89
19
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7955 |
EB-3D
|
Apoptosis; AMPK; AChR | Apoptosis; Chromatin/Epigenetic; Neuroscience; PI3K/Akt/mTOR signaling |
EB-3D 是一种选择性胆碱激酶 α 抑制剂,对 ChoKα1 的IC50值为 1 μM。它影响 ChoKα 表达、AMPK 激活、细胞凋亡、内质网应激和脂质代谢,具有抗癌活性。 | |||
T15432 |
GSK256073
|
GPR; Others | Endocrinology/Hormones; GPCR/G Protein; Others |
GSK256073 是一种口服有活性的GPR109A 选择性激动剂,也是一种持久的人HCA2激动剂(pEC50:7.5) 。它能够减少脂降解,而显著改善葡萄糖稳态,对 2 型糖尿病和血脂异常具有潜在的研究价值。 | |||
T8988 |
PythiDC
|
Others | Others |
PythiDC 是一种选择性胶原脯氨酰 4-羟化酶抑制剂,既不会引起一般毒性,也不会破坏铁稳态。 | |||
T31014 |
Corrector C4
Corr 4a,Corrector C-4,Corr4a,Corrector C 4,Corr-4a |
Others | Others |
Corrector C4 是一种常用于研究囊性纤维化突变体的校正子,通过减轻CFTR跨膜结构域突变体与蛋白稳态的相互作用来发挥作用。 | |||
T64342 |
DC-TEADin02
|
YAP | Stem Cells |
DC-TEADin02 是 TEAD 自棕榈酰化抑制剂 (IC50 = 197 nM)。 DC-TEADin02 可用于有关发育、再生和组织稳态的研究。 | |||
TP1028L |
Calcitonin eel acetate
Calcitonin eel acetate (57014-02-5 Free base),降钙素,Thyrocalcitonin eel |
Others | Others |
Calcitonin eel acetate (Calcitonin eel acetate (57014-02-5 Free base)) 是调节钙稳态的甲状腺激素肽。 | |||
T36522 |
Isoallolithocholic acid
Alloisolithocholic Acid,AILCA,3β-Hydroxy-5α-cholanic acid |
Others | Others |
Isoallolithocholic acid (3β-Hydroxy-5α-cholanic acid) 是一种 T 细胞调节剂,是一种胆汁酸代谢物,具有抗炎活性,与人类免疫稳态有关。 | |||
T5627 |
Methoxychlor
|
Others | Others |
Methoxychlor 是一种有机氯农药,被认为是一种内分泌干扰物,会影响不同细胞模型中的 Ca²⁺ 稳态和细胞活力。 | |||
TP1305 |
LEP(116-130)(mouse)
|
Others | Others |
LEP(116-130)(mouse) 是合成的瘦素肽片段之一。 | |||
T40498L |
Dentonin acetate
Dentonin acetate (400090-20-2 Free base) |
Others | Others |
Dentonin acetate 增强骨生成并促进未成熟贴壁细胞的存活。 Dentonin acetate 是一种源自 MEPE 的合成片段,可用于磷酸盐稳态和骨代谢的研究。 | |||
T35707 |
3'-Sialyllactose sodium
3'-SL sodium |
NF-κB | NF-κB |
3'-Sialyllactose sodium 是一种益生元,具有抗炎活性,可维持免疫稳态。3'-Sialyllactose sodium 可减少压力源引起的焦虑样行为,可用于研究炎症和关节炎。 | |||
T60122 |
Aldometanib
Compound IA-47 (Br- base 2246625-81-8) |
Others; AMPK | Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling |
Aldometanib (LXY-05-029) 是一种具有口服活性的醛缩酶抑制剂,可以阻止FBP 与v-ATPase 相关的醛缩酶结合,并激活溶酶体 AMPK 。Aldometanib 可用于代谢稳态的研究。 | |||
T23543 |
YIL 781
|
GHSR | GPCR/G Protein |
YIL 781是一种选择性ghrelin 受体拮抗剂(GHS-R1a) (Ki = 17 nM)),对运动素受体显示出较弱的亲和力(K = 6 μ M)。YIL 781通过阻断胃饥饿素分泌对体内和体外胰岛素分泌改善体内葡萄糖稳态。 | |||
T2134 |
Dorzolamide hydrochloride
MK507 hydrochloride,L671152 hydrochloride,MK-507 (L-671152) HCl,盐酸多佐胺,Dorzolamide HCl |
Carbonic Anhydrase | Metabolism |
Dorzolamide hydrochloride (MK507 hydrochloride) 是一种碳酸酐酶carbonic anhydrase II 抑制剂,能够抑制红细胞CA-II(IC50:0.18 nM) 和CA-I(IC50:600 nM) 。 | |||
T4567 |
Sulfaphenazole
Plisulfan,Raziosulfa,Depocid,磺胺苯吡唑,Depotsulfonamide |
P450; Antibacterial | Metabolism; Microbiology/Virology |
Sulfaphenazole (Plisulfan) 是一种 CYP2C9的特异性抑制剂,抑制 CYP2C9介导的亚油酸动脉粥样硬化和促炎症效应,增加 AP-1的氧化应激和激活。 | |||
T4535L |
Etomoxir
(R)-(+)-Etomoxir |
Antioxidant; CPT | Metabolism; oxidation-reduction |
Etomoxir 是肉碱棕榈酰转移酶 1a (CPT-1a) 抑制剂,通过抑制 CPT-1a 来抑制脂肪酸氧化,且抑制人、大鼠和豚鼠中棕榈酸酯的氧化。Etomoxir 对腺嘌呤核苷酸转位酶有抑制作用,可通过破坏CoA稳态来抑制巨噬细胞极化。 | |||
T63349 |
Treprostinil diethanolamine
UT-15C |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Treprostinil diethanolamine (UT-15C) 是EP2、DP1和IP 的有效激动剂,对EP2、DP1、IP、EP1、EP4、EP3 和 FPKi 的值分别为 3.6、4.4、32.1、212、826、2505 和 4680 nM。Treprostinil diethanolamine 能够促使 cAMP 的上调,进而维持血管系统内的稳态,并造成人肺动脉的血管扩张。 | |||
T28020 |
Mesendogen
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
Mesendogen 是瞬时受体电位阳离子通道、亚家族 M、成员 6 (TRPM6) 和 7 (TRPM7) 的抑制剂,通过抑制 TRPM6/TRPM7 镁通道活性起作用。 | |||
T30203 | Atrinositol | ||
Atrinositol improves energy homeostasis in a mouse model of pancreatic cancer. | |||
T34963 |
TSPA
|
||
TSPA is an ATF6α translocation inducer which effectively promotes ATF6α translocation into the nucleus and ameliorates glucose homeostasis on db/db mice. | |||
T20274 |
Dibenzyl phthalate
AI300364,AI3-00364 |
||
Dibenzyl phthalate is an endocrine-disrupting chemical. It also interferes with different cell signaling pathways involved in weight and glucose homeostasis. | |||
TP1464 |
Risuteganib hydrochloride
|
||
Risuteganib hydrochloride is an anti-integrin that downregulates oxidative stress and restores homeostasis, and targets three integrin receptors that are implicated in dry age-related macular degeneration (AMD) in order to restore homeostasis in the retin | |||
T10046 |
16,16-Dimethyl prostaglandin E2
16,16-dimethyl PGE2 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
16,16-Dimethyl prostaglandin E2 is an orally active vertebrate Hematopoietic stem cells homeostasis critical regulator. It can act through EP2/EP4 and has an interaction with the Wnt pathway. | |||
TP1027 |
Calcitonin, eel TFA (57014-02-5 free base)
Thyrocalcitonin eel (TFA),Calcitonin, eel TFA |
||
Calcitonin,eel TFA is a thyroid hormone polypeptide that can regulate calcium homeostasis and is widely used in the study of postmenopausal osteoporosis. | |||
T40898 |
DMHCA
|
||
DMHCA, a potent, selective LXR agonist, specifically activates the LXR pathway's cholesterol efflux arm, avoiding triglyceride synthesis stimulation. This compound exhibits anti-inflammatory properties and is utilized in researching cholesterol homeostasis and diabetes. | |||
T39244 |
Atrial Natriuretic Peptide (1-28), human, porcine, Biotin-labeled
|
||
Atrial Natriuretic Peptide (1-28), human, porcine, Biotin-labeled, is one of three mammalian natriuretic peptides (NPs) that exerts endocrine effects on fluid homeostasis and blood pressure. Atrial Natriuretic Peptide holds promise for cardiovascular diseases research. | |||
T41109 |
Phytochelatin 2 (PC2)
|
||
Phytochelatin 2, a short plant peptide, serves as an essential metal-binding compound. Phytochelatins are a diverse group of plant compounds that play a crucial role in chelating metals, safeguarding against metal toxicity, and maintaining metal homeostasis. | |||
T40498 |
Dentonin
AC-100 |
||
Dentonin (AC-100) is a synthetic fragment derived from MEPE that enhances osteogenesis by promoting osteoprogenitor adhesion and facilitating the survival of immature adherent cells. It does not have a significant effect on mature osteoblasts. Dentonin is useful for research on phosphate homeostasis and bone metabolism. | |||
T78372 |
Calcitonin, eel TFA
Thyrocalcitonin eel TFA |
||
Calcitonin, eel TFA,一种甲状腺激素多肽,调节钙稳态,主要应用于绝经后骨质疏松症研究。 | |||
T70605 | NaPi2b Inhibitor 15 | ||
NaPi2b is primarily expressed in the small intestine, lungs, and testes and plays an important role in phosphate homeostasis. The inhibition of NaPi2b, responsible for intestinal phosphate absorption, is considered to reduce serum phosphate levels, making it a promising therapeutic approach for hyperphosphatemia | |||
T61806 |
Antitumor agent-44
|
||
Antitumor agent-44 (Compound 5n) elicits potent antitumor effects by inducing disruption of mitochondrial homeostasis, cell cycle arrest, and apoptosis in human adenocarcinoma cells. Moreover, Antitumor agent-44 demonstrates significant anti-tumor activity in a lung cancer cell xenograft mice model [1]. | |||
T80556 |
wt hMLN
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
wt hMLN为抑制SR Ca2+泵(SERCA)的微量蛋白,对骨骼肌钙稳态具有关键作用。 | |||
T78330 |
Peresolimab
|
PD-1/PD-L1 | Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation |
Peresolimab是一种人源化IgG1-κ单克隆抗体,专门针对PD-1受体。该药物通过激活生理免疫抑制途径,有助于重建免疫平衡。 | |||
T61496 | NPR-C activator 1 | ||
NPR-C activator 1 (Compound 1) is a potent activator of natriuretic peptide receptor C (NPR-C), a receptor involved in the regulation of vascular homeostasis. It acts as a potent agonist (EC50 ~ 1 μM) of C-type natriuretic peptide (CNP), showing promising in vivo pharmacokinetic properties [1]. | |||
T80870 | VE-PTP-IN-1 | ||
VE-PTP-IN-1 (compound 2) 为一种选择性VE-PTP抑制剂,呈弱酸性,涉及调控血管稳态及血管生成。 | |||
T22575 | Angiotensin Fragment 1-7 (acetate) | Others | Others |
Angiotensin Fragment 1-7 is a type 1 angiotensin II receptor agonist. In the renin-angiotensin system, angiotensin I is cleaved by the angiotensin-converting enzyme to form angiotensin II, which has effects on fluid and electrolyte, as well as homeostasis | |||
T40255 |
VCP/p97 inhibitor-1
VCP/p97 inhibitor-1 |
||
VCP/p97 inhibitor-1, a highly effective compound, inhibits VCP/p97 (also known as Cdc48, CDC-48, or Ter94) with an IC 50 of 54.7 nM. This inhibitor induces a disruption in protein homeostasis and interferes with the degradation process of misfolded polypeptides by the ubiquitin-proteasome system (UPS). | |||
TP2093 |
Apelin-36(human)
Apelin-36 (human) |
||
Endogenous APJ receptor agonist (EC50 = 20 nM) that is secreted by adipocytes. Binds with high affinity to human APJ receptors expressed in HEK 293 cells (pIC50= 8.61). Involved in regulation of cardiovascular function, fluid homeostasis and feeding. Bloc | |||
TP1209 |
BNP (1-32), rat TFA (133448-20-1 free base)
Brain Natriuretic Peptide (BNP) (1-32), rat TFA,BNP (1-32), rat TFA |
||
Acts as a cardiac hormone with a variety of biological actions including natriuresis, diuresis, vasorelaxation, and inhibition of renin and aldosterone secretion. It is thought to play a key role in cardiovascular homeostasis. Helps restore the body\'s sa | |||
T70639 |
AM-9514
|
||
AM-9514 is a novel, potent Glucokinase (GK) activator. AM-9514 showed a favorable combination of in vitro potency, enzyme kinetic properties, acceptable pharmacokinetic profiles in preclinical species, and robust efficacy in a rodent PD model. Glucokinase (GK) activators represent a class of type 2 diabetes therapeutics actively pursued due to the central role that GK plays in regulating glucose homeostasis. | |||
T80770 |
wt hMLN TFA
|
||
wt hMLN (TFA) 是一种微量蛋白,能够抑制SR Ca2+泵 (SERCA);在骨骼肌的钙稳态调节中具有重要功能。 | |||
T35595 | Cyclic di-AMP (sodium salt) | ||
Cyclic di-AMP (c-di-AMP) is a second messenger produced by bacteria but not by mammals. Generated by a family of diadenylate cyclases, c-di-AMP can impact bacterial cell growth, cell wall homeostasis, pathogenicity, and other cellular functions. Bacteria-derived cyclic dinucleotides, including c-di-AMP, trigger the expression of interferon genes in mammalian cells. | |||
T37827 |
CAY10506
CAY10506 |
||
Anti-diabetic drugs of the thiazolidinedione (TZD) structural class as well as α-lipoic acid activate peroxisome proliferator-activated receptor γ (PPARγ), a nuclear transcription factor that controls glucose metabolism and lipid homeostasis. CAY10506 is a hybrid lipoic acid-TZD derivative that transactivates human PPARγ with an EC50 value of 10 μM. | |||
T82199 |
HIF-1 alpha (556-574) (TFA)
|
HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism |
HIF-1 alpha (556-574) TFA 是一种由19个氨基酸组成的缺氧诱导因子-1 (HIF-1) 短肽段,起着调控氧稳态响应的关键作用。 | |||
T35785 |
N-Oleoyl Leucine
|
||
N-Oleoyl leucine is an N-acyl amide generated by PM20D1 that uncouples mitochondrial respiration independent of uncoupling protein 1 (UCP1) in vitro. N-Oleoyl leucine (25 mg/kg, i.p.) decreases body weight and food intake, preferentially decreasing fat mass in a diet-induced obesity mouse model. It improves glucose homeostasis in a fasting glucose tolerance test and increases VO2 while slightly decreasing overall locomotor activity. | |||
T80438 |
Atrial natriuretic peptide (3-28) (human)
ANP (3-28) (human) |
Endothelin Receptor | GPCR/G Protein |
Atrial natriuretic peptide (3-28) (human) 是由心房心肌细胞合成并分泌的肽类激素,主要在调节血压、体液平衡及电解质稳态方面发挥作用。 | |||
T68482 | CE-326597 | ||
CE-326597 is a potent and selective CCK1R agonist. The type 1 cholecystokinin receptor (CCK1R) has multiple physiologic roles relating to nutrient homeostasis,including mediation of postcibal satiety. The type 1 cholecystokinin (CCK) receptor (CCK1R) is a key mediator of postcibal satiety and a potential target for drugs that may be useful to prevent and/or treat obesity. | |||
T36492 | CMC2.24 | ||
CMC2.24 (TRB-N0224) is an orally active tricarbonylmethane agent that demonstrates effectiveness in inhibiting Ras activation and the downstream effector ERK1/2 pathway, thus effectively combating pancreatic tumor formation in mice. Additionally, CMC2.24 exerts potent inhibitory effects on zinc-dependent MMPs, with IC50s ranging from 2.0-69 μM. Furthermore, CMC2.24 aids in alleviating the progression of osteoarthritis by restoring cartilage homeostasis and inhibiting chondrocyte apoptosis throug... | |||
TP2094 |
Apelin-36(rat, mouse)
Apelin-36 (rat, mouse) |
||
Endogenous APJ receptor agonist that is secreted by adipocytes. Binds with high affinity to APJ receptors (IC50 = 5.4 nM) and potently inhibits cAMP production in vitro (EC50 = 0.52 nM). Involved in regulation of cardiovascular function, fluid homeostasis | |||
T64293 |
SLN124
|
||
SLN124 是一种 GalNac-siRNA,靶向跨膜丝氨酸蛋白酶 6 (Tmprss6),由与 TMPRSS6-siRNA 结合的三聚体 GalNAc 配体组成。SLN124 具有潜力用做 siRNA 剂,恢复铁调素表达并使 β-地贫中铁稳态正常化。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7999 |
7-Hydroxyflavanone
|
Anti-infection | Microbiology/Virology |
7-Hydroxyflavanone 对肺炎链球菌临床分离株显示出抗菌活性。 | |||
T4461 |
3,5-Diiodo-L-thyronine
3,5-二碘-L-甲状腺素,Diiodothyronine |
Thyroid hormone receptor(THR); Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
3,5-Diiodo-L-thyronine (Diiodothyronine) 是内源性代谢产物的一种。 | |||
TN1480 |
Cephaeline
吐根鹼,吐根酚碱 |
Virus Protease; Influenza Virus; HIF | Angiogenesis; Chromatin/Epigenetic; Microbiology/Virology |
Cephaeline 对受保护的原代 CLL 细胞具有高度活性(相对 IC50 为 35nM),并通过抑制 HIF-1α± 和扰乱细胞内氧化还原稳态发挥作用。 | |||
T6S2038 |
Ziyuglycoside II
|
Apoptosis; Antioxidant; Reactive Oxygen Species | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction |
Ziyuglycoside II 是从地榆中提取的一种三萜皂苷,可诱导活性氧 产生和凋亡,具有抗炎和抗癌作用。 | |||
T4238 |
Glycocyamine
乙酸胍,2-Guanidinoacetic acid,Guanidoacetic acid |
Others; Endogenous Metabolite | Metabolism; Others |
Glycocyamine (2-Guanidinoacetic acid) 是一种肌酸的前体,能够为鸟类的体内平衡提供能量,也能够成为食用精氨酸的替代物。 | |||
T3834 |
8-Epideoxyloganic acid
8-表去氧马钱酸 |
ROS; Immunology/Inflammation related | Immunology/Inflammation |
8-Epideoxyloganic acid 是从 Incarvillea delavayi 中分离得到的一种环烯醚萜苷。它具有微弱的缓解疼痛活性。 | |||
T6368 |
Abscisic Acid
Abscisin II,Dormin,(+)-脱落酸,(+)-ABA,Abscisic Acid (Dormin) |
Others; Proton pump; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Others |
Abscisic Acid (Dormin) 是具有口服活性的植物激素,存在于蔬菜和水果中,也是内源性的哺乳动物激素。它是生长抑制剂,可以调节植物生长发育。他抑制质子泵,并导致 Ca2+依赖性的质膜去极化。它是 LANCL2 的天然配体,属于胰岛素敏感化合物,在糖尿病前期,2 型糖尿病和代谢综合征的研究中具有价值。 | |||
T20089 |
ATP
Atipi,ATP disodium salt hydrate,Triphosphoric acid adenosine ester,Ara-ATP,Triphosphaden,Adenosine triphosphate;Ara-ATP,Adenosine triphosphate |
Endogenous Metabolite | Metabolism |
ATP (Adenosine triphosphate) 可为细胞提供能量,参与整体能量平衡,维持细胞内稳态。ATP 可以通过与特异性嘌呤能受体的相互作用充当细胞外信号分子,以介导神经传递、炎症、细胞凋亡和骨重塑等多种过程。 | |||
T3386 |
Kaempferitrin
Lespedin,Kaempferol,Lespenephryl,Lespenefril,Kaempferol 3,7-dirhamnoside,山奈苷 |
cell cycle arrest; Glucokinase; IGF-1R | Cell Cycle/Checkpoint; Metabolism; Tyrosine Kinase/Adaptors |
Kaempferitrin (Lespenephryl) 是天然黄酮苷类化合物,具有缓解疼痛、抗糖尿病、消炎、抗肿瘤和化疗作用,可激活胰岛素信号传导。 | |||
TN6694 |
5,6-Benzoflavone
β-Naphthoflavone,beta-NF |
Antioxidant | oxidation-reduction |
5,6-Benzoflavone (β-Naphthoflavone) 是芳烃受体的外源配体,可破坏人肝癌 HepG2 细胞中的锌稳态。5,6-Benzoflavone (β-Naphthoflavone) 具有抗炎和抗氧化活性,抑制通过 AKT/Nrf-2/HO-1-NF-kappaB 信号转导轴,抑制 LPS 诱导的炎症,抑制TNF-α诱导的ICAM-1和VCAM-1表达,可用于研究神经退行性疾病。 | |||
T5065 |
GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD
Monosodium-GMP,cGMP sodium salt,鸟苷-3',5'-环磷酸一钠盐,Cyclic GMP |
PKA | Tyrosine Kinase/Adaptors |
GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD (cGMP sodium salt) 也称为 cGMP,是一种细胞调节剂,被描述为第二信使。它的水平随着各种激素的增加而增加,包括乙酰胆碱、胰岛素和催产素。 cGMP 激活蛋白激酶 G(PKG) 并调节离子通道电导,信号传导影响多种过程,包括平滑肌松弛和增殖、光转导和能量稳态。 | |||
T4S2126 |
Ginkgetin
银杏双黄酮,银杏素 |
Apoptosis; Wnt/beta-catenin; COX; STAT; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Stem Cells |
Ginkgetin 是从银杏叶中分离得到的一种双黄酮,具有抗肿瘤、抗炎、神经保护、抗真菌的作用。它也是 Wnt 信号抑制剂,IC50值为 5.92 μM。 | |||
TMA0805 |
Lupanine
|
ATPase; Potassium Channel; Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Lupanine has a weak sedative effect on the central nervous system, interaction with specific drugs used for treatment of the CNS and for analgesic activity. Lupanine improves glucose homeostasis by influencing KATP-channels of pancreatic beta cells. | |||
TN4016 |
Ethyl 2,4,6-trihydroxybenzoate
|
Liver X Receptor | Metabolism |
Ethyl 2,4,6-trihydroxybenzoate is a dual-LXR modulator that regulates the expression of key genes in cholesterol homeostasis in multiple cells without inducing lipid accumulation in HepG2 cells. It suppresses cellular cholesterol accumulation in a dose-dependent manner and induces the transcriptional activation of LXR-α/-β-responsive genes. | |||
T60789 |
L-Cystine dihydrochloride
|
||
L-Cystine dihydrochloride 是合成谷胱甘肽 (GSH) 的含硫前体。L-Cystine dihydrochloride 的稳态对谷胱甘肽的功能很重要。L-Cystine dihydrochloride 可用作细胞培养组分。 | |||
T39605 |
β-D-Glucopyranosyl abscisate
ABA-GE,β-D-Glucopyranosyl abscisate,(S)-cis,trans-Abscisicacidglucosylester |
||
β-D-Glucopyranosyl abscisate (ABA-GE) is a hydrolyzable conjugate of abscisic acid (ABA), which predominantly accumulates in the vacuole and likely in the endoplasmic reticulum. The deconjugation of β-D-Glucopyranosyl abscisate enables a swift release of free ABA in response to abiotic stress factors like dehydration and salt stress. β-D-Glucopyranosyl abscisate plays a crucial role in maintaining ABA homeostasis. | |||
TN2876 |
3,4-Dihydroxy-2-methoxyxanthone
|
Antibacterial; Antifection | Microbiology/Virology |
3,4-Dihydroxy-2-methoxyxanthone 显示出抗菌和保肝活性,它能防止叔丁基过氧化氢诱导的新鲜离体大鼠肝细胞的脂质过氧化和细胞死亡,并在一定程度上有效防止细胞谷胱甘肽平衡的扰乱。 | |||
TN4223 |
Homopterocarpin
|
Antifection | Microbiology/Virology |
Homopterocarpin and Pterocarpus extract offer gastroprotection against indomethacin- induced ulcer by antioxidative mechanism and the modulation of gastric homeostasis, homopterocarpin may be responsible for, or contribute to the antiulcerogenic property | |||
TN2641 | 15-Methoxypinusolidic acid | ERK; IL Receptor; p38 MAPK; Calcium Channel; NOS; NF-κB; COX; JNK; NMDAR; PPAR | DNA Damage/DNA Repair; Immunology/Inflammation; MAPK; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB |
15-Methoxypinusolidic acid has anti-inflammatory effects, it inhibits LPS-induced iNOS expression and NO production, independent on MAPK and NF-kappaB. 15-Methoxypinusolidic acid suppresses adipocyte differentiation through the inhibition of PPARgamma-dep |