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Search Results for " m. tuberculosis "

74

抑制剂 & 化合物

11

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T38359	Dup-721	Antibacterial	Microbiology/Virology
	DuP-721 是广谱的口服有效的抗菌剂，可以抑制多种临床敏感和耐药细菌，特别是结核杆菌M. tuberculosis。
T8411	C-215	Others	Others
	C-215 是MmpL3抑制剂。它在 HTS 中被鉴定为对结核分枝杆菌具有独立的甘油活性，对哺乳动物细胞的非特异性毒性较低，对结核分枝杆菌的IC90=16 μM，并且能够有效抑制在巨噬细胞中生长的结核分枝杆菌。
T16339	Norverapamil hydrochloride (±)-Norverapamil hydrochloride,D591 hydrochloride,盐酸去甲维拉帕米	Calcium Channel; P-gp; Drug Metabolite	Membrane transporter/Ion channel; Metabolism; Neuroscience
	Norverapamil hydrochloride (D591 hydrochloride) 是 Verapamil 的 N-去甲基代谢物，是 L 型钙通道阻滞剂和 P-糖蛋白 (P-gp) 功能抑制剂。
T5400	Q203 IAP6,Telacebec	Antibacterial; Antibiotic	Microbiology/Virology
	Q203 (Telacebec)是一种中氮杂吡啶酰胺。在培养基中抑制结核分枝杆菌H37Rv 活性的MIC50值为2.7 nM。
T9830	GSK2556286 GSK286	Antibacterial	Microbiology/Virology
	GSK2556286 (GSK286) 是一种具有口服活性的结核分枝杆菌 (M. tuberculosis) 抑制剂。GSK2556286 对人巨噬细胞 (macrophages) 生长具有抑制作用，IC50值为 0.07 μM。GSK2556286对多重耐药 (MDR) 或广泛耐药 (XDR) 和药物敏感 (DS) 结核分枝杆菌均有效。
T25817	Mitonafide NSC-300288,米托萘胺,NSC300288,NSC 300288	Antibacterial	Microbiology/Virology
	Mitonafide (NSC-300288) 抑制 M. tuberculosis NAD+ 依赖性 DNA 连接酶 A 的活性。它是一种 DNA 嵌入剂。
T5997	TBAJ-587	Antibacterial; Antibiotic	Microbiology/Virology
	TBAJ-587 是一种抗结核药物，在 MABA 和 LORA 试验中抑制 M.tb 菌株 H37Rv 的生长，MIC90 分别为 0.006 和 <0.02 µg/mL。它对 M. tuberculosis 具有更有效的活性，并且在 TB 动物模型中具有更好的功效。
T7312	AX20017	Others; Antibacterial	Microbiology/Virology; Others
	AX20017是蛋白激酶G 的一个小分子抑制剂，IC50值为 0.39 μM。
T7342	BM212	Antibacterial	Microbiology/Virology
	BM212 是一种分枝杆菌膜蛋白 MmpL3抑制剂。它抑制结核分枝杆菌和部分非结核分枝杆菌，抗结核杆菌 H37Rv 菌株的 MIC 值为 5 µM。
T0020	Sodium 4-aminosalicylate dihydrate 对氨基水杨酸钠二水合物,Sodium 4-Aminosalicylate,4-Amino-salicylic acid sodium salt	Free radical scavengers; NF-κB; Antibacterial; Antibiotic	Microbiology/Virology; NF-κB; oxidation-reduction
	Sodium 4-aminosalicylate dihydrate (4-Amino-salicylic acid sodium salt) 是一种抗耐药性结核化合物。
T27482	GSK572A	Others	Others
	GSK572A 是一种新型且强效的EchA6强效抑制剂，可用来治疗肺结核。
T4531	GSK2200150A	Antibacterial	Microbiology/Virology
	GSK2200150A 是一种通过高通量筛选活动确定的抗结核剂，对 H37Rv 的 MIC 是 0.38 μM。
T10563	BM635	Others	Others
	BM635 is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).
T60446	LCS3	Apoptosis; Glutathione reductase	Apoptosis; oxidation-reduction
	LCS3是一种可逆和非竞争性的谷胱甘肽二硫化物还原酶（GSR）和硫氧还蛋白还原酶1（TXNRD1）的协同抑制剂，IC50分别为3.3μM 和3.8μM。LCS3具有抗肿瘤活性，可诱导细胞凋亡，可用于研究肺腺癌（LUAD）。
T10563L2	BM635 mesylate (1493762-74-5 free base) BM635 mesylate	Others	Others
	BM635 mesylate is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).
T10563L	BM635 hydrochloride (1493762-74-5 free base) BM635 hydrochloride	Others	Others
	BM635 hydrochloride is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).
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.
T75168	Homo-BacPROTAC7
	Homo-BacPROTAC7 是一个 ClpC1NTDBacPROTAC 降解剂，可以靶向 ClpC2。Homo-BacPROTAC7 能有效杀死 M. tuberculosis。
T27206	DprE1-IN-377790
	DprE1-IN-377790 is a novel DprE1 inhibitor, killing M. tuberculosis.
T38773	LeuRS-IN-1 hydrochloride
	LeuRS-IN-1 hydrochloride is a potent and orally active inhibitor of M. tuberculosis leucyl-tRNA synthetase (M.tb LeuRS). It has IC 50 and Kd values of 0.06 μM and 0.075 μM, respectively, for M.tb LeuRS. Additionally, LeuRS-IN-1 hydrochloride inhibits human cytoplasmic LeuRS with an IC 50 of 38.8 μM and HepG2 protein synthesis with an EC 50 of 19.6 μM.
T29505	A039 A-039,A 039
	A039 is a highly active bactericidal agent against M. tuberculosis.
T68809	Trichomonacid
	Trichomonacid is a novel inhibitor of Mycobacterium marinum MelF (Rv1936), exhibiting bacteriostatic/bactericidal activity against M. marinum and M. tuberculosis in vitro.
T10887	CRS400393	Antibacterial	Microbiology/Virology
	CRS400393 is an effective anti-mycobacterial drug , with MIC of 0.03, 2, and ≤ 0.12 µg/mL against M. abs., M. avium, M. intracellulare, and M. tuberculosis, respectively.
T39109	ML338 ML338
	ML338 is a selective small molecule inhibitor probe specifically targeting non-replicating Mycobacterium tuberculosis bacilli. It exhibits potent activity against non-replicating M. tuberculosis, with IC90 and IC99 values of 1 μM and 4 μM, respectively, as determined by CFU. This compound, ML338, is an invaluable tool for identifying essential functions and vulnerabilities of M. tuberculosis bacilli under nutrient deprivation conditions. Additionally, ML338 is highly useful for studying M. tuber...
T61573	MtTMPK-IN-5
	MtTMPK-IN-5 (compound 17) is a highly effective inhibitor of M. tuberculosis thymidylate kinase (Mtb TMPK), demonstrating remarkable enzyme inhibitory activity with an IC50 value of 34 μM. Additionally, MtTMPK-IN-5 exhibits notable activity against M. tuberculosis, as evidenced by a minimum inhibitory concentration (MIC) of 12.5 μM. Given its potent properties, MtTMPK-IN-5 serves as a valuable tool for tuberculosis research [1].
T69488	CB5255829
	CB5255829 is a novel inhibitor of Mycobacterium marinum MelF (Rv1936), exhibiting bacteriostatic/bactericidal activity against M. marinum and M. tuberculosis in vitro.
T71846	CB6513745
	CB6513745 is a novel inhibitor of Mycobacterium marinum MelF (Rv1936), exhibiting bacteriostatic/bactericidal activity against M. marinum and M. tuberculosis in vitro.
T63755	Antitubercular agent-22
	Antitubercular agent-22 (Compound 2) 是有效的抗念珠菌和抗结核剂，能够作用于 Candida albicansMTCC 3017 (MIC: 2.34 μg/ml) 和 M. tuberculosis(H37Rv) (MIC: 2 μg/ml)。
T61781	MtTMPK-IN-6
	MtTMPK-IN-6 (compound 1) is a highly effective inhibitor (IC 50 = 29 μM) of M. tuberculosis thymidylate kinase (Mtb TMPK). It is a valuable compound for tuberculosis research [1].
T75167	Homo-BacPROTAC6
	Homo-BacPROTAC6 是一个 ClpC1NTDBacPROTAC 降解剂，可以靶向 ClpC2。Homo-BacPROTAC7 能有效杀死M. tuberculosis。
T61303	MmpL3-IN-1
	MmpL3-IN-1, also known as compound 32, is a highly effective inhibitor of Mycobacterial membrane protein large 3 (MmpL3). With an anti-tuberculosis activity exhibiting a minimum inhibitory concentration (MIC) of less than 0.016 μg/mL in M. tuberculosis, MmpL3-IN-1 is a valuable compound for research on drug-resistant tuberculosis [1].
T61520	Antitubercular agent-24
	Antitubercular agent-24 (Compound 1) exhibits anti-tubercular properties against M. tuberculosis H37Rv. It demonstrates an extracellular IC50 of 0.83 μM and an intracellular IC50 of 0.17 μM [1].
T63525	Antitubercular agent-23
	Antitubercular agent-23 是有效的抗念珠菌及抗结核剂，能够作用于 Candida albicansMTCC 3017 (MIC: 1.1 μg/ml) 和 M. tuberculosis(H37Rv) (MIC: 1 μg/ml)。
T40317	α/β-Hydrolase-IN-1
	α/β-Hydrolase-IN-1 demonstrates exceptional potency, with MICs of 50 μM (25 μg/mL) against M. smegmatis and 16 μM (8.4 μg/mL) against M. tuberculosis H37Ra, establishing it as a superior compound in this class.
T28480	Q-203 Ditosylate Q203,Q-203,Q 203
	Q-203 Ditosylate, also known as Q-203, is a mycobacterium tuberculosis protein potentially for the treatment of tuberculosis. The optimized IPA compound Q203 inhibited the growth of MDR and XDR M. tuberculosis clinical isolates in culture broth medium in
T71449	Capreomycin free base
	Capreomycin is a polypeptide antibiotic originally isolated from S. capreolus. It is active against M. tuberculosis (MIC = 10 µg/ml). Capreomycin binds to both the 30S and 50S ribosomal subunits, inhibiting protein synthesis.
T38355	Lariatin A
	Lariatin A is an antimycobacterial lasso peptide originally isolated from R. jostii. It is active against M. tuberculosis and M. smegmatis in vitro (MICs = 0.39 and 0.1 μg/ml, respectively). Lariatin A increases survival in a silkworm model of M. smegmatis infection (ED50 = 0.5 μg/g).
T61170	Antibacterial agent 96
	Antibacterial agent 96 (compound 4k) 是一种有效的抗菌剂。Antibacterial agent 96 对药物敏感和耐多药的结核分枝杆菌 (M.tuberculosis)显示出抗结核活性。Antibacterial agent 96 对 HepG2 和 Vero 细胞有毒性。
T63786	WX-081
	WX-081 是抗结核剂 (anti-tuberculosis)，对 M. tuberculosisH37Rv 表现出明显的抗分枝杆菌效果，并能够作用于药物敏感结核病 (DS-TB) 杆菌 (MIC: 0.083 μg/ml) 和耐多药结核病 (MDR-TB) 菌株 (MIC: 0.11 μg/ml)，对 hERG 通道表现出抑制作用 (IC50: 1.89 μM)。
T72262	Antituberculosis agent-6
	Antituberculosis agent-6 是一种有效的抗结核分枝杆菌 (antimycobacterial) 剂。Antituberculosis agent-6 对M. tuberculosis 显示出显著的抑制活性，MIC 为 3.49 μM。Antituberculosis agent-6 还对A. niger 表现出良好的抗真菌 (antifungal) 活性，MIC 为 62.50 μM。 Antituberculosis agent-6 表现出高胃肠道吸收。
T61665	Antibacterial agent 118
	Antibacterial agent 118 (also known as compound 20) is a potent antimycobacterial compound with activity against various mycobacterial strains, including Mtb H37Ra, M. aurum, M. smegmatis, Mtb H37Rv, and M. avium. The minimum inhibitory concentration (MIC) values for Antibacterial agent 118 against these strains are 40.7 μM, 10.2 μM, 163.0 μM, 62.5 μM, and 62.5 μM, respectively. This compound holds potential for tuberculosis research [1].
T37880	OPC-167832
	OPC-167832 is a potent and orally active dprE1 Inhibitor with an IC50 of 0.258 μM. OPC-167832 has antituberculosis activity and can be used for the research of tuberculosis caused by Mycobacterium tuberculosis[1]. OPC-167832 exhibits very low MICs against laboratory strains of M. tuberculosis H37Rv (MIC: 0.0005 μg/ml) and Kurono (MIC: 0.0005 μg/ml) and strains with monoresistance to rifampin (RIF), isoniazid (INH), ethambutol (EMB), streptomycin (STR), and pyrazinamide (PZA) (MIC: 0.00024-0.001 ...
T72263	Antituberculosis agent-8
	Antituberculosis agent-8 是一种抗结核剂，对M. tuberculosis H37Rv 的 MIC 值为 3.53 μM (1.6 μg/mL)。Antituberculosis agent-8 对A. niger 也显示出良好的抗真菌 (antifungal) 活性，MIC 为 62.50 μM。
T60971	Antitubercular agent-14
	Antitubercular agent-14 (Compound 1) 具有抗结核活性。Antitubercular agent-14 对结核分枝杆菌的 MIC 值为 0.3 μg/mL。
T61772	PknB-IN-1
	PknB-IN-1 (Compound 2) is an inhibitor of protein kinase B (PknB) with a concentration causing 50% inhibition (IC50) of 14.4 μM. This compound demonstrates anti-mycobacterial activity by effectively suppressing the growth of M. tuberculosis H37Rv strain, with a minimum inhibitory concentration (MIC) of 6.2 μg/mL [1].
T36541	Nornidulin
	Nornidulin is a depsidone originally isolated from A. nidulans that has antibacterial activity against M. tuberculosis and M. ranoe as well as antifungal activity against T. tonsurans and M. audouini. It also inhibits the growth of methicillin-resistant S. aureus (MRSA; MIC = 2 μg/ml) and has larvicidal activity toward Artemia (LC50 = 1.7 μg/ml). Nornidulin has cytotoxic activity in MOLT-3 cells (IC50 = 35.7 μM) but not HuCCA-1, HepG2, or A549 cells (IC50s = >116.4 μM).
T38073	Thiocarlide Isoxyl
	Thiocarlide (isoxyl) is a thiourea derivative that was used in the 1960s to successfully treat tuberculosis (TB). It has considerable antimycobacterial activity in vitro and is effective against multi-drug resistant strains of Mycobacterium tuberculosis in the range of 1-10 &#181g/ml. [1] [2] At concentrations of 10 &#181M, isoxyl inhibits the synthesis of M. bovis during six hours of exposure which is similar to isoniazid (INH) and ethionamide (ETH), two other predominant anti-tuberculosis drug...
T37070	Pyridomycin
	Pyridomycin is a structurally unusual antimycobacterial cyclodepsipeptide whose composition includes two rare moieties: 3-(3-pyridyl)-L-alanine and 2-hydroxy-3-methylpent-2-enoic acid. It inhibits NADH-dependent enoyl (Acyl-Carrier-Protein) reductase InhA, preventing mycolic acid synthesis in M. tuberculosis, including isoniazid-resistant strains (MICs = 0.31-0.63 μg/ml).
T73032	MtInhA-IN-1
	MtInhA-IN-1是一种口服活性的选择性结核分枝杆菌NADH依赖性烯酰基载体蛋白还原酶(MtInhA)抑制剂，IC50值为0.23 μM。对结核分枝杆菌H37Rv菌株，其MIC为0.4 μM。
T74771	Diaporthein B
	Diaporthein B 是氧化程度极高的 pimarane 二萜之一。Diaporthein B 表现出抗结核分枝杆菌的活性，MIC 为 3.1 μg/mL。Diaporthein B 显示对 HCT 116 和 LoVo 结肠癌细胞的 IC50为 1.5-3 μM/L。

化合物

Cat.No: T38359

Target: Antibacterial

Cat.No: T8411

Target: Others

Norverapamil hydrochloride

Cat.No: T16339

Synonym: (±)-Norverapamil hydrochloride,D591 hydrochloride,盐酸去甲维拉帕米

Target: Calcium Channel, P-gp, Drug Metabolite

Cat.No: T5400

Synonym: IAP6,Telacebec

Target: Antibacterial, Antibiotic

Cat.No: T9830

Synonym: GSK286

Target: Antibacterial

Cat.No: T25817

Synonym: NSC-300288,米托萘胺,NSC300288,NSC 300288

Target: Antibacterial

Cat.No: T5997

Target: Antibacterial, Antibiotic

Cat.No: T7312

Target: Others, Antibacterial

Cat.No: T7342

Target: Antibacterial

Sodium 4-aminosalicylate dihydrate

Cat.No: T0020

Synonym: 对氨基水杨酸钠二水合物,Sodium 4-Aminosalicylate,4-Amino-salicylic acid sodium salt

Target: Free radical scavengers, NF-κB, Antibacterial, Antibiotic

Cat.No: T27482

Target: Others

Cat.No: T4531

Target: Antibacterial

Cat.No: T10563

Target: Others

Cat.No: T60446

Target: Apoptosis, Glutathione reductase

BM635 mesylate (1493762-74-5 free base)

Cat.No: T10563L2

Synonym: BM635 mesylate

Target: Others

BM635 hydrochloride (1493762-74-5 free base)

Cat.No: T10563L

Synonym: BM635 hydrochloride

Target: Others

Polyketide synthase 13-IN-3

Cat.No: T39693

Homo-BacPROTAC7

Cat.No: T75168

DprE1-IN-377790

Cat.No: T27206

LeuRS-IN-1 hydrochloride

Cat.No: T38773

Cat.No: T29505

Synonym: A-039,A 039

Cat.No: T68809

Cat.No: T10887

Target: Antibacterial

Cat.No: T39109

Synonym: ML338

Cat.No: T61573

Cat.No: T69488

Cat.No: T71846

Antitubercular agent-22

Cat.No: T63755

Cat.No: T61781

Homo-BacPROTAC6

Cat.No: T75167

Cat.No: T61303

Antitubercular agent-24

Cat.No: T61520

Antitubercular agent-23

Cat.No: T63525

α/β-Hydrolase-IN-1

Cat.No: T40317

Q-203 Ditosylate

Cat.No: T28480

Synonym: Q203,Q-203,Q 203

Capreomycin free base

Cat.No: T71449

Cat.No: T38355

Antibacterial agent 96

Cat.No: T61170

Cat.No: T63786

Antituberculosis agent-6

Cat.No: T72262

Antibacterial agent 118

Cat.No: T61665

Cat.No: T37880

Antituberculosis agent-8

Cat.No: T72263

Antitubercular agent-14

Cat.No: T60971

Cat.No: T61772

Cat.No: T36541

Cat.No: T38073

Synonym: Isoxyl

Cat.No: T37070

Cat.No: T73032

Cat.No: T74771

Cat. No.	Product Name	Target	Signaling Pathways
T1426	Pyrazinamide Pyrazinoic acid amide,Pyrazinecarboxamide,吡嗪酰胺	Antibacterial; Antibiotic; Autophagy; Fatty Acid Synthase	Autophagy; Metabolism; Microbiology/Virology
	Pyrazinamide (Pyrazinecarboxamide) 是一种口服抗结核类抗生素。它是一种前药，通过结核分枝杆菌pncA 基因编码的 PZase/烟酰胺酶转化为活性吡嗪酸形式。
TQ0184	Chebulinic acid	ATPase; Proton pump; DNA/RNA Synthesis; Antibacterial; TGF-beta/Smad	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Stem Cells
	Chebulinic acid 是从诃子果中提取的一种天然产物，结核分枝杆菌 DNA 促旋酶的有效抑制剂。它也能抑制 SMAD-3 phosphorylation 和 H+ K+-ATPase 的活性。
T4964	steviolbioside CCRIS-6025,菊双糖甙,甜菊双糖苷	Others	Others
	Steviolbioside (CCRIS-6025) 是一种存在于甜菊叶中的罕见甜味剂。它对几种人类癌细胞有抑制作用，对乳腺癌具有潜在的研究价值。
TN3674	Clauszoline M	Antifection	Microbiology/Virology
	Clauszoline M shows a significant anti-tuberculosis activity.
TN3422	Anisofolin A	Antifection	Microbiology/Virology
	Anisofolin A has promising antimalarial activity (IC50 4.39 ± 0.25 uM). It has promising antimycobacterium activity [IC50 4.50 ± 0.75 uM (3.31 ug/mL)] against M. tuberculosis H37Ra and at 100 ug/mL, shows 55.6 % inhibition of M. bovis.
T38019	Nybomycin
	Nybomycin is a fungal metabolite originally isolated from Streptomyces sp. A717 and has antibacterial activity. It is active against B. subtilis, B. cereus, B. mycoides, M. smegmatis, and K. pneumoniae (MICs = 0.025, 2, 0.8, 0.2, and 0.003 μg/ml, respectively). Nybomycin is also active against M. tuberculosis and M. bovis (MICs = 4.5 and 1 μg/ml, respectively).
T69368	GKK1032B
	GKK1032B is a fungal metabolite that has antiproliferative and antibacterial activities. GKK1032B inhibits the growth of HeLa S3 cervical and MCF-7 breast cancer cells and Vero cells. It also inhibits the growth of B. subtilis and M. tuberculosis.
TN5404	(+)-Conocarpan
	Conocarpan has antinociceptive effects. Conocarpan is quite active against S. aureus and B. subtilis with MIC of 6.25 micrograms/ml, it also shows activity against M. tuberculosis (MIC=15.6 ug/ml). Conocarpan shows considerable activity against epimastigo
T75676	Orotidine 5′-monophosphate trisodium
	Orotidine 5'-monophosphate trisodium 是一种嘧啶核苷酸。Orotidine 5'-monophosphate trisodium 是通过从头合成途径合成的，用于在大量微生物中合成 DNA，包括 M. tuberculosis、S. cerevisiae、S. typhimurium 和 P. falciparum 等等。乳清酸磷酸核糖基转移酶 (OPRT) 以磷酸核糖焦磷酸 (PRPP) 和乳清酸 (OA) 作为底物催化合成 Orotidine 5'-monophosphate trisodium[1]
T36815	Chevalone C
	Chevalone C is a meroterpenoid fungal metabolite originally isolated from E. chevalieri. It is active against M. tuberculosis H37Ra (MIC = 6.3 μg/ml) and is cytotoxic to BC1 human breast cancer cells (IC50 = 8.7 μg/ml). Chevalone C inhibits the growth of multidrug-resistant isolates of E. coli, S. aureus, and E. faecium in a disc diffusion assay when used at a concentration of 15 μg/disc. It also induces cell death in HCT116 colorectal carcinoma cells.
T38330	Collinin
	Collinin is a coumarin that has been found in Z. schinifolium and has diverse biological activities.1,2,3,4 It is active against drug-susceptible and -resistant strains of M. tuberculosis (MIC50s = 3.13-6.25 μg/ml).1 Collinin inhibits LPS-induced nitric oxide (NO) production (IC50 = 5.9 μM) and reduces COX-2 protein levels in RAW 264.7 cells.2 It completely inhibits aggregation of isolated rabbit platelets induced by arachidonic acid , collagen, or platelet activating factor (PAF) when used at a...

天然产物

Cat.No: T1426

Synonym: Pyrazinoic acid amide,Pyrazinecarboxamide,吡嗪酰胺

Target: Antibacterial, Antibiotic, Autophagy, Fatty Acid Synthase

Chebulinic acid

Cat.No: TQ0184

Target: ATPase, Proton pump, DNA/RNA Synthesis, Antibacterial, TGF-beta/Smad

Cat.No: T4964

Synonym: CCRIS-6025,菊双糖甙,甜菊双糖苷

Target: Others

Cat.No: TN3674

Target: Antifection

Cat.No: TN3422

Target: Antifection

Cat.No: T38019

Cat.No: T69368

Cat.No: TN5404

Orotidine 5′-monophosphate trisodium

Cat.No: T75676

Cat.No: T36815

Cat.No: T38330

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