237
89
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T17372 |
Ald-Ph-NHS ester
|
Others | Others |
Ald-Ph-NHS ester 是用于抗体-药物偶联的不可切割接头。 | |||
T38721 |
ALD-PEG4-OPFP
ALD-PEG4-OPFP |
||
ALD-PEG4-OPFP is a cleavable ADC linker consisting of four units of PEG. It is specifically formulated for use in the synthesis of antibody-drug conjugates (ADCs). | |||
T38853 |
Methyl-PEG3-Ald
Methyl-PEG3-Ald |
||
Methyl-PEG3-Ald 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. | |||
T38632 |
Ald-Ph-amido-PEG11-NH-Boc
Ald-Ph-amido-PEG11-NH-Boc |
||
Ald-Ph-amido-PEG11-NH-Boc is a non-cleavable 11-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs). | |||
T39535 |
Ald-Ph-amido-PEG3-NHS ester
Ald-Ph-amido-PEG3-NHS ester |
||
Ald-Ph-amido-PEG3-NHS ester is a non-cleavable 3-unit PEG linker specifically designed for the synthesis of antibody-drug conjugates (ADCs). It is utilized as a chemical compound in connecting antibodies and drugs, forming stable conjugates. | |||
T17371 |
Ald-Ph-amido-PEG4-propargyl
Ald-benzyl-amide-PEG4-propargyl |
Others | Others |
Ald-Ph-amido-PEG4-propargyl is a non-cleavable 4-unit polyethylene glycol (PEG) antibody-drug conjugate (ADC) linker employed in ADC synthesis[1]. | |||
T38971 |
Me-triacetyl-β-D-glucopyranuronate-Ph-ald-NO2
Me-triacetyl-β-D-glucopyranuronate-Ph-ald-NO2 |
||
Me-triacetyl-β-D-glucopyranuronate-Ph-ald-NO2 is a cleavable linker employed in ADC synthesis for conjugation with antibodies, ultimately producing antibody-drug conjugates (ADCs). | |||
T38733 |
Ald-Ph-amido-PEG11-C2-NH2
Ald-Ph-amido-PEG11-C2-NH2 |
||
Ald-Ph-amido-PEG11-C2-NH2 is an 11-unit polyethylene glycol (PEG) linker that is non-cleavable. It is specifically designed for use in the synthesis of antibody-drug conjugates (ADCs). | |||
T17382 | Ald-Ph-amido-PEG2 | Others | Others |
Ald-Ph-amido-PEG2 is a noncleavable ADC linker for antibody-drug conjugate[1]. | |||
T14169 |
Ald-Ph-PEG6-acid
|
Others | Others |
Ald-Ph-PEG6-acid 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. | |||
T17375 |
Ald-Ph-PEG24-NHS ester
|
Others | Others |
Ald-Ph-PEG24-NHS ester 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. | |||
T14157 |
Ald-CH2-PEG4-Boc
|
Others | Others |
Ald-CH2-PEG4-Boc 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. | |||
T17374 |
Ald-Ph-PEG2-Boc
|
Others | Others |
Ald-Ph-PEG2-Boc 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. | |||
T14167 |
Ald-Ph-PEG4-Boc
|
Others | Others |
Ald-Ph-PEG4-Boc 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. | |||
T17377 |
Ald-Ph-PEG5-Boc
|
Others | Others |
Ald-Ph-PEG5-Boc 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. | |||
T14160 |
Ald-CH2-PEG5-Boc
|
Others | Others |
Ald-CH2-PEG5-Boc is a PEG- and Alkyl/ether-based PROTAC linker suitable for synthesizing PROTACs[1]. | |||
T14159 |
Ald-CH2-PEG5-azide
|
Others | Others |
Ald-CH2-PEG5-azide is a non-cleavable linker consisting of a five unit PEG chain, commonly employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T14170 |
Ald-Ph-PEG6-Boc
|
Others | Others |
Ald-Ph-PEG6-Boc 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. | |||
T17366 |
Ald-CH2-PEG10-Boc
|
Others | Others |
Ald-CH2-PEG10-Boc 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. | |||
T17367 |
Ald-CH2-PEG8-azide
|
Others | Others |
Ald-CH2-PEG8-azide 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. | |||
T14156 |
Ald-CH2-PEG3-azide
|
Others | Others |
Ald-CH2-PEG3-azide is a cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T14161 |
Ald-PEG1-C2-Boc
|
Others | Others |
Ald-PEG1-C2-Boc is an alkyl-ether-based linker utilized for the synthesis of PROTACs, a class of small molecules that induce targeted protein degradation[1]. | |||
T14155 |
Ald-C2-PEG4-azide
N3-PEG4-CH2CH2CHO |
Others | Others |
Ald-C2-PEG4-azide 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. | |||
T17378 |
Ald-Ph-amido-C2-nitrate
|
Others | Others |
Ald-Ph-amido-C2-nitrate (Example XXIVb) is a thiazolidine derivative primarily employed as a noncleavable ADC linker[1]. | |||
T17370 |
Ald-Ph-amido-PEG24-acid
|
Others | Others |
Ald-Ph-amido-PEG24-acid is a polyethylene glycol (PEG)-based linker used for the synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T14166 |
Ald-Ph-PEG2-NH-Boc
|
Others | Others |
Ald-Ph-PEG2-NH-Boc 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. | |||
T17373 |
Ald-Ph-PEG12-TFP ester
|
Others | Others |
Ald-Ph-PEG12-TFP ester 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. | |||
T14168 |
Ald-Ph-PEG4-NH-Boc
|
Others | Others |
Ald-Ph-PEG4-NH-Boc 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. | |||
T17369 |
Ald-Ph-amido-PEG23-OPSS
|
Others | Others |
Ald-Ph-amido-PEG23-OPSS is a cleavable 23-unit polyethylene glycol linker commonly employed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T14158 |
Ald-CH2-PEG3-CH2-Boc
|
Others | Others |
Ald-CH2-PEG3-CH2-Boc, a PEG- and Alkyl/ether-based PROTAC linker, is utilized for the synthesis of SGK3 kinase PROTAC degrader[1]. | |||
T17383 |
Ald-Ph-amido-PEG3-C-COOH
|
Others | Others |
Ald-Ph-amido-PEG3-C-COOH is a noncleavable linker utilized in the formation of antibody-drug conjugates (ADCs). | |||
T17376 |
Ald-Ph-PEG24-TFP ester
|
Others | Others |
Ald-Ph-PEG24-TFP ester 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. | |||
T14173 |
Ald-Ph-amido-PEG3-C2-NH2
|
Others | Others |
Ald-Ph-amido-PEG3-C2-NH2 is a PEG-based PROTAC linker employed in PROTACs synthesis[1]. | |||
T17368 |
Ald-Ph-amido-C2-PEG3-azide
|
Others | Others |
Ald-Ph-amido-C2-PEG3-azide 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. | |||
T14163 |
Ald-Ph-amido-C2-PEG3-NH-Boc
|
Others | Others |
Ald-Ph-amido-C2-PEG3-NH-Boc is a polyethylene glycol (PEG)-based bifunctional linker utilized for the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1]. | |||
T14171 |
Ald-Ph-amido-PEG2-C2-acid
|
Others | Others |
Ald-Ph-amido-PEG2-C2-acid is a PEG-based PROTAC linker utilized for synthesizing PROTACs[1]. | |||
T17384 |
Ald-Ph-amido-PEG3-C1-Boc
|
Others | Others |
Ald-Ph-amido-PEG3-C1-Boc is a polyethylene glycol (PEG) linker specific to antibody-drug conjugates (ADC). | |||
T14174 |
Ald-Ph-amido-PEG4-C2-acid
|
Others | Others |
Ald-Ph-amido-PEG4-C2-acid is a noncleavable linker utilized in the development of antibody-drug conjugates (ADC). | |||
T14162 |
Ald-Ph-amido-C2-PEG2-amine
|
Others | Others |
Ald-Ph-amido-C2-PEG2-amine is a polyethylene glycol (PEG)-based linker utilized for the synthesis of PROteolysis TArgeting Chimeras (PROTACs)[1]. | |||
T14164 |
Ald-Ph-amido-PEG2-C2-Boc
|
Others | Others |
Ald-Ph-amido-PEG2-C2-Boc is a polyethylene glycol (PEG)-based linker utilized for the synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T17380 |
Ald-Ph-amido-PEG1-C2-Pfp ester
|
Others | Others |
Ald-Ph-amido-PEG1-C2-Pfp ester is a non-cleavable 1-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs. | |||
T17385 |
Ald-Ph-amido-PEG3-C2-Pfp ester
|
Others | Others |
Ald-Ph-amido-PEG3-C2-Pfp ester is a noncleavable antibody-drug conjugate (ADC) linker that falls under the category of polyethylene glycol (PEG) linkers. | |||
T14165 |
Ald-Ph-amido-PEG4-C2-NHS ester
|
Others | Others |
Ald-Ph-amido-PEG4-C2-NHS ester is a non-cleavable 4-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs. | |||
T14172 |
Ald-Ph-amido-PEG2-C2-NHS ester
|
Others | Others |
Ald-Ph-amido-PEG2-C2-NHS ester is a non-cleavable 2-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs. | |||
T17379 |
Ald-Ph-amido-PEG1-C2-NHS ester
|
Others | Others |
Ald-Ph-amido-PEG1-C2-NHS ester is a non-cleavable 1-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs. | |||
T17381 |
Ald-Ph-amido-PEG2-C2-Pfp ester
|
Others | Others |
Ald-Ph-amido-PEG2-C2-Pfp ester is a non-cleavable 2-unit PEG linker employed in antibody-drug conjugation (ADC) to connect antibodies with drugs. | |||
T9578 |
ELOVL1-IN-1
1-(2-Fluorophenyl)-N-(1-(2-fluoropyridin-4-YL)-1H-pyrazol-3-YL)cyclopropane-1-carboxamide |
Others | Others |
ELOVL1-IN-1 (1-(2-Fluorophenyl)-N-(1-(2-fluoropyridin-4-YL)-1H-pyrazol-3-YL)cyclopropane-1-carboxamide) 是ELOVL1抑制剂,能够降低超长链脂肪酸的水平,可用于肾上腺脑白质营养不良的研究。 | |||
T0219 |
Valdecoxib
伐地考昔,代他考昔,SC 65872 |
COX | Immunology/Inflammation; Neuroscience |
Valdecoxib (SC 65872) 是可口服的高选择性 COX-2抑制剂,对 COX-2 和 COX-1 的 IC50值分别为 5 nM 和 140 μM,可用于治疗骨关节炎、类风湿性关节炎以及痛经和经期症状。 | |||
T24398 |
Lenaldekar
LDK |
Akt; IGF-1R; S6 Kinase | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
Lenaldekar (LDK) 抑制 T 细胞扩增和自身免疫性脑脊髓炎。 Lenaldekar 导致 PI3 激酶/AKT/mTOR 通路成员的去磷酸化并延迟有丝分裂晚期的敏感细胞。 | |||
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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.。 | |||
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。 | |||
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]. | |||
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。 | |||
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), a natural polyphenol compound derived from radix Salviae Miltiorrhizae roots, exhibits diverse biological activities and finds extensive medicinal applications as an antioxidant, anti-aging, antibacterial, and anti-inflammatory agent. | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
TN7214 |
Galdosol
|
Others | Others |
Galdosol 是一种天然产物,存在于植物分药花分药花Perovskia abrotanoides。 | |||
TN6748 |
3-Methoxysalicylaldehyde
|
Others | Others |
3-Methoxysalicylaldehyde 是一种天然产物。 | |||
T7973 |
BENZOFURAN-3-CARBALDEHYDE
|
Others | Others |
BENZOFURAN-3-CARBALDEHYDE 是一种天然产物。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T36786 |
2-Hydroxy-4-methylbenzaldehyde
|
Endogenous Metabolite | Metabolism |
2-Hydroxy-4-methylbenzaldehyde 是人内源性代谢产物。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T4930 |
ISOBUTYRALDEHYDE OXIME
|
Others | Others |
ISOBUTYRALDEHYDE OXIME 是衍生自 2-methylpropanal 的醛肟。它来源于异丁醛。 | |||
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。 | |||
T8086 |
Decyl aldehyde
|
Others; Endogenous Metabolite | Metabolism; Others |
Decyl aldehyde 是细菌荧光素酶底物,是十碳醛。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T0908 |
Chlorquinaldol
5,7-Dichloro-8-hydroxy-2-methylquinoline,Chloquinan,氯喹那多 |
Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Chlorquinaldol (5,7-Dichloro-8-hydroxy-2-methylquinoline) 是一种抗菌剂, 有潜力研究局部皮肤病症和阴道感染。 | |||
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。 | |||
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。 | |||
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。 | |||
T22470 |
10Z-Hymenialdisine
|
Others | Others |
Pan kinase inhibitor | |||
TN6657 |
4-(Dimethylamino)cinnamaldehyde
|
||
4-Dimethylaminocinnamaldehyde is a photometric reagent for primary aromatic amines. The 4-(dimethylamino)cinnamaldehyde assay is currently used to quantify proanthocyanidin (PAC) content in cranberry products. | |||
TN4455 |
Lucialdehyde B
|
Integrase; HSV | Microbiology/Virology |
Lucialdehyde B exhibits potent inhibitory activity against herpes simplex virus. It shows cytotoxic effects on Lewis lung carcinoma (LLC), T-47D, Sarcoma 180, and Meth-A tumor cell lines. | |||
T35596 |
Debromohymenialdisine
|
||
Debromohymenialdisine 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 T35596,CAS号为 75593-17-8。 | |||
TN2956 |
3-Methoxy-4,5-methylenedioxycinnamaldehyde
|
Others | Others |
3-Methoxy-4,5-methylenedioxycinnamaldehyde is a natural product from Artemisia annua L. | |||
TN4025 | Eucamalduside A | Others | Others |
Eucamalduside A is a natural product from Eucalyptus camaldulensis var. obtusa. | |||
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