50
8
4
3
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T25492 |
Hepln-13
Hepln 13,Hepln13 |
c-Met/HGFR | Tyrosine Kinase/Adaptors |
Hepln-13 是具有口服活性的Hepsin 抑制剂(IC50:0.33 µM)。它可用于研究转移性前列腺癌。 | |||
TP1253 |
Argireline
六胜肽,Acetyl hexapeptide-3,阿基瑞林 |
Others | Others |
Argireline (Acetyl hexapeptide-3) 是可渗透皮肤的、无毒的抗皱肽。它对神经肌肉接头处依赖 Ca2+的神经递质释放具有显著的抑制作用。它具有抗皱和抗衰老的活性。 | |||
T6456 |
CRT0044876
NSC 69877,7-NO2-ICA,7-硝基吲哚-2-甲酸,NSC 69877,7-Nitroindole-2-Carboxylic Acid |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
CRT0044876 (7-NO2-ICA) 是一种高选择性的嘌呤/嘧啶核苷核酸内切酶 1 抑制剂,IC50约为 3 μM。它也是 APE1 所属的核酸外切酶 III 家族的特异性抑制剂,可抑制 APE1 的 AP 内切酶、3′-磷酸二酯酶和 3′-磷酸酶活性,可增强几种 DNA 碱基靶向化合物的细胞毒性。 | |||
T30582 |
BRD56491
BRD-56491,BRD 56491 |
Others | Others |
BRD56491 is a non-toxic reactive oxygen species (ROS) enhancer that strongly elevates markers of oxidative stress without causing cell death. | |||
T5314 |
pyridoxal isonicotinoyl hydrazone
吡哆醛异烟酰肼,PIH |
Others | Others |
pyridoxal isonicotinoyl hydrazone (PIH) 是亲脂的三价铁螯合剂,具有高铁螯合特性。 | |||
T15379 |
GGsTop
Nahlsgen |
Others | Others |
GGsTop is a non-toxic and irreversible inhibitor of γ glutamyl transpeptidase (GGT) (Ki: 170 μM for Human GGT). GGsTop protects hepatic ischemia-reperfusion injury in the rat model. GGsTop shows Kons of 150±10 and 51±3 /(M·s) against E.coli GGT and human GGT, respectively. | |||
T19232 |
CMC-Na (Viscosity:800-1200 mPa.s)
羧甲基纤维素钠,Sodium carboxymethyl cellulose,CMC-Na (Viscosity:800-1200 mPa.s) |
Others | Others |
Sodium carboxymethyl cellulose (CMC-Na) (Viscosity:800-1200 mPa.s) 是一种水溶性纤维素,常用作动物实验的助溶剂,对动物基本没有毒性。 | |||
T8669 |
BTDA
3,3',4,4'-Benzophenonetetracarboxylic dianhydride |
Others | Others |
3,3',4,4'-Benzophenonetetracarboxylic dianhydride 是一种化合物,用于生产聚酰亚胺薄膜和粘合剂的聚酰亚胺前体。它是一种无毒材料,对人体健康没有已知的不良影响。 | |||
T0914 |
Metacetamol
酰胺苯酚,3-Acetamidophenol |
Others | Others |
Metacetamol (3-Acetamidophenol) 是对乙酰氨基酚的衍生物,为其无毒区域异构体,是一种非处方镇痛剂和解热剂,也可用作有机合成中间体。 | |||
T14922 |
Cefodizime
|
Antibacterial; Antibiotic | Microbiology/Virology |
Cefodizime 是一种新型头孢菌素抗生素,具有广泛的生物活性。Cefodizime 对肾脏没有毒性且具有良好的耐受性和免疫调节活性,具有抗菌活性,可用于研究呼吸系统和泌尿系统的严重感染。 | |||
T14319 |
Aripiprazole Lauroxil
|
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Aripiprazole lauroxil 是一种长效注射剂 (LAI) 的抗精神病药物,是阿立哌唑的 N-酰氧基甲基前药形式。它能够被体内酯酶裂解为 N-羟甲基阿立哌唑(月桂酸),再裂解为阿立哌唑,无毒性。 | |||
T15602 |
ITX3
|
Others; Rho | Cell Cycle/Checkpoint; Others |
ITX3 是特异的、无毒的、有活性的、具有选择性的TrioN RhoGEF 抑制剂,IC50 值为 76 μM。 ITX3具有抗癌作用,能抑制trion 介导的GTP 在RhoG 和Rac1上的交换,抑制ngf 介导的PC12细胞神经突的生长和trion 诱导的REF52成纤维细胞结构的形成。 | |||
T38063 |
N-Acetyl lysyltyrosylcysteine amide
|
Glutathione Peroxidase | Metabolism |
N-Acetyl lysyltyrosylcysteine amide 是一种无毒的髓过氧化物酶 (MPO) 三肽抑制剂,具有有效性,可逆性和特异性。N-Acetyl lysyltyrosylcysteine amide 在体内可有效抑制 MPO 产生。N-Acetyl lysyltyrosylcysteine amide 减轻中风后大脑的神经元损伤,并保留脑组织和神经功能。N-Acetyl lysyltyrosylcysteine amide 抑制MPO依赖性次氯酸 (HOCl) 的生成,蛋白质硝化和 LDL 氧化。N-Acetyl lysyltyrosylcysteine amide 可用于研究支气管发育不良。 | |||
T33923 |
Pentyl rhamnoside
Selectiose |
Others | Others |
Pentyl rhamnoside is a new non-toxic cosurfactant to formulate microemulsions. | |||
T34391 |
Rosmarinine
|
Others | Others |
Rosmarinine is a non-toxic pyrrolizidine alkaloid. | |||
T16082 |
Mivotilate
YH439 |
Others | Others |
Mivotilate, a potent, non-toxic aryl hydrocarbon receptor (AhR) activator, functions as a hepatoprotective agent. | |||
T22255 | Amastatin | Others | Others |
Amastatin is a non-toxic inhibitor of aminopeptidase A and leucine aminopeptidase, and its Ki for aminopeptidase A is 1 µM . | |||
T33388 |
Mimosine methyl ester
L-Mimosine methyl ester |
Others | Others |
Mimosine methyl ester is a toxic non-protein amino acid chemically similar to tyrosine, that was first isolated from Mimosa pudica. | |||
T71501 |
GBS-149
|
Others | Others |
GBS-149 is a novel non-toxic and mammalian-specific LINE-1 inhibitor. | |||
T31437 |
Dicobalt edetate
Ba-2724,Ba2724,Ba 2724,Kelocyanor |
Others | Others |
Cobalt edylic acid is a cobalt compound whose mechanism is that cyanide binds cobalt to form a relatively non-toxic complex. | |||
T11051 |
DIQ3
|
Others | Others |
DIQ3 is non-toxic to normal human cell lines and is an effective anti-cancer agent. | |||
T30581 |
BRD5459
BRD-5459,BRD 5459 |
Others | Others |
BRD5459 is a kind of reactive oxygen species enhancer that is non-toxic or leads to genotype selective cell death. Brd5459 can selectively kill cancer cells in various in vitro and in vivo models. | |||
T28110 |
MRZ-99030
EG 030,EG030,EG-030,MRZ 99030 |
Others | Others |
MRZ-99030 is an Aβ aggregation modulator. MRZ-99030 triggers a non-amyloidogenic aggregation pathway, thereby reducing the amount of intermediate toxic soluble oligomeric Aβ species. | |||
T61470 |
NMDA receptor antagonist 5
|
Others | Others |
NMDA receptor antagonist 5 (Compound 10e), a potent and non-toxic NMDA receptor antagonist, exhibits brain permeability. It is of significance in studying neurological disorders [1]. | |||
T13609L |
Chlorazanil
|
Others | Others |
Chlorazanil 是一种三嗪衍生物,也是一种口服有效的新型非毒性利尿剂,可以阻止钠和氯在远曲小管的吸收。 | |||
T60855 |
Elastase-IN-1
|
Others | Others |
Elastase-IN-1 (Compound Q11) 是无毒的弹性蛋白酶抑制剂,IC50值为 0.897 μM。 | |||
T3694L |
Tebanicline tosylate
|
Others | Others |
Tebanicline is a potent synthetic nicotinic (non-opioid) analgesic drug. It was developed as a less toxic analogue of the potent poison dart frog-derived compound epibatidine. Like epibatidine, tebanicline showed potent analgesic activity against neuropat | |||
T73356 |
Ac32Az19
|
Others | Others |
Ac32Az19 是一种有效、无毒、高选择性的 BCRP 抑制剂,在BCRP 过度表达的HEK293/R2细胞中,EC50值为13 nM。 | |||
T39322 |
Temporin A
|
||
Temporin A, a short alpha-helical antimicrobial peptide derived from the skin of Rana temporaria, exhibits a wide-ranging efficacy against Gram-positive bacteria. It directly interacts with the cell membrane of microorganisms and remains non-toxic to erythrocytes at antimicrobial concentrations. Additionally, Temporin A demonstrates antifungal properties against yeast-like Candida albicans. | |||
T74526 |
Antifungal agent 29
|
Others | Others |
Antifungal agent 29 (化合物 9d) 是一种有效的、选择性的、无毒的抗真菌剂。Antifungal agent 29 对新隐球菌具有抗真菌活性 (MIC≤ 0.23 μM)。 | |||
T23207 |
Q-VD(OMe)-OPh
|
Others | Others |
Q-VD-OPh (quinolyl-valyl-O-methylaspartyl-[-2,6-difluorophenoxy]-methyl ketone) is a broad-spectrum caspase inhibitor, provides a cost-effective, non-toxic, and highly specific means of apoptotic inhibition and provides new insight into the design of new | |||
T62697 |
BuChE-IN-3
|
Others | Others |
BuChE-IN-3 (Compound C4) 是一种 BuChE 的有效抑制剂 (IC50: 8.3 nM)。BuChE-IN-3 具有温和的抗氧化能力、无毒、亲脂性和神经保护效果。 | |||
T34029 |
Phosmet oxon
R-1571,R 1571,ENT 25707,ENT-25707,R1571 |
Others | Others |
Phosmet oxon is a toxic metabolite of phosmet, a phthalimide-derived, non-systemic, organophosphate insecticide used on plants and animals. It is mainly used on apple trees for control of codling moth, though it is also used on a wide range of fruit crops | |||
T76244 |
Amp1EP9
|
||
Amp1EP9为一抗菌肽,作为开发有效无毒抗菌活性分子的强大工具,具备针对多重耐药细菌感染进行研究的潜力。 | |||
T63472 |
HDAC6-IN-4
|
Others | Others |
HDAC6-IN-4 (C10) 是一种口服具有活力的、高度选择性的、有效的、无明显毒性的 HDAC6 抑制剂 (IC50: 23 nM)。HDAC6-IN-4 能够诱导肿瘤细胞凋亡 (apoptosis),表现出高效的抗肿瘤效果。 | |||
T61462 |
EV-A71-IN-1
|
Others | Others |
EV-A71-IN-1 is a potent inhibitor of the human enterovirus A71 (EV-A71) capsid protein, with an EC50 of 0.27 μM against EV-A71. Acting as a capsid binder, EV-A71-IN-1 disrupts the crucial interaction between the viral VP1 protein and the host receptor hSCARB2. It displays broad-spectrum antiviral activity against various human enteroviruses, while being non-toxic to human cells (CC50 > 56.2 μM) [1]. | |||
T63628 |
AChE-IN-19
|
Others | Others |
AChE-IN-19 是 AChE 的高效抑制剂 (IC50: 0.56 μM),对 Aβ 聚集也表现出抑制作用。AChE-IN-19 表现出神经保护作用,对 SH-SY5Y 细胞几乎没有毒性。AChE-IN-19 能够用于研究阿尔兹海默症。 | |||
T40341 |
SARS-CoV-2-IN-11
|
Others | Others |
SARS-CoV-2-IN-11 is a highly potent and non-toxic inhibitor of the 3C-like protease (3CLpro) of SARS-CoV-2, demonstrating IC50 and EC50 values of 0.17 nM and 1.45 nM, respectively. This compound targets the essential viral replication enzyme, 3CLpro, making it an attractive candidate for intervention strategies. SARS-CoV-2-IN-11 holds significant promise in the development of specific antivirals against SARS-CoV-2. | |||
T74494 |
Antitumor agent-63
|
Others | Others |
Antitumor agent-63(Compound 40),一种20 (S)-O-linked camptothecin (CPT) 糖复合物,作为抗肿瘤剂,对正常细胞展现出无毒性。该化合物表现出高稳定性和低topoisomeraseI (Topo I)直接抑制活性。 | |||
T78305 |
Briquilimab
JSP-191 |
||
Briquilimab (JSP-191) 是针对 CD117 (c-Kit) 的无毒人源化单克隆抗体,用于消耗造血干细胞 (HSC)。它被应用于重度联合免疫缺陷 (SCID) 治疗中,以清空宿主骨髓生态位,为供体造血干细胞移植及免疫重建创造条件。 | |||
T82388 |
Fluorescein-6-carbonyl-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone
|
Caspase | Apoptosis; Proteases/Proteasome |
Fluorescein-6-carbonyl-Asp(OMe)-Glu(OMe)-Val-DL-Asp(OMe)-fluoromethylketone 是一种细胞渗透性且无毒的抑制剂,它能与活化的caspase-3在凋亡细胞内不可逆结合。该抑制剂的荧光强度可通过流式细胞仪、微孔板读数器或荧光显微镜检测。 | |||
T40340 |
SARS-CoV-2-IN-10
|
Others | Others |
SARS-CoV-2-IN-10 is a powerful and non-toxic inhibitor of SARS-CoV-2 3CL protease, with IC50 and EC50 values of 0.13 nM and 1.03 nM, respectively. The SARS-CoV-2 3C-like protease (3CLpro) is a critical enzyme for viral replication and serves as an ideal target for intervention. By targeting the SARS-CoV-2 3CL protease, SARS-CoV-2-IN-10 has the potential to facilitate the development of effective antiviral drugs specific to SARS-CoV-2. | |||
T79559 |
Mtb-IN-4
|
Others | Others |
Mtb-IN-4(化合物17h)是一种异恶唑类化合物,显示出针对结核分枝杆菌(Mtb)的抗活性,其IC50值为0.70 μM。它能阻断巨噬细胞内Mtb的呼吸和生物膜形成,并可以增强抗生素异烟肼(INH)对耐INH Mtb突变体的抑制效果。 | |||
T36475 |
TunR2
|
Others | Others |
TunR2 is an antibiotic and derivative of tunicamycin .1It is active againstB. subtilis(MIC = 0.3 μg/ml) and increases the efficacy of the β-lactam antibiotics oxacillin , methicillin , and penicillin G againstB. subtiliswhen used at a concentration of 0.4 μg/ml. Unlike tunicamycin, TunR2 is non-toxic toS. cerevisiae(MIC = >10 μg/ml) and does not inhibit glycosylation in a protein N-glycosylation assay. TunR2 also has reduced antiproliferative activity against MDA-MB-231 and CHO cells compared wi... | |||
T11896 |
LV-320
|
Cysteine Protease | Proteases/Proteasome |
LV-320 是一种有效且非竞争性的ATG4B 抑制剂,其IC50值为 24.5 μM,Kd 值为 16 μM。 LV-320 抑制ATG4B 的酶促活性,阻断细胞自噬,并且稳定无毒,在体内具有活性。 | |||
T78964 |
Antileishmanial agent-17
|
Parasite | Microbiology/Virology |
Antileishmanial agent-17是香豆素杂化化合物,展现出优越的抗利什曼原虫活性(IC50<0.78 μM),同时对VERO细胞具备安全性。该化合物通过抑制叶酸代谢途径发挥效用,且在对抗利什曼原虫不同生长阶段表现显著,其IC50值分别对前鞭毛体为0.40 μM,对无鞭毛体为0.68 μM。 | |||
T69657 |
GS-441524 HCl
|
Others | Others |
GS-441524 is a potent inhibitor of feline infectious peritonitis (FIP) virus with an EC50 of 0.78 μM.. GS-441524 strongly inhibits feline infectious peritonitis (FIP) virus in tissue culture and experimental cat infection studies. GS-441524 is a molecular precursor to a pharmacologically active nucleoside triphosphate molecule. These analogs act as an alternative substrate and RNA-chain terminator of viral RNA dependent RNA polymerase. GS-441524 was non-toxic in feline cells at concentrations ... | |||
T63735 |
SP inhibitor 1
|
Others | Others |
SP inhibitor 1 是体外无毒浓度 (0.3250<5.98 μM) 的 SARS-CoV-2 复制抑制剂。SP inhibitor 1 是 SARS-CoV-2 刺突蛋白 (SP) 的选择性抑制剂,能够作用于 SP 蛋白 (IC50: 3.26 μM)、Mpro 蛋白 (IC50>25 μM)和 PLpro 蛋白 (IC50>25 μM),具有细胞抗病毒作用。 | |||
T62729 |
MS31 trihydrochloride
|
Others | Others |
MS31 trihydrochloride 是一种选择性的、高亲和性的、片段样的甲基赖氨酸读写蛋白 spindlin 1 (SPIN1) 抑制剂。MS31 trihydrochloride 有效破坏 SPIN1 与 H3K4me3 蛋白互相作用 (IC50: 77 nM,AlphaLISA;243 nM,FP),选择性结合 SPIN1 的 Tudor 结构域 II (Kd: 91 nM)。MS31 trihydrochloride 对含三甲基赖氨酸肽与 SPIN1 的结合具有有效抑制作用,对非肿瘤性细胞没有毒性。 | |||
T66029 |
3,4-Dehydro-L-proline
|
||
The leguminous shrub,Leucaena leucocephala(Leucaena) is wide‐spread in tropical and subtropical agricultural systems and provides a ready source of protein for livestock. However, the presence of mimosine, a non‐protein, amino acid comprising about 12% of the dry matter in growing tips ofLeucaena, is toxic to animals. Mimosine is degraded rapidly in the rumen to produce 3,4‐dihydroxypyridine (3,4‐DHP) and 2,3‐dihydroxypyridine (2,3‐DHP), both of which remain toxic to animals[1]. 3,4-DHP, as a de... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5757 |
Loganetin
|
Antibacterial | Microbiology/Virology |
Loganetin 是无毒的天然产物,来源于Cornus officinalis Sieb. et Zucc.,可用于耐多药革兰氏阴性菌感染的研究。 | |||
T5279 |
Ethylmalonic acid
alpha-Carboxybutyrate,2-Ethylmalonic acid,乙基丙二酸 |
Others; Endogenous Metabolite | Metabolism; Others |
Ethylmalonic acid 是潜在有毒物质,非致癌性,与神经性厌食和甲氧基脱羧酶缺乏症有关。 | |||
T4S1521 |
1,4-Dicaffeoylquinic acid
1,4-二咖啡酰奎宁酸,洋蓟素 |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
1,4-Dicaffeoylquinic acid 是一种苯丙素类物质,从苍耳子中获得,可以减少 LPS 诱导的 TNF-α 的生成,具有抗炎活性。 | |||
T3321 |
Oleanonic acid
3-Oxooleanolic acid,3-Oxoolean-12-en-28-oic Acid,Oleanonic Acid,齐墩果酮酸,3-Ketooleanolic Acid |
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Oleanonic acid (3-Ketooleanolic Acid) 是一种三萜,可以抑制 HIV-1 对细胞的感染。它具有保肝作用,并具有抗肿瘤和抗病毒特性。 | |||
TN1704 |
Glycyrrhetic acid 3-O-β-D-glucuronide
Glycyrrhetic acid 3-O-mono-beta-D-glucuronide,单葡萄糖醛酸甘草次酸 |
Others | Others |
Glycyrrhetic acid 3-O-mono-beta-D-glucuronide 是从甘草中分离出的甘草酸 3-O-β-D-葡萄糖醛酸,是甘草甜素的重要衍生物。它具有抗过敏活性,可作为甜味剂。 | |||
T4776 |
Glycerol
Glycerin,甘油 |
Endogenous Metabolite | Metabolism |
Glycerol 是甘油三酯(即脂肪和油)和磷脂的重要成分。它在食品工业中被广泛用作甜味剂和保湿剂以及药物制剂。 | |||
T15703 |
Lactimidomycin
|
Others | Others |
Lactimidomycin, isolated from Streptomyces, is an inhibitor of eukaryotic translation elongation. It is also a potent and non-toxic inhibitor of dengue virus 2 and other RNA viruses. Lactimidomycin has an antiproliferative effect on tumor cell lines. It i | |||
T75447 |
Asperaculane B
|
Others | Others |
Asperaculane B,一种真菌代谢产物,以IC50 7.89 µM抗恶性疟原虫传播,同时以IC50 3 µM抑制无性恶性疟原虫的发育,对人类细胞无毒。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00771 |
Ferritin-2 Protein, Glycine max, Recombinant (His & SUMO)
Ferritin-2, chloroplastic,SFerH-2 |
Glycine max | E. coli |
Stores iron in a soluble, non-toxic, readily available form. Important for iron homeostasis. Has ferroxidase activity. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. | |||
TMPJ-00761 |
FTH Protein, Human, Recombinant (His)
FTHL6,Cell proliferation-inducing gene 15 protein,Ferritin h... |
Human | E. coli |
Ferritin heavy polypeptide 1(FTH1), is a ubiquitous intracellular protein which stores iron in a soluble, non-toxic, readily available form. FTH1 has ferroxidase activity and is important for iron homeostasis. Iron is taken up in the ferrous form and deposited as ferric hydroxides after oxidation. Ferritin is composed of 24 subunits of the light and heavy ferritin chains. It plays a role in delivery of iron to cells and mediates iron uptake in capsule cells of the developing kidney. Variation of... | |||
TMPY-02711 |
Ferritin heavy chain 1/FTH1 Protein, Human, Recombinant
FHC,FTHL6,FTH,PIG15,PLIF,ferritin, heavy polypeptide 1,HFE5 |
Human | E. coli |
FTH1 (ferritin, heavy polypeptide 1) is the heavy subunit of ferritin which is the major intracellular iron storage protein in prokaryotes and eukaryotes. It is composed of 24 subunits of the heavy and light ferritin chains. Variation in ferritin subunit composition may affect the rates of iron uptake and release in different tissues. A major function of ferritin is the storage of iron in a soluble and nontoxic state. Defects in ferritin proteins are associated with several neurodegenerative dis... | |||
TMPY-02299 |
ALDH3A1 Protein, Human, Recombinant (His)
ALDHIII,aldehyde dehydrogenase 3 family, member A1,ALDH3 |
Human | Baculovirus Insect Cells |
Aldehyde dehydrogenase 3A1 (ALDH3A1) is a metabolic enzyme that catalyzes the oxidation of various aldehydes. Certain types of epithelial tissues in mammals, especially those continually exposed to environmental stress (e.g., corneal epithelium), express ALDH3A1 at high levels and its abundance in such tissues is perceived to help to maintain cellular homeostasis under conditions of oxidative stress. Metabolic as well as non-metabolic roles for ALDH3A1 have been associated with its mediated resi... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T35521 |
Aflatoxin G2-13C17
Aflatoxin G2-13C17 |
||
Aflatoxin G2-13C17is intended for use as an internal standard for the quantification of aflatoxin G2by GC- or LC-MS. Aflatoxin G2is a mycotoxin that has been found inAspergillus.1It is lethal to ducklings (LD50= 2.83 mg/kg) but is non-toxic to rats when administered at a dose of 200 mg/kg.2 1.Bennett, J.W., and Klich, M.MycotoxinsClin. Microbiol. Rev.16(3)497-516(2003) 2.Wogan, G.N., Edwards, G.S., and Newberne, P.M.Structure-activity relationships in toxicity and carcinogenicity of aflatoxins a... | |||
T11934 |
Macitentan-d4
Macitentan D4,ACT-064992 D4 |
Endothelin Receptor | GPCR/G Protein |
Macitentan-d4 (ACT-064992 D4) 是一种 Macitentan 氘代物,可被当作非多肽 ETA 和 ETB (内皮素受体)双拮抗剂。Macitentan-d4 比 Macitentan 毒性更低,半衰期更长,可用于研究由内皮素受体介导介导的疾病。 | |||
TMID-0097 |
Ethyl-d5-malonic Acid
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Ethyl-d5-malonic Acid 是 Ethyl-malonic Acid 的氘代化合物。Ethyl-malonic Acid 的 CAS 号为 601-75-2。Ethylmalonic acid 是潜在有毒物质,非致癌性,与神经性厌食和甲氧基脱羧酶缺乏症有关。 |