140
28
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38359 |
Dup-721
|
Antibacterial | Microbiology/Virology |
DuP-721 是广谱的口服有效的抗菌剂,可以抑制多种临床敏感和耐药细菌,特别是结核杆菌M. tuberculosis。 | |||
T9734 |
InhA-IN-2
|
CDK | Cell Cycle/Checkpoint |
InhA-IN-2直接抑制 InhA,不需要过氧化氢酶过氧化物酶 KatG 的激活。 | |||
T7342 |
BM212
|
Antibacterial | Microbiology/Virology |
BM212 是一种分枝杆菌膜蛋白 MmpL3抑制剂。它抑制结核分枝杆菌和部分非结核分枝杆菌,抗结核杆菌 H37Rv 菌株的 MIC 值为 5 µM。 | |||
T10411 |
AU1235
|
Antibacterial | Microbiology/Virology |
AU1235是金刚烷脲,是一种MmpL3抑制剂。结核分枝杆菌蛋白MmpL3在细胞壁合成中起重要作用,它影响海藻糖单支霉菌酸酯跨内膜转运。 | |||
T8694 |
ML406
|
Antibacterial; Antibiotic | Microbiology/Virology |
ML406 是一种小分子探针,通过抑制M.tuberculosisBioA(DAPA 合酶) 显示出抗结核活性,IC50为 30 nM。 | |||
T5315 |
TCA1
TCA-1,TCA 1 |
Antibacterial; Antibiotic | Microbiology/Virology |
TCA1 (TCA 1) 是一种小分子,具有抗耐药性和持续性结核病的活性。 | |||
T0827 |
Cefsulodin sodium
Cefsulodine sodium,Sulcephalosporin,头孢磺啶钠 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefsulodin sodium (Sulcephalosporin) 是β内酰胺抗生素,对缘脓杆菌和肠杆菌有活性。 | |||
T77730 |
QST4
|
Antifungal | Microbiology/Virology |
QST4 具有抗结核、抗真菌活性,在结核分枝杆菌 Mycobacterium tuberculosis H37Rv 中的 MIC 值为 6.25 μM。 | |||
T3642 |
TBA-354
TBA 354 |
Antibacterial; Antibiotic | Microbiology/Virology |
TBA-354 有抗结核作用,对结核分枝杆菌 H37Rv 菌株具有活性。 | |||
T61411 |
InhA-IN-4
|
Antibacterial | Microbiology/Virology |
InhA-IN-4 (TU14) 是一种有效的结核分枝杆菌InhA(烯酰 ACP 还原酶) 抑制剂,具有潜在的抗癌和抗增殖活性,可用于研究结核分枝杆菌感染。 | |||
T60866 |
InhA-IN-3
|
Antibacterial | Microbiology/Virology |
InhA-IN-3 (TU13) 是一种有效的结核分枝杆菌InhA(烯酰 ACP 还原酶) 抑制剂,具有潜在的抗癌和抗增殖活性,可用于研究结核分枝杆菌感染。 | |||
T60073 |
Antimycobacterial agent-4
4-nitro-N-[4-(2-pyridyl)thiazol-2-yl]benzamide |
Antibacterial | Microbiology/Virology |
Antimycobacterial agent-4 (4-nitro-N-[4-(2-pyridyl)thiazol-2-yl]benzamide) 对结核分枝杆菌具有抗菌活性。 | |||
T3582 |
BTZ043
|
Antibacterial; Antibiotic; DprE1 | Microbiology/Virology; Others |
BTZ043 是一种 DprE1 的抑制剂,它对结核分枝杆菌 H37Rv 和耻垢分枝杆菌具有纳摩尔杀菌活性,MIC 值分别为 2.3 nM 和 9.2 nM。 | |||
T9830 |
GSK2556286
GSK286 |
Antibacterial | Microbiology/Virology |
GSK2556286 (GSK286) 是一种具有口服活性的结核分枝杆菌 (M. tuberculosis) 抑制剂。GSK2556286 对人巨噬细胞 (macrophages) 生长具有抑制作用,IC50值为 0.07 μM。GSK2556286对多重耐药 (MDR) 或广泛耐药 (XDR) 和药物敏感 (DS) 结核分枝杆菌均有效。 | |||
T72576 |
Transketolase-IN-4
|
Antibacterial | Microbiology/Virology |
Transketolase-IN-4 是一种转酮酶抑制剂 ,IC50值为3.9 μM。Transketolase-IN-4 对结核分枝杆菌 DXS 有抑制作用,IC50 为 114.1 μM。 Transketolase-IN-4 抑制 SW620、LS174T 和 MIA PaCa-2 的肿瘤细胞增殖。 | |||
T27453 |
GSK1733953A
DG70 |
Antibacterial | Microbiology/Virology |
GSK1733953A 可作为一种小分子结核分枝杆菌呼吸抑制剂,对 MenG 活性有抑制作用,IC50 值为 2.6 ± 0.6 μM。GSK1733953A 是一种具有选择性的联苯苯甲酰胺,对结核分枝杆菌去甲基萘醌甲基转移酶的催化甲基化有抑制作用,对结核分枝杆菌H4Rv的MIC为8.37 μg/ml,对耐药菌株的MIC为1.2至9.6 μg/ml。GSK1733953A 是治疗结核病的候选化合物。 | |||
T13346L |
WQ3810 TFA
WQ3810 TFA(888032-58-4 Free base),KPI-10 TFA |
Antifungal | Microbiology/Virology |
WQ3810 TFA 是一种可口服的氟喹诺酮,具有抗菌活性,对结核分枝杆菌有抑制作用,抑制氧氟沙星耐药麻风分枝杆菌的 DNA 旋转酶活性。 | |||
T11497 |
Ganfeborole HCl
GSK3036656 HCl,GSK656 HCl |
Antibacterial | Microbiology/Virology |
Ganfeborole HCl (GSK3036656 HCl) 是一种具有抗结核活性的小分子化合物,是结核分枝杆菌(Mtb)亮氨酰-tRNA 合成酶(LeuRS;IC50:0.2 μM)的抑制剂。 | |||
T77683 |
Methyl quinoline-2-carboxylate
Methyl 2-quinolinecarboxylate |
Antibacterial | Microbiology/Virology |
Methyl quinoline-2-carboxylate (Methyl 2-quinolinecarboxylate) 对结合结核杆菌具有抑制作用。 | |||
T78745 |
Mtb-IN-2
|
Antibiotic | Microbiology/Virology |
Mtb-IN-2 是一种具有抗菌活性和低毒性的结核分枝杆菌(Mtb)的小分子化合物,干预蛋氨酸代谢过程,可用于研究结核病。 | |||
T2585 |
Bedaquiline
R207910,TMC207,贝达喹啉 |
Antibacterial; Antibiotic | Microbiology/Virology |
Bedaquiline (R207910) 是一种二芳基喹啉药物,能同时靶向 c-亚基和 ε-亚基,抑制结核分枝杆菌 (Mtb) F1FO-ATP 合酶。它具有解偶联活性和有用于耐多药结核病的潜力。 | |||
T12231 |
NITD-349
|
Others; Antibacterial | Microbiology/Virology; Others |
NITD-349 是MmpL3的抑制剂,它对毒性结核分枝杆菌 H37Rv 显示出高效的抗分枝杆菌活性,MIC50 为 23 nM。 | |||
T67827 |
Urease Inhibitor 07
|
Others | Others |
Urease Inhibitor 07 是一种异取代金属蛋白酶抑制剂 , 对结核分枝杆菌H37Rv 菌株的潜在活性。 | |||
T21023 |
Bedaquiline fumarate
TMC 207,R403323,TMC-207,TMC207,R-403323,贝达喹啉富马酸盐,R 403323 |
Antibacterial; Antibiotic | Microbiology/Virology |
Bedaquiline fumarate (TMC207) 是二芳基喹啉抗生素,作用于 ATP 合成酶,常用于结核杆菌感染的研究。 | |||
T1940 |
BTB06584
|
RAAS; ATPase | Endocrinology/Hormones; Membrane transporter/Ion channel |
BTB06584 是选择性依赖 IF1 的线粒体F1Fo-ATPase 抑制剂,可延迟缺血性细胞死亡。 | |||
T0020 |
Sodium 4-aminosalicylate dihydrate
对氨基水杨酸钠二水合物,Sodium 4-Aminosalicylate,4-Amino-salicylic acid sodium salt |
Free radical scavengers; NF-κB; Antibacterial; Antibiotic | Microbiology/Virology; NF-κB; oxidation-reduction |
Sodium 4-aminosalicylate dihydrate (4-Amino-salicylic acid sodium salt) 是一种抗耐药性结核化合物。 | |||
T67765 |
MenA-IN-2
|
Others | Others |
MenA-IN-2是一种有效的 1,4-二羟基-2-萘甲酸酯异戊二烯转移酶 (MenA) 抑制剂,对 MenA 的 IC50 值为 22 µM,对结核分枝杆菌 (Mtb) 的 GIC50 值为 10 µM。MenA-IN-2 Mtb 的持续传播具有抑制作用。 | |||
T7877 |
Thiacetazone
氨硫脲,Diazam,Thioacetazone,Neustab,Neotibil |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Thiacetazone (Diazam) 是一种氨基硫脲抗结核剂,也是一种具有口服活性抗生素。它具有抗菌作用,可抑制结核分枝杆菌 H37Rv 的生长,MIC 值为 0.1 μg/mL。 | |||
T5400 |
Q203
IAP6,Telacebec |
Antibacterial; Antibiotic | Microbiology/Virology |
Q203 (Telacebec)是一种中氮杂吡啶酰胺。 在培养基中抑制结核分枝杆菌H37Rv 活性的MIC50值为2.7 nM。 | |||
T40520 |
Thiophene-2
Thiophene-2,TP2 |
||
Thiophene-2 (TP2) is a targeted inhibitor of polyketide synthase 13 (Pks13), specifically designed to disrupt mycolic acid biosynthesis. By doing so, it effectively induces rapid cell death in mycobacteria. Thiophene-2 demonstrates notable anti-tuberculosis activity and exhibits a minimum inhibitory concentration (MIC) value of 1 μM against Mycobacterium tuberculosis. | |||
T11594 |
I2906
|
Others | Others |
I2906 showed antimycobacterial and cytotoxic activity against mycobacterium tuberculosis. | |||
T27477 | GSK366A | ||
GSK366A is an anti-TB agent against Mycobacterium bovis BCG and Mycobacterium tuberculosis, targeting MmpL3 and inhibiting EchA6. | |||
T69470 | HC103A | ||
HC103A is an inhibitor of Mycobacterium tuberculosis DosRST signaling and persistence. | |||
T11817 | Lansoprazole Sulfide D4 | Proton pump | Membrane transporter/Ion channel |
Lansoprazole Sulfide D4 is a deuterium labeled Lansoprazole Sulfide. Lansoprazole Sulfide is an orally active anti-TB (Mycobacterium tuberculosis) agent with IC50 values of 0.59 μM intracellularly and 0.46 μM in broth.Lansoprazole Sulfide is an active metabolite of the proton pump inhibitor Lansoprazole. | |||
T26733 |
B 746
B-746,B746 |
||
B 746 is an antibacterial agent primarily. B 746 is used in therapy for leprosy and Mycobacterium avium infections as well as against Mycobacterium tuberculosis, including those with multi-drug resistance. | |||
T20799 |
Lobenzarit
Lobenzaritum |
||
Lobenzarit, an immunomodulator, is most frequently used to treat arthritis. Its chemical scaffold has been repurposed to tryptophan biosynthesis in Mycobacterium tuberculosis | |||
T25468 |
GSK1829820A
GSK-1829820-A,GSK 1829820A,GSK 1829820 A,GSK-1829820A |
||
GSK1829820A is a Mycobacterium tuberculosis H37Rv non-cytotoxic inhibitor. | |||
T34177 |
Pseudopterosin E
|
||
Pseudopterosin E can act towards Mycobacterium tuberculosis and other pathogens. | |||
T29701 |
AG 85
AG85,AG-85 |
||
AG 85 is a major secretion protein of Mycobacterium tuberculosis. | |||
T24765 |
SB-790594-A
SB790594A,SB 790594 A |
||
SB-790594-A is a non-cytotoxic Mycobacterium tuberculosis H37Rv inhibitor. | |||
T24397 |
ZTB23(R)
ZTB 23(R),ZTB-23(R) |
||
ZTB23(R) is the first potent and selective inhibitor of Mycobacterium tuberculosis Zmp1. | |||
T31688 |
Ethambutol, (R,R)-
L-Ethambutol |
||
Ethambutol, (R, R)- can be used to treat tuberculosis. It is usually used in combination with other tuberculosis medications. It may also be used to treat Mycobacterium avium complex, and Mycobacterium kansasii. | |||
T79511 |
Tuberculosis inhibitor 8
|
||
Tuberculosis inhibitor 8 (compound 3b) 是 3-甲氧基-2-苯基咪唑并[1,2-b]哒嗪衍生物,具有针对结核分枝杆菌 (MIC90为 0.69 μM) 和海洋分枝杆菌 (MIC90为 0.69 μM) 的高抗菌活性。 | |||
T71727 |
HC102A
|
||
HC102A is an inhibitor of Mycobacterium tuberculosis DosRST signaling and persistence. | |||
T61096 |
Antibacterial agent 95
|
||
Antibacterial agent 95 (2-(quinoline-4-methoxy) acetamide), a new antituberculotic agent, exhibited a minimum inhibitory concentration (MIC) of only 0.3 μM against the reference strain of Mycobacterium tuberculosis H37Rv. Additionally, it effectively suppressed the growth of Mycobacterium tuberculosis in the macrophage model of tuberculosis infection. | |||
T110951 |
Compound F0447-0245
|
||
Antitubercular agent-33 是一种 2-氨基噻唑衍生物,对于结核分枝杆菌 (Mycobacterium tuberculosis,Mtb)显示出有效的抗结核活性。 | |||
T70671 |
IC2418
|
||
IC2418 is an MmpL3 inhibitor, being active against drug-resistant Mycobacterium tuberculosis. | |||
T11983 |
MDRTB-IN-1
|
Others | Others |
MDRTB-IN-1 (5aα) is an antibiotic which is against Mycobacterium tuberculosis H37Rv(MIC90 :10.5 μM). | |||
T29527 |
ABT-255
ABT 255,ABT255,UNII-YA04O24J4T |
||
ABT-255 is a novel 2-pyridone antimicrobial agent for the treatment of tuberculosis. Both drug-sensitive and drug-resistant strains of Mycobacterium tuberculosis showed efficacy in vitro and in vivo. | |||
T27848 |
LP10
LP-10,LP 10 |
||
LP10 is a reverse type I inhibitor of Mycobacterium tuberculosis CYP125A1 and a Potent type II inhibitor of Trypanosoma cruzi CYP51. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1426 |
Pyrazinamide
Pyrazinoic acid amide,Pyrazinecarboxamide,吡嗪酰胺 |
Antibacterial; Antibiotic; Autophagy; Fatty Acid Synthase | Autophagy; Metabolism; Microbiology/Virology |
Pyrazinamide (Pyrazinecarboxamide) 是一种口服抗结核类抗生素。它是一种前药,通过结核分枝杆菌pncA 基因编码的 PZase/烟酰胺酶转化为活性吡嗪酸形式。 | |||
TN1466 |
Canthin-6-one
NSC 103003 |
Antifungal | Microbiology/Virology |
Canthin-6-one(NSC 103003) 是一种从 Allium neapolitanum 分离出来的生物碱,具有抗菌活性,对结核分枝杆菌具有抑制作用。 | |||
TN2279 |
Totarol
(+)-Totarol,桃柁酚 |
Antibacterial; Antifection | Microbiology/Virology |
Totarol ((+)-Totarol) 对几种致病性革兰氏阳性细菌、结核分枝杆菌具有抗菌作用。 | |||
TN5503 |
Linaroside
|
Antibacterial | Microbiology/Virology |
Linaroside 在 6.25 microg mL(-1) 浓度下对结核分枝杆菌、菌株 H(37)Rv 的抗分枝杆菌活性表现出 30%的抑制作用。 | |||
T5041 |
Faropenem sodium
法罗培南,法罗培南钠 |
Antibacterial; Antibiotic | Microbiology/Virology |
Faropenem sodium 是一种口服生物可利用的青霉烯类抗生素,能有效杀灭结核分枝杆菌,治疗结核病和社区获得性肺炎。 | |||
T5722 |
Nevadensin
Pedunculin,石吊兰素,5,7-二羟基-6,8,4'-三甲氧基黄酮 |
Anti-infection; Antibacterial | Microbiology/Virology |
Nevadensin 是一种重要的草本成分,可抑制雌二醇的生物活化。 它具有抗结核分枝杆菌、镇咳、抗炎、抗高血压等多种药理作用。 | |||
TN2086 |
Piperlotine A
|
Antibacterial | Microbiology/Virology |
Piperlotine A 是一种可从罗洛胡椒中提取得到的生物碱,具有抗血小板聚集活性。Piperlotine A 在体外试验中显示出对结核分枝杆菌的抑制作用,MIC 值为 50 ug/mL。 | |||
TN1019 |
Beta-mangostin
β-Mangostin,beta-倒捻子素 |
Apoptosis; Antibacterial; Parasite | Apoptosis; Microbiology/Virology |
Beta-mangostin (β-Mangostin) 是存在 Cratoxylum arborescens 中的一种氧杂蒽酮类天然产物,有抗癌和抗菌活性,对结核分枝杆菌的 MIC 值为 6.25 μg/mL。它在体外有抗疟活性,对恶性疟原虫的 IC50值为 3.00 μg/mL。 | |||
T3S1612 |
kuwanon G
桑黄酮G,Moracenin B,桑黄酮 G,Kuwanone G |
Phosphatase; Antibacterial; Bombesin Receptor; AChR; AChE; Glucosidase | GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Kuwanon G (Moracenin B) 是一种从桑树中得到的黄酮类蛙皮素受体拮抗剂,具有杀菌作用。 | |||
TN5684 |
5,6-Desmethylenedioxy-5-methoxyaglalactone
|
||
5,6-Desmethylenedioxy-5-methoxyaglalactone is cytotoxic to small cell lung cancer (NCI-H187) cell line. It has antimycobacterial activity against Mycobacterium tuberculosis H(37)Ra. | |||
TN5657 | Goniotriol | ||
Goniotriol shows antimycobacterial activity against Mycobacterium tuberculosis (MIC =100 microg/mL). It exhibits antiplasmodial activity against Plasmodium falciparum (IC50=2.6 microg/mL). Goniotriol shows cytotoxicity against cancer cells, KB, BC1, NCI-H | |||
T75564 | Pomolic acid 3-acetate | ||
Pomolic acid 3-acetate 是一种抗结核 (antitubercular) 剂,对 Mycobacterium tuberculosisH37Rv 的 MIC 为 32 μM。 | |||
TN5648 | Porson | ||
Porson exhibited anti-tubercular activity against Mycobacterium tuberculosis H37Rv in vitro and MICs values of 40.0 μg/mL. | |||
TN4944 | Santamarine | Caspase | Apoptosis; Proteases/Proteasome |
Santamarine has significant anticancer activity, can inhibit L1210 cells because of its cytotoxic,cytostatic and blocking mitosis and reducing uptake of thymidine. Santamarine and reynosin show bactericidal activity against clinical strains of Mycobacterium tuberculosis. | |||
TN4336 | Isothymusin | Antifection | Microbiology/Virology |
Isothymusin( MIC= 200 microg/mL) exhibits inhibition activity against Mycobacterium tuberculosis. It ( IC50=7.7 microg/mL ) exhibits antioxidant activity against the radical scavenging ability of DPPH. | |||
TN3924 | Eichlerialactone | Others | Others |
Eichlerialactone and ethyl eichlerianoate show antimycobacterial activity against mycobacterium tuberculosis H37Ra, with minimum inhibitory concentration in the range of 25-50ug/mL; eichlerialactone exhibits good antibacterial activity against both the Gr | |||
TN4953 |
Sativan
三叶草 |
Antifection | Microbiology/Virology |
Sativan possesses a broad spectrum of antimicrobial activity against bacteria and phytopathogenic fungi, it exhibits antituberculosis activity against Mycobacterium tuberculosis H37Rv, with the MIC value of 50 ug/mL. | |||
TN4776 | Physalin D | TNF; Antifection | Apoptosis; Microbiology/Virology |
Physalin D shows antimalarial activity; it also exhibits a minimum inhibitory concentration value (MIC) against Mycobacterium tuberculosis H(37)Rv strain of 32 microg/mL. Physalin D displays considerable cytotoxicity against several cancer cell lines. It | |||
TN3560 |
Cabralealactone
|
Antifection | Microbiology/Virology |
Cabralealactone displays antimycobacterial activity against Mycobacterium tuberculosis, it is weakly cytotoxic to a breast cancer (BC) cell line, it is moderately active against a small-cell lung cancer (NCI-H187) cell line. | |||
TN3559 |
Cabraleahydroxylactone
|
HSV | Microbiology/Virology |
Cabraleahydroxylactone displays antimycobacterial activity against Mycobacterium tuberculosis, it is weakly cytotoxic to a breast cancer (BC) cell line.It shows antiviral activity against herpes simplex virus type-1 with an IC50 value of 3.20 ug/mL, in comparison with the standard acyclovir (IC50=1.90ug/mL). | |||
T75631 | Ganorbiformin B | ||
Ganorbiformin B是一种具有与灵芝酸相同羊毛甾烷骨架的羊毛甾烷三萜类化合物。其C-3差向异构体灵芝酸T对结核分枝杆菌H37Ra显示出强抗分枝杆菌活性。 | |||
TN3557 |
Cabraleadiol
|
ATPase; Antifection | Membrane transporter/Ion channel; Microbiology/Virology |
Cabraleadiol displays antimycobacterial activity against Mycobacterium tuberculosis, it also is weakly cytotoxic to a breast cancer (BC) cell line. Cabraleadiol inhibits photosystem II (PS II) and induces the appearance of small G band which is related wi | |||
T75633 | (22S,24E)-3β,22-Diacetoxylanosta-7,9(11),24-trien-26-oic acid | ||
(22S,24E)-3β,22-Diacetoxylanosta-7,9(11),24-trien-26-oic acid (compound 15) 为具有抗结核活性的化合物,对结核分枝杆H37Ra的最小抑菌浓度(MIC)为12.5 μg/mL,并展现出对Vero细胞的细胞毒性,其半数抑制浓度(IC50)值为32 μM[1]。 | |||
TN5014 | Shoreic acid | Antifection; HSV | Microbiology/Virology |
Shoreic acid exhibits antibacterial activity against E. coli, P. aeruginosa, S. aureus, and B. subtilis with activity indices (AI) of 0.2, 0.3, 0.5 and 0.4, respectively, it also shows antifungal activity against C. albicans and T. mentagrophytes with AI | |||
T72742 |
(-)-Pinocembrin
(-)-乔松素 |
||
(-)-Pinocembrin 对 H37Ra 结核分枝杆菌展示了抗菌活性,无论是休眠还是活跃期,其 IC50 值分别为1.11 mg/mL 和 1.21 mg/mL。作为一种抗增殖剂,(-)-Pinocembrin 对于 THP-1、A549、Panc-1、HeLa 和 MCF7 细胞系,IC50 值范围为 1.88 至 11.00 mg/mL。 | |||
TN1694 |
Gliotoxin
|
Apoptosis; NF-κB; Wnt/beta-catenin; COX; PKA; Antibacterial; Antifection | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; Microbiology/Virology; Neuroscience; NF-κB; Stem Cells; Tyrosine Kinase/Adaptors |
Gliotoxin 是一种次生代谢产物,由A. fumigatus 分泌,可以抑制巨噬细胞的吞噬作用和其他免疫细胞的免疫功能。它通过阻止 IκB 降解来抑制诱导型NF-κB 活性,从而诱导宿主细胞凋亡。它可以激活PKA 并增加细胞内 cAMP 浓度,调节肌动蛋白细胞骨架重排以促进A. fumigatus 内化到肺上皮细胞。 | |||
T38330 |
Collinin
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Collinin is a coumarin that has been found in Z. schinifolium and has diverse biological activities.1,2,3,4 It is active against drug-susceptible and -resistant strains of M. tuberculosis (MIC50s = 3.13-6.25 μg/ml).1 Collinin inhibits LPS-induced nitric oxide (NO) production (IC50 = 5.9 μM) and reduces COX-2 protein levels in RAW 264.7 cells.2 It completely inhibits aggregation of isolated rabbit platelets induced by arachidonic acid , collagen, or platelet activating factor (PAF) when used at a... | |||
TN1378 |
α-Viniferin
ALPHA-VINIFERIN,Alpha-葡萄素 |
P450; NO Synthase; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism |
α-Viniferin 也称为2-芳基苯并呋喃类黄酮,是前列腺素H2合成酶抑制剂。具有抗阿尔茨海默病、抗结核、抗肿瘤、抗炎、抗糖尿病等多种药理活性 |