75
27
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T62125 | Colistin adjuvant-1 | ||
Colistin adjuvant-1 是一种粘菌素佐剂 (colistin adjuvant),对革兰氏阴性细菌具有增强的粘菌素增强活性。Colistin adjuvant-1 对 NF-κB 表现出抑制作用 (IC50: 0.209 μM)。 | |||
T61154 | Colistin adjuvant-2 | ||
Colistin adjuvant-2 is a compound that acts as a potentiation agent for colistin, effectively enhancing its activity against Gram-negative bacteria [1]. | |||
T10466 |
BAY-1797
|
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
BAY-1797 是具有口服活性的选择性P2X4高效拮抗剂,对人 P2X4 的IC50为 211 nM,具有抗伤害和抗炎作用。 | |||
T2067 |
NS11394
NS 11394 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
NS11394 是可口服GABAA 的阳性变构调节剂 (PAM),Ki 值为 0.5 nM。它对GABAA 的选择性依次为 α5、α3、α2 和α1 受体,具有抗炎和抗焦虑活性。 | |||
T2125 |
Trametinib
GSK1120212,曲美替尼,JTP-74057 |
Apoptosis; MEK; Autophagy | Apoptosis; Autophagy; MAPK |
Trametinib (GSK1120212) 是一种 MEK 抑制剂,抑制 MEK1 和 MEK2 (IC50=0.7/0.9 nM),具有 ATP 非竞争性和口服活性。Trametinib 可以激活自噬,诱导凋亡。 | |||
T5857 |
Trametinib (DMSO solvate)
Trametinib DMSO solvate,GSK-1120212 (DMSO solvate),Trametinib dimethyl sulfoxide,JTP-74057 (DMSO solvate) |
Apoptosis; MEK | Apoptosis; MAPK |
Trametinib (DMSO solvate) (GSK-1120212 (DMSO solvate)) 是一种口服有效的 MEK 抑制剂,抑制 MEK1 和 MEK2 的 IC50分别为 2 nM。它还能激活自噬,诱导凋亡。 | |||
T16871 |
Semustine
|
DNA Alkylator/Crosslinker | DNA Damage/DNA Repair |
Semustine 是一种 DNA 烷化剂,是一种癌症化疗化合物,在接受辅助化疗的恶性黑色素瘤患者中具有肾毒性,可用于辅助治疗白血病。 | |||
T67912 |
PA3552-IN-1
|
||
PA3552-IN-1 是一种抗生素佐剂, 可以降低 PA3552 的表达,恢复 MDR 铜绿假单胞菌 DK2 菌株对 Polymyxin B 的敏感性。 | |||
T4027 |
KIN1148
|
Influenza Virus | Microbiology/Virology |
KIN1148 是一种新型小分子佐剂,是IRF3激动剂,用于增强流感疫苗效率。 | |||
T68088 |
Iodofiltic acid
|
||
Iodofiltic acid 可用于辅助治疗急性冠脉综合征(Zeus-ACS),可成像以检测心肌缺血。 | |||
T13545 |
Aluminum Hydroxide
|
Others | Others |
Aluminum Hydroxide 是一种具有口服活性的铝佐剂的主要形式。它也可作为佐剂补偿亚单位疫苗的低固有免疫原性。基于它辅助的研究包括储存库效应、促吞噬作用和激活促炎症的 NLRP3 通路。 | |||
T19967 |
Fendosal
芬度柳,HP 129,P 71-0129,P71-0129,P-71-0129,HP129,HP-129 |
Immunology/Inflammation related | Immunology/Inflammation |
Fendosal (HP-129) 是一种非甾体抗炎药。在预防性和治疗性辅助诱导的慢性炎症多关节炎模型中,它的活性是阿司匹林的 6.9 至 9.5 倍。 | |||
T14513 |
BBIQ
|
TLR | Immunology/Inflammation |
BBIQ 是一种有效且选择性的 toll 样受体 7 (TLR7) 激动剂,对人 TLR7 的 EC50 为 59.1 nM。BBIQ 还是一种功能强大的疫苗佐剂,可增强机体的先天免疫应答。 | |||
T0806 |
Flunarizine dihydrochloride
Flunarizine 2HCl,KW-3149,R14950,盐酸氟桂利嗪 |
Calcium Channel; Dopamine Receptor; Sodium Channel | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Flunarizine dihydrochloride (R14950) 是 Na+/Ca2+(T 型) 通道双重阻滞剂。它也是 D2多巴胺受体拮抗剂。它具有用于扩张外周血管和预防偏头痛的潜力。 | |||
T72253 |
AXC-715 trihydrochloride
T785 trihydrochloride |
TLR | Immunology/Inflammation |
AXC-715 trihydrochloride (T785 trihydrochloride) 是一种 TLR7/TLR8 双激动剂, 可用于合成抗体佐剂免疫偶联物。偶联物多为程序性死亡配体 1 (PD-L1) 连接到一个或多个佐剂的抗体结构上。 | |||
T63056 |
Dovramilast
|
||
Dovramilast (CC-11050) 是一种口服具有活力的磷酸二酯酶 4 (PDE4) 抑制剂,可以降低炎症反应,改善 INH 介导的肺部细菌清除。Dovramilast (CC-11050) 能够作为辅助试剂,用于研究结核病。 | |||
T77796 |
DL-Borneol
(endo)-Borneol,Borneol,(±)-Borneol |
GABA Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
DL-Borneol ((endo)-Borneol) 是一种从中药中提取的小分子,是一种可口服的生物佐剂,可以改善药物向大脑的输送,常用作治疗心脑血管疾病的中药的辅助成分。 | |||
TP1938L |
RS09 2TFA (1449566-36-2 free base)
RS09 2TFA 1449566-36-2(free base) |
TLR | Immunology/Inflammation |
RS09 2TFA (1449566-36-2 free base) 是一种 TLR4 激动剂。促进 NF-κB 核转位并在体外诱导 RAW264.7 巨噬细胞分泌炎性细胞因子。它在体内充当佐剂并提高 X-15 特异性抗体血清浓度。 | |||
T21320 |
Methoxyamine HCl
甲氧基胺盐酸盐,TRC102,TRC 102,Methoxyamine,TRC-102 |
Others | Others |
Methoxyamine HCl (Methoxyamine) 与脱嘌呤/脱嘧啶 (AP) DNA 损伤位点共价结合并抑制碱基切除修复 (BER),这可能导致 DNA 链断裂和细胞凋亡增加。 Methoxyamine 是一种具有潜在佐剂活性的口服生物可利用的小分子抑制剂。该药剂可增强烷化剂的抗肿瘤活性。 | |||
T64914 |
Vitamin E succinate
D-α-Tocopherol Succinate |
Apoptosis | Apoptosis |
Vitamin E succinate (D-α-Tocopherol Succinate) 是一种具有抗氧化作用的生育酚,属于维生素 E 类化合物。Vitamin E succinate 具有抗肿瘤活性,可诱导细胞凋亡,可用于辅助治疗癌症和合成 INVITE (一种生物偶联物)。 | |||
T21543 |
AP 18
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
AP-18 是选择性的 TRPA1 抑制剂。AP-18 可以抑制 50 μM 肉桂醛诱导的 TRPA1 激活,在小鼠和人中的 IC50 分别为 4.5 μM 和 3.1 μM。AP-18 可以逆转 CFA 诱导的小鼠机械性痛觉过敏。AP-18 可以浓度依赖的方式减弱 30 μM AITC 诱导的 Yo-Pro 摄取(IC50= 10.3 μM)。 | |||
T15003 |
CP-20961
|
Others | Others |
CP-20961 is a synthetic non-immunogenic adjuvant. It induces arthritis. | |||
T29846 |
Alcuronium free base
Alcuronium,Alcuronum,Diallylnortoxiferine,Alcuronium kation,Alloferine |
||
Alcuronium free base is a non-depolarizing skeletal muscle relaxant similar to Tubocurarine. It is used as an anesthesia adjuvant. | |||
T39527 |
Se-DMC
|
||
Se-DMC effectively reduces the inflammatory response, nociception, and neurobehavioral deficits induced by complete Freund's adjuvant (CFA) in mice. | |||
T19590 |
Trehalose 6-behenate
|
Others | Others |
Trehalose 6-behenate is a Th1/Th17 skewing vaccine adjuvant. | |||
T31914 |
Gantacurium chloride
GW 280430A,AV4430A,AV 4430A,GW280430,GW 280430,GW-0430 |
||
Gantacurium chloride is a benzylisoquinoline alkaloid, which may be used as an adjuvant in anesthesia. | |||
T68926 | Indomethacin salicylate | ||
Indomethacin salicylate is an antiinflammatory drug. It has shown remarkable inhibitory effects on carrageenin edema, ultraviolet erythema and adjuvant arthritis. | |||
T32085 |
HM30181AK
HM-30181AK,HM 30181AK |
||
HM30181AK is an inhibitor of the adenosine triphosphate (ATP) binding cassette (ABC) transporter P-glycoprotein (P-gp) with adjuvant activity. | |||
T24994 |
MreB Perturbing Compound A22 hydrochloride
A22 hydrochloride,MreB Perturbing Compound A22 |
||
A22 is an inhibitor of MreB, an actin-like bacterial protein, and has been proved to be an antibiotic adjuvant. A22 inhibition of MreB disrupts the bacterial actin cytoskeleton, which can cause an increase in cell permeability and altered transport. | |||
T28916 |
TAK-603
TAK603,TAK 603 |
||
TAK-603 is an anti-rheumatic drug and is also anti-inflammatory compound. It selectively suppresses Th1 cytokine production and inhibits the progression of adjuvant arthritis. | |||
T69385 | Baicalein monohydrate | ||
Baicalein monohydrate is an inhibitor of 12-lipoxygenase, leukotriene biosynthesis and release of lysosomal enzymes. It also inhibits cellular Ca2+ uptake and mobilization and adjuvant-induced arthritis. | |||
T6287L |
Tariquidar dimesylate
D 06008,XR9576,D06008,XR 9576,Tariquidar dimesilate,XR-9576 |
||
Tariquidar is a P-glycoprotein inhibitor undergoing research as an adjuvant against multidrug resistance in cancer. Tariquidar non-competitively binds to the p-glycoprotein transporter, thereby inhibiting transmembrane transport of anticancer drugs. | |||
T21392 |
Flunarizine
Flunarizinum,Flunarizin,Sibelium,Flunarizina,R-14950 |
||
Flunarizine is a non-selective calcium entry blocker and a histamine H1 receptor blocker. It is effective in the prophylaxis of migraine, occlusive peripheral vascular disease, vertigo of central and peripheral origin, and as an adjuvant in the therapy of | |||
T40152 | AXC-715 hydrochloride | ||
AXC-715 hydrochloride is a TLR7/TLR8 dual agonist, can be used for synthesis of antibody-adjuvant immunoconjugates, comprising an antibody construct that binds programmed death-ligand 1 (PD-L1) linked to one or more adjuvants. | |||
T38619 |
GSK1795091
CRX-601 |
||
GSK1795091 (CRX-601) is a synthetic TLR4 agonist and immunologic stimulator with demonstrated antitumor activity. It serves as a vaccine adjuvant, enhancing both mucosal and systemic immunity to influenza virus vaccines. | |||
T15167 |
Draflazine
R-75231 |
Others | Others |
Draflazine is an ENT1 inhibitor. It completely reverses the hypersensitivity in the complete Freund’s adjuvant (CFA) model of mechanical hyperalgesia. Draflazine also completely reverses the hypersensitivity of the carrageenan inflammation model of therma | |||
T74916 | ODN M362 | ||
ODN M362 是一种 C 类寡核苷酸,是 TLR-9激动剂,可用作疫苗佐剂。ODN M362 诱导癌细胞凋亡(apoptosis)。 | |||
T74240 |
Vaxfectin
|
||
Vaxfectin 是一种阳离子脂质佐剂,可用于基于质粒 DNA 和蛋白质的疫苗。 | |||
T69451 |
R-130823
|
||
R-130823 is a ighly selective inhibition against mitogen-activated protein kinase p38alpha (IC50=22 nM). The release of tumor necrosis factor-alpha, interleukin-1beta, -6 and -8 was inhibited in lipopolysaccharide-stimulated human blood pretreated by R-130823 , with IC50 values of 0.089, 0.066, 0.95 and 0.16 microM, respectively. R-130823 reduced the established hind paw swelling in rat adjuvant-induced arthritis, while methotrexate showed no suppression. In the same model, R-130823 ameliorated ... | |||
T14035 |
3M-011
|
TLR | Immunology/Inflammation |
3M-011, a potent dual toll-like receptor TLR7/8 agonist and cytokine inducer, serves as a powerful adjuvant to radiotherapy, eliciting significant local and systemic immune responses. Additionally, it effectively inhibits H3N2 influenza viral replication in the nasal cavity and exhibits strong antitumor activity[1][2][3]. | |||
T72871 |
IMD-biphenylC
|
NF-κB | NF-κB |
IMD-biphenylC是一款新型NF-κB免疫调节剂二聚体,能够有效抑制肿瘤增殖,并诱导较低的全身性炎症反应,同时减轻佐剂的毒性。 | |||
T74909 |
ODN 2395
|
||
ODN 2395为C类寡核苷酸,作为疫苗佐剂和TLR9激动剂应用。其序列为5'-tcgtcgttttcggcgc:gcgccg-3'。(注:碱基为硫代磷,ODN 2395特征为包含部分回文序列cggcgc:gcgccg) | |||
T38327 |
Cryogenine
|
||
Cryogenine is an alkaloid originally isolated from H. salicifolia that has anti-inflammatory activity.1 It inhibits prostaglandin synthetase (IC50 = 424 μM). Cryogenine (100 mg/kg per day, p.o.) reduces paw edema and the mean arthritic index in a rat model of adjuvant-induced polyarthritis.2 |1. Lema, W.J., Blankenship, J.W., and Malone, M.H. Prostaglandin synthetase inhibition by alkaloids of Heimia salicifolia. J. Ethnopharmacol. 15(2), 161-167 (1986).|2. Kosersky, D.S., Brown, J.K., and Malon... | |||
T70268 |
3A-MPLA
|
||
Monophosphoryl lipid A (MPLA) is a natural agonist for the toll-like receptor-4 (TLR4). It is useful as an adjuvant in immunization. MPLA is a safe prophylactic agent and has immunotherapeutic applications. It induces tumor necrosis factor and interleukin (IL)-1β, however not as efficient as lipopolysaccharide (LPS). MPLA improves immune response during bacterial sepsis infection. | |||
T5317L |
Cridanimod sodium
XBIO-101,XBIO 101,Cycloferon,Sodium Cridanimod,Cridanimod Na,XBIO101 |
||
Cridanimod can increase progesterone receptor (PR) expression, with potential antineoplastic adjuvant activity. Cridanimod is able to induce the expression of PR in endometrial cancer. In combination with a progestin, cancer cells could be eradicated thro | |||
T72869 |
IMD-biphenylA
|
NF-κB | NF-κB |
IMD-biphenylA是NF-κB免疫调节二聚体中的新型咪唑喹啉酮类化合物,具有增强小分子免疫增强剂免疫佐剂性的能力。 | |||
T74902 |
ODN 1018
|
||
ODN 1018 (1018 ISS)为一种寡脱氧核苷酸,兼具TLR-9激动剂与合成免疫刺激序列的特性,广泛应用作疫苗佐剂。序列为5′-TGACTGTGAACGTTCGAGATGA-3′。 | |||
T72870 |
IMD-biphenylB
|
NF-κB | NF-κB |
IMD-biphenylB作为NF-κB免疫调节剂二聚体,具有抑制肿瘤增殖的功能,并能诱导低全身炎症反应,同时减少佐剂毒性。 | |||
T72688 |
STING agonist-20
|
||
STINGagonist-20 是一种有效的STING 激动剂,用于合成 XMT-2056。STINGagonist-20 可作为疫苗佐剂,用于癌症以及其他炎症,免疫性疾病的研究。 | |||
T78672 |
I-287
|
||
I-287为一种口服活性PAR2选择性抑制剂,能对Gαq和Gα12/13的活性以及其下游效应物施加负异构调控。该化合物能够减轻Complete Freund's adjuvant引发的小鼠炎症,适用于免疫炎症研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12500 |
Platycoside E
Platycodin E,桔梗苷E |
Others | Others |
Platycoside E (Platycodin E) 是一种桔梗皂苷元型皂苷,从桔梗的根中分离获得,能够促进 ovalbumin 免疫小鼠中血清 OVA 特异性IgG2a 和IgG2b 抗体的产生。它具有溶血活性和佐剂潜力。 | |||
TJS2216 |
Aurantiamide acetate
金色酰胺醇酯,Asperglaucide |
Cysteine Protease | Proteases/Proteasome |
Aurantiamide acetate (Asperglaucide) 是抑制口服有活性的 cathepsin 选择性抑制剂,分离自 Portulaca oleracea L。它具有抗炎作用,可用于研究炎性相关疾病。 | |||
TN6925 |
Pristane
姥鲛烷,2,6,10,14-tetramethylpentadecane |
Others | Others |
Pristane (2,6,10,14-tetramethylpentadecane) 是一种天然存在的烃油,是矿物油中最活跃的成分,较少存在于许多植物、各种海洋生物中。它是一种非抗原性佐剂,可诱导大鼠中 MHC II 类限制性关节炎 T 细胞。 | |||
TN2232 |
Soyasaponin Ab
|
NOS; NF-κB; COX | Immunology/Inflammation; Neuroscience; NF-κB |
Soyasaponin Ab 是一种大豆皂苷。Soyasaponin Ab 在 3T3-L1 脂肪细胞中通过下调 PPARγ 产生抗肥胖的作用。 | |||
T6431 |
Levoleucovorin Calcium
左亚叶酸钙,Calcium Levofolinate,CL307782 |
Others; Antifolate | Cell Cycle/Checkpoint; Others |
Levoleucovorin Calcium (CL307782) 是一种亚叶酸的钙盐,在癌症化疗中用作辅助剂。 | |||
T24403 |
Folinic acid
HSDB 6544,Leucovorin |
Endogenous Metabolite; Antifolate | Cell Cycle/Checkpoint; Metabolism |
Folinic acid (Leucovorin) 是一种可用于治疗甲氨蝶呤的生物叶酸,通常与 Methotrexate (MTX) 联用来降低 MTX 诱导的毒性,可用于辅助治疗结肠癌。 | |||
T6S1485 |
Ginsenoside Rh4
人参皂苷Rh4 |
Others | Others |
Ginsenoside Rh4 可以安全地用作佐剂,具有低溶血作用或无溶血作用。它具有细胞毒活性,其苷元对癌细胞系具有杀伤作用。 | |||
T5781 |
taraxasteryl acetate
蒲公英甾醇醋酸酯,醋酸蒲公英酯 |
Antibacterial | Microbiology/Virology |
Taraxasteryl acetate 是分离自矢状疟原虫中,具有广谱的抗炎活性。它能够改善右旋糖酐、酵母聚糖及花生四烯酸诱导的大鼠后爪水肿。它可用于研究局部炎症。 | |||
TN2088 |
Platycodin D2
桔梗皂苷D2 |
IL Receptor; HBV | Immunology/Inflammation; Microbiology/Virology |
Platycodin D2 是分离自桔梗的皂苷类物质,显示除抗癌活性。 | |||
TJS0339 |
Coumarin-3-carboxylic acid
香豆素-3-羧酸,3-Carboxycoumarin |
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Coumarin-3-carboxylic acid (3-Carboxycoumarin) 是一种合成香豆素的重要起始化合物。其中香豆素是具有多种生物活性的天然产物。它的镧系复合物对 K-562 细胞具有抗增殖活性。 | |||
T7028 |
Licochalcone C
LICOCHALCONEC,甘草查尔酮C |
Phosphatase; Antioxidant; Glucosidase | Metabolism; oxidation-reduction |
Licochalcone C (LICOCHALCONEC) 能够抑制 α-葡萄糖苷酶,其对 α-葡萄糖苷酶的 IC50 <100 nM,对蛋白酪氨酸磷酸酶 1B 的 IC50=92.43 μM 。 | |||
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。 | |||
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。 | |||
T35000 |
Uproleselan sodium
GMI 1271,GMI1271,GMI-1271 |
||
Uproleselan sodium (GGI-1271) is a small molecule E-selector antagonist originally targeted at AML as an adjuvant to standard chemotherapy for hematological malignancies. | |||
T11392 |
Germacrene D
|
Antibacterial | Microbiology/Virology |
Germacrene D has antibacterial and antifungal activities and can be used as an adjuvant agent in the application of aminoglycosides and azoles. Germacrene D is isolated from Bursera species. | |||
T13472 | α-Carotene | Others | Others |
α-Carotene is isolated from yellow-orange and dark-green vegetables. α-Carotene is used as an anti-metastatic agent or as an adjuvant for anti-cancer drugs. | |||
TN4804 |
Platycoside A
|
Antifection | Microbiology/Virology |
Platycoside A has hemolytic activity and adjuvant potential on the immune responses to Newcastle disease virus-based recombinant avian influenza vaccine. It induces the IgG and IgG1 antibody responses in the immunized mice. | |||
TN3383 |
α-Amyrin palmitate
alpha-Amyrin palmitate |
PKA | Tyrosine Kinase/Adaptors |
alpha-Amyrin palmitate is antiarthritic in the adjuvant model of arthritis in rats. alpha-Amyrin palmitate is a potent non-competitive inhibitor of chymotrypsin (Ki=6 microM), it also shows weak cytotoxicity against the A2780 human ovarian cancer cell line. | |||
TN4410 | Lappaol C | P-gp; JNK | MAPK; Membrane transporter/Ion channel; Neuroscience |
Lappaol C has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. Lappaol C also has potential chemosensitizing activity, it may be candidates for developing novel adjuvant an | |||
T38838 |
QS-21
Stimulon,QS-21 |
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QS-21, an immunostimulatory saponin, is a powerful vaccine adjuvant that stimulates both Th2 humoral and Th1 cell-mediated immune responses by interacting with antigen presenting cells (APCs) and T cells. Additionally, QS-21 activates the NLRP3 inflammasome, leading to the release of cytokines IL-1β and IL-18, which are dependent on caspase-1. | |||
TN1072 |
Lappaol A
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P-gp; JNK | MAPK; Membrane transporter/Ion channel; Neuroscience |
Lappaol A has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. Lappaol A also has potential chemosensitizing activity, it may be candidates for developing novel adjuvant an | |||
T38241 |
2-Aminoimidazole
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2-Aminoimidazole is a potent antibiofilm agent and adjuvant to antimicrobial treatments, which effectively disrupts bacterial self-protection mechanisms by inhibiting biofilm formation and genetically-encoded antibiotic resistance traits. Additionally, 2-Aminoimidazole acts as a weak noncompetitive inhibitor of human arginase I, with a Ki value of 3.6 mM[1][2][3]. | |||
T78492 |
D-Mannuronic acid sodium
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D-Mannuronic acid sodium,一种可从Macrocystis pyrifera中分离得到的化合物,显示出在自身免疫性脑脊髓炎(EAE)、佐剂性关节炎(AIA)、肾病综合征以及急性肾小球肾炎的研究中具有潜在应用价值。 | |||
TN5530 |
Volkensiflavone
Talbotaflavone |
Others | Others |
Volkensiflavone (Talbotaflavone) 是一种天然产物,存在于黄芪和藤黄中。它具有植物代谢物的作用,是一种次生代谢产物。Volkensiflavone 是一种双类黄酮,属于羟黄酮和羟黄酮。Volkensiflavone 可以作为佐剂用于过表达外排泵的多药耐药金黄色葡萄球菌的抗生素治疗。 | |||
T13606L |
cGAMP disodium
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cGAMP disodium 是在细菌中发现的一种环二核苷酸 (CDN) ,可作为内源性第二信使,影响干扰素的产生以响应胞浆 DNA。cGAMP disodium 通过激活干扰素基因刺激因子 (STING)使 I 型干扰素和其他免疫介质的信号产生级联现象。cGAMP disodium 是一种有效的舌下免疫佐剂,能使免疫功能(血清抗 PA 中和和气道分泌物抗 PA SIgA 反应) 更好的发挥作用。 | |||
TN4411 |
Lappaol F
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CDK; P-gp; JNK | Cell Cycle/Checkpoint; MAPK; Membrane transporter/Ion channel; Neuroscience |
1. Lappaol F has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. <br/> 2. Lappaol F has potential chemosensitizing activity, it may be candidates for developing novel adju | |||
T37272 |
9(S),12(S),13(S)-TriHOME
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9(S),12(S),13(S)-TriHOME is a linoleic acid-derived oxylipin that has diverse biological activities.1,2,3,4It has been found in various plants and is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble epoxide hydrolase-independent manner.1,59(S),12(S)13(S)-TriHOME inhibits antigen-induced β-hexosaminidase release from RBL-2H3 mast cells (IC50= 28.7 μg/ml).2It inhibits LPS-induced nitric oxide (NO) production in BV-2 microglia (IC50= 40.95 μM).3In vivo, 9(S),12(S),13(S)-TriHOME... |