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86

抑制剂 & 化合物

64

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Cat. No. Product Name Target Signaling Pathways
T5491 GSK3179106

c-RET Apoptosis; Tyrosine Kinase/Adaptors
GSK3179106 是选择性的、具有口服活性的RET 激酶抑制剂,对人和大鼠 RET 的 IC50 分别为 0.4 nM 和 0.2 nM。它能够减轻炎症后和应激引起的内脏超敏反应,对肠易激综合征具有潜在的应用价值。
TP1889 MCL0020

MCL 0020

Melanocortin Receptor GPCR/G Protein; Neuroscience
MCL0020 是一种有效的选择性黑素皮质素MC4受体拮抗剂,IC50为 11.63 nM。它剂量依赖性减轻束缚应激诱发的厌食症,在体内表现出抗焦虑样活性。
T1997 JNJ-31020028

JNJ 31020028

Neuropeptide Y Receptor GPCR/G Protein; Neuroscience
JNJ-31020028是神经肽Y2受体选择性可脑渗透抑制剂,对人Y2和鼠源Y2受体pIC50值分别为8.07和8.22,其神经肽 Y2 受体的选择性比人 Y1/Y4/Y5 受体高 100 倍。
T16481 PF-04995274

5-HT Receptor GPCR/G Protein; Neuroscience
PF-04995274 是强效,高亲和力,口服活性血清素 4 受体的部分激动剂。它是可脑渗透的,可用于与阿尔茨海默症相关的认知障碍的研究。
T5913 Sulbutiamine

舒布硫胺,Bisibuthiamine

Antioxidant oxidation-reduction
Sulbutiamine (Bisibuthiamine) 是合成的维生素 B1 类似物,可用于研究无力症。
T13867 RH01386

Others Others
RH01386是可以预防 ER 应激诱导的β细胞功能障碍和死亡、抑制促凋亡基因表达的小分子。它恢复内质网应激受损的葡萄糖刺激的胰岛素分泌反应。对2型糖尿病具有潜在的研究价值。
T20797 NE-100 hydrochloride

NE100 Hydrochloride,NE 100 HCl,NE 100 Hydrochloride,NE-100 Hydrochloride,NE-100 HCl

Sigma receptor GPCR/G Protein
NE-100 hydrochloride (NE-100 HCl) 是选择性sigma-1 受体拮抗剂,IC50为 4.16 nM。它在体内具有抗精神病活性。它也能抑制内质网应激诱导的海马细胞死亡。
T4125 HSF1A

HSP Cytoskeletal Signaling; Metabolism
HSF1A 是一种可渗透细胞的 HSF1 激活剂,可保护哺乳动物细胞免受应激诱导的细胞凋亡。它还是 TRiC/CCT 的特异性抑制剂。
T5500 DORA-22

OX Receptor GPCR/G Protein; Neuroscience
DORA-22 是一种双食欲素受体拮抗剂,可改善轻度压力引起的失眠,对记忆的影响很小。
T14491 B022

NF-κB NF-κB
B022 是一种具有选择性和高效性的 NF-κB 诱导激酶(NIK)抑制剂(Ki:4.2 nM),是治疗肝脏炎症和损伤的化学探针。B022 可避免肝脏免受氧化应激和毒素引起的炎症和损伤。
T22577 Antalarmin hydrochloride

CRFR; Immunology/Inflammation related GPCR/G Protein; Immunology/Inflammation
Antalarmin hydrochloride 是促肾上腺皮质激素释放因子 1 (CRF1) 的拮抗剂。 Antalarmin hydrochloride 具有抗炎作用并抑制与肠易激综合征相关的应激性胃溃疡。
T21824 Sephin1

NSC 65390,IFB-088

Phosphatase Metabolism
Sephin1 (IFB-088) 是 GADD34 (PPP1R15A) 的选择性抑制剂,这是一种应激诱导的蛋白磷酸酶 1 复合物调节亚基,可将 eIF2α 去磷酸化。
T8869 B355252

Others Others
B355252 是苯氧基噻吩磺酰胺小分子,NGF 受体激动剂。它能增强 NGF 诱导的神经突生长。它可减轻 DNA 损伤、抑制 ROS 生成、降低 LDH 水平以及预防神经元凋亡,保护缺血性神经元免受神经元损失。它具有抗细胞凋亡作用。
T4400 DIM-C-pPhOH

CDIM8

Apoptosis; Others Apoptosis; Others
DIM-C-pPhOH (CDIM8) 是一种核受体 4A1(NR4A1) 拮抗剂,可降低细胞增殖,对 ACHN 细胞和 786-O 细胞的IC50值分别为 13.6 μM 和 13.0 μM。它抑制癌细胞的生长和 mTOR 信号传导,诱导细胞凋亡和细胞应激。
T9564 IRE1α kinase-IN-1

IRE1 Cell Cycle/Checkpoint
IRE1α kinase-IN-1 是IRE1α 的选择性抑制剂(IC50为 77 nM),对 IRE1α 的选择性高于 IRE1β 亚型 100 倍。它抑制内质网诱导的 IRE1α 寡聚和自磷酸化,并抑制 IRE1α RNase 活性 (IC50=80 nM)。
T34081 Piromelatine

NEU-P-11,NEU-P 11,NEU-P11

P2X Receptor; 5-HT Receptor; MT Receptor; Sodium Channel; TRP/TRPV Channel GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience
Piromelatine 是褪黑激素 MT1/MT2 受体、5-HT1A 和 5-HT1D 的激动剂,也是 5-HT2B 的拮抗剂。Piromelatine 具有抗痛觉活性,对 P2X3、TRPV1 和 Nav1.7 通道有抑制作用,可用于促进睡眠、缓解疼痛、抗神经退行性疾病和抗抑郁疾病的研究。
T16550 PKR-IN-C16

Others Others
PKR-IN-C16 是一种特异性蛋白激酶抑制剂。它能够抑制 PKR 的自磷酸化,解除 PKR 在原代神经元细胞培养中诱导的翻译阻断。
T26684 Auten-99 HBr

Auten-99,Auten-99 hydrochloride. Auten-99 HBr,Auten99,Auten 99

Phosphatase Metabolism
Auten-99 HBr (Auten-99) 是新型肌管蛋白磷酸酶 Jumpy( MTMR14) 的抑制剂,可通过血脑屏障,具有强大的神经保护作用。
T50032 5-(2-furyl)-N-propylisoxazole-3-carboxamide

Others Others
5-(2-furyl)-N-propylisoxazole-3-carboxamide 是一种用作分子结构单元的化合物,被认为是 NMDA 受体的调节剂,已被证明对神经元细胞中谷氨酸诱导的兴奋性毒性和氧化应激具有保护作用。它也被发现具有抗炎活性,使其成为阿尔茨海默病和帕金森病等疾病的潜在治疗剂。
T7042 1,5-Isoquinolinediol

PARP Chromatin/Epigenetic; DNA Damage/DNA Repair
1,5-Isoquinolinediol 是一种多聚(ADP-核糖)合成酶抑制剂,对PARP1的IC50值为 0.39 µM。它用于研究 PARP1 在 DNA 修复和氧化应激诱导的细胞死亡中的作用。
T35449 α-(difluoromethyl)-DL-Arginine

DFMA,RMI 71897,α-(difluoromethyl)-DL-Arginine

Others Others
α-(difluoromethyl)-DL-Arginine (RMI 71897) 是一种酶激活的、不可逆的大肠杆菌(Ki = 800 μM)、铜绿假单胞菌和肺炎克雷伯菌精氨酸脱羧酶抑制剂。在0.01 mM 时,它已被证明可以防止渗透胁迫诱导的燕麦叶片细胞精氨酸脱羧酶活性和腐胺合成的增加。当α-(difluoromethyl)-DL-Arginine 与多种多胺类似物联用时,能在10 mM 的最低浓度下抑制克氏锥虫在哺乳动物宿主细胞中的生长,并在T 细胞受体α缺陷小鼠模型中阻止小锥虫的生长。
T13488 2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide

2-_E-2-decenoylamino_ethyl_2-_cyclohexylethyl__sulfide

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide is a compound known to inhibit stress-induced ulcers, effectively maintaining the levels of phospholipase A2 and prostaglandin E2 in rats subjected to water immersion-restrained stress-induced ulceration.
T26002 Pyclen

Pyclen is an inhibitor of cell death induced by oxidative stress and an inhibitor of AB1-40 aggregation induced by Cu2+ ion. It can both prevent and disrupt Cu(2+) induced AB(1-40) aggregation.
T25807 MHY884

MHY 884,MHY-884

MHY884 is an inhibitor of tyrosinase that acts by inhibiting UVB-induced activation of the NF-κB signaling pathway through the downregulation of oxidative stress.
T31263 Deanol aceglumate

Otrun,Deanolo aceglumato,Risatarun,Deanoli aceglumas

Deanol aceglumate is combination of deanol and N-acetyl-L-glutamic acid. deanol aceglumate can effect Hepatoprotective on stress-induced gastropathy and diabetes mellitus.
T10809 CHPG

Others Others
CHPG is a selective agonist of mGluR5. In BV2 microglial cells, it attenuates SO2-induced oxidative stress and inflammation through the TSG-6/NF-κB pathway.
T26596 Allylpyrocatechol

Allylpyrocatechol is an antioxidant. Allylpyrocatechol attenuates collagen-induced arthritis via attenuation of oxidative stress secondary to modulation of the MAPK, JAK/STAT, and Nrf2/HO-1 pathways.
T68398 MI-223

MI-223 is an inhibitor of Mcl-1-stimulated homologous recombination (HR) DNA repair, which leads to sensitization of cancer cells to hydroxyurea- or olaparib-induced DNA replication stress.
T26172 S3QEL-2

S3QEL2,S3QEL 2

S3QEL-2 is a retrograde signaling modulator. It acts by strongly mitigating the oxidative stress-induced apoptosis that limits the yield of functional ß-cells from intact islets.
T71479 Kahweol oleate

Kahweol oleate is emi-syntetic derivative of kahweol, a natural product found in coffee beans. It exhibits a wide variety of biological activities, including inhibiting RANKL-induced osteoclast generation, inducing cell cycle arrest and apoptosis in oral squamous cell carcinoma cells, preventing aflatoxin B1 induced DNA adduct formation, and suppressing H2O2-induced DNA damage and oxidative stress.
T68959 Fenobam hydrate

Fenobam hydrate is a noncompetitive antagonist and inverse agonist of metabotropic glutamate receptor 5 (mGluR5). It inhibits intracellular calcium mobilization induced by the glutamate analog quisqualate and inhibits basal activity of mGluR5. Fenobam reduces stress-induced hyperthermia, exhibits anxiolytic-like activity, and may induce analgesia.
T27107 CYM-5478

CYM 5478,CYM5478

CYM-5478 is a potent and selective S1P2 agonist. Under nutrient-deprivation stress produced by serum-starvation, CYM-5478 induced a significant increase in the viability of C6 cells in a dose dependent manner at concentrations above 100 nM.
T68642 Kahweol palmitate

Kahweol palmitate is a semi-synthetic derivative of kahweol, a natural product found in coffee beans. It exhibits a wide variety of biological activities, including inhibiting RANKL-induced osteoclast generation, inducing cell cycle arrest and apoptosis in oral squamous cell carcinoma cells, preventing aflatoxin B1-induced DNA adduct formation, and suppressing H2O2-induced DNA damage and oxidative stress.
T34811 Terrein

NSC 291308,土曲霉酮,Terrain,(+)Terrein,NSC291308,NSC-291308

Terrain, also known as NSC 291308, is a fungal metabolite with diverse biological activities. Terrein reduces age-related inflammation induced by oxidative stress through Nrf2/ERK1/2/HO-1 signalling in aged HDF cells. (+)-terrein suppresses interleukin-6/
T71478 Kahweol stearate

Kahweol stearate is a semi-synthetic derivative of kahweol, a natural product found in coffee beans. It exhibits a wide variety of biological activities, including inhibiting RANKL-induced osteoclast generation, inducing cell cycle arrest and apoptosis in oral squamous cell carcinoma cells, preventing aflatoxin B1-induced DNA adduct formation, and suppressing H2O2-induced DNA damage and oxidative stress.
T68641 Kahweol Acetate

Kahweol Acetate is a semi-synthetic derivative of kahweol, a natural product found in coffee beans. It exhibits a wide variety of biological activities, including inhibiting RANKL-induced osteoclast generation, inducing cell cycle arrest and apoptosis in oral squamous cell carcinoma cells, preventing aflatoxin B1 induced DNA adduct formation, and suppressing H2O2-induced DNA damage and oxidative stress.
T25576 KF 392

KF392,KF-392

KF 392 is antiulcer. It was found that KF-392 given orally to rats at 1.0 to 5.0 mg/kg had a marked suppression on the developments of Shay ulcer as well as the aspirin-, stress-, and reserpine-induced gastric lesions.
T71480 Kahweol linoleate

Kahweol linoleate is a semi-syntetic derivative of kahweol, a natural product found in coffee beans. It exhibits a wide variety of biological activities, including inhibiting RANKL-induced osteoclast generation, inducing cell cycle arrest and apoptosis in oral squamous cell carcinoma cells, preventing aflatoxin B1 induced DNA adduct formation, and suppressing H2O2-induced DNA damage and oxidative stress.
T73096 Z-LEVD-FMK

Z-LEVD-FMK 是一种细胞渗透性的caspase-4抑制剂。 Z-LEVD-FMK 阻断 ER 应激诱导的癌细胞凋亡。
T3689L Ruboxistaurin mesylate

LY-333531,LY333531,LY 333531,LY-333531 Mesylate

Ruboxistaurin is a PKC beta inhibitor. Ruboxistaurin reduces oxidative stress and attenuates left ventricular hypertrophy and dysfunction in rats with streptozotocin-induced diabetes. Ruboxistaurin attenuates diabetic nephropathy via modulation of TGF-β1/
T69068 Aspulvinone H

Aspulvinone H is a natural inhibitor of glutamic oxaloacetate transaminase 1 (GOT1), suppressing glutamine metabolism, making PDAC cells sensitive to oxidative stress and inhibiting cell proliferation, exhibiting potent in vivo antitumor activity in an SW1990-cell-induced xenograft model.
T38228 R 121919 hydrochloride

High affinity corticotropin releasing factor receptor1 (CRF1) antagonist (Ki = 3.5 nM). Reduces stress-induced elevations of plasma ACTH. Anxiolytic and antidepressant in vivo. Orally bioavailable. Chen and Grigoriadis (2005) NBI 30775 (R121919), an orally active antagonist of the corticotropin-releasing factor (CRF) type-1 receptor for the treatment of anxiety and depression. Drug Dev.Res. 65 216 |Jutkiewicz et al (2005) The effects of CRF antagonists, antalarmin, CP154,526, LWH234, and R121919...
T36328 Termitomycamide B

Endoplasmic reticulum (ER) stress, caused by accumulation of misfolded proteins and a disruption of calcium homeostasis, has been linked to several neuronal diseases including, Parkinson's, Alzheimer's, and prion diseases. A screen for protective activity against ER stress-dependent cell death identified termitomycamides, extracts from the fruiting bodies of T. titanicus, a notably large edible mushroom that is cultivated symbiotically in the nests of termites Termitomycamide B is a fatty acid i...
T83050 Anti-inflammatory agent 62

Anti-inflammatory agent 62 减轻乙酰氨基酚诱导的HepG2肝毒性,其机制是通过调节炎症和氧化应激途径。
T76195 Stresscopin-related peptide (human)

Stresscopin-related peptide (human) 是 2 型 CRH 受体的特异性配体。Stresscopin-related peptide (human) 抑制食物摄入,延迟胃排空,并减少热引起的水肿。Stresscopin-related peptide (human) 在应激后维持体内平衡,可用于应激相关疾病的研究。
T72543 BOLD-100 free base

NKP-1339 free base ; IT-139 free base ; KP-1339 free base,KP-1339 free base,NKP-1339 free base,IT-139 free base

BOLD-100 (NKP-1339; IT-139) free base 是一款钌基抗癌药物。作为GRP78应激诱导上调的抑制剂,它破坏内质网(ER)的稳态,从而诱发ER应激和未折叠蛋白反应(UPR)。此外,BOLD-100 free base 干预了内质网应激反应、溶酶体动力学以及细胞自噬(autophagy)间的复杂交互作用。
T81970 Kuwanon T

Kuwanon T为一种源自桑树根皮的异戊二烯黄酮类化合物,能抵御t-BHP诱导的氧化应激,其EC50值为30.32 μM。
T35670 Miro1 Reducer

Promotes proteasomal degradation of Miro1 (mitochondrial Rho GTPase 1). Reduces Miro1 levels in fibroblasts from Parkinson's disease (PD) patients (IC50 = 7.8 μM). Exhibits no significant effect on related outer mitochondrial membrane protein Mitofusin. Reduces stress-induced degeneration of dopaminergic neurons derived from PD patient iPSCs. Rescues age-dependent neuronal loss and prolongs lifespan in fly PD models.
T24883 Tingenin B

22-Hydroxytingenone

Tingenin B is a potent anticancer agent due to its cytotoxic activity on cancer stem cells of breast cancer in vitro. Tingenin b was cytotoxic against MCF-7s (IC50: 2.38 μM for 48 h) by inducing apoptosis. Endoplasmic reticulum stress was also found to be
T70987 AT-1001

AT-1001 is an α3β4 nAChR partial agonist. AT-1001 attenuates stress-induced reinstatement of nicotine seeking in a rat model of relapse and induces minimal withdrawal in dependent rats. AT-1001 also potently and reversibly blocks epibatidine-induced inward currents in HEK cells transfected with α3β4 nAChR. Importantly, AT-1001 potently and dose-dependently blocks nicotine self-administration in rats, without affecting food responding. When tested in a nucleus accumbens (NAcs) synaptosomal prepar...

化合物

GSK3179106
Cat.No: T5491
Synonym:
Target: c-RET
MCL0020
Cat.No: TP1889
Synonym: MCL 0020
Target: Melanocortin Receptor
JNJ-31020028
Cat.No: T1997
Synonym: JNJ 31020028
Target: Neuropeptide Y Receptor
PF-04995274
Cat.No: T16481
Synonym:
Target: 5-HT Receptor
Sulbutiamine
Cat.No: T5913
Synonym: 舒布硫胺,Bisibuthiamine
Target: Antioxidant
RH01386
Cat.No: T13867
Synonym:
Target: Others
NE-100 hydrochloride
Cat.No: T20797
Synonym: NE100 Hydrochloride,NE 100 HCl,NE 100 Hydrochloride,NE-100 Hydrochloride,NE-100 HCl
Target: Sigma receptor
HSF1A
Cat.No: T4125
Synonym:
Target: HSP
DORA-22
Cat.No: T5500
Synonym:
Target: OX Receptor
B022
Cat.No: T14491
Synonym:
Target: NF-κB
Antalarmin hydrochloride
Cat.No: T22577
Synonym:
Target: CRFR, Immunology/Inflammation related
Sephin1
Cat.No: T21824
Synonym: NSC 65390,IFB-088
Target: Phosphatase
B355252
Cat.No: T8869
Synonym:
Target: Others
DIM-C-pPhOH
Cat.No: T4400
Synonym: CDIM8
Target: Apoptosis, Others
IRE1α kinase-IN-1
Cat.No: T9564
Synonym:
Target: IRE1
Piromelatine
Cat.No: T34081
Synonym: NEU-P-11,NEU-P 11,NEU-P11
Target: P2X Receptor, 5-HT Receptor, MT Receptor, Sodium Channel, TRP/TRPV Channel
PKR-IN-C16
Cat.No: T16550
Synonym:
Target: Others
Auten-99 HBr
Cat.No: T26684
Synonym: Auten-99,Auten-99 hydrochloride. Auten-99 HBr,Auten99,Auten 99
Target: Phosphatase
5-(2-furyl)-N-propylisoxazole-3-carboxamide
Cat.No: T50032
Synonym:
Target: Others
1,5-Isoquinolinediol
Cat.No: T7042
Synonym:
Target: PARP
α-(difluoromethyl)-DL-Arginine
Cat.No: T35449
Synonym: DFMA,RMI 71897,α-(difluoromethyl)-DL-Arginine
Target: Others
2-(E-2-decenoylamino)ethyl 2-(cyclohexylethyl) sulfide
Cat.No: T13488
Synonym: 2-_E-2-decenoylamino_ethyl_2-_cyclohexylethyl__sulfide
Target: Prostaglandin Receptor
Pyclen
Cat.No: T26002
Synonym:
Target:
MHY884
Cat.No: T25807
Synonym: MHY 884,MHY-884
Target:
Deanol aceglumate
Cat.No: T31263
Synonym: Otrun,Deanolo aceglumato,Risatarun,Deanoli aceglumas
Target:
CHPG
Cat.No: T10809
Synonym:
Target: Others
Allylpyrocatechol
Cat.No: T26596
Synonym:
Target:
MI-223
Cat.No: T68398
Synonym:
Target:
S3QEL-2
Cat.No: T26172
Synonym: S3QEL2,S3QEL 2
Target:
Kahweol oleate
Cat.No: T71479
Synonym:
Target:
Fenobam hydrate
Cat.No: T68959
Synonym:
Target:
CYM-5478
Cat.No: T27107
Synonym: CYM 5478,CYM5478
Target:
Kahweol palmitate
Cat.No: T68642
Synonym:
Target:
Terrein
Cat.No: T34811
Synonym: NSC 291308,土曲霉酮,Terrain,(+)Terrein,NSC291308,NSC-291308
Target:
Kahweol stearate
Cat.No: T71478
Synonym:
Target:
Kahweol Acetate
Cat.No: T68641
Synonym:
Target:
KF 392
Cat.No: T25576
Synonym: KF392,KF-392
Target:
Kahweol linoleate
Cat.No: T71480
Synonym:
Target:
Z-LEVD-FMK
Cat.No: T73096
Synonym:
Target:
Ruboxistaurin mesylate
Cat.No: T3689L
Synonym: LY-333531,LY333531,LY 333531,LY-333531 Mesylate
Target:
Aspulvinone H
Cat.No: T69068
Synonym:
Target:
R 121919 hydrochloride
Cat.No: T38228
Synonym:
Target:
Termitomycamide B
Cat.No: T36328
Synonym:
Target:
Anti-inflammatory agent 62
Cat.No: T83050
Synonym:
Target:
Stresscopin-related peptide (human)
Cat.No: T76195
Synonym:
Target:
BOLD-100 free base
Cat.No: T72543
Synonym: NKP-1339 free base ; IT-139 free base ; KP-1339 free base,KP-1339 free base,NKP-1339 free base,IT-139 free base
Target:
Kuwanon T
Cat.No: T81970
Synonym:
Target:
Miro1 Reducer
Cat.No: T35670
Synonym:
Target:
Tingenin B
Cat.No: T24883
Synonym: 22-Hydroxytingenone
Target:
AT-1001
Cat.No: T70987
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T3S0488 Syringaresinol diglucoside

Syringaresinol-di-O-glucoside,丁香树脂醇双葡萄糖苷

Others Others
Syringaresinol diglucoside (Syringaresinol-di-O-glucoside) 是一种提取自竹叶中的天然化合物。
T8704 4-hydroxyphenyl acetate

Nrf2 Immunology/Inflammation
4-hydroxyphenyl acetate 通过作为 NRF2 稳定剂防止 RPE 氧化应激诱导的坏死。
T0632 3,4,5-Trimethoxybenzoic acid

Gallic acid trimethyl ether,Eudesmic acid,3,4,5-三甲氧基苯甲酸,Trimethylgallic Acid,Benzoic acid,Tri-O-methylgallic acid,没食子酸三甲醚

Antioxidant oxidation-reduction
3,4,5-Trimethoxybenzoic acid (Gallic acid trimethyl ether) 是一种苯甲酸衍生物,可用作医药和有机合成中的砌块。
T5665 Geraniol

Others; Endogenous Metabolite; Antifungal Metabolism; Microbiology/Virology; Others
Geraniol 对糖尿病引起的心脏功能障碍起保护作用,抑制氧化应激。
TN1058 Pelargonidin chloride

NOS; Reactive Oxygen Species; Nrf2; NO Synthase Immunology/Inflammation; Metabolism; NF-κB
Pelargonidin chloride 是一种氧化氮自由基的清除剂,具有抗氧化作用。
T6S1768 Narcissin

水仙苷,Isorhamnetin 3-Rutinoside,Narcissoside

Antioxidant oxidation-reduction
Narcissin (Isorhamnetin 3-Rutinoside) 是一种黄连糖苷,能够清除 ONOO-(IC50:3.5 μM)和 SIN-1 衍生的 ONOO-(IC50:9.6 μM),具有抗氧化作用。
T2805 Chlorogenic Acid

NSC-407296,3-O-Caffeoylquinic acid,Heriguard,绿原酸

Others; Influenza Virus; Reactive Oxygen Species; HIF/HIF Prolyl-Hydroxylase; Endogenous Metabolite; Antibacterial Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; Others
Chlorogenic Acid (NSC-407296) 是咖啡和茶中的主要酚类化合物。它具有多种生物作用。
TN1600 Eclalbasaponin I

Others Others
Eclalbasaponin I 分离自鳢肠中,具有抗肿瘤作用,能够抑制肝癌细胞 smmc-7721 的增殖(IC50:111.1703 μg/ml)。
TN1594 DL-Syringaresinol

(±)-Syringaresinol

Antioxidant; Antifungal Microbiology/Virology; oxidation-reduction
DL-Syringaresinol ( (±)-Syringaresinol) 是一种来自与人参浆果的木质素,具有抗炎、抗氧化、镇痛活性和较弱的抗分枝杆菌活性。DL-Syringaresinol 可通过自噬延缓氧化应激诱导的皮肤老化,通过抑制炎症反应来缓解奥沙利铂诱导的神经性疼痛和脓毒症引起的心功能障碍。
T3860 Isoliquiritin apioside

MMP; p38 MAPK; NF-κB MAPK; NF-κB; Proteases/Proteasome
Isoliquiritin apioside 可抑制癌细胞和内皮细胞的侵袭和血管生成,显著降低 PMA 诱导的MMP9活性增加,并抑制 PMA 诱导的MAPK 和NF-κB 活化。
T2S0690 Ecliptasaponin A

早莲苷 A,旱莲苷A,Echinocystic acid-3-o-glucoside

Others Others
Ecliptasaponin A (Echinocystic acid-3-o-glucoside) 是一种墨旱莲 (Eclipta prostrate) 中分离得到的五环三萜皂苷。其中墨旱莲是一种具有多效作用的滋补草药,如抗炎、保肝、抗氧化和免疫调节。
TN1461 (-)-Butin

Butin,漆黄素 ( 紫铆素)

Akt; PI3K; Nrf2 Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling
(-)-Butin (Butin) 是 Butin 的 S 对映体。其中 Butin 是一种分离自黄檀的心材中的生物活性黄酮类化合物,具有显著的抗血小板、抗氧化、抗炎作用。
T4868 gamma-Linolenic acid

gamolenic acid,γ-Linolenic acid,γ-亚麻酸

Endogenous Metabolite Metabolism
gamma-Linolenic acid (gamolenic acid) 是一种 omega-6 (n-6),18 碳 (18C-) 多不饱和脂肪酸 (PUFA),可以从人乳和植物种子油中提取。
T5255 5-Hydroxymethyluracil

5-(Hydroxymethyl)uracil,5-羟甲基脲嘧啶,Hydroxymethyl Uracil,a-Hydroxythymine

Others; Endogenous Metabolite Metabolism; Others
5-Hydroxymethyluracil (a-Hydroxythymine) 是一种氧化性 DNA 损伤的产物,能够增强或抑制细菌 RNA 聚合酶转录的潜在表观遗传标记。
T11685 Isolongifolene

异长叶烯,(-)-Isolongifolene

Apoptosis; Others Apoptosis; Others
Isolongifolene ((-)-Isolongifolene) 是一种从调料九里香中分离的三环倍半萜烯,具有抗氧化,抗炎,抗癌和神经保护的特性。它通过调节 PI3K/AKT/GSK-3β 信号通路来减轻鱼藤酮诱导的氧化应激,线粒体功能障碍和细胞凋亡。
TN1957 Mulberrofuran Q

MulberrofuranQ

Mulberrofuran Q是一种有活性的化合物,可抑制12-羟基-5,8,10-十七碳三烯酸(HHT)和血栓烷B2(环加氧酶产物)的形成 ,可保护神经细胞免受缺氧-缺糖(OGD)诱导的氧化应激的影响。
T6S1966 Curculigoside

Curculigoside A,仙茅苷

Antioxidant; NF-κB; JAK; STAT Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; NF-κB; oxidation-reduction; Stem Cells
Curculigoside (Curculigoside A) 是仙茅中的主要皂苷,具有显著的抗氧化、抗骨质疏松、抗抑郁和神经保护作用。它通过调节JAK/STAT/NF-κB 信号传导途径,具有抗关节炎作用。
T3395 Timosaponin AIII

Filiferin B,知母皂苷 A-III,AneMarsaponin A3,Timosaponin A3

AChE; mTOR Neuroscience; PI3K/Akt/mTOR signaling
Timosaponin AIII (Timosaponin A3) 是一种乙酰胆碱酯酶活性抑制剂,其IC50=35.4 μM。
TN1601 Effusol

灯心草菲酚,厄弗酚

Caspase Apoptosis; Proteases/Proteasome
Effusol 是一种从 Juncus effuses 中分离到的酚类物质,对 DPPH 自由基(IC50:79 μM) 及 ABTS 自由基(IC50:2.73 μM)具有较强的清除活性。它能挽救皮质酮减弱的 CA1 LTP,保护海马功能对抗应激诱导的认知能力下降。
T6S0221 Eriocitrin

eriodictyol 7-rutinoside,圣草次甙,Eriodictyol-7-O-Rutinoside,Eriodictioside,圣草次甙;圣草次苷,Eriodictyol glycoside

Apoptosis; Carbonic Anhydrase Apoptosis; Metabolism
Eriocitrin (Eriodictyol-7-O-Rutinoside) 是从柠檬中分离出来的一种黄酮类天然产物,是强效的抗氧化剂。它通过激活线粒体涉及的内在信号传导途径来触发细胞凋亡。它通过上调 p53、cyclin A、cyclin D3 和 CDK6 使 S 期细胞周期停滞,从而抑制肝癌细胞的增殖。
T3795 Corilagin

Apoptosis; TLR; Reverse Transcriptase; Antibacterial; Autophagy Apoptosis; Autophagy; Immunology/Inflammation; Microbiology/Virology
Corilagin 是一种鞣酸,有抑制 RNA 肿瘤病毒逆转录酶的活性。它抑制金黄色葡萄球菌的生长,MIC 为 25 μg/mL。它有抗肿瘤活性,可用于肝癌和卵巢癌。
T4001 Euxanthone

1,7-Dihydroxyxanthone

Autophagy Autophagy
Euxanthone (1,7-Dihydroxyxanthone) 是一种从 Polygala tenuifolia Willd 的根中提取的氧杂蒽酮衍生物,具有抗肿瘤、神经保护和血管松弛活性,可通过诱导自噬 (autophagy) 来减弱 Aβ1-42 诱导的氧化应激和细胞凋亡。Euxanthone 可诱导神经母细胞瘤神经 2A (BU-1) 细胞的分化。
T3753 Sinapinic Acid

Sinapic acid,芥子酸,Synapoic acid

Apoptosis; RAAS; Reactive Oxygen Species; HDAC Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Endocrinology/Hormones; Immunology/Inflammation; Metabolism; NF-κB
Sinapinic Acid (Synapoic acid) 是从 Hydnophytum formicarumJack. 根中分离到的酚类,是HDAC 抑制剂,对ACE-I 的活性也有抑制作用。它有抗肿瘤活性,诱导肿瘤细胞凋亡,具有抗氧化、抗糖尿病的作用。
T6S1572 Sauchinone

ERK; p38 MAPK; NF-κB MAPK; NF-κB
Sauchinone 是一种从Saururus chinensis 中获得的非对映异构的木脂素。它通过抑制I-κBα磷酸化和p65核易位来抑制 LPS 诱导的 iNOS,TNF-α 和 COX-2 表达。它具有抗炎和抗氧化活性。
TWS1977 Kamebakaurin

尾叶香茶菜丙素,Kamebakaurine

NF-κB NF-κB
Kamebakaurin (Kamebakaurine) 是一种提取自Isodon japonicus 中的天然产物,是一种NF-κB 的抑制剂,能够抑制 p50 的 DNA 结合活性。
T2909 Fraxetin

7,8-dihydroxy-6-methoxy coumarin,秦皮素,弗拉西汀

Apoptosis; Others Apoptosis; Others
Fraxetin (7,8-dihydroxy-6-methoxy coumarin) 是从秦皮中分离出来的一种天然产物,可诱导细胞凋亡,具有抗肿瘤、抗氧化作用和抗炎作用。
T2854 Phillyrin

Forsythin,连翘苷

P450; Influenza Virus; AMPK Chromatin/Epigenetic; Metabolism; Microbiology/Virology; PI3K/Akt/mTOR signaling
Phillyrin (Forsythin) 是从连翘中分离出来的一种天然产物,具有抗甲型流感病毒的活性,以及抗菌和消炎作用。
TN1413 Atranorin

荔枝素,巴美灵,荔枝素

Endogenous Metabolite; NO Synthase; Ras GPCR/G Protein; Immunology/Inflammation; MAPK; Metabolism
Atranorin 是地衣的次生代谢产物,具有显着的抗伤害、抗炎和氧化还原活性,对 H(2)O(2) 诱导的氧化应激下的细胞具有细胞保护作用。
T6S1784 Brazilin

Natural Red 24,巴西苏木素;苏枋精,Braziletto,Brasilin,Superbresiline,巴西苏木素

Apoptosis; Others; AMPK; Autophagy Apoptosis; Autophagy; Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling
Brazilin (Braziletto) 是来自几种热带硬木的心材的一种红色染料前体,有软骨保护和抗炎活性。它抑制细胞增殖,促进细胞凋亡并通过 AMPK/mTOR 途径诱导自噬。
T40615 N,N'-Dimethylthiourea

N,N-二甲基硫脲,DMTU

Antioxidant oxidation-reduction
N,N'-Dimethylthiourea (DMTU) 是一种分离自黑蒜的化合物。N,N'-Dimethylthiourea 具有口服活性的羟基自由基 (•OH) 的清除剂,通过活化的中性粒细胞在体外阻止 •OH 的产生。N,N'-Dimethylthiourea 通过发挥 •OH 清除和抗炎作用,防止水浸限制应激诱导的大鼠胃粘膜损伤。
T4S2326 Cornuside

7-Galloylsecologanol,7-O-Galloylsecologanol,山茱萸新苷,Comuside

ERK; p38 MAPK; NF-κB; JNK MAPK; NF-κB
Cornuside (Comuside) 是从山茱萸的果实中分离出的环烯醚萜苷,可用于炎症疾病的研究和促进血液循环。 它通过下调 MAPK 和 NF-κB 信号通路抑制肥大细胞介导的过敏反应,用于炎性过敏性疾病中的潜能。
T5S1805 5,7-Dihydroxychromone

5,7-Dihydroxy-4H-Chromen-4-One,5,7-二羟基色酮,5,7-二羟基色原酮

Others; Virus Protease; PARP; Caspase; Nrf2 Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology; Others; Proteases/Proteasome
5,7-Dihydroxychromone (5,7-Dihydroxy-4H-Chromen-4-One) 是一种Cudrania tricuspidata 的提取物,通过激活 Nrf2/ARE 信号对 6-OHDA 诱导的氧化应激和细胞凋亡发挥神经保护作用。它抑制 6-OHDA 诱导的 SH-SY5Y 细胞中活化的caspase-3,caspase-9以及切割的PARP 表达。
T3414 Morroniside

莫诺苷,奎宁树

Apoptosis; MMP; Pyroptosis Apoptosis; Immunology/Inflammation; Proteases/Proteasome
Morroniside 通过抑制神经元凋亡和 MMP9/2 的表达从而发挥神经保护作用,可作为 db/db 小鼠肝脏炎症反应和脂质代谢的调节剂。它通过抑制高血糖和氧化应激表现出对糖尿病肾损伤和人脐静脉内皮细胞的保护作用。
T4719 1,4-D-Gulonolactone

D-Gulonic acid γ-lactone,D-(-)-古洛糖酸-1,4-内酯

Others; Endogenous Metabolite Metabolism; Others
1,4-D-Gulonolactone (D-Gulonic acid γ-lactone) (也称为还原性抗坏血酸,RAA) 是 L-gulono-1,4-lactone oxidoreductase (EC 1.1.3.8)的底物,催化植物和动物中l -抗坏血酸(维生素C)生物合成的最后一步。enzyme L-Gulono-1,4-lactone oxidase 在容易患坏血病、缺乏维生素c的动物(如人类)中缺失。1,4-D-Gulonolactone 存在于人体血液中,并被用作比较运动引起的氧化应激变化的标志物之一。
T6S0735 Flavokawain B

黄卡瓦胡椒素B,Flavokavain B,Flavokawin B,2'-Hydroxy-4',6'-Dimethoxychalcone

Apoptosis; Others Apoptosis; Others
Flavokawain B (Flavokavain B) 是从卡瓦醉椒的根提取物中,分离出的查尔酮。它是一种凋亡诱导剂,可抑制各种癌细胞株生长。它以极低的无毒浓度抑制人脑内皮细胞的迁移和血管形成,具有抗血管生成活性。
T3779 Crocin II

Crocin 2,西红花苷II,Crocetin gentiobiosylglucosyl ester,藏红花,Tricrocin,Crocin B

Caspase; COX; NO Synthase Apoptosis; Immunology/Inflammation; Neuroscience; Proteases/Proteasome
Crocin II (Crocetin gentiobiosylglucosyl ester) 是从栀子果实中分离出来的一种天然产物,具有抗氧化、抗癌和抗抑郁活性。它抑制 iNOS 和 COX-2的蛋白质和 m-RNA 的表达,还抑制NO 产生,IC50值为 31.1 μM。
T4S0969 Obtusifolin

决明蒽醌,决明蒽醌;美决明子素

Antioxidant; NF-κB NF-κB; oxidation-reduction
Obtusifolin 是分离自决明子的种子中,能够抑制NF-kB 通路,调节气道上皮细胞中 MUC5AC 粘蛋白的基因表达和产生。它通过靶向甲状旁腺激素相关蛋白来抑制邻苯二甲酸酯诱导的乳腺癌骨转移。
TN1163 2'-Hydroxychalcone

Others Others
2'-Hydroxychalcone 是一种药物合成中间体,可用于合成黄酮类化合物。负载在纳米乳液中的2'-Hydroxychalcone 在Danio rerio 模型对副球孢子菌显示出杀真菌活性。2'-Hydroxychalcone 通过负载脂质的Hepg2细胞中的氧化应激诱导细胞毒性。2'-Hydroxychalcone 抑制通过逆转录聚合酶链反应确定的肿瘤坏死因子-α诱导ICAM-1,VCAM-1和E-选择素的稳态转录水平,因此可能会干扰其基因的转录。
T37512 cis-4-Hydroxy-L-proline

Endogenous Metabolite Metabolism
cis-4-Hydroxy-L-proline 是脯氨酸的一种类似物,抑制胶原蛋白的产生。它通过阻止三层螺旋胶原在细胞层上的沉积从而抑制成纤维细胞的生长。它还可抑制原发性N-亚硝基甲基脲诱导的大鼠乳腺肿瘤的生长。
T24025 Eckol

Eckol inhibits ultraviolet B-induced cell damage by a decrease in oxidative stress in human keratinocytes.
TN1581 Dihydroguaiaretic acid

二氢愈创木酸

COX; DNA/RNA Synthesis Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Neuroscience
Dihydroguaiaretic acid has antioxidative activity, can significantly protect primary cultured neuronal cells against glutamate-induced oxidative stress.
T19576 Tetrahydrocortisone

Others Others
Tetrahydrocortisone, a stress-induced hormone and a urinary metabolite of Cortisone, originates from the reduction of Cortisone facilitated by 5-reductase.
TN4941 Sanggenon N

Others Others
Sanggenon N shows protective effects on t-BHP-induced oxidative stress with the EC50 value of 23.45 ± 4.72 uM. It inhibits lipopolysaccharide-induced nitric oxide production in RAW 264.7 macrophages.
TN1542 Cycloheterophyllin

NADPH-oxidase; PKA; PKC Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; Tyrosine Kinase/Adaptors
Cycloheterophyllin has an antioxidant effect, it is a photoprotective agent that inhibits ultraviolet A (UVA)-induced oxidative stress and damage, and could be used in the research on and prevention of skin photoaging.
TN3618 Cedrin

Beta Amyloid; BCL; Caspase Apoptosis; Neuroscience; Proteases/Proteasome
Cedrin has protective effects on PC12 cells against the neurotoxicity induced by amyloid β1-42, the protective effect is related to the inhibition of oxidative stress, improvement of mitochondrial dysfunction and suppression of apoptosis.
TN2287 Turkesterone

Calcium Channel Membrane transporter/Ion channel; Metabolism
Turkesterone is a phytoecdysteroid possessing an 11alpha-hydroxyl group, also is an analogue of the insect steroid hormone 20-hydroxyecdysone. It has immunomodulating and antistress activity, can increase the adaptation capacity of mice under immobilization-induced stress conditions.
TN3473 Axillarin

Axillarin has antioxidant activity, it shows xanthine oxidase inhibitory activity ( IC(50) :36.0 uM). Axillarin can strongly protect primary cultured neurons against glutamate-induced oxidative stress.
TN4587 Mulberrofuran C

HSV Microbiology/Virology
Mulberrofuran C shows protective effects on t-BHP-induced oxidative stress with the EC50 value of 0.41 ± 0.48 uM ; it also shows protective effects on glutamate-induced cell death with the EC50 value of 16.50 ± 7.82 uM. Mulberrofuran C has antiviral effects against herpes simplex virus type 1 and 2 (HSV-1 and HSV-2).
TN4465 Luvangetin

COX; Prostaglandin Receptor; Antifection GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience
Luvangetin may have anti-inflammatory activity, it can inhibit NO and PGE2 production in LPS-stimulated BV2 cells. Luvangetin shows significant protection against pylorus-ligated and aspirin-induced gastric ulcers in rats and cold restraint stress-induced
T83257 7(8)-Dehydroschisandrol A

7(8)-Dehydroschisandrol A (Compound 4a)为从Schizandra chinensis Baill分离的木脂素,对激性胃溃疡表现出较弱抑制效果。
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天然产物

Syringaresinol diglucoside
Cat.No: T3S0488
Synonym: Syringaresinol-di-O-glucoside,丁香树脂醇双葡萄糖苷
Target: Others
4-hydroxyphenyl acetate
Cat.No: T8704
Synonym:
Target: Nrf2
3,4,5-Trimethoxybenzoic acid
Cat.No: T0632
Synonym: Gallic acid trimethyl ether,Eudesmic acid,3,4,5-三甲氧基苯甲酸,Trimethylgallic Acid,Benzoic acid,Tri-O-methylgallic acid,没食子酸三甲醚
Target: Antioxidant
Geraniol
Cat.No: T5665
Synonym:
Target: Others, Endogenous Metabolite, Antifungal
Pelargonidin chloride
Cat.No: TN1058
Synonym:
Target: NOS, Reactive Oxygen Species, Nrf2, NO Synthase
Narcissin
Cat.No: T6S1768
Synonym: 水仙苷,Isorhamnetin 3-Rutinoside,Narcissoside
Target: Antioxidant
Chlorogenic Acid
Cat.No: T2805
Synonym: NSC-407296,3-O-Caffeoylquinic acid,Heriguard,绿原酸
Target: Others, Influenza Virus, Reactive Oxygen Species, HIF/HIF Prolyl-Hydroxylase, Endogenous Metabolite, Antibacterial
Eclalbasaponin I
Cat.No: TN1600
Synonym:
Target: Others
DL-Syringaresinol
Cat.No: TN1594
Synonym: (±)-Syringaresinol
Target: Antioxidant, Antifungal
Isoliquiritin apioside
Cat.No: T3860
Synonym:
Target: MMP, p38 MAPK, NF-κB
Ecliptasaponin A
Cat.No: T2S0690
Synonym: 早莲苷 A,旱莲苷A,Echinocystic acid-3-o-glucoside
Target: Others
(-)-Butin
Cat.No: TN1461
Synonym: Butin,漆黄素 ( 紫铆素)
Target: Akt, PI3K, Nrf2
gamma-Linolenic acid
Cat.No: T4868
Synonym: gamolenic acid,γ-Linolenic acid,γ-亚麻酸
Target: Endogenous Metabolite
5-Hydroxymethyluracil
Cat.No: T5255
Synonym: 5-(Hydroxymethyl)uracil,5-羟甲基脲嘧啶,Hydroxymethyl Uracil,a-Hydroxythymine
Target: Others, Endogenous Metabolite
Isolongifolene
Cat.No: T11685
Synonym: 异长叶烯,(-)-Isolongifolene
Target: Apoptosis, Others
Mulberrofuran Q
Cat.No: TN1957
Synonym: MulberrofuranQ
Target:
Curculigoside
Cat.No: T6S1966
Synonym: Curculigoside A,仙茅苷
Target: Antioxidant, NF-κB, JAK, STAT
Timosaponin AIII
Cat.No: T3395
Synonym: Filiferin B,知母皂苷 A-III,AneMarsaponin A3,Timosaponin A3
Target: AChE, mTOR
Effusol
Cat.No: TN1601
Synonym: 灯心草菲酚,厄弗酚
Target: Caspase
Eriocitrin
Cat.No: T6S0221
Synonym: eriodictyol 7-rutinoside,圣草次甙,Eriodictyol-7-O-Rutinoside,Eriodictioside,圣草次甙;圣草次苷,Eriodictyol glycoside
Target: Apoptosis, Carbonic Anhydrase
Corilagin
Cat.No: T3795
Synonym:
Target: Apoptosis, TLR, Reverse Transcriptase, Antibacterial, Autophagy
Euxanthone
Cat.No: T4001
Synonym: 1,7-Dihydroxyxanthone
Target: Autophagy
Sinapinic Acid
Cat.No: T3753
Synonym: Sinapic acid,芥子酸,Synapoic acid
Target: Apoptosis, RAAS, Reactive Oxygen Species, HDAC
Sauchinone
Cat.No: T6S1572
Synonym:
Target: ERK, p38 MAPK, NF-κB
Kamebakaurin
Cat.No: TWS1977
Synonym: 尾叶香茶菜丙素,Kamebakaurine
Target: NF-κB
Fraxetin
Cat.No: T2909
Synonym: 7,8-dihydroxy-6-methoxy coumarin,秦皮素,弗拉西汀
Target: Apoptosis, Others
Phillyrin
Cat.No: T2854
Synonym: Forsythin,连翘苷
Target: P450, Influenza Virus, AMPK
Atranorin
Cat.No: TN1413
Synonym: 荔枝素,巴美灵,荔枝素
Target: Endogenous Metabolite, NO Synthase, Ras
Brazilin
Cat.No: T6S1784
Synonym: Natural Red 24,巴西苏木素;苏枋精,Braziletto,Brasilin,Superbresiline,巴西苏木素
Target: Apoptosis, Others, AMPK, Autophagy
N,N'-Dimethylthiourea
Cat.No: T40615
Synonym: N,N-二甲基硫脲,DMTU
Target: Antioxidant
Cornuside
Cat.No: T4S2326
Synonym: 7-Galloylsecologanol,7-O-Galloylsecologanol,山茱萸新苷,Comuside
Target: ERK, p38 MAPK, NF-κB, JNK
5,7-Dihydroxychromone
Cat.No: T5S1805
Synonym: 5,7-Dihydroxy-4H-Chromen-4-One,5,7-二羟基色酮,5,7-二羟基色原酮
Target: Others, Virus Protease, PARP, Caspase, Nrf2
Morroniside
Cat.No: T3414
Synonym: 莫诺苷,奎宁树
Target: Apoptosis, MMP, Pyroptosis
1,4-D-Gulonolactone
Cat.No: T4719
Synonym: D-Gulonic acid γ-lactone,D-(-)-古洛糖酸-1,4-内酯
Target: Others, Endogenous Metabolite
Flavokawain B
Cat.No: T6S0735
Synonym: 黄卡瓦胡椒素B,Flavokavain B,Flavokawin B,2'-Hydroxy-4',6'-Dimethoxychalcone
Target: Apoptosis, Others
Crocin II
Cat.No: T3779
Synonym: Crocin 2,西红花苷II,Crocetin gentiobiosylglucosyl ester,藏红花,Tricrocin,Crocin B
Target: Caspase, COX, NO Synthase
Obtusifolin
Cat.No: T4S0969
Synonym: 决明蒽醌,决明蒽醌;美决明子素
Target: Antioxidant, NF-κB
2'-Hydroxychalcone
Cat.No: TN1163
Synonym:
Target: Others
cis-4-Hydroxy-L-proline
Cat.No: T37512
Synonym:
Target: Endogenous Metabolite
Eckol
Cat.No: T24025
Synonym:
Target:
Dihydroguaiaretic acid
Cat.No: TN1581
Synonym: 二氢愈创木酸
Target: COX, DNA/RNA Synthesis
Tetrahydrocortisone
Cat.No: T19576
Synonym:
Target: Others
Sanggenon N
Cat.No: TN4941
Synonym:
Target: Others
Cycloheterophyllin
Cat.No: TN1542
Synonym:
Target: NADPH-oxidase, PKA, PKC
Cedrin
Cat.No: TN3618
Synonym:
Target: Beta Amyloid, BCL, Caspase
Turkesterone
Cat.No: TN2287
Synonym:
Target: Calcium Channel
Axillarin
Cat.No: TN3473
Synonym:
Target:
Mulberrofuran C
Cat.No: TN4587
Synonym:
Target: HSV
Luvangetin
Cat.No: TN4465
Synonym:
Target: COX, Prostaglandin Receptor, Antifection
7(8)-Dehydroschisandrol A
Cat.No: T83257
Synonym:
Target:
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