIs)。
T61632	Glucosylceramide synthase-IN-3
	Glucosylceramide synthase-IN-3 (compound BZ1) is a highly potent, brain-penetrant, and orally active inhibitor of glucosylceramide synthase (GCS), exhibiting an IC50 value of 16 nM for human GCS. This compound, designated as Glucosylceramide synthase-IN-3, finds potential applications in Gaucher's disease research [1] [2].
T62898	Glucosylceramide synthase-IN-1
	Glucosylceramide synthase-IN-1 (T-036) 是一种有效的、口服具有活力的、具有血脑屏障通透性的 glucosylceramide synthase (GCS) 抑制剂，作用于人 GCS (IC50: 31 nM) 和小鼠 GCS (IC50: 51 nM)。Glucosylceramide synthase-IN-1 能够用于研究戈谢病。
T61188	Chitin synthase inhibitor 2
	Chitin synthase inhibitor 2 (compound 2b) is a highly potent inhibitor of chitin synthase, with an IC50 value of 0.09 mM and a K i value of 0.12 mM. This compound exhibits antimicrobial activities in vitro and demonstrates synergistic or additive effects when combined with fluconazole or polyoxin B [1].
T62739	Chitin synthase inhibitor 9
	Chitin synthase inhibitor 9 是一种几丁质合成酶 (chitin synthase, CHS) 抑制剂，表现出广谱抗真菌效果。Chitin synthase inhibitor 9 能够用于进行真菌感染相关研究。
T78886	Chitin synthase inhibitor 14
	Chitin synthase inhibitor 14 (compound 4n)，一种CHS抑制剂，展现出优异的抗真菌活性和对耐药真菌变异的有效抗性。
T74956	Chitin synthase inhibitor 10
	Chitin synthase inhibitor 10为一种高效的几丁质合酶(CHS)抑制剂，具有0.11 mM的IC50，表现出显著的CHS抑制活性。作为抗真菌剂，该化合物对包括C. albicans和C. neoformans在内的耐药真菌变体有效，适合用于侵袭性真菌感染(IFI)研究。
T9987	GSK3-IN-1	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	GSK3-IN-1是一种 GSK3B-糖原合酶激酶3β抑制剂。
T60877	Mtb ATP synthase-IN-1
	Mtb ATP synthase-IN-1 (compound 6ab) 可用于研究抗结核分枝杆菌。Mtb ATP synthase-IN-1 具有低细胞毒性 (Vero IC50> 64 μg/mL)和可接受的口服生物利用度，具有良好的代谢稳定性。Mtb ATP synthase-IN-1 是结核分枝杆菌 (Mtb) ATP 合成酶的有效抑制剂（MIC 值为 0.452 ~ 0.499 μg/mL）。
T79004	ATP synthase inhibitor 2 TFA
	ATP synthase inhibitor2 (Compound 22) TFA 为针对铜绿假单胞菌 (PA) ATP synthase 的抑制剂，具IC50值为10 μg/mL，在浓度达到128 μg/mL 时能够全面阻断铜绿假单胞菌 (PA) ATP的合成活性。
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。
T1965	Bikinin Abrasin	Others; GSK-3	Others; PI3K/Akt/mTOR signaling; Stem Cells
	Bikinin (Abrasin) 是一种非甾体类的，ATP 竞争性的，植物性 GSK-3/Shaggy-like kinases 抑制剂，可激活 BR 信号通路。
T61598	Polyketide synthase 13-IN-2
	Polyketide synthase 13-IN-2 (comp 42) is a potent inhibitor of polyketide synthase 13 in Mycobacterium tuberculosis. It demonstrates a minimum inhibitory concentration (MIC) of 0.25 μg/mL [1].
T10202	A 1070722	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	A 1070722 是高效的糖原合成酶激酶 3 (GSK-3)选择性抑制剂，与 GSK-3α 和 GSK-3β 结合的Ki 为 0.6 nM。A 1070722 可以穿透血脑屏障并在脑区积聚，具有作为PET 放射性跟踪剂定量测定脑部 GSK-3的潜力。
T1741	AZD1080	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	AZD1080 是一种选择性GSK3抑制剂。它抑制重组人GSK3α和GSK3β，pKi(IC50) 分别为 8.2 (6.9 nM) 和 7.5 (31 nM)。
T5843L	(S)-Flurbiprofen esflurbiprofen,(S)-氟比洛芬	COX; PGE Synthase	Immunology/Inflammation; Neuroscience
	Esflurbiprofen 是 Flurbiprofen 的活性对映体，是 COX-1 和 COX-2 的抑制剂，对 COX-1和 COX-2的 IC50分别为0.48 和 0.47 μM。
T2166	TWS119	GSK-3; Autophagy	Autophagy; PI3K/Akt/mTOR signaling; Stem Cells
	TWS119 是一种GSK-3β特异性抑制剂，IC50值为 30 nM，它可激活 wnt/β-catenin 信号通路，能够诱导神经元分化。
T2261	IM-12 IM 12	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	IM-12 是一种 GSK-3β的抑制剂，其 IC50=53 nM，可提高 Wnt 信号传导。
T3077	SB 216763 SB216763	GSK-3; Autophagy	Autophagy; PI3K/Akt/mTOR signaling; Stem Cells
	SB 216763 (SB216763) 是一种选择性和ATP 竞争性的GSK-3α/β抑制剂，IC50为34.3 nM。
T14066	9-ING-41	Apoptosis; GSK-3; Autophagy	Apoptosis; Autophagy; PI3K/Akt/mTOR signaling; Stem Cells
	9-ING-41 是基于马来酰亚胺的 ATP 竞争性和选择性的糖原合酶激酶-3β 抑制剂，IC50为 0.71 μM。它显著导致癌细胞的细胞周期停滞，自噬和凋亡，具有增强化疗药物抗肿瘤作用的潜力，有抗癌活性。
T5956	VP3.15 dihydrobromide	GSK-3; PDE	Metabolism; PI3K/Akt/mTOR signaling; Stem Cells
	VP3.15 dihydrobromide 是一种口服具有活力的、高效的、CNS 可渗透的PDE7-GSK3双重抑制剂，对 PDE7 和 GSK3 作用的IC50值分别为 1.59 μM 和 0.88 μM。它具有神经保护和神经修复作用，可用于研究多发性硬化症 (MS) 潜在的抗炎和促髓鞘再生联合。
T1957	AZD2858	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	AZD2858 是具有口服活性的GSK-3抑制剂，可以抑制 GSK-3α (IC50:0.9 nM) 和 GSK-3β (IC50:5 nM) 的活性，可用于骨折愈合的研究。
T9213	G140	cGAS	Immunology/Inflammation
	G140 是选择性环状GMP-AMP 合酶抑制剂，具有抗炎活性，对 h-cGAS 和 m-cGAS 的IC50值分别为 14.0 和 442 nM。
T61784	GlcN-6-P Synthase-IN-1
	GlcN-6-P Synthase-IN-1 (Compound 4d) is a potent inhibitor of Glucosamine-6-phosphate (GlcN-6-P) synthase, with an IC50 of 3.47 μM. This compound demonstrates remarkable antimicrobial activity and exhibits excellent penetration in the central nervous system. Additionally, GlcN-6-P Synthase-IN-1 is capable of inhibiting cytochrome P450, specifically the CYP3A4 isoform [1].
T9611	PF-04802367	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	PF-04802367是 GSK-3高选择性抑制剂，对 GSK-3β酶的 IC50为 2.1 nM。它抑制两种 GSK-3 亚型（GSK-3α和GSK-3β）效果差不多，IC50值分别为 10.0 和 9.0 nM。它具有理想的中枢神经系统特性和效力。
T1755	LY2090314	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	LY2090314 是GSK-3抑制剂，抑制 GSK-3α (IC50:1.5 nM) 和 GSK-3β (IC50:0.9 nM)。
T15373	Gboxin	ATPase; Mitochondrial Metabolism	Membrane transporter/Ion channel; Metabolism
	Gboxin 是一种氧化磷酸化抑制剂，可靶向抑制胶质母细胞瘤生长，还抑制 F0F1 ATP 合成，具有抗肿瘤活性。

化合物

ATP synthase inhibitor 1

Cat.No: T10404

Target: ATPase

Ac-CoA Synthase Inhibitor1

Cat.No: T4380

Synonym: ACSS2 inhibitor

Target: RSV, Fatty Acid Synthase

Prostaglandin G/H synthase 1 inhibitor

Cat.No: T27066

Synonym: CP74006,CP 74006,2-Amino-N-(4-chlorophenyl)benzamide

Target: Others

Chitin synthase inhibitor 4

Cat.No: T61147

Target: Antibiotic

Polyketide synthase 13-IN-1

Cat.No: T39883

Polyketide synthase 13-IN-3

Cat.No: T39693

Phospho-Glycogen Synthase Peptide-2(substrate)

Cat.No: T40945

S.pombe lumazine synthase-IN-1

Cat.No: T38168

Hyaluronan synthase (PmHAS)

Cat.No: T75397

Chitin synthase inhibitor 7

Cat.No: T62475

Chitin synthase inhibitor 13

Cat.No: T79481

ATP synthase inhibitor 2

Cat.No: T61649

Chitin synthase inhibitor 3

Cat.No: T61398

Dihydropteroate synthase-IN-1

Cat.No: T62701

Chitin synthase inhibitor 6

Cat.No: T62738

Chitin synthase inhibitor 8

Cat.No: T62246

Glucosylceramide synthase-IN-2

Cat.No: T62664

Chitin synthase inhibitor 11

Cat.No: T63353

Squalene synthase-IN-1

Cat.No: T81109

Chitin synthase inhibitor 1

Cat.No: T62068

Chitin synthase inhibitor 5

Cat.No: T63392

Cat.No: T1866

Target: Others, PGE Synthase

Nitric Oxide Synthase (599-613) Blocking Peptide, Bovine Endothelial Cell

Cat.No: TP2195

Target: Others

Chitin synthase inhibitor 12

Cat.No: T63077

Glucosylceramide synthase-IN-3

Cat.No: T61632

Glucosylceramide synthase-IN-1

Cat.No: T62898

Chitin synthase inhibitor 2

Cat.No: T61188

Chitin synthase inhibitor 9

Cat.No: T62739

Chitin synthase inhibitor 14

Cat.No: T78886

Chitin synthase inhibitor 10

Cat.No: T74956

Cat.No: T9987

Target: GSK-3

Mtb ATP synthase-IN-1

Cat.No: T60877

ATP synthase inhibitor 2 TFA

Cat.No: T79004

Cat.No: T2681

Target: PGE Synthase

Cat.No: T1965

Synonym: Abrasin

Target: Others, GSK-3

Polyketide synthase 13-IN-2

Cat.No: T61598

Cat.No: T10202

Target: GSK-3

Cat.No: T1741

Target: GSK-3

(S)-Flurbiprofen

Cat.No: T5843L

Synonym: esflurbiprofen,(S)-氟比洛芬

Target: COX, PGE Synthase

Cat.No: T2166

Target: GSK-3, Autophagy

Cat.No: T2261

Synonym: IM 12

Target: GSK-3

Cat.No: T3077

Synonym: SB216763

Target: GSK-3, Autophagy

Cat.No: T14066

Target: Apoptosis, GSK-3, Autophagy

VP3.15 dihydrobromide

Cat.No: T5956

Target: GSK-3, PDE

Cat.No: T1957

Target: GSK-3

Cat.No: T9213

Target: cGAS

GlcN-6-P Synthase-IN-1

Cat.No: T61784

Cat.No: T9611

Target: GSK-3

Cat.No: T1755

Target: GSK-3

Cat.No: T15373

Target: ATPase, Mitochondrial Metabolism

Cat. No.	Product Name	Target	Signaling Pathways
T2S2335	Dehydroevodiamine DHED,去氢吴茱萸碱	Others; NF-κB; COX; PGE Synthase; NO Synthase	Immunology/Inflammation; Neuroscience; NF-κB; Others
	Dehydroevodiamine (DHED) 是从吴茱萸中分离出的一种喹唑啉生物碱，可抑制 LPS 诱导的小鼠巨噬细胞中iNOS、COX-2、PGE2和NF-κB 的表达，对豚鼠心室肌细胞具有抗心律失常作用。
TQ0260	Cerulenin	Antibiotic; Antifungal; Fatty Acid Synthase	Metabolism; Microbiology/Virology
	Cerulenin 是广泛使用的天然脂肪酸合成酶抑制剂。它是由真菌Cephalosporium caeruleus 产生的。它抑制拓扑异构酶I 催化活性并增强 SN-38 诱导的细胞凋亡。它具有抗真菌和抗肿瘤活性。
T5681	ETHYL CAFFEATE 咖啡酸乙酯,ETHYL 3,4-DIHYDROXYCINNAMATE	NF-κB; COX; PGE Synthase; NO Synthase	Immunology/Inflammation; Neuroscience; NF-κB
	Ethyl Caffeate (ETHYL 3,4-DIHYDROXYCINNAMATE) 是从鬼针草分离的一种酚类天然产物，在体外或在小鼠皮肤中抑制NF-κB 活化及其下游炎症介质的诱导型一氧化氮合酶、环氧合酶 2 和前列腺素 E2。
TQ0301	Kuwanon A	NO Synthase	Immunology/Inflammation
	Kuwanon A 抑制一氧化氮的产生 (IC50: 10.5 μM)。Kuwanon A 是从桑树 (Morus alba L.) 中分离出来的黄酮衍生物。
T6S1665	Irisflorentin	Others; NO Synthase	Immunology/Inflammation; Others
	Irisflorentin 是天然存在的异黄酮，是大量存在于 Rhizoma Belamcandae 中的活性成分。它明显抑制了诱导型一氧化氮合酶的转录和翻译以及 NO 产生。
T4S0227	Sinensetin Pedalitin permethyl ether,甜橙素	TNF; PGE Synthase	Apoptosis; Immunology/Inflammation
	Sinensetin (Pedalitin permethyl ether) 是从水果中发现的一种甲基化黄酮，有很强的抗血管和抗炎症的能力。
T6S2023	Harpagoside	Others; COX; NO Synthase	Immunology/Inflammation; Neuroscience; Others
	Harpagoside 是从爪钩草中分离出来的一种天然产物，可抑制COX-1和COX-2活性，并抑制 NO 的产生。
T5727	CAFESTOL 咖啡醇,咖啡油醇	ERK; NF-κB; COX; PGE Synthase	Immunology/Inflammation; MAPK; Neuroscience; NF-κB
	Cafestol 是咖啡特有的一种二萜，可靶向 AP-1 抑制ERK，有化学预防、抗肿瘤、保肝、抗氧化和抗炎作用。它通过抑制NF-kB 活化途径强烈的抑制 PGE2的产生，还抑制 LGE 激活的 RAW264.7 细胞中的PGE2产生和环氧合酶(COX-2)的 mRNA 表达。
T7682	Asymmetric dimethylarginine	Endogenous Metabolite; NO Synthase; NOD	Immunology/Inflammation; Metabolism; NF-κB
	Asymmetric dimethylarginine 是内源性一氧化氮合成酶抑制剂，可以作为内皮功能障碍的标志。
T2824	Pedunculoside	Others; Fatty Acid Synthase	Metabolism; Others
	Pedunculoside 是从 Ilex rotunda Thunb 中提取的，通过对脂质形成和脂肪酸 β-氧化的调节而发挥降脂作用。
T3847	Asperuloside Asperulosid,车叶草苷	Others; NO Synthase	Immunology/Inflammation; Others
	Asperuloside (Asperulosid) 是一种来源于蛇舌草的环烯醚萜，具有抗炎作用。它可抑制诱导型一氧化氮合酶，抑制 NF-κB 和 MAPK 信号通路。
T2S0765	Epibetulinic acid	NO Synthase; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation
	Epibetulinic acid 对细菌内毒素刺激的小鼠巨噬细胞 (RAW 264.7) 中 NO 和前列腺素 E(2) 的产生具有有效的抑制作用，IC50分别为 0.7 和 0.6 μM，具有抗炎活性。
T5838	L-Canavanine sulfate	NO Synthase; NOD	Immunology/Inflammation; NF-κB
	L-Canavanine sulfate 是一种诱导型 NO 合酶的选择性抑制剂。
TN6772	Malabaricone C	Others	Others
	Malabaricone C 是天然的鞘磷脂合成酶抑制剂，对 SMS 1 和 SMS 2 的IC50分别为 3 和 1.5 μM。
T5S0285	Cistanoside A 肉苁蓉苷 A,肉苁蓉苷A	Others	Others
	Cistanoside A 是一种肉苁蓉中的苯丙素类化合物，能够抑制 NO 的聚集，但不影响诱导型一氧化氮合酶 iNOS 的 mRNA 和蛋白水平及其活性。它具有抗炎作用。
T5S0246	Pseudoprotodioscin 山药	Others; Fatty Acid Synthase	Metabolism; Others
	Pseudoprotodioscin 是一种呋喃葡糖苷，抑制SREBP1/2和microRNA 33a/b 水平，降低胆固醇和甘油三酯合成相关的基因表达。
T4808	Agmatine sulfate Agmatine sulfate salt,硫酸胍基丁胺	Endogenous Metabolite; NO Synthase; Imidazoline Receptor	Immunology/Inflammation; Metabolism; Neuroscience
	Agmatine sulfate (Agmatine sulfate salt) 是咪唑啉受体的内源性激动剂和一氧化氮合酶抑制剂。它靶向神经递质系统，离子通道和一氧化氮合成。
T6323	Oligomycin A MCH 32,寡霉素A	ATPase; Antibiotic; Antifungal	Membrane transporter/Ion channel; Microbiology/Virology
	Oligomycin A (MCH 32) 是从链霉菌属中得到的一种线粒体F0F1-ATPase 抑制剂，抑制氧化磷酸化和线粒体偶联膜上发生的所有 ATP 依赖性过程。
TJS0387	Desoxyrhaponticin 去氧土大黄苷,Deoxyrhapontin,脱氧土大黄苷,Deoxyrhaponticin	Apoptosis; Fatty Acid Synthase	Apoptosis; Metabolism
	Desoxyrhaponticin (Deoxyrhaponticin) 是来自西藏营养食品唐古特大黄中的一种二苯乙烯苷。它是脂肪酸合成酶抑制剂，抑制细胞内 FAS 活性，下调人乳腺癌 MCF-7细胞中 FAS 的表达。它是控制糖尿病餐后高血糖的潜在药物。
T2980	Chondroitin sulfate Chonsurid,Chondroitin polysulfate,硫酸软骨素	MMP; Others; Endogenous Metabolite; NO Synthase	Immunology/Inflammation; Metabolism; Others; Proteases/Proteasome
	Chondroitin sulfate (Chonsurid) 是一种糖胺聚糖，被广泛用于骨关节炎的研究。它能够减少炎症介质和凋亡过程，并能够减少炎性细胞因子，iNOS 和MMPs 产生。
TN2139	Regaloside B 鸦胆子苦醇,王百合苷 B	NOS; COX; NO Synthase	Immunology/Inflammation; Neuroscience
	Regaloside B 是从麝香百合中分离出来的一种苯丙烷，可抑制iNOS 和COX-2的表达，具有抗炎活性。
T7597	6-Biopterin L-生物喋呤,L-Biopterin	Endogenous Metabolite; NO Synthase; NOD	Immunology/Inflammation; Metabolism; NF-κB
	6-Biopterin (L-Biopterin) 是一种蝶呤衍生物，是一氧化氮合酶 (NO synthase) 辅因子。
T2791	Pectolinarin 柳穿鱼叶苷,大蓟苷	Apoptosis; Others; NO Synthase; Prostaglandin Receptor; Interleukin	Apoptosis; GPCR/G Protein; Immunology/Inflammation; Others
	Pectolinarin 抑制 IL-6和 IL-8分泌以及 PGE2和 NO 产生，可通过抑制 PI3K/Akt 途径来抑制细胞增殖和炎症反应并诱导凋亡，具有抗炎活性。
T3121	Betulin Trochol,betulinic alcohol,betuline,betulinol,桦木醇,Betulol,白桦脂醇	Apoptosis; Endogenous Metabolite; Lipid; Fatty Acid Synthase	Apoptosis; Metabolism
	Betulin (betulinol) 是从桦树树皮中分离出来的一种天然三萜，是 SREBP 抑制剂。
T3S0364	L-Arginine L-精氨酸,L-Arg,(S)-(+)-Arginine	IL Receptor; Endogenous Metabolite; NO Synthase	Immunology/Inflammation; Metabolism
	L-Arginine (L-Arg) 是内皮型一氧化氮合酶(eNOS) 的底物。L-Arginine 通过阳离子氨基酸转运体家族转运到血管平滑肌细胞，并被代谢成一氧化氮、多胺或 L-脯氨酸。
T1310	2-Thiouracil Thiouracil,硫代由雪,Deracil,2-硫脲嘧啶	Thyroid hormone receptor(THR); NO Synthase	Endocrinology/Hormones; Immunology/Inflammation
	2-Thiouracil (Deracil) 是神经型一氧化氮合酶 (nNOS) 的选择性抑制剂(Ki:20 μM)，是一种抗甲状腺化合物，可用作高度特异性的黑色素瘤探测物。
TN1373	α-Humulene Alpha-caryophyllene,ALPHA-律草烯	TNF; NOS; COX	Apoptosis; Immunology/Inflammation; Neuroscience
	α-Humulene (Alpha-caryophyllene) 是 Tanacetum vulgareL. 精油的主要成分，显示出抗炎作用，IC50=15±2 μg/mL。它抑制 iNOS 和COX-2表达。
T7030	anemarsaponin B 知母皂苷B,知母皂苷 B	p38 MAPK; NF-κB; MEK; COX; NO Synthase	Immunology/Inflammation; MAPK; Neuroscience; NF-κB
	Anemarsaponin B 是一种甾体皂苷，可降低iNOS 和COX-2的蛋白和 mRNA 水平，减少促炎细胞因子的表达和产生。它通过阻断 IκBα 的磷酸化来抑制NF-κB 的 p65 亚基的核转位，还抑制 MAP 激酶激酶 3/6 (MKK3/6) 和混合谱系激酶 3 的磷酸化。
T5684	Ethyl 3,4-dihydroxybenzoate	Apoptosis; Others; Reactive Oxygen Species; HIF/HIF Prolyl-Hydroxylase; NO Synthase; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; NF-κB; Others
	Ethyl 3,4-dihydroxybenzoate 是从花生种子的种皮中发现的脯氨酰羟化酶抑制剂，是一种抗氧化剂。它是胶原蛋白合成抑制剂，具有骨骼保护作用。它通过激活 NO 合酶并产生线粒体 ROS 来保护心肌，可诱导 ESCC 细胞自噬和凋亡。
T3322	trans-Chalcone Chalcone,反-查耳酮,查尔酮,Cinnamophenone,Chalkone	Apoptosis; Others; Antifungal; Fatty Acid Synthase	Apoptosis; Metabolism; Microbiology/Virology; Others
	trans-Chalcone (Chalkone) 是从 Aronia melanocarpa 果皮中分离出来的一种天然产物，是类黄酮前体的双酚核心结构。它是脂肪酸合酶和 α-淀粉酶的抑制剂，具有抗真菌和抗癌活性。
T7786	Tryptanthrin	DNA gyrase	DNA Damage/DNA Repair
	Tryptanthrin 是一种口服具有活性的细胞内Leukotriene (LT) biosynthesis 抑制剂。它能够降低大鼠胸膜炎模型中的 LTB4 水平，并抑制人全血中Leukotriene 的形成 (IC50= 10 µM)。
T3918	Ginsenoside Rb3 人参皂苷 Rb3,Gypenoside IV,人参皂苷Rb3	NF-κB; COX; NO Synthase	Immunology/Inflammation; Neuroscience; NF-κB
	Ginsenoside Rb3 (Gypenoside IV) 是从三七中提取的一种天然产物。它在 293T 细胞系中抑制 TNFα 诱导的NF-κB 转录活性，IC50为 8.2 μM。它还抑制COX-2和iNOSmRNA 的诱导。
T4S1173	Agrimol B 仙鹤草酚B,仙鹤草酚 B	Sirtuin; PPAR	Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism
	Agrimol B 是从仙鹤草中分离得到的一种多酚衍生物，可抑制脂肪形成，降低PPARγ的表达，诱导SIRT1易位和表达。
T0983	Penicillamine 青霉胺,d-penicillamin,Dimethyl Cysteine,D-青霉胺,Artamine,D-(-)-Penicillamine	Antibiotic	Microbiology/Virology
	Penicillamine (Artamine) 是一种 penicillin 的代谢降解产物，是一种螯合剂，可作用于威尔逊氏病。
T3811	Ginsenoside C-K 20(S)-人参皂苷 C-K,Ginsenoside compound K,Ginsenoside K,人参皂苷 C-K	P450; cell cycle arrest; COX; NO Synthase	Cell Cycle/Checkpoint; Immunology/Inflammation; Metabolism; Neuroscience
	Ginsenoside C-K (Ginsenoside K) 是 Ginsenoside Rb1 的细菌代谢物，可通过抑制诱生型一氧化氮合酶和COX-2来发挥抗炎作用。它在人肝微粒体中抑制CYP2C9和CYP2A6活性，IC50分别为 32.0±3.6 和 63.6±4.2 μM。
T3779	Crocin II Crocin 2,西红花苷II,Crocetin gentiobiosylglucosyl ester,藏红花,Tricrocin,Crocin B	Caspase; COX; NO Synthase	Apoptosis; Immunology/Inflammation; Neuroscience; Proteases/Proteasome
	Crocin II (Crocetin gentiobiosylglucosyl ester) 是从栀子果实中分离出来的一种天然产物，具有抗氧化、抗癌和抗抑郁活性。它抑制 iNOS 和 COX-2的蛋白质和 m-RNA 的表达，还抑制NO 产生，IC50值为 31.1 μM。
T3805	Prim-O-glucosylcimifugin 升麻苷,Cimifugin beta-D-glucopyranoside,Cimifugin 7-glucoside	TNF; COX; JAK; NO Synthase	Angiogenesis; Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Stem Cells
	Prim-O-glucosylcimifugin (Cimifugin 7-glucoside) 具有强效的抗炎作用。通过调节 JAK2/STAT3 信号传导可抑制iNOS 和COX-2表达。
T3S0401	Piceatannol 3'-O-glucoside 白皮杉醇 3'-O-葡萄糖苷,Piceatannol 3-glycoside,Quzhaqigan,曲札茋苷、白皮杉醇-3'-O-葡萄糖苷	Arginase; NO Synthase	Immunology/Inflammation
	Piceatannol 3'-O-glucoside (Piceatannol 3-glycoside) 是大黄的一种活性成分，通过抑制精氨酸酶活性激活内皮细胞一氧化氮合酶，抑制Arginase I 和Arginase II，IC50值分别为 11.22 和 11.06 μM。它可增加肺血氧分压，减少肺间质水肿，从而保护肺损伤。
T3324	Lycorine Galanthidine,Narcissine,石蒜碱,Amarylline,Belamarine,Licorine,番石榴碱	Apoptosis; Virus Protease; Antibacterial; AChR; Fatty Acid Synthase	Apoptosis; Metabolism; Microbiology/Virology; Neuroscience
	Lycorine (Narcissine) 是从金眼科植物科中提取的一种天然生物碱。它是一种具有口服活性的SCAP 抑制剂，Kd 值 15.24 nM。它也是黑色素瘤血管生成抑制剂，有用于前列腺癌和代谢疾病的研究潜力。
T2758	Madecassic acid 6-Deoxy-L-Galactose,羟基积雪草酸,L-Fucose,Brahmic acid,L-fucopyranose	Others; TNF; COX; NO Synthase; Interleukin	Apoptosis; Immunology/Inflammation; Neuroscience; Others
	Madecassic acid (L-fucopyranose) 是分离自积雪草的一种天然产物，抑制iNOS、COX-2、TNF-α、IL-1beta 和IL-6，可通过在 RAW 264.7 巨噬细胞中下调NF-κB 激活而具有抗炎作用。
T5S0754	Isoquercetin 3-Glucosylquercetin,Hirsutrin,Isoquercitrin,异槲皮苷,Quercetin 3-o-glucopyranoside,槲皮素-3-葡萄糖苷	NF-κB; Wnt/beta-catenin; NO Synthase	Cytoskeletal Signaling; Immunology/Inflammation; NF-κB; Stem Cells
	Isoquercetin (3-Glucosylquercetin) 是天然存在的多酚，具有抗氧化，抗增殖和抗炎特性。它通过调节核因子-κB 转录调节系统调节一氧化氮合酶 2 的表达。它通过 Nrf2/ARE 抗氧化剂信号传导途径减轻乙醇诱导的肝毒性，氧化应激和炎症反应。它具有高生物利用度和低毒性，是预防糖尿病妊娠出生缺陷的有希望的候选药物。
T0670	L-Arginine hydrochloride (S)-(+)-Arginine hydrochloride,左旋精氨酸单盐酸盐,L-Arginine HCl (L-Arg),L-arginine monohydrochloride	Amino Acids and Derivatives; Endogenous Metabolite; NO Synthase	Immunology/Inflammation; Metabolism
	L-Arginine hydrochloride 为合成一氧化氮的氮供体，是血管扩张剂。
T4S1421	Praeruptorin B Praeruptorin D,(+)-川白芷内酯	NPC1L1; Fatty Acid Synthase	Membrane transporter/Ion channel; Metabolism
	Praeruptorin B 是一种固醇调控元件结合蛋白(SREBPs)的抑制剂。
TN1102	Physalin L 酸浆苦味素L,酸浆苦味素 L	Others; NO Synthase	Immunology/Inflammation; Others
	Physalin L 抑制巨噬细胞中 LPS 诱导的 NO 生成，平均抑制率是 70.97%。它具有抗炎作用。
TN1109	3-O-Acetyl-16α-hydroxydehydrotrametenolic acid 3-O-Acetyl-16 alpha-hydroxydehydrotrametenolic acid,3-O-乙酰基-16Α-羟基松苓新酸	NOS; NO Synthase; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation
	3-O-Acetyl-16α-hydroxydehydrotrametenolic acid (3-O-Acetyl-16 alpha-hydroxydehydrotrametenolic acid) 是三萜类化合物。它能够作用于 LPS 刺激的 Raw264.7 细胞，减少NO 产生和 iNOS 表达，具有消炎作用。
T7344	SDMA NG,NG'-Dimethyl-L-arginine,Symmetric dimethylarginine,对称N,N-二甲基精氨酸	Endogenous Metabolite	Metabolism
	SDMA (Symmetric dimethylarginine) 是一氧化氮 (NO) 合酶的内源性抑制剂。
T9267	Aureobasidin A	Others; Antifungal	Microbiology/Virology; Others
	Aureobasidin A 是一种环肽和抗真菌抗生素。它是肌醇磷酸神经酰胺合酶 AUR1 的抑制剂。
T12039	Miglustat N-Butyldeoxynojirimycin,OGT918,美格鲁特,NB-DNJ,N-丙基脱氧野尻霉素	Others	Others
	Miglustat (NB-DNJ) 是一种葡萄糖神经酰胺合成酶抑制剂，可用于I 型戈谢病。
T5267	N-Acetyl-L-glutamic acid Ac-L-Glu-OH,N-乙酰-L-谷氨酰胺,N-Acetylglutamic acid	Others; Endogenous Metabolite	Metabolism; Others
	N-Acetyl-L-glutamic acid (Ac-L-Glu-OH) 是一种 N-Acyl-L-氨基酸，是动物细胞培养基的组成成分，是一种酿酒酵母和人类的代谢物。
T17056	Tetrahydrobiopterin Sapropterin,BH4,(Rac)-Sapropterin	NOS; Endogenous Metabolite	Immunology/Inflammation; Metabolism
	Tetrahydrobiopterin (BH4) 是芳香族氨基酸羟化酶的辅因子, 也是一氧化氮合酶 (NOS) 的必需辅因子，可用于研究如高血压、高胆固醇血症、糖尿病等内皮功能障碍。
------------------------ 更多 ------------------------

天然产物

Dehydroevodiamine

Cat.No: T2S2335

Synonym: DHED,去氢吴茱萸碱

Target: Others, NF-κB, COX, PGE Synthase, NO Synthase

Cat.No: TQ0260

Target: Antibiotic, Antifungal, Fatty Acid Synthase

Cat.No: T5681

Synonym: 咖啡酸乙酯,ETHYL 3,4-DIHYDROXYCINNAMATE

Target: NF-κB, COX, PGE Synthase, NO Synthase

Cat.No: TQ0301

Target: NO Synthase

Cat.No: T6S1665

Target: Others, NO Synthase

Cat.No: T4S0227

Synonym: Pedalitin permethyl ether,甜橙素

Target: TNF, PGE Synthase

Cat.No: T6S2023

Target: Others, COX, NO Synthase

Cat.No: T5727

Synonym: 咖啡醇,咖啡油醇

Target: ERK, NF-κB, COX, PGE Synthase

Asymmetric dimethylarginine

Cat.No: T7682

Target: Endogenous Metabolite, NO Synthase, NOD

Cat.No: T2824

Target: Others, Fatty Acid Synthase

Cat.No: T3847

Synonym: Asperulosid,车叶草苷

Target: Others, NO Synthase

Epibetulinic acid

Cat.No: T2S0765

Target: NO Synthase, Prostaglandin Receptor

L-Canavanine sulfate

Cat.No: T5838

Target: NO Synthase, NOD

Cat.No: TN6772

Target: Others

Cat.No: T5S0285

Synonym: 肉苁蓉苷 A,肉苁蓉苷A

Target: Others

Pseudoprotodioscin

Cat.No: T5S0246

Synonym: 山药

Target: Others, Fatty Acid Synthase

Agmatine sulfate

Cat.No: T4808

Synonym: Agmatine sulfate salt,硫酸胍基丁胺

Target: Endogenous Metabolite, NO Synthase, Imidazoline Receptor

Cat.No: T6323

Synonym: MCH 32,寡霉素A

Target: ATPase, Antibiotic, Antifungal

Desoxyrhaponticin

Cat.No: TJS0387

Synonym: 去氧土大黄苷,Deoxyrhapontin,脱氧土大黄苷,Deoxyrhaponticin

Target: Apoptosis, Fatty Acid Synthase

Chondroitin sulfate

Cat.No: T2980

Synonym: Chonsurid,Chondroitin polysulfate,硫酸软骨素

Target: MMP, Others, Endogenous Metabolite, NO Synthase

Cat.No: TN2139

Synonym: 鸦胆子苦醇,王百合苷 B

Target: NOS, COX, NO Synthase

Cat.No: T7597

Synonym: L-生物喋呤,L-Biopterin

Target: Endogenous Metabolite, NO Synthase, NOD

Cat.No: T2791

Synonym: 柳穿鱼叶苷,大蓟苷

Target: Apoptosis, Others, NO Synthase, Prostaglandin Receptor, Interleukin

Cat.No: T3121

Synonym: Trochol,betulinic alcohol,betuline,betulinol,桦木醇,Betulol,白桦脂醇

Target: Apoptosis, Endogenous Metabolite, Lipid, Fatty Acid Synthase

Cat.No: T3S0364

Synonym: L-精氨酸,L-Arg,(S)-(+)-Arginine

Target: IL Receptor, Endogenous Metabolite, NO Synthase

Cat.No: T1310

Synonym: Thiouracil,硫代由雪,Deracil,2-硫脲嘧啶

Target: Thyroid hormone receptor(THR), NO Synthase

Cat.No: TN1373

Synonym: Alpha-caryophyllene,ALPHA-律草烯

Target: TNF, NOS, COX

anemarsaponin B

Cat.No: T7030

Synonym: 知母皂苷B,知母皂苷 B

Target: p38 MAPK, NF-κB, MEK, COX, NO Synthase

Ethyl 3,4-dihydroxybenzoate

Cat.No: T5684

Target: Apoptosis, Others, Reactive Oxygen Species, HIF/HIF Prolyl-Hydroxylase, NO Synthase, Autophagy

Cat.No: T3322

Synonym: Chalcone,反-查耳酮,查尔酮,Cinnamophenone,Chalkone

Target: Apoptosis, Others, Antifungal, Fatty Acid Synthase

Cat.No: T7786

Target: DNA gyrase

Ginsenoside Rb3

Cat.No: T3918

Synonym: 人参皂苷 Rb3,Gypenoside IV,人参皂苷Rb3

Target: NF-κB, COX, NO Synthase

Cat.No: T4S1173

Synonym: 仙鹤草酚B,仙鹤草酚 B

Target: Sirtuin, PPAR

Cat.No: T0983

Synonym: 青霉胺,d-penicillamin,Dimethyl Cysteine,D-青霉胺,Artamine,D-(-)-Penicillamine

Target: Antibiotic

Ginsenoside C-K

Cat.No: T3811

Synonym: 20(S)-人参皂苷 C-K,Ginsenoside compound K,Ginsenoside K,人参皂苷 C-K

Target: P450, cell cycle arrest, COX, NO Synthase

Cat.No: T3779

Synonym: Crocin 2,西红花苷II,Crocetin gentiobiosylglucosyl ester,藏红花,Tricrocin,Crocin B

Target: Caspase, COX, NO Synthase

Prim-O-glucosylcimifugin

Cat.No: T3805

Synonym: 升麻苷,Cimifugin beta-D-glucopyranoside,Cimifugin 7-glucoside

Target: TNF, COX, JAK, NO Synthase

Piceatannol 3'-O-glucoside

Cat.No: T3S0401

Synonym: 白皮杉醇 3'-O-葡萄糖苷,Piceatannol 3-glycoside,Quzhaqigan,曲札茋苷、白皮杉醇-3'-O-葡萄糖苷

Target: Arginase, NO Synthase

Cat.No: T3324

Synonym: Galanthidine,Narcissine,石蒜碱,Amarylline,Belamarine,Licorine,番石榴碱

Target: Apoptosis, Virus Protease, Antibacterial, AChR, Fatty Acid Synthase

Madecassic acid

Cat.No: T2758

Synonym: 6-Deoxy-L-Galactose,羟基积雪草酸,L-Fucose,Brahmic acid,L-fucopyranose

Target: Others, TNF, COX, NO Synthase, Interleukin

Cat.No: T5S0754

Synonym: 3-Glucosylquercetin,Hirsutrin,Isoquercitrin,异槲皮苷,Quercetin 3-o-glucopyranoside,槲皮素-3-葡萄糖苷

Target: NF-κB, Wnt/beta-catenin, NO Synthase

L-Arginine hydrochloride

Cat.No: T0670

Synonym: (S)-(+)-Arginine hydrochloride,左旋精氨酸单盐酸盐,L-Arginine HCl (L-Arg),L-arginine monohydrochloride

Target: Amino Acids and Derivatives, Endogenous Metabolite, NO Synthase

Cat.No: T4S1421

Synonym: Praeruptorin D,(+)-川白芷内酯

Target: NPC1L1, Fatty Acid Synthase

Cat.No: TN1102

Synonym: 酸浆苦味素L,酸浆苦味素 L

Target: Others, NO Synthase

3-O-Acetyl-16α-hydroxydehydrotrametenolic acid

Cat.No: TN1109

Synonym: 3-O-Acetyl-16 alpha-hydroxydehydrotrametenolic acid,3-O-乙酰基-16Α-羟基松苓新酸

Target: NOS, NO Synthase, Prostaglandin Receptor

Cat.No: T7344

Synonym: NG,NG'-Dimethyl-L-arginine,Symmetric dimethylarginine,对称N,N-二甲基精氨酸

Target: Endogenous Metabolite

Cat.No: T9267

Target: Others, Antifungal

Cat.No: T12039

Synonym: N-Butyldeoxynojirimycin,OGT918,美格鲁特,NB-DNJ,N-丙基脱氧野尻霉素

Target: Others

N-Acetyl-L-glutamic acid

Cat.No: T5267

Synonym: Ac-L-Glu-OH,N-乙酰-L-谷氨酰胺,N-Acetylglutamic acid

Target: Others, Endogenous Metabolite

Tetrahydrobiopterin

Cat.No: T17056

Synonym: Sapropterin,BH4,(Rac)-Sapropterin

Target: NOS, Endogenous Metabolite

--------- 更多 ---------

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼