1273
105
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11615 |
IDO-IN-12
|
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-12 是吲哚胺 2,3-双加氧酶抑制剂。 | |||
T11616 |
IDO-IN-13
GS-4361 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-13 (GS-4361) 是 indoleamine 2,3-dioxygenase 1 抑制剂,EC50=17 nM。 | |||
T7660 |
IDO inhibitor 1
4-[[2-[(氨基磺酰基)氨基]乙基]氨基]-N'-(3-溴-4-氟苯基)-N-羟基-1,2,5-恶二唑-3-甲脒 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO inhibitor 1 是一种有效的吲哚胺-2,3 双加氧酶 (IDO) 抑制剂 (IC50 <100 nM)。具有潜在的免疫调节和抗肿瘤活性。 | |||
T7181 |
IDO-IN-1
4-氨基-N-(3-溴-4-氟苯基)-N'-羟基-1,2,5-恶二唑-3-甲脒 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-1 是吲哚胺-2,3-双加氧酶抑制剂,IC50=59 nM。 | |||
T1806 |
IDO-IN-7
NLG919,Navoximod,NLG-919 analogue,GDC-0919 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-7 (NLG-919 analogue) 是 IDO1 抑制剂,IC50=38 nM。 | |||
T4142 |
PCC0208009
IDO inhibitor 1,DO-IN-2,IDO-IN-2 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
PCC0208009 (IDO-IN-2) 是一种有效的 IDO 抑制剂,其在 HeLa 细胞中的 IC50=4.52 nM。它调节 ACC 和杏仁核的突触可塑性,减少神经性疼痛和合并症。 | |||
T3548 |
Epacadostat
INCB 024360,艾卡哚司他,IDO Inhibitor 1 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Epacadostat (INCB 024360) 是选择性的IDO1抑制剂,IC50=71.8 nM。 | |||
T11901 |
IDO1-IN-5
|
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO1-IN-5 是可透过血脑屏障的、选择性的IDO1抑制剂,能够与缺乏血红素的 apo-IDO1 结合,但无法与成熟血红素的 IDO1 结合。 | |||
T40093 | IDO-IN-15 | ||
IDO-IN-15 is an IDO1 inhibitor ( IC 50 < 0.51 nM). | |||
T11618 |
IDO-IN-4
|
Others | Others |
IDO-IN-4 is an indoleamine 2,3-dioxygenase 1 (IDO-1) inhibitor. | |||
T11619 |
IDO-IN-5
NLG-1489 |
IDO | Metabolism |
IDO-IN-5 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM). | |||
T11617 | IDO-IN-3 | IDO | Metabolism |
IDO-IN-3 is a potent indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 290 nM). | |||
T11622 |
IDO-IN-9
|
IDO | Metabolism |
IDO-IN-9 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.011 μM (Kinase) and 0.0018 μM (Hela Cell). | |||
T11614 | IDO-IN-11 | IDO | Metabolism |
IDO-IN-11 is an indoleamine-2,3-dioxygenase (IDO) inhibitor with IC50s of 0.18 μM (Kinase) and 0.014 μM (Hela Cell). | |||
T11623 |
IDO/TDO-IN-1
|
Others | Others |
IDO/TDO-IN-1 is an orally active dual indoleamine-2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO) inhibitor (IC50s: 9.7 and 47 nM). | |||
T11621 |
IDO-IN-8
NLG-1487 |
IDO | Metabolism |
IDO-IN-8 is an indoleamine 2,3-dioxygenase (IDO) inhibitor (IC50: 1-10 μM). | |||
T11620 |
IDO-IN-6
NLG-1486 |
IDO | Metabolism |
IDO-IN-6 is an indoleamine 2,3-dioxygenase (IDO) inhibitor. | |||
T11626 |
IACS-8968
IDO/TDO Inhibitor |
IDO | Metabolism |
IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO). | |||
T11627 |
IACS-8968 R-enantiomer
IDO/TDO Inhibitor (R-enantiomer) |
IDO | Metabolism |
IACS-8968 R-enantiomer is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO). | |||
T62130 | IDO-IN-16 | ||
IDO-IN-16 (compound 5) 是一种 IDO 抑制剂 (IC50: 36 nM)。 | |||
T2647 |
IDO5L
INCB024360 analogue,INCB14943 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO5L (INCB024360 analogue) 是一种有效的吲哚胺-2,3-双加氧酶 (IDO) 抑制剂,IC50=67 nM。 | |||
T62270 |
IDO-IN-14
|
||
IDO-IN-14 是一种 IDO 抑制剂 (IC50: 0.6928 nM)。 | |||
T11628 |
IACS-8968 S-enantiomer
IDO/TDO Inhibitor (S-enantiomer) |
IDO | Metabolism |
IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO). | |||
T74536 | IDO/Tubulin-IN-2 | ||
IDO/Tubulin-IN-2 (HT2) 是一种对TDO和微管蛋白 (tubulin)展现出高效抑制作用的化合物。该抑制剂对多种癌细胞系(包括U87、HepG2、A549、HCT-116和LO2)均表现出强抗肿瘤活性,其半抑制浓度(IC50)分别为0.43、0.036、0.041、0.095和1.04 μM,有效提升了抗肿瘤效果。 | |||
T39888 |
IDO1-IN-7
IDO1-IN-7 |
||
IDO1-IN-7, a potent and selective indoleamine-2,3-dioxygenase-1 (IDO1) inhibitor, exhibits high potency with an IC 50 of 6.1 nM in the cellular assay (SKOV3). Apart from its inhibitory properties, IDO1-IN-7 also demonstrates immunomodulatory effects, contributing to its potential applications in cancer research. | |||
T39839 |
IDO1-IN-11
IDO1-IN-11 |
||
IDO1-IN-11 is an IDO1 inhibitor with an IC 50 value of 0.6 nM. | |||
T39946 |
IDO1-IN-12
IDO1-IN-12 |
||
IDO1-IN-12 is a potent and orally available IDO1 inhibitor. | |||
T37329 |
PROTAC IDO1 Degrader-1
PROTAC IDO1 Degrader-1 |
||
PROTAC IDO1 Degrader-1 is the first potent IDO1 (indoleamine 2,3-dioxygenase 1) degrader that hijacks IDO1 to CRBN E3 ligase to introduce IDO1 into UPS and eventually achieve ubiquitination and degradation (DC50=2.84 μM). PROTAC IDO1 Degrader-1 moderately improves the tumor-killing activity of H ER2 CAR-T cells[1]. PROTAC IDO1 Degrader-1 (compound 2c) (10 μM; 24 hours) notably decreases IDO1 level induced by IFN-γ[1].PROTAC IDO1 Degrader-1 and IFN-γ (5 ng/mL) are incubated with HeLa cells for 24... | |||
T10199 |
GNF-PF-3777
8-Nitrotryptanthrin |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
GNF-PF-3777 (8-Nitrotryptanthrin) 是人吲哚胺2,3-双加氧酶 2 (hIDO2) 抑制剂,能够降低IDO2活性,Ki=为 0.97 μM。 | |||
T9164 |
BMS-986242
BMS986242 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
BMS-986242 是具有口服具有活力、强效的、选择性的 indoleamine-2,3-dioxygenase 1 抑制剂,可用于研究癌症。 | |||
T4307 |
PF-06840003
EOS200271,PF 06840003 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
PF-06840003 (EOS200271) 是口服具有活力的、选择性的IDO-1抑制剂,抑制 hIDO-1, dIDO-1和 mIDO-1 的IC50分别为 0.41 μM, 0.59 μM,和 1.5 μM。 | |||
TQ0071 |
Navoximod
GDC-0919,NLG-919 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Navoximod (GDC-0919) 是 IDO(indoleamine-(2,3)-dioxygenase) 抑制剂,Ki=7 nM/,EC50=75 nM。 | |||
T4532 |
Linrodostat
BMS-986205 |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Linrodostat (BMS-986205) 是选择性的、不可逆的吲哚胺 2,3-双加氧酶 1(IDO1) 抑制剂,能够有效抑制 IDO1-HEK293 细胞,其IC50=1.1 nM。它在晚期癌症中具有良好的药理特性。 | |||
T1847 |
Necrostatin-1
Nec-1,Necrostatin 1 |
Indoleamine 2,3-Dioxygenase (IDO); Ferroptosis; Autophagy; RIP kinase | Apoptosis; Autophagy; Metabolism; NF-κB |
Necrostatin-1 (Nec-1) 是一种坏死性凋亡抑制剂和 RIP1 抑制剂,具有特异性。Necrostatin-1 抑制 TNF-α 诱导的坏死性凋亡。Necrostatin-1 也可以抑制 IDO。 | |||
T20513 |
IDO1-IN-1
IDO1 inhibitor 1,2 HzBTZ,2-肼基苯并噻唑,IDO1IN1,2-HzBTZ,IDO1-inhibitor-1 |
IDO | Metabolism |
IDO1-IN-1 (2 HzBTZ) 是一种吲哚胺 2,3-双加氧酶 1 (IDO1) 抑制剂。 | |||
T11624 | IDO1-IN-2 | IDO | Metabolism |
IDO1-IN-2 is a potent and selective IDO1 inhibitor with IC50s of 81 nM, 59 nM (mouse), and 28 nM (rat), respectively. It has anti-cancer activity. | |||
T11625 | IDO1 and HDAC1 Inhibitor | Others | Others |
IDO1 and HDAC1 Inhibitor is a dual IDO1 and HDAC1 inhibitor (IC50s: 69.0 nM and 66.5 nM). | |||
T6543 |
Indoximod
NLG-8189,Indoximod (NLG-8189),1-Methyl-D-tryptophan,吲哚莫德 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Indoximod (Indoximod (NLG-8189)) 是一种具有口服具有活力的吲哚胺2,3-双加氧酶(IDO) 途径抑制剂。它在调节 mTOR 中充当 Trp 模拟物。它是一种可用于癌症研究的免疫代谢佐剂。 | |||
T12801 |
(S)-IDO1-IN-5
|
Others | Others |
(S)-IDO1-IN-5 is an active S-isomer of IDO1-IN-5. (S)-IDO1-IN-5 binds to IDOL(IC50 value less than 1.5 µΜ). | |||
T12668 |
(Rac)-IDO1-IN-5
|
Others | Others |
(Rac)-IDO1-IN-5 is a racemate of IDO1-IN-5, a potent, selective, and brain-penetrating inhibitor of Indoleamine 2,3-Dioxygenase 1 (IDO1) activity. It specifically binds to apo-IDO1, which lacks heme, instead of mature heme-bound IDO1. | |||
T61789 | IDO1-IN-14 | ||
IDO1-IN-14 (compound 4a) is a highly effective inhibitor of the IDO1 enzyme, exhibiting an IC50 value of 396.9 nM. Additionally, IDO1-IN-14 demonstrates excellent suppression of cellular IDO1 activity, as observed in HeLa cells with an EC50 value of 3393 nM [1]. | |||
T82082 | IDO1-IN-23 | Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO1-IN-23(化合物41)是一种有效的人类IDO1抑制剂,具备13 μM的IC50值。 | |||
T78687 | IDO1-IN-21 | Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO1-IN-21(化合物10m)为IDO1抑制剂,其IC50值为0.64 μM。该化合物在小鼠体内可有效抑制肿瘤生长。 | |||
T61944 |
IDO1-IN-15
|
||
IDO1-IN-15 是有效的IDO1抑制剂,IC50为127 nM。IDO1-IN-15与Epacadostat 在体外对抗 IDO1 酶的效力相当。 | |||
T74507 |
IDO1-IN-20
|
||
IDO1-IN-20是一种催化色氨酸氧化代谢的酶,能在肿瘤微环境中对肿瘤进行免疫抑制。 | |||
T63814 |
IDO2-IN-1
|
||
IDO2-IN-1 是一种口服活性的强效IDO2抑制剂,其IC50为112 nM。该化合物适用于炎症性自身免疫研究。 | |||
T7504 |
Necrostatin 2 racemate
5-[(7-氯-1H-吲哚-3-基)甲基]-3-甲基-2,4-咪唑烷二酮,Necrostatin-2 racemate |
RIP kinase | Apoptosis; NF-κB |
Necrostatin 2 racemate (Necrostatin-2 racemate) 是一种特异性的RIPK1抑制剂,是一种稳定型 Nec-1。 | |||
T63034 | IDO1-IN-13 | ||
IDO1-IN-13 (compound 27a) 是一种 IDO1 的有效抑制剂 (IC50: 61.6 nM)。IDO1-IN-13 能够抑制细胞 IDO1,对 HeLa 的 EC50 值为 30 nM。在 SK-OV-3 异种移植肿瘤组织中,IDO1-IN-13 减少了 51% 的 kyn/trp 比率。 | |||
T73111 | IDO1-IN-17 | ||
IDO1-IN-17 (I-4) 是IDO1的抑制剂,其在 hela 细胞中的IC50值为 0.44 μM。 | |||
T63082 |
IDO1-IN-19
|
||
IDO1-IN-19 (Compound 17) 是一种 IDO1 的有效抑制剂,具有潜力进行癌症疾病的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4S0051 |
Coptisine sulfate
|
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Coptisine Sulfate 是一种从黄连中分离到的生物碱,是非竞争性的IDO 抑制剂,Ki=为 5.8 μM,IC50=6.3 μM。 | |||
T3S1967 |
(S)-Indoximod
N-ME-Tryptophan,Abrine,相思豆碱,L-Abrine |
Others; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism; Others |
(S)-Indoximod (L-Abrine) 是一种吲哚胺-2,3-双加氧酶 (IDO) 抑制剂,可用于研究癌症。 | |||
T5S0053 |
Coptisine
黄连碱,Coptisin |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Coptisine (Coptisin) 是一种从黄连中分离到的生物碱,是非竞争性的IDO 抑制剂,Ki=为 5.8 μM,IC50=6.3 μM。 | |||
T2718 |
Palmatine chloride
|
Others; Indoleamine 2,3-Dioxygenase (IDO); Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Others |
Palmatine chloride 是口服具有活力的不可逆 IDO-1抑制剂。它能够减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,并改善 DSS 诱发的结肠炎。 | |||
T5S0802 |
Palmatine
巴马汀,Berbericinine,Burasaine |
Indoleamine 2,3-Dioxygenase (IDO); AChR; AChE; Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Metabolism; Neuroscience |
Palmatine (Burasaine) 是口服具有活力的、不可逆IDO-1抑制剂。它可以减轻结肠损伤,预防肠道菌群失调和调节色氨酸分解代谢,从而改善DSS (Dextran Sulphate Sodium Salt) 诱发的结肠炎。它有用于结肠炎的研究潜力。 | |||
T5S0056 |
Coptisine chloride
盐酸黄连碱,氯化黄连碱,Q-100696,NSC-119754 |
Indoleamine 2,3-Dioxygenase (IDO); Influenza Virus; Antibacterial | Metabolism; Microbiology/Virology |
Coptisine chloride (NSC-119754) 是从黄连中分离到的一种生物碱,是一种非竞争性 IDO 抑制剂,Ki 值为 5.8 μM,IC50值为 6.3 μM。它是一种 H1N1 神经氨酸酶抑制剂,可用于甲型流感病毒感染,IC50为 104.6 μg/mL。 | |||
T8214 |
Kushenol E
苦参醇E,Flemiphilippinin D |
IDO; Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
Kushenol E (Flemiphilippinin D) 是一种分离自Sophora flavescens 中的类黄酮,是一种IDO1的非竞争性抑制剂,其IC50=7.7 µM,Ki=为 9.5 µM,具有抗肿瘤特性。 | |||
T5085 |
Pyridoxal 5'-phosphate hydrate
Codecarboxylase,Pyridoxal 5'-phosphate hydrate(1:x),5-磷酸吡多醛水合物,PLP,Pyridoxal 5'-phosphate hydrate |
Others; Endogenous Metabolite | Metabolism; Others |
Pyridoxal 5'-phosphate hydrate (PLP) 是内源性代谢产物的一种。 | |||
T7916 |
4-Acetamidobenzenesulfonyl azide
|
Others | Others |
4-Acetamidobenzenesulfonyl azide 用于各种科学研究应用,包括药物、肽和其他生物活性分子的合成,也被用作聚合反应和聚合物合成中的催化剂。 | |||
T14011 |
2-Arachidonoylglycerol
|
Cannabinoid Receptor; Endogenous Metabolite | GPCR/G Protein; Metabolism |
2-Arachidonoylglycerol 属于人内源性代谢物,是中枢神经系统中的一种内源性大麻素配体。 | |||
T19962 |
Xyloidone
NSC-106453,NSC106453,Dehydro-α-lapachone,NSC 106453,Dehydrolapachone,脱氢拉帕醌,NSC 629748 |
Antifungal | Microbiology/Virology |
Xyloidone (NSC-106453) 具有抗真菌活性,在 0.4-33.3 mg/L 的范围内完全抑制 B. cinerea、Colletotrichum acutatum Simmonds、Colletotrichum gloeosporioides Simmonds、M. grisea 和 Pythium ultimum Trow 的菌丝生长。 | |||
T4728 |
4-Acetamidobutanoic acid
N-acetyl GABA,4-ACETAMIDOBUTYRIC ACID,4-乙酰氨基丁酸 |
GABA Receptor; Endogenous Metabolite; Antibacterial | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience |
4-Acetamidobutanoic acid (4-ACETAMIDOBUTYRIC ACID) 可在血液、粪便和尿液以及人体前列腺组织中找到,也存在于从酵母到人类的所有真核生物中。它是GABA 衍生物,具有抗氧化和抗菌活性。 | |||
T0076 |
Paliperidone
9-羟基利培酮,帕潘立酮,9-hydroxyrisperidone |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Paliperidone (9-hydroxyrisperidone) 是 Risperidone 的主要活性代谢产物,是多巴胺 D2 拮抗剂和5-HT2A 拮抗剂。它用作非典型抗精神病药,用于精神分裂症的急性及维持治疗。它对α1和α2肾上腺素能受体和 H1组胺能受体也有拮抗作用。 | |||
T5226 |
2-(2-Methylbenzamido)acetic acid
2-Methylhippuric acid,2-甲基马尿酸,O-Toluric acid,N-(O-Toluoyl)glycine |
Others; Endogenous Metabolite | Metabolism; Others |
2-(2-Methylbenzamido)acetic acid (O-Toluric acid) 是一种能够在尿液中检测到的代谢物。 | |||
T4805 |
α-Pyridone
2-Hydroxypyridine,2-羟基吡啶 |
Others; Endogenous Metabolite | Metabolism; Others |
α-Pyridone (2-Hydroxypyridine) 是内源性代谢产物的一种。 | |||
T0436 |
6-Acetamidohexanoic acid
醋氨己酸,6-Acetamidocaproic acid,Acexamic Acid |
Amino Acids and Derivatives; COX | Immunology/Inflammation; Metabolism; Neuroscience |
6-Acetamidohexanoic acid (Acexamic Acid) 是一种医药中间体。 | |||
T9279 |
nerolidol acetate
|
Others | Others |
Nerolidol acetate是一种具有抗癌、抗炎、抗菌和抗虫的活性的天然倍半萜。Nerolidol acetate可抑制寄生虫活动,抑制吸血虫病、线虫病以及疟疾等。Nerolidol acetate可保护细胞免受脂质、蛋白质和 DNA 的氧化损伤,对小鼠海马神经细胞具有保护作用。 | |||
T5217 |
2-(2-Phenylacetamido)acetic acid
Phenaceturic acid,Phenyl-ac-Gly-OH,苯乙酰甘氨酸,Phenylacetyl glycine |
Others; Endogenous Metabolite | Metabolism; Others |
2-(2-Phenylacetamido)acetic acid (Phenyl-ac-Gly-OH) 是内源性代谢产物的一种。 | |||
TN1035 |
Irisolidone
尼泊尔鸢尾异黄酮,葛花苷元 |
IL Receptor; NF-κB; Chloride channel | Immunology/Inflammation; Membrane transporter/Ion channel; NF-κB |
Irisolidone 是葛根花中的一种异黄酮,具有较强的保肝活性。它是一种有效的体积调节阴离子通道 (VRAC) 电流抑制剂,有高效阻断作用,IC50 为 5-13 μM。 | |||
T20003 |
Acridone
|
Antibacterial; ABC | Membrane transporter/Ion channel; Microbiology/Virology |
Acridone 具有抗菌、抗疟、抗病毒和抗肿瘤活性。它可诱导细胞凋亡,抑制 ABCG2 蛋白,并调节激素水平。 | |||
T3578 |
Pyridoxal phosphate
PLP,PAL-P,磷酸吡哆醛,pyridoxal 5'-phosphate,Pyridoxyl phosphate,Pyridoxal 5′-phosphate,Vitamin B6 phosphate |
Reverse Transcriptase; Endogenous Metabolite | Metabolism; Microbiology/Virology |
Pyridoxal phosphate (Vitamin B6 phosphate) 是维生素 B6 的活性形式,可抑制逆转录酶活性,用于研究迟发性运动障碍症。 | |||
T5S0055 |
Chelidonine
Helidonine,Khelidonin,白屈菜碱,Stylophorin |
Apoptosis; Others; Influenza Virus | Apoptosis; Microbiology/Virology; Others |
Chelidonine (Stylophorin) 是白屈菜中的一种异喹啉生物碱,有抗肿瘤和抗病毒作用。它可导致细胞周期 G2/M 停滞,诱导 caspase 依赖和非依赖性的细胞凋亡。 | |||
T12588 |
Pyridoxylamine
pyridoxamine,吡多胺 |
Endogenous Metabolite | Metabolism |
Pyridoxylamine (pyridoxamine) 是脂质化终产物和糖基化终产物抑制剂,能够防止糖尿病引起的视网膜血管病变。 | |||
T0973 |
Pyridoxine
吡哆醇,Pyridoxol,Vitamin B6,Gravidox,吡多素(维生素B6) |
PLK; Nrf2; Endogenous Metabolite | Cell Cycle/Checkpoint; Immunology/Inflammation; Metabolism |
Pyridoxine (Vitamin B6) 是一种吡啶衍生物,通过 Nrf-2/HO-1 途径发挥抗氧化作用,作用于阿尔茨海默病细胞模型。 | |||
T2790 |
Oridonin
NSC-250682,Rubescenin,冬凌草甲素,Isodonol,Rubescensin A |
Akt; Antibacterial | Cytoskeletal Signaling; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Oridonin (NSC-250682) 是从Rabdosia rubescens 中得到的二萜,是一种AKT 抑制剂,对 AKT1 和 AKT2 的IC50值分别为 8.4 和 8.9 μM,具有抗菌、抗炎、抗肿瘤等功效。 | |||
T5558 |
Chelidonic acid
Jervaic acid,Jerva acid,白屈菜酸,γ-Pyrone-2,6-dicarboxylic acid |
NF-κB; Caspase | Apoptosis; NF-κB; Proteases/Proteasome |
Chelidonic acid (Jervaic acid) 是从白屈菜中分到的酸类物质,用作温和的镇痛剂、抗菌剂和中枢神经系统镇静剂。它是谷氨酸脱羧酶抑制剂,Ki 值为 1.2 μM。它可能通过抑制 NF-κB 和caspase-1来降低 IL-6 的产生抗炎作用。 | |||
T6795 |
Carbidopa
卡比多巴,(S)-(-)-Carbidopa,Lodosyn |
Decarboxylase; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism; Others |
Carbidopa (Lodosyn) 是一种选择性芳香烃受体(AhR)调节剂,是外周型脱羧酶抑制剂,抑制胰腺癌细胞和肿瘤生长,可用于帕金森病的研究。 | |||
T25114 |
Ascaridole
NSC-406266,NSC 406266,NSC406266 |
Parasite | Microbiology/Virology |
Ascaridole (NSC-406266) 可作为驱虫化合物,能驱除人体和植物中的寄生蠕虫(蠕虫),具有较弱的抗疟活性。 | |||
TN7032 |
4'-O-Methylpyridoxine
4-methoxymethylpyridoxine,Ginkgotoxin |
Antioxidant | oxidation-reduction |
4'-O-Methylpyridoxine(MPN)是从银杏叶中发现的维生素类化合物,具有抗氧化活性和细胞毒性。 | |||
T8083 |
Pyridoxal 5'-phosphate monohydrate
Pyridoxal phosphate monohydrate,Pyridoxal 5-phosphate monohydrate,5-磷酸吡哆醛 |
Others | Others |
Pyridoxal 5'-phosphate monohydrate 是维生素 B6的活性形式,也是多种酶的重要辅因子。它是维生素 B6 在细胞内磷酸化过程中重要的辅酶变异体,能够与其他变异体(如 PNP 、 PMP)发生互换。 | |||
T7324 |
Chelidonine hydrochloride
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Others | Others |
Chelidonine hydrochloride 是 Chelidonium majus 的生物碱之一,具有广泛的药理活性。 | |||
T36473 |
trans-Nerolidol
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trans-Nerolidol is a sesquiterpene that has been found in various plants, includingC. sativa, and has diverse biological activities, including antimicrobial, antioxidant, anticancer, and insecticidal properties.1,2,3,4In a disc assay,trans-nerolidol inhibits the growth ofS. aureus,B. subtilis,E. coli, andS. cerevisiaewith zones of inhibition measuring 10, 9, 10, and 4 mm, respectively.2It reduces viability of CaCo-2 adenocarcinoma cells with an IC50value of 28.7 mg/L and reduces production of re... | |||
T4754 |
Pyridoxylamine dihydrochloride
盐酸吡多胺,Pyridorin,Pyridoxamine dihydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Pyridoxylamine dihydrochloride (Pyridorin) 是一种糖基化终产物和脂质化终产物抑制剂,能够防止糖尿病引起的视网膜血管病变。 | |||
T4129 |
Arachidonic acid
Immunocytophyte,花生四烯酸,arachidonate,Immunocytophyt,Vevodar |
Others; Endogenous Metabolite | Metabolism; Others |
Arachidonic acid (Immunocytophyte) 是不饱和的必需脂肪酸。 它存在于动物和人类脂肪以及肝脏、大脑和腺体器官中,是动物磷脂的成分。 它由膳食亚油酸合成而成,是前列腺素、血栓素和白三烯生物合成的前体。 | |||
T2S2172 |
nerolidol
(±)-Nerolidol,Peruviol,橙花叔醇 |
Others; Endogenous Metabolite; Antibacterial; Parasite; Antifungal | Metabolism; Microbiology/Virology; Others |
Nerolidol (Peruviol) 是天然膜活性倍半萜,有抗肿瘤、抗细菌、抗真菌和抗寄生虫活性。它对动物有镇静作用,氧化过程对神经元病理后果起关键作用。 | |||
T3799 |
Isorhamnetin-3-O-neohespeidoside
Isorhamnetin 3-O-neohesperidin,异鼠李素-3-O-新橙皮糖苷,Isorhamnetin 3-O-neohesperoside,Calendoflavoside,异鼠李素-3-O-新橙皮苷 |
Antioxidant | oxidation-reduction |
Isorhamnetin-3-O-neohespeidoside (Calendoflavoside) 是一种黄酮类化合物,分离自Pollen typhae 中。 | |||
T0973L |
Pyridoxine hydrochloride
Pyridoxine HCl,吡哆醇盐酸盐,Pyridoxol (hydrochloride),吡哆醇盐酸盐(维生素B6),Vitamin B6 (hydrochloride),Vitamin B6 |
Nrf2; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
Pyridoxine hydrochloride (Vitamin B6) 是一种吡啶衍生物。在于阿尔茨海默病细胞模型中,通过 Nrf-2/HO-1 途径发挥抗氧化作用。 | |||
T4761 |
Pyridoxal hydrochloride
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Others; Endogenous Metabolite | Metabolism; Others |
Pyridoxal hydrochloride 是内源性代谢产物的一种。 | |||
T4107 |
4-Pyridoxic Acid
4-吡哆酸,Pyridoxic Acid,4-Pyridoxinsaeure |
Endogenous Metabolite | Metabolism |
4-Pyridoxic Acid (4-Pyridoxinsaeure) 是一种维生素B6的分解代谢产物,从尿液中分泌得到。 | |||
T4919 |
Ureidopropionic acid
Carbamoyl-b-alanine,3-酰脲丙酸,3-Ureidopropionic acid |
Endogenous Metabolite | Metabolism |
Ureidopropionic acid (3-Ureidopropionic acid) 是尿嘧啶代谢的中间体。更具体地说,它是二氢尿嘧啶的分解产物,由二氢嘧啶酶产生。它通过β -脲丙酸酶进一步分解为β -丙氨酸。尿素丙酸本质上是β -丙氨酸的尿素衍生物。高水平的尿丙酸存在于β -尿丙酸酶(UP)缺乏的个体中。嘧啶代谢中的酶缺乏与抗肿瘤药物5-氟尿嘧啶的严重毒性风险有关。 | |||
T4933 |
(S)-2-acetamido-4-amino-4-oxobutanoic acid
Nα-Acetyl-L-asparagine,N-乙酰-L-天门冬酰胺 |
Endogenous Metabolite | Metabolism |
(S)-2-acetamido-4-amino-4-oxobutanoic acid (Nα-Acetyl-L-asparagine),也称为acasn,属于一种内源性代谢产物。 | |||
TN1819 |
Kaempferol 3-neohesperidoside
Kaempferol 3-O-neohesperidoside,堪非醇 3-新橙皮糖苷 |
GSK-3; MEK; PI3K | MAPK; PI3K/Akt/mTOR signaling; Stem Cells |
Kaempferol 3-neohesperidoside (Kaempferol 3-O-neohesperidoside) 是一种类黄酮,对大鼠比目鱼肌具有拟胰岛素作用。 | |||
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 | |||
T82325 | Gentiiridosides A | ||
Gentiiridosides A为从龙胆中提取的一种化合物,采用无水乙醇作为萃取溶剂。 | |||
T72730 | D-Isofloridoside | ||
D-Isofloridoside 是多糖前体之一,具有清除自由基、抑制ROS 表达、抑制MMP-2和MMP-9的活性。 | |||
T79980 |
Flaccidoside III
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Glucosidase | Metabolism |
Flaccidoside III, 分离自黑种草(N. sativa)地上部分的一种类黄酮和三萜类化合物,具有抑制α-Glucosidase(IC50:256.7 μM)的活性,表现出潜在的抗氧化和抗糖尿病效应。 | |||
TN6244 |
Hainanolidol
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Hainanolidol 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 TN6244,CAS号为 73213-63-5。 | |||
T19885 |
Methyllucidone
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Methyllucidone is an inhibitor of STAT3 that acts by regulating the expression of the protein tyrosine phosphatase MEG2. | |||
TN2590 |
11alpha,12alpha-Oxidotaraxerol palmitate
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Others | Others |
11alpha,12alpha-Oxidotaraxerol palmitate shows selective cytotoxicity against HCT-8, Bel-7402, BGC-823, A549 and A2780. | |||
TN1044 |
Quercetin 3-O-neohesperidoside
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Others | Others |
Quercetin 3-O-neohesperidoside shows anti-atherosclerosis, and antiplatelet aggregation activities. | |||
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