56
11
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9372 |
D-Histidine
|
Mitochondrial Metabolism | Metabolism |
D-Histidine 是一种 L-histidine 的对映体。其中 L-histidine 是婴儿必需的氨基酸,是一种线粒体谷氨酰胺转运的抑制剂。 | |||
T40122 |
L-Histidine benzyl ester bistosylate
|
Others | Others |
L-Histidine benzyl ester bistosylate可作为HutP(一种RNA结合蛋白)的激活剂。 | |||
T32080 |
Histidine oxoglurate
Histidine alpha-ketoglutarate |
||
Histidine oxoglurate is a bioactive chemical. | |||
T81677 |
N-Formyl-L-histidine
Formyl-L-histidine |
||
N-Formyl-L-histidine 通过与组氨酸-tRNA合成酶结合展示其活性,其Ki值为4.6 μM。此外,N-Formyl-L-histidine作为L-组氨酸解氨酶的竞争性抑制剂,具有4.26 mM的Ki值,能够有效抑制该酶对L-组氨酸的解氨反应,阻止尿苷酸的生成。 | |||
T20382 |
Diglycyl-histidine
NSC334195,NSC-334195,Gly-gly-his,Glycylglycyl-L-histidine,NSC 334195 |
||
Diglycyl-histidine is a tripeptide complexed with cupric ion designed to mimic specific Cu(II) transport site of ascorbate on albumin molecule. | |||
T67981 |
Copper histidine
|
||
Copper histidine 抑制了Ctr1介导的奥沙利铂在体外的细胞摄取,而不会改变奥沙利铂在体内DRG 组织中的铂或神经毒性的积累。Copper histidine 通过口服治疗 Menkes 疾病。 | |||
T68950 | Hepta-histidine | ||
Hepta-histidine is a novel inhibitor of Tau aggregation against Tau-related neurodegenerative diseases including Alzheimer's disease (AD). | |||
T33702 |
N-Mercaptoacetyl-L-histidine
SA 120,L-Histidine, N-(mercaptoacetyl)-,SA120,SA-120 |
||
N-Mercaptoacetyl-L-histidine is a peptide. | |||
T66645 |
Fmoc-His-OH
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoic acid,(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-histidine,FMOC-L-Histidine |
||
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoic acid 是一种组氨酸衍生物。 | |||
T9494 |
Imidazole-5-propionic acid
Imidazolylpropionic acid,3-(咪唑-4-基)丙酸,SALOR-INT L480258-1EA,Deamino-histidine |
Dehydrogenase | Metabolism |
Imidazole-5-propionic acid (Imidazolylpropionic acid) 是组氨酸代谢的产物,可能涉及氧化或转氨作用。它是 G. candidum 组氨醇脱氢酶的有效抑制剂,IC50 值低至 3.17 microM。 | |||
T32735 |
L-Histidine S-malate
|
||
L-Histidine S-malate is a bioactive chemical. | |||
T3937 |
Methyl L-histidinate dihydrochloride
L-Histidine methyl ester dihydrochloride,L-组氨酸甲酯二盐酸盐 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Methyl L-histidinate dihydrochloride (L-Histidine methyl ester dihydrochloride) 在Sprague-Dawley 大鼠胃中组氨酸脱羧酶的抑制作用被评估为 14CO2 产生减少,活性值为 1.8 μM。 | |||
T66788 |
DL-Histidine
|
||
T33760 |
N-Stearoylhistidine
N-Stearoyl-L-histidine |
||
N-Stearoylhistidine is a bioactive chemical. | |||
T24974 |
2-Iodohistidine
2-Iodo-L-histidine |
||
2-Iodohistidine shows potent antimalarial activity. | |||
T65767 | N-Cbz-L-histidine | ||
N-Cbz-L-histidine 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 T65767。 | |||
T66680 |
Fmoc-1-methyl-L-histidine
|
||
Fmoc-1-methyl-L-histidine 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 T66680,CAS号为 202920-22-7。 | |||
TP1088 |
N-Acetylcarnosine
N-Acetyl-L-carnosine,N-乙酰肌肽 |
Others | Others |
N-Acetylcarnosine (N-Acetyl-L-carnosine) 是一种含有组氨酸的天然二肽,是药理学上主要的 L-carnosine 的来源。它是一种眼科药物,对人类白内障具有潜在的应用价值。 | |||
T83633 |
1-N-Methyl-4-mercaptohistidine disulfide
|
Others | Others |
1-N-Methyl-4-mercaptohistidine disulfide 是一种潜在的杜氏菌叶绿体偶联因子1氧化还原调节剂,是氧化形式的卵硫醇A,抑制光触发的CF1 ATP酶活性。 | |||
T26374 |
(S)-alpha-Fluoromethylhistidine 2 HCl
|
||
(S)-alpha-Fluoromethylhistidine 2 HCl is a potent irreversible inhibitor of histidine decarboxylase (HDC) and glutathione S-transferase. | |||
T80908 |
Tyrosylhistidine
|
||
Tyrosylhistidine是由酪氨酸和组氨酸构成的二肽(Tyr-His)。作为一种口服降血压肽,它能够降低自发性高血压模型小鼠的血压。 | |||
T34033 |
Phosphohistidine
3-Phosphohistidine |
||
Phosphohistidine is a eukaryotic enzyme dephosphorylating proteins and peptides. | |||
T34208 |
Pyroglutamylhistidine
Pglu-his |
||
Pyroglutamylhistidine is a dipeptide. | |||
T33611 | N-Carbethoxyhistidine | ||
N-Carbethoxyhistidine can be used to protect amine functional groups. | |||
TP1401 |
HAE
His-Ala-Glu |
Others | Others |
HAE (His-Ala-Glu) 由组氨酸、丙氨酸和谷氨酸组成。 | |||
TP1280 |
Hexa-His
|
Others | Others |
Hexa-His 是融合蛋白的金属结合位点,是一种由 6 个组氨酸构成的六肽。 | |||
T6605 |
NH125
|
CaMK; Virus Protease; PKA; Antibacterial; PKC; Autophagy; Antifungal | Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; Microbiology/Virology; Neuroscience; Tyrosine Kinase/Adaptors |
NH125 是一种真核延长因子 2 激酶(eEF-2K/CaMKIII)的高效选择性抑制剂,诱导 eEF2 磷酸化,对 eEF-2K 作用的 IC50值为 60 nM。 | |||
T65118 |
DEPC
Diethyl pyrocarbonate |
Others | Others |
DEPC (Diethyl pyrocarbonate) 是一种有效的、不可逆的含有组氨酸残基的 RNase 抑制剂。DEPC 可用碳氧基化修饰组氨酸残基从而导致酶失活,可用于防止RNA 酶降解RNA。DEPC 对兔子的中枢化学敏感性具有抑制作用。DEPC 可以修饰 His,Tyr,Ser 和 Thr 残基。 | |||
T15650 |
KDM5A-IN-1
|
Histone Demethylase | Chromatin/Epigenetic |
KDM5A-IN-1 是一种可口服且具有高效性和选择性的泛组氨酸赖氨酸脱甲基酶 5 KDM5 抑制剂,抑制 KDM5A,KDM5B,KDM5C,IC50 值分别为 45 nM,56 nM 和 55 nM。KDM5A-IN-1 抑制 PC9 H3K4Me3,可用于研究癌症。 | |||
T32098L |
Homocarnosine acetate
|
GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Homocarnosine acetate 是大脑特有的二肽,由 γ-氨基丁酸 (GABA) 和组氨酸组成。它具有抗氧化和抗炎作用、预防 DNA 损伤和抑制晚期糖基化终产物形成 | |||
T7454 |
4-Bromo-3-hydroxybenzoic acid
|
Decarboxylase; Endogenous Metabolite | Metabolism; Others |
4-Bromo-3-hydroxybenzoic acid 是一种组氨酸脱羧酶抑制剂,是一种 Brocresine 的代谢产物,对大鼠胎儿和大鼠胃HDC 的IC50均为 1 mM。它还能够在体外抑制猪肾脏和大鼠胃粘膜中的芳香族 L-氨基酸脱羧酶,两种酶的IC50均为 1 mM。 | |||
T22243 |
Anserine
L-鹅肌肽,L-Anserine |
Endogenous Metabolite | Metabolism |
Anserine (L-Anserine) 是 Carnosine 的甲基化形式,是口服具有活性的天然二肽,存在于脊椎动物的骨骼肌。它不会被血清肌肽酶裂解,能够作为生化缓冲液,螯合剂,抗糖化剂和抗氧化剂。它能够改善阿尔茨海默氏病模型小鼠的记忆功能。 | |||
T26480 |
A331440
A-331440,A331440 free base,A 331440 |
||
A331440 is an modulator of L-histidine and histamine H3 receptor. | |||
T31851 |
Formiminoglutamic acid
NSC-334078,NSC334078,NSC 334078 |
||
Formiminoglutamic acid is used to indicate folic acid deficiency and megaloblastic anemia of pregnancy with the measurement in the urine after oral administration of histidine. | |||
T33440 |
MK785
MK-785,MK 785 |
||
MK785 is part of the association between inhibition of aortic histamine formation, aortic albumin permeability, and atherosclerosis. Aortic histamine synthesis was inhibited by partial inhibition of aortic histidine decarboxylase (HD) by application of MK | |||
TP1401L |
HAE acetate(64111-99-5 free base)
|
Others | Others |
HAE acetate(64111-99-5 free base) 是由组氨酸、丙氨酸和谷氨酸组成的3个氨基酸肽。 | |||
T38472 |
Phosphoribosyl pyrophosphate pentasodium
PRPPpentasodium,磷酸核糖焦磷酸 |
||
Phosphoribosyl pyrophosphate (PRPP) pentasodium is a vital metabolite essential for the biosynthesis of purine and pyrimidine nucleotides, as well as the amino acids histidine and tryptophan. It also acts as a precursor for the important cofactors NAD and NADP. | |||
T37547 |
trans-Urocanic Acid
|
||
trans-Urocanic acid is a major epidermal chromophore for the immunosuppressive effects of UV radiation that is produced in mammalian stratum corneum by the action of histidine ammonialyase on L-histidine. It contributes to the acidification of the surface of the stratum corneum, and its function has been proposed as that of an endogenous sunscreen, endowing a low-level of protection (SPF ~ 1.5) against UV-induced DNA damage and excessive keratinocyte apoptosis. Upon UVB exposure, trans-urocanic ... | |||
T17166 |
Tritoqualine
Hypostamine,酞茂异喹,Inhibostamin |
Decarboxylase | Metabolism; Others |
Tritoqualine is used as an inhibitor of histidine decarboxylase. | |||
T38382 | 8Br-HA | ||
8Br-HA is an inhibitor of fragile histidine triad diadenosine triphosphatase (FHIT; IC50= 0.12 μM).1It inhibits the growth of HCC827 and H460 lung cancer cells (GI50s = 0.87 and 5.9 μM, respectively). 1.Kawaguchi, M., Sekimoto, E., Ohta, Y., et al.Synthesis of fluorescent probes targeting tumor-suppressor protein FHIT and Identification of apoptosis-inducing FHIT inhibitorsJ. Med. Chem.64(13)9567-9576(2021) | |||
T27995 |
MDK-3046
HK-inhibitor-2,MDK3046,HK inhibitor 2 |
||
MDK-3046 is a YycG histidine kinase (HK) inhibitor with potent antibiofim activity against Staphylococcus epidermidis. | |||
T82863 |
Biotin-X-NTA
|
||
Biotin-X-NTA,用于定性检测硝基纤维素膜上固定的组氨酸标记蛋白。 | |||
TP2181 |
Hexa His tag peptide
|
Others | Others |
Hexa His is an amino acid sequence consisting of 6 His residues in a row, it is also known as Hexa histidine-tag, 6 x His-tag, and by the trademarked name His-tag. | |||
T36973 |
5-Phospho-D-ribose 1-diphosphate (sodium salt hydrate)
|
||
5-Phospho-D-ribose 1-diphosphate (PRPP) is a natural intermediate involved in the pentose phosphate pathway leading to purine, pyrimidine, and histidine metabolism. It is also an intermediate in the synthesis of plant hormones, alkaloids, and other secondary metabolites from glucose. Several phosphoribosyltransferases (PRTases) use PRPP as a substrate to add a 5-phosphoribosyl group to another substrate, as in the production of adenosine monophosphate from adenine and PRPP by adenine PRTase. N/A | |||
T17274 |
YM022
|
CCR | Immunology/Inflammation; Microbiology/Virology |
YM022 is a highly effective and selective gastrin/cholecystokinin (CCK)-B receptor antagonist. YM022 can inhibit gastrin-induced gastric acid secretion and histidine decarboxylase activation in vivo. YM022 shows the Ki values of 68 pM and 63 nM for CCK-B and CCK-A receptor, respectively. | |||
T76577 |
Antiulcer Agent 2
|
||
Antiulcer Agent 2 是一种四肽,组成包括天冬氨酸、丙氨酸、组氨酸和赖氨酸,存在于人白蛋白N端,并在溃疡及活性氧生成中显示出潜在应用。 | |||
T76585 |
Hepcidin-20 (human)
|
||
Hepcidin-20 (human) 是一种β-折叠结构肽,含有组氨酸和丰富的半胱氨酸,具备抗真菌活性,并能抑制多糖细胞间粘附素 (PIA) 阳性及阴性菌株的生物膜形成及细菌细胞代谢[3]。 | |||
TP1088L |
N-Acetylcarnosine acetate
N-Acetyl-L-carnosine acetate,N-Acetyl carnosine acetate,N-乙酰肌肽醋酸盐 |
Others | Others |
N-Acetylcarnosine acetate (N-Acetyl-L-carnosine acetate) 是一种天然的,含有组氨酸的二肽,是药理学上主要的 L-carnosine 的来源。N-Acetylcarnosine 是一种有效的眼科药物,有用于人类白内障的潜力。 | |||
T77105 | Odesivimab | ||
Odesivimab 是一种人源化单克隆抗体,靶向埃博拉病毒糖蛋白,重组组氨酸标记的马科纳毒株埃博拉病毒糖蛋白胞外域蛋白的 KD 值为 7.74 nM。Odesivimab 可用于埃博拉病毒感染的研究。 | |||
T35646 |
4-oxo-2-Nonenal
4-oxo-2-Nonenal,4-ONE |
||
4-hydroxy Nonenal is a lipid peroxidation product derived from oxidized ω-6 polyunsaturated fatty acids such as arachidonic acid and linoleic acid. [1] [2] It exhibits various biological activities such as cytotoxicity, growth inhibiting activity, genotoxicity, and chemotactic activity and has been widely used as a marker of lipid peroxidation.[1][2][3] 4-oxo-2-Nonenal is a more recently identified product of lipid peroxidation.[4][5][6] It actively modifies histidine and lysine residues on prot... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2A2532 |
L-Histidine
Glyoxaline-5-alanine,L-(-)-Histidine,L-组氨酸,histidine,组氨酸,L-Hisidine |
Mitochondrial Metabolism; Endogenous Metabolite | Metabolism |
L-Histidine (L-(-)-Histidine) 是人类生长和组织修复所需的一种半必需氨基酸(儿童应从食物中获得)。 L-Histidine 是线粒体谷氨酰胺转运的抑制剂。 | |||
T4934 |
1-Methyl-L-histidine
1-甲基-L-组氨酸,3-(1-Methylimidazol-4-yl)-L-alanine,Nτ-Methyl-L-histidine |
Endogenous Metabolite | Metabolism |
1-Methyl-L-histidine (3-(1-Methylimidazol-4-yl)-L-alanine),一种人内源性代谢物,是肉类和外源性 3-methylhistidine 摄入的客观生物标记。 | |||
T4826 |
L-Histidine monohydrochloride monohydrat
|
Others; Endogenous Metabolite | Metabolism; Others |
L-Histidine monohydrochloride monohydrat 是一种 α-氨基酸。 L-异构体是 22 种蛋白质氨基酸之一,即蛋白质的组成部分。 | |||
T8274 |
3-Methyl-L-histidine
|
Endogenous Metabolite | Metabolism |
3-Methyl-L-histidine 是一种肉类尤其是鸡肉摄入和大豆制品摄入的生物标记。 | |||
T4732 |
L-Carnosine
Karnozin,L-肌肽,beta-Alanyl-L-histidine |
Antioxidant; Endogenous Metabolite | Metabolism; oxidation-reduction |
L-Carnosine (Karnozin) 是 由beta-丙氨酸和组氨酸组成的二肽,具有抑制衰老的作用。 | |||
T38094 |
N-Acetyl-L-histidine monohydrate
|
||
N-Acetyl-L-histidine monohydrate 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 T38094,CAS号为 39145-52-3。 | |||
T37298 |
Spinacine
|
Endogenous Metabolite | Metabolism |
Spinacine 是人内源性代谢产物。 | |||
T8790 |
1-Methylhistamine dihydrochloride
|
Endogenous Metabolite | Metabolism |
1-Methylhistamine dihydrochloride 是组胺代谢物。 | |||
T0965 |
Histamine
Ergamine,组胺 |
5-HT Receptor; Endogenous Metabolite; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Histamine (Ergamine) 是通过组胺的酶促脱羧衍生的胺。它是一种强大的胃分泌兴奋剂、支气管平滑肌的收缩剂、血管扩张剂以及中枢作用的神经递质。 | |||
T19443L |
N-Acetylhistamine acetate
|
Endogenous Metabolite; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
N-Acetylhistamine acetate 是一种组胺代谢物。 它可用作过敏反应的组氨酸代谢的潜在生物标志物。 | |||
TN4505 | Masticadienolic acid | Others | Others |
Masticadienolic acid is a specific competitive inhibitor of secreted phospholipase A2, it not only protects the active site histidine from alkylation but also inhibits the action of secreted from pancreas, synovial fluid, and bee venom. Masticadienolic ac |