178
90
Cat. No. | Product Name | Target | Signaling Pathways |
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T39232 |
Azido-PEG3-aldehyde
Azido-PEG3-aldehyde |
||
Azido-PEG3-aldehyde is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T37039 |
Betulinic Aldehyde oxime
|
||
Betulinic aldehyde oxime is a pentacyclic triterpenoid and derivative of the cholesterol biosynthesis inhibitor betulin .1It is active againstE. aerogenes,E. coli,E. faecalis,P. aeruginosa,S. aureus, andC. albicans, as well asL. donovaniamastigotes, when used at a concentration of 50 μM.1,2Betulinic aldehyde oxime (50 μM) is cytotoxic to Huh7 hepatocellular carcinoma cells.2 | |||
T36056 |
Betaine Aldehyde (chloride)
|
||
Betaine aldehyde is the physiological intermediate in the oxidation of choline to betaine. This step is involved in glycine, serine, and threonine metabolism. | |||
T35412 | (+)-JQ-1-aldehyde | ||
(+)-JQ-1-aldehyde is the aldehyde derivative of (+)-JQ1, commonly used as a precursor for the synthesis of PROTACs targeting the BET bromine domain[1]. | |||
T24633 |
Phlebiakauranol aldehyde
|
||
Phlebiakauranol aldehyde is an antifungal and cytotoxic metabolite. | |||
T35575 | Aldehyde Reactive Probe (trifluoroacetate salt) | ||
DNA is continually damaged by endogenous and environmental agents leading to the formation of abasic (apurinic/apyrimidinic, AP) sites that are disruptive to DNA synthesis. Aldehyde Reactive Probe (ARP) is a biotinylated reagent for the detection and quantification of AP sites in damaged DNA. ARP reacts with aldehyde groups formed when reactive oxygen species depurinate DNA, resulting in covalent linkage of biotin to these AP sites. The biotin-tagged DNA can then be detected using common avidin-... | |||
T15867 |
m-PEG4-aldehyde
|
Others | Others |
m-PEG4-aldehyde is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T33490 |
m-PEG12-aldehyde
|
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m-PEG12-aldehyde is a PEG derivative containing an aldehyde group. Aldehyde is reactive to hydrazide and aminooxy groups which are commonly used in biomolecular probes for labeling and crosslinking carbonyls (oxidized carbohydrates). The hydrophilic PEG s | |||
T17573 |
Biotin-PEG3-aldehyde
|
Others | Others |
Biotin-PEG3-aldehyde is a three-unit PEG linker with cleavable properties, specifically designed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18065 |
Lenalidomide-C9-aldehyde
|
Others | Others |
Lenalidomide-C9-aldehyde is a synthesized E3 ligase ligand-linker conjugate that incorporates the Lenalidomide based cereblon ligand and a linker. Lenalidomide-C9-aldehyde can be used in the synthesis of a series of PROTACs, such as INY-03-041. INY-03-041 | |||
T15850 |
m-PEG3-aldehyde
|
Others | Others |
m-PEG3-aldehyde is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T18474 |
N3-PEG5-aldehyde
|
Others | Others |
N3-PEG5-aldehyde is a 5-unit cleavable polyethylene glycol (PEG) linker specifically designed for antibody-drug conjugates (ADCs) synthesis[1]. | |||
T17563 |
Biotin-PEG2-aldehyde
|
Others | Others |
Biotin-PEG2-aldehyde is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17811 | DBCO-SS-aldehyde | Others | Others |
DBCO-SS-aldehyde is an ADC linker employed for ADC synthesis[1]. This cleavable linker is designed to facilitate the conjugation of antibodies and drugs, resulting in antibody-drug conjugates (ADCs). | |||
T35132 |
Wieland-gumlich aldehyde
Desacetyldiaboline,Caracurine VII,Deacetyldiaboline |
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Wieland-Gumlich aldehyde is an indoline derived by chemical degradation from strychnine. | |||
T15876 |
m-PEG4-CH2-aldehyde
|
Others | Others |
m-PEG4-CH2-aldehyde is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T36739 | Prednisone 21-aldehyde/22-hydroxy Prednisone | ||
Prednisone 21-aldehyde is a derivative of the synthetic corticosteroid prednisone that has antiviral activity against influenza virus A-PR8 in embryonated chicken eggs. 22-hydroxy Prednisone is an unstable adduct of prednisone. It has been observed following incubation of prednisone with nornicotine. This product is a mixture of prednisone 21-aldehyde and 22-hydroxy prednisone. | |||
T17564 | Biotin-PEG2-C1-aldehyde | Others | Others |
Biotin-PEG2-C1-aldehyde is a polyethylene glycol (PEG)-based linker utilized in synthesizing proteolysis targeting chimeras (PROTACs) [1]. | |||
T18800 | Tetrazine-Ph-PEG4-Ph-aldehyde | Others | Others |
Tetrazine-Ph-PEG4-Ph-aldehyde is a polyethylene glycol (PEG) derived linker, specifically designed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1]. | |||
T29820 |
Alaninal
Alanine aldehyde |
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Alaninal is useful to study the role of the different ceramide synthases and the resulting N-acyl (dihydro)ceramides in cell fate. | |||
T17281 |
Z-Ile-Leu-aldehyde
Z-IL-CHO,GSI-XII,γ-Secretase inhibitor XII |
Others | Others |
Z-Ile-Leu-aldehyde is an effective and competitive peptide aldehyde inhibitor of γ-secretase and notch. | |||
T124586 | Phloroglucinol aldehyde triethylether | ||
Phloroglucinol aldehyde triethylether 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 T124586,CAS号为 59652-88-9。 | |||
T76159 | Aldehyde dehydrogenase (NAD(P)) | ||
Aldehyde dehydrogenaseNAD(P) (ALDH) 催化醛氧化成相应的羧酸,伴随辅因子 NAD(P) 还原成 NAD(P)H,常用于生化研究。Aldehyde dehydrogenaseNAD(P) 是人体用来缓解乙醛应激的许多酶系统之一。 | |||
T7835 |
CM10
CM 10 |
Dehydrogenase | Metabolism |
CM10是一种有效的乙醛脱氢酶 1A (ALDH1A) 家族选择性抑制剂,对于 ALDH1A1,ALDH1A2 和 ALDH1A3 的IC50分别为 1700、740 和 640 nM。CM 10 可以调节新陈代谢并具有抗癌活性。 | |||
T76599 |
Ac-Leu-Val-Lys-Aldehyde
|
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Ac-Leu-Val-Lys-Aldehyde 是有效的组织蛋白酶 B (cathepsin B) 抑制剂,其 IC50 值为 4 nM。该化合物能显着降低喹啉酸引起的纹状体细胞死亡,并促使 LC3-II 积累。 | |||
T124473 | threo-Guaiacylglycerol-beta-coniferyl aldehyde ether | ||
threo-Guaiacylglycerol-beta-coniferyl aldehyde ether 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 T124473。 | |||
T80106 |
Z-Pro-Pro-aldehyde-dimethyl acetal
|
Prolyl Endopeptidase (PREP) | Metabolism; Proteases/Proteasome |
Z-Pro-Pro-aldehyde-dimethyl acetal 是一种高效的脯氨酸内肽酶(PRE P)抑制剂,其IC50值为12 nM。该化合物在衰老过程和神经退行性疾病,诸如阿尔茨海默病中认知功能障碍的研究中具有重要作用。 | |||
T72184 |
Ac-Tyr-Val-Lys-Asp-aldehyde
|
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Ac-Tyr-Val-Lys-Asp-aldehyde,一种caspase-1抑制剂,适用于慢性疾病相关贫血、化疗诱导贫血及钻石黑扇贫血的研究。 | |||
T31015 |
Coumarin, 3-glyoxyloyl-
3-Glyoxylcoumaric aldehyde,3-Glyoxyloylcoumarin,Aldeide cumarin-3-gliossilica |
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Coumarin, 3-glyoxyloyl-, is a coumarin analogue for treatment of various diseases. Substituting new functional groups at different positions of coumarin nucleus may be useful in the development of novel compounds for the treatment of cancer. | |||
T76600 |
Ac-Trp-Glu-His-Asp-Aldehyde
|
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Ac-Trp-Glu-His-Asp-Aldehyde 是一种有效的选择性 caspase-1抑制剂,Ki 值为 56 pM。 | |||
T124284 | Erythro-Guaiacylglycerol-beta-coniferyl aldehyde ether | ||
Erythro-Guaiacylglycerol-beta-coniferyl aldehyde ether 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 T124284。 | |||
T10140 |
4-Diethylaminobenzaldehyde
|
Dehydrogenase | Metabolism |
4-Diethylaminobenzaldehyde 是醛脱氢酶(ALDHs)的可逆抑制剂,对 ALDH1 的 Ki 为 4 nM,具有较强的抗雄激素作用 ,IC50为1.71 μM。 | |||
T31016 |
Coumarin, 3-glyoxyloyl-8-methoxy-
3-Glyoxyloyl-8-methoxycoumarin,3-Glyoxyl-8-methoxycoumaric aldehyde |
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Coumarin, 3-glyoxyloyl-8-methoxy- is a coumarin analogue for treatment of various diseases. Substituting new functional groups at different positions of coumarin nucleus may be useful in the development of novel compounds for the treatment of cancer. | |||
T12196 |
NCT-505
|
Dehydrogenase | Metabolism |
NCT-505是乙醛脱氢酶的选择性抑制剂,IC50为 7 nM。对 hALDH1A2,hALDH1A3,hALDH2,hALDH3A1的抑制作用较弱,IC50分别为 >57,22.8,20.1,>57 μM。 | |||
T6903 |
NCT-501
NCT501 |
Dehydrogenase | Metabolism |
NCT-501 是一种茶碱类化合物,有效抑制醛脱氢酶 1A1(ALDH1A1), 抑制 hALDH1A1 IC50为 40 nM, 选择性超过其它 ALDH 同工酶和其它脱氢酶 (作用于 hALDH1B1, hALDH3A1, 和 hALDH2 时,IC50值 >57 UM)。 | |||
T2662 |
Alda-1
Alda 1 |
Apoptosis; Dehydrogenase | Apoptosis; Metabolism |
Alda-1是一种 ALDH2 激动剂,是野生型 ALDH2*1 和亚洲 E487K 突变体 ALDH2*2 形式的线粒体醛脱氢酶 2 的细胞渗透激活剂。 | |||
T23533 |
WIN 18446
|
Dehydrogenase | Metabolism |
Win 18446 是口服有效的睾丸特异性的ALDH1a2的抑制剂,IC50为 0.3 μM。Win 18446 抑制睾丸内视黄醇合成视黄酸,可逆的抑制多个物种的精子形成,。 | |||
T7838 |
Losartan Carboxaldehyde
|
COX | Immunology/Inflammation; Neuroscience |
Losartan Carboxaldehyde 是氯沙坦的中间醛代谢产物。它不能阻断 AT1-R ,但可以抑制内皮环氧合酶 (COX)-2 的表达,起到抗炎作用。 | |||
T69244 |
Betulonaldehyde
|
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Betulonaldehyde is a pentacyclic triterpenoid and derivative of the cholesterol biosynthesis inhibitor betulin that has been found in Betula. It is active against P. falciparum (IC50 = 3.36 µg/ml) and cytotoxic to NCI H187 lung cancer cells and non-cancerous Vero cells (IC50s = 19.23 and 17.09 µg/ml, respectively). Topical application of betulonaldehyde (1 mg/ear) reduces ear edema induced by phorbol 12-myristate 13-acetate (TPA; Item No. 10008014) in mice. It has also been used a precursor in t... | |||
T0054 |
Disulfiram
双硫伦,Tetraethylthiuram disulfide,双硫仑,NSC 190940,TETD |
Dehydrogenase; Interleukin; Pyroptosis | Apoptosis; Immunology/Inflammation; Metabolism |
Disulfiram (TETD) 是一种乙醛脱氢酶 ALDH 的抑制剂,抑制 hALDH1 和 hALDH2 (IC50=0.15/1.45 μM),具有特异性。Disulfiram 对酒精产生急性敏感性,还可以抑制 GSDMD 孔形成。 | |||
T1389 |
Dyclonine hydrochloride
盐酸达克罗宁,Dyclocaine hydrochloride,Dyclonine HCl |
Sodium Channel; Antibacterial; Antifungal | Membrane transporter/Ion channel; Microbiology/Virology |
Dyclonine hydrochloride (Dyclonine HCl) 是润喉片的有效成分,具有显著的杀菌和杀真菌作用。 | |||
T2154 |
MG-132
Z-LLL-al,Z-Leu-Leu-Leu-CHO |
Apoptosis; Proteasome; Autophagy | Apoptosis; Autophagy; Proteases/Proteasome; Ubiquitination |
MG-132 (Z-Leu-Leu-Leu-al) 是一种 26S 蛋白酶体抑制剂 (IC50=100 nM),具有细胞渗透性、可逆性。MG-132 可作为自噬激活剂,可诱导凋亡。 | |||
T15022 |
CVT-10216
3-[[[3-[4-[(甲基磺酰基)氨基]苯基]-4-氧代-4H-苯并吡喃-7-基]氧基]甲基]苯甲酸 |
Dehydrogenase | Metabolism |
CVT-10216 是可逆的、选择性的醛脱氢酶 2(ALDH-2)抑制剂,IC50为 29 nM。对 ALDH-1的抑制作用较弱,IC50为 1.3 μM。 它可以减少偏爱酒精的大鼠过量饮酒,并表现出抗焦虑作用。 | |||
T20350 | Benzaldehyde, oxime | Others | Others |
Benzaldehyde, oxime 是合成色酮的中间体。 | |||
T0527 |
2,3,4-Trimethoxybenzaldehyde
Benzaldehyde,三甲氧基苯甲醛,Trimethoxybenzaldehyde |
Others | Others |
2,3,4-Trimethoxybenzaldehyde (Trimethoxybenzaldehyde) 用作医药中间体。 | |||
T4239 |
1,3-dimethyl-2-oxobenzimidazole-5-carbaldehyde
1,3-DIMETHYL-2-OXO-2,3-DIHYDRO-1H-BENZIMIDAZOLE-5-CARBALDEHYDE |
Others | Others |
1,3-dimethyl-2-oxobenzimidazole-5-carbaldehyde 是中间体。 | |||
T9354 |
2,4-Difluorobenzaldehyde
2,4-Difluoro-benzaldehyde,2,4-二氟苯甲醛 |
Others | Others |
2,4-Difluorobenzaldehyde 靶点-A 型肉毒杆菌神经毒素(肉毒杆菌)。 | |||
T18595 |
Dasatinib carbaldehyde
PROTAC ABL binding moiety 4,BMS-354825 carbaldehyde |
Others; Ligands for Target Protein for PROTAC | Others; PROTAC |
Dasatinib carbaldehyde (PROTAC ABL binding moiety 4) 基于 ABL 抑制剂达沙替尼,通过接头与 IAP 配体结合,形成 SNIPER [1]。 | |||
T9367 |
3-(Trifluoromethyl)benzaldehyde
3-三氟甲基苯甲醛,3-Trifluoromethylbenzaldehyde |
Others | Others |
3-(Trifluoromethyl)benzaldehyde (3-Trifluoromethylbenzaldehyde) 有强烈的甜味,被用作调味剂,香水和化妆品的生产,以及作为中间体合成各种化合物。 | |||
T5151 |
5-Methoxyindole-3-carboxaldehyde
|
Others | Others |
5-Methoxyindole-3-carboxaldehyde 用作中间体。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8086 |
Decyl aldehyde
|
Others; Endogenous Metabolite | Metabolism; Others |
Decyl aldehyde 是细菌荧光素酶底物,是十碳醛。 | |||
T7972 |
Gallic aldehyde
3,4,5-三羟基苯甲醛,五倍子醛 |
HSV | Microbiology/Virology |
Gallic aldehyde 对 HSV-1 显示出有效的抗病毒活性。 | |||
T4S1551 |
Cinnamaldehyde
Cinnamic Aldehyde,肉桂醛 |
HIF | Angiogenesis; Chromatin/Epigenetic |
Cinnamaldehyde (Cinnamic Aldehyde) 具有解热作用。 它是镇静剂。它抑制MDA-MB-435S 细胞的侵袭能力与下调miR-27a 的表达有关。它诱导活性氧的产生,发挥血管扩张和抗癌作用。 它似乎是一种有希望的候选药物,可作为与 5-氟尿嘧啶 (5-FU) 和奥沙利铂 (OXA) 这两种用于 CRC 治疗的化疗药物联合治疗的辅助剂。其作用的可能机制可能涉及药物代谢基因的调节。 它在抑制黑色素瘤的发生和发展方面具有一定的作用,其作用机制可能表现为抑制VEGF 和HIF-α的表达,从而使血管模拟和黑色素瘤细胞新生血管的形成,促进肿瘤的生长。 | |||
T3747 |
syringaldehyde
Syringic aldehyde,丁香醛,Springaldehyde |
COX | Immunology/Inflammation; Neuroscience |
syringaldehyde 是可从厚朴和木薯中分离得到的黄酮类多酚,具有抗氧化、抗高血糖和抗炎活性,可适度抑制COX-2活性,IC50为 3.5 μg/mL。 | |||
T20312 |
3-Phenylpropanal
NSC-9271,Phenylpropyl aldehyde,NSC9271,NSC 9271 |
Others | Others |
3-Phenylpropanal (Phenylpropyl aldehyde) 是RIFM 香料成分,可用于制作香水。3-Phenylpropanal 是杀螨剂的主要成分。3-Phenylpropanal 可作为苍蝇引诱剂使用。 | |||
T4918 |
DL-Glyceraldehyde
Glyceric aldehyde,DL-甘油醛晶体 |
Reductase | Endocrinology/Hormones; Metabolism |
DL-Glyceraldehyde (Glyceric aldehyde) 是由酶甘油醛脱氢酶的作用产生的,该酶使用 NADP 作为辅因子将甘油转化为甘油醛。它是一种高活性化合物,可以修饰和交联蛋白质。 | |||
T3796 |
Betulinaldehyde
Betulinic aldehyde,Betulinal,Betunal,白桦脂醛 |
Apoptosis; Antibacterial | Apoptosis; Microbiology/Virology |
Betulinaldehyde (Betunal) 是五环三萜,有抗金黄色葡萄球菌等细菌和真菌作用。 | |||
T7441 |
Cuminaldehyde
Cuminic aldehyde,4-异丙基苯甲醛,Cuminal |
Endogenous Metabolite | Metabolism |
Cuminaldehyde (Cuminal) 是一种具有抑制 α-突触核蛋白纤颤和细胞毒性作用的天然醛,是一种 Cuminum cyminum 的主要成分。它显示抗癌特性。 | |||
T2S1907 |
Coniferaldehyde
Ferulaldehyde,Ferulyl aldehyde,4-HYDROXY-3-METHOXYCINNAMALDEHYDE,松柏醛,Coniferyl aldehyde,松柏醛;4-羟基-3-甲氧基肉桂醛 |
Apoptosis; Antioxidant | Apoptosis; oxidation-reduction |
Coniferaldehyde (Ferulaldehyde) 是一种血红素加氧酶-1 的有效诱导剂,具有抗炎作用。在 RAW264.7 巨噬细胞中,它通过 PKCα/βII/Nrf-2/HO-1 依赖性途径来抑制 LPS 诱导的细胞凋亡。 | |||
T19536 |
Pyruvic aldehyde
|
Others | Others |
Pyruvic aldehyde is a flavoring agent, and in tanning. | |||
T3018 |
Protocatechualdehyde
Protocatechuic aldehyde,3,4-Dihydroxybenzaldehyde,Rancinamycin IV,Catechaldehyde,原儿茶醛 |
Reactive Oxygen Species; Antibacterial | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Protocatechualdehyde (3,4-Dihydroxybenzaldehyde),源自丹参根的天然多酚化合物,展现多样生物活性,并作为抗氧化剂、抗衰老剂、抗菌剂和抗炎剂在医药领域广泛应用。 | |||
T5256 |
All-trans-retinal
视黄醛,All trans-Retinal,Retinaldehyde,Vitamin A aldehyde |
Others; Endogenous Metabolite | Metabolism; Others |
All-trans-retinal (Vitamin A aldehyde) 是视网膜中维生素A 代谢物之一。 生理条件下,它再生为视觉发色团,11-顺式-视黄醛。 | |||
TN5382 |
Changweikang aldehyde
|
||
Changweikang aldehyde 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 TN5382,CAS号为 2119605-13-7。 | |||
TN5207 |
Ursolic aldehyde
|
Others | Others |
Ursolic aldehyde can inhibit phosphatase of regenerating liver-3, with the IC(50) value of 50 +/- 0.3 mu M. | |||
T3S1553 |
trans-Cinnamaldehyde
Cinnamaldehyde,Cinnamic aldehyde,桂皮醛,反式肉桂醛,Cinnamal,Phenylacrolein |
COX; Endogenous Metabolite | Immunology/Inflammation; Metabolism; Neuroscience |
trans-Cinnamaldehyde (Phenylacrolein) 是一种能够用于合成反式肉桂醛-β-环糊精复合物,一种能够食用的抗菌涂层,能够延长鲜切水果的保质期。它是一种能够通过烷基异氰化物与乙炔二羧酸二烷基酯的反应来合成高度多官能的呋喃环。 | |||
T7910 |
4-Methoxybenzaldehyde
大茴香醛,Anisaldehyde,p-Anisaldehyde,Anisic aldehyde,4-Anisaldehyde,4-甲氧基苯甲醛,P-Methoxybenzaldehyde |
Others; Endogenous Metabolite | Metabolism; Others |
4-Methoxybenzaldehyde (p-Anisaldehyde) 是一种天然存在的芳香酚类化合物,存在于许多植物物种中,包括辣根,茴香,八角茴香等。它是一种能够能的神经毒物,已经表现出致死亡率,吸引力和干扰宿主寻求的影响。 | |||
T79993 |
Oleanolic aldehyde
|
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Oleanolic aldehyde 是一种具有抗菌性质的化合物,能够抑制口腔内细菌生长。该化合物对变形链球菌和牙龈卟啉单胞菌——与龋齿和牙周病有关的细菌——显示出显著的抑制效果,其最低抑菌浓度(MICs)分别为488 μg/mL和250 μg/mL。 | |||
T4778 |
3-Hydroxybenzaldehyde
|
Others; Dehydrogenase | Metabolism; Others |
3-Hydroxybenzaldehyde 是很多酚类化合物的前体分子。它是人和大鼠醛脱氢酶 (ALDH) 的底物 (substrate)。它具有血管保护的作用。 | |||
TN4662 |
Nonanal
|
Others | Others |
Nonanal 是木材腐烂真菌的生长因子。 Nonanal 是松梢甲虫的潜在引诱剂。 | |||
TJS1382 |
Taraxerone
蒲公英赛酮 |
Dehydrogenase | Metabolism |
Taraxerone 是分离自景天的天然产物。它可以增强乙醇脱氢酶和乙醛脱氢酶活性,EC50分别为 512.42 μM 和 500.16 μM。 | |||
T4S0878 |
Prunetin
樱黄素,Prunusetin |
ERK; Dehydrogenase; NF-κB | MAPK; Metabolism; NF-κB |
Prunetin (Prunusetin) 是一种O-甲基化异黄酮,具有抗炎的作用。它是人醛脱氢酶的有效抑制剂。 | |||
T10148 |
4-Hydroxynonenal
4-羟基壬烯醛,4-HNE |
Dehydrogenase; Endogenous Metabolite | Metabolism |
4-Hydroxynonenal (4-HNE) 是一种 α,β 不饱和羟基烯醛,可作为氧化/亚硝化应激生物标志物。它是ALDH2的底物和抑制剂。它可以调节许多信号传导过程,主要是通过与蛋白质,核酸和膜脂质中具有亲核官能团的共价加合物形成的。它通过线粒体在癌症中起重要作用。 | |||
T5090 |
2-Methylbutyraldehyde
2-Ethylpropanal,RS)-2-Methylbutanal,2-甲基丁醛 |
Others | Others |
2-Methylbutyraldehyde (2-Ethylpropanal) 属于短链醛类化合物,白术饮片中的焦香味物质之一。 | |||
TN7184 |
5,6-dibromo-1H-indole-3-carbaldehyde
ZINC198368276,5,6-二溴吲哚-3-甲醛 |
Others | Others |
5,6-dibromo-1H-indole-3-carbaldehyde 是一种海洋来源的天然产物,存在于Smenospongia sp.。 | |||
T35704 |
2-Methoxybenzaldehyde
o-Anisaldehyde |
Antibacterial; Antifungal | Microbiology/Virology |
2-Methoxybenzaldehyde (o-Anisaldehyde) (o-Anisaldehyde), obtained from cinnamon essential oil (CEO), exhibits antibacterial and antifungal properties [1]. | |||
T67670 |
4-Ethylbenzaldehyde
|
Endogenous Metabolite | Metabolism |
4-Ethylbenzaldehyde 是一种 RIFM 香料,存在于自然发酵的罗非鱼香肠和大豆植株中。4-Ethylbenzaldehyde 在250 g/ml 时显示出杀线虫活性,可被当作一种新型杀线虫剂。 | |||
TN7136 |
1,7-dimethyl-1H-indole-3-carbaldehyde
1,7-dimethylindole-3-carbaldehyde,ZINC14592128,N,7-Dimethylindole-3-carbaldehyde |
Others | Others |
1,7-dimethyl-1H-indole-3-carbaldehyde (ZINC14592128) 是一种海洋来源的天然产物,存在于 Lyngbya majuscula。 | |||
T5657 |
Veratraldehyde
3,4-Dimethoxybenzaldehyde,藜芦醛 |
Antifungal | Microbiology/Virology |
Veratraldehyde (3,4-Dimethoxybenzaldehyde) 是一种能够使用于香料,农业化学和制药工业中的重要化学品。 | |||
TCS1857 |
2-Phenylacetaldehyde
Phenylacetaldehyde,Benzeneacetaldehyde,苯乙醛,Phenylethanal,Hyacinthin |
Others; Endogenous Metabolite | Metabolism; Others |
2-Phenylacetaldehyde (Hyacinthin) 是内源性代谢产物的一种。 | |||
TN3048 |
4-Methoxycinnamaldehyde
p-Methoxycinnamaldehyde |
RSV | Microbiology/Virology |
4-Methoxycinnamaldehyde (p-Methoxycinnamaldehyde) 是 Agastache rugosa 的一种活性成分。4-Methoxycinnamaldehyde 对人喉癌细胞系中的呼吸道合胞病毒 (RSV) 具有细胞保护活性,有助于控制 RSV 感染诱发的疾病,IC50 约为 0.055 μg/mL。 | |||
TN7051 |
2,4-Dihydroxybenzaldehyde
2,4-二羟基苯甲醛,4-Formylresorcinol,beta-Resorcylaldehyde,4-Hydroxysalicylaldehyde |
Endogenous Metabolite | Metabolism |
2,4-Dihydroxybenzaldehyde (4-Formylresorcinol) 是内源性代谢产物的一种。 | |||
TN2281 |
Sinapaldehyde
trans-3,5-Dimethoxy-4-hydroxy cinnamaldehyde,TRANS-3,5-二甲氧基-4-羟基肉桂醛,芥子醛 |
Antibacterial | Microbiology/Virology |
Sinapaldehyde (trans-3,5-Dimethoxy-4-hydroxy cinnamaldehyde) 对耐甲氧西林的金黄色葡萄球菌和大肠杆菌有抗菌作用,MIC 值都为 128 μg/mL。 | |||
T7973 |
BENZOFURAN-3-CARBALDEHYDE
|
Others | Others |
BENZOFURAN-3-CARBALDEHYDE 是一种天然产物。 | |||
TN6748 |
3-Methoxysalicylaldehyde
|
Others | Others |
3-Methoxysalicylaldehyde 是一种天然产物。 | |||
TN2730 |
2,5-Dihydroxybenzaldehyde
Gentisaldehyde,2,5-二羟基苯甲醛 |
Anti-infection; Antibacterial | Microbiology/Virology |
2,5-Dihydroxybenzaldehyde (Gentisaldehyde) 是一种天然抗微生物剂,可抑制Mycobacterium avium subsp. paratuberculosis 的生长。它还抑制金黄色葡萄球菌菌株,MIC50为 500 mg/L。 | |||
T2S1814 |
p-Hydroxybenzaldehyde
4-Formylphenol,4-羟基苯甲醛;对羟基苯甲醛,4-hydroxybenzaldehyde,对羟基苯甲醛,p-Oxybenzaldehyde |
Transaminase; GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
p-Hydroxybenzaldehyde (p-Oxybenzaldehyde) 是从天麻中提取的一种天然产物,对 GABA 转氨酶有抑制作用,有助于抗癫痫和抗惊厥活性。 | |||
TN1206 |
2,4,6-Trihydroxybenzaldehyde
|
Others | Others |
2,4,6-Trihydroxybenzaldehyde 是一种天然产物。 2,4,6-三羟基苯甲醛是一种潜在的抗肥胖治疗药物,可抑制 C57BL/6 小鼠的 3T3-L1 细胞中的脂肪细胞分化和高脂饮食诱导的脂肪积累。它也是一种有效的抗糖尿病药物。 2,4,6-三羟基苯甲醛具有潜在的抗癌活性。 | |||
TN5757 |
p-Hydroxybenzaldehyde glucoside
4-formylphenyl b-d-glucopyranoside,Gastrodin Impurity |
||
p-Hydroxybenzaldehyde glucoside (4-formylphenyl b-d-glucopyranoside) 是抑制天麻素衍生物,具有镇痛活性,可以用于研究神经源性疼痛。 | |||
T7452 |
2-methoxycinnamaldehyde
2'-甲氧基肉桂醛,O-methoxycinnamaldehyde |
Apoptosis; Others | Apoptosis; Others |
2-methoxycinnamaldehyde 是一种肉桂中的天然产物。它能通过使线粒体膜电位 (ΔΨm) 损失 、激活 caspase-3 和 caspase-9,来抑制细胞增殖和诱导细胞凋亡,具有抗肿瘤活性。它还能抑制血小板衍生生长因子诱导的 HASMC 迁移。 | |||
T2A2524 |
2-Hydroxy-4-methoxybenzaldehyde
4-甲氧基水杨醛,4-Methoxysalicylaldehyde,2-羟基-4-甲氧基苯甲醛 |
Tyrosinase; Antibacterial | Microbiology/Virology; Proteases/Proteasome |
2-Hydroxy-4-methoxybenzaldehyde (4-Methoxysalicylaldehyde) 是一种来自三种东非药用植物,Mondia whitei、Rhus vulgaris Meikle 和Sclerocarya caffra Sond 的酪氨酸酶抑制剂。它是香兰素的异构体,可用于合成尿苷M7。 | |||
TN3694 |
Coniferaldehyde
|
NOS; COX; Nrf2; PKC; Autophagy | Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; Neuroscience |
Coniferaldehyde 能显着抑制酒球菌菌株的生长活力。 Coniferaldehyde 通过诱导血红素加氧酶 1 (HO-1) 发挥抗炎特性。 | |||
T9599 |
3,4,5-Trimethoxybenzaldehyde
|
Anti-infection; Antibacterial | Microbiology/Virology |
3,4,5-Trimethoxybenzaldehyde 是合成各种药物,特别是治疗细菌感染的甲氧苄啶的中间体,它有抗念珠菌功效并抑制粘附和生物膜。 | |||
T19154 |
5-Methyl-2-thiophenecarboxaldehyde
|
Others | Others |
5-Methyl-2-thiophenecarboxaldehyde 是一种候选的微观三阶非线性光学(NLO)材料。5-Methyl-2-thiophenecarboxaldehyde 具有广泛的生物活性,如抗癌活性。 | |||
T2975 |
2,3-Dimethoxybenzaldehyde
5,6-Dimethoxybenzaldehyde,邻藜芦醛,o-Veratraldehyde |
Antifungal | Microbiology/Virology |
2,3-Dimethoxybenzaldehyde (5,6-Dimethoxybenzaldehyde) 是苯甲酸类似物,具有高抗真菌活性(MIC=2.5 mM)。2,3-Dimethoxybenzaldehyde 可用于合成小檗碱。 | |||
TN6975 |
Cirsiumaldehyde
5,5’-oxydimethylenebis(2-furfural) |
Platelet aggregation | Others |
Cirsiumaldehyde 是一种从Lobelia chinensis、Cornus officinalis 成熟果实和 Hippophae rhamnoides 果实中分分离出的化合物。Cirsiumaldehyde 在胶原蛋白存在下对 U46619 诱导(1~5 uM)的大鼠血小板聚集的抑制浓度为 0.8~1.0 ug/mL。 | |||
T2826 |
Asaraldehyde
Asarylaldehyde,2,4,5-trimethoxy-Benzaldehyde,Asaronaldehyde,细辛醛 |
COX | Immunology/Inflammation; Neuroscience |
Asaraldehyde (2,4,5-trimethoxy-Benzaldehyde) 是COX-2抑制剂,能够明显降低环加氧酶 II (COX-2) 的活性(IC50:100 μg/mL)。 | |||
T8105 |
Indole-3-carboxaldehyde
3-Formylindole,3-吲哚甲醛 |
Endogenous Metabolite | Metabolism |
Indole-3-carboxaldehyde (3-Formylindole) 是由黄化豌豆幼苗的粗酶制剂氧化降解IAA 的产物,是一种卷心菜提取物。它可用于制备吲哚类植物抗毒素环芸香素类似物。 | |||
TN6514 | 2-Carboxybenzaldehyde | ||
The major peak of 2-Carboxybenzaldehyde reductase activity in human liver co-purifies with hAFAR protein. Sulphydryl substances and some proteins play important roles in preserving the molecular and catalytic properties of 2-Carboxybenzaldehyde reductase. | |||
T9112 | (-)-Perillaldehyde | AhR; ROS; Nrf2 | Immunology/Inflammation; Metabolism |
L-Perillaldehyde 是紫苏草精油的主要成分,吸入后经由嗅觉神经功能表现出抗抑郁功能。 | |||
TN5027 |
Sinapaldehyde glucoside
|
Others | Others |
Sinapaldehyde glucoside是一种天然产物,属于芸香科黄柏属,其产品编号为 TN5027,CAS号为 154461-65-1。Sinapaldehyde glucoside可用作对照参考。 | |||
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