98
28
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T18514 |
PAC
|
Others | Others |
PAC is a chemical conjugate consisting of an ADCs linker and PROTACs linked to an antibody. When PAC is conjugated to an antibody, it exhibits enhanced degradation of estrogen receptor-alpha (ERα) in comparison to PROTAC alone. | |||
T2503 |
PAC-1
Procaspase activating compound 1 |
Apoptosis; Caspase; Autophagy | Apoptosis; Autophagy; Proteases/Proteasome |
PAC-1 (Procaspase activating compound 1) 是一种 procaspase-3激活剂,诱导癌细胞凋亡,EC50为 2.08 μM,可用于研究淋巴瘤、黑色素瘤、实体瘤、乳腺癌和胸癌等治疗的试验。 | |||
T37139 |
5'-O-DMT-PAC-dA
|
||
5’-O-DMT-PAC-dA can be used in the synthesis of oligoribonucleotides[1]. [1]. Schulhof JC, et, al. The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups. Nucleic Acids Res. 1987 Jan 26;15(2):397-416. | |||
T16426 |
Asivatrep
PAC-14028 |
Others | Others |
Asivatrep is an effective and selective transient receptor potential vanilloid type I antagonist. | |||
T18603 | PROTAC BRD4 degrader for PAC-1 | Others | Others |
PROTAC BRD4 degrader for PAC-1 (compound 5) is a chimeric BET degrader GNE-987 conjugated with a disulfide-containing linker[1]. This PROTAC-linker conjugate specifically targets and degrades BRD4, enabling selective proteolysis of PAC-1. | |||
T74121 |
DMT-dA(PAc) Phosphoramidite
|
||
DMT-dA(PAc) Phosphoramidite 是一种亚磷酰胺单体,可用于 DNA 或 RNA 的合成。 | |||
T78105 |
PAC1R antagonist 1
|
PACAP | GPCR/G Protein |
PAC1R antagonist 1为一种具有口服活性的 PAC1 受体拮抗剂,可抑制由垂体腺苷酸环化酶激活多肽(PACAP)及神经损伤所诱导的异常性疼痛,可用于研究肿瘤和与免疫相关的疾病。 | |||
TNU1202 |
3’,5’-TIPS-N-PAc-Guanosine
|
||
Nucleoside Derivatives - Protected nucleosides with NH2/OH open | |||
TP1618L |
PACAP-38 (31-38), human, mouse, rat acetate
PACAP-38 (31-38), human, mouse, rat acetate(138764-85-9 Free base) |
PACAP | GPCR/G Protein |
PACAP-38 (31-38), human, mouse, rat acetate 是 PAC1 受体的激活剂。PACAP-38 (31-38), human, mouse, rat acetate 对交感神经元 NPY 和儿茶酚胺的产生具有强效、有效和持续的刺激作用,可用于神经营养和神经保护研究。 | |||
T41277 |
PACMA 31
|
Others | Others |
PACMA 31 是一种不可逆的共价蛋白二硫键异构酶 (PDI) 抑制剂,IC50 为 10 μM。 PACMA 31 显着抑制卵巢肿瘤生长并表现出肿瘤靶向能力。 | |||
TQ0245 |
Sapacitabine
CS682,CYC682 |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Sapacitabine is a nucleoside analog prodrug with antitumor activity. | |||
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。 | |||
TP1878L |
PACAP 1-38 acetate
|
PACAP | GPCR/G Protein |
PACAP 1-38 acetate 是一种垂体腺苷酸环化酶激活多肽 (PACAP) 类似物。它与 PACAP I 型受体 (IC50 = 4 nM) 和 PACAP II 型 VIP2 受体 (IC50 = 1 nM) 结合,但不与 PACAP II 型 VIP1 受体结合。 | |||
T24449 |
Mepacrine
Haffkinine,Erion |
Others | Others |
Mepacrine (Erion) 是一种吖啶衍生物,以前广泛用作抗疟药。它在细胞生物学实验中用作磷脂酶A2的抑制剂。 | |||
T6020 |
Pacritinib
SB1518 |
FLT; Tyrosine Kinases; JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Pacritinib (SB1518) 是一种野生型 JAK2和 JAK2V617F 突变型抑制剂,IC50分别为 23 和 19 nM。它也抑制 FLT3及其突变型 FLT3D835Y,IC50分别为 22 和 6 nM。 | |||
T27635 |
Isoxepac
伊索克酸,Olopatadine USP Related Compound C |
Others | Others |
Isoxepac (Olopatadine USP Related Compound C) 是非甾体抗炎剂,显示出抗炎、镇痛和解热活性,已在多种动物模型中进行了相关研究。 | |||
TP1722L |
PACAP (6-38), human, ovine, rat acetate
|
PACAP | GPCR/G Protein |
PACAP (6-38), human, ovine, rat acetate 是一种有效的 PACAP 受体拮抗剂。PACAP (6-38) 作用于 PACAP I 型受体,PACAP II 型受体 VIP1 和 PACAP II 型受体 VIP2,IC50 分别为 30 nM,600 nM 和 40 nM。 | |||
T11212 |
EPAC 5376753
5-{[5-(2,4-dichlorophenyl)furan-2-yl]methylidene}-2-thioxodihydropyrimidine-4,6(1H,5H)-dione |
cAMP | GPCR/G Protein |
EPAC 5376753 是 EPAC1 的变构抑制剂,在瑞士 3T3 细胞中的 IC50 为 4 µM。 | |||
T38273 |
Paclobutrazol
(2R,3R)-Paclobutrazol,多效唑,(R,R)-paclobutrazol,2R,3R-Paclobutrazol |
Antifungal | Microbiology/Virology |
Paclobutrazol ((R,R)-paclobutrazol) 是一种含有三唑的植物生长延缓剂,能抑制赤霉素的生物合成。Paclobutrazol 还具有抗真菌 (antifungal) 活性。Paclobutrazol 能抑制脱落酸的合成,诱导植物的耐冷性植物。Paclobutrazol 通常用于赤霉素在植物生物学中作用的研究。 | |||
T29067L |
Upacicalcet HCl
Upacicalcet HCl(1333218-50-0 Free base) |
CaSR | GPCR/G Protein |
Upacicalcet HCl 是一种静脉内拟钙剂,通过直接作用于甲状旁腺细胞膜钙敏感受体来抑制过量的甲状旁腺激素 (PTH) 分泌,从而降低血液中的 PTH 水平。Upacicalcet HCl 可用于治疗血液是一种新型继发性甲状旁腺功能亢进化合物,靶向钙敏感受体的氨基酸结合位点。 | |||
T4545 |
Propacetamol Hydrochloride
盐酸丙帕他莫,Propacetamol HCL |
Others | Others |
Propacetamol Hydrochloride (Propacetamol HCL) 是 paracetamol(acetaminophen) 的前药,具有改善的水溶性。当口服非甾体抗炎药不合适或矛盾时,丙帕西莫是一种静脉给药的镇痛药。 | |||
TP1070L |
PACAP (1-27), human, ovine, rat acetate
PACAP 1-27 acetate,PACAP (1-27), human, ovine, rat acetate(127317-03-7 free base) |
PACAP | GPCR/G Protein |
PACAP (1-27), human, ovine, rat acetate (PACAP 1-27 acetate)(127317-03-7 free base) 是一种新的神经肽,最初从牛下丘脑中分离出来,也存在于人和大鼠中。 | |||
T29067 |
Upacicalcet
PLS-240,SK-1403,AJT-240 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Upacicalcet (AJT-240) 是一种静脉内拟钙剂,是一种可用于人血液透析的 SHPT, 通过直接作用于甲状旁腺细胞膜钙敏感受体来抑制过量的甲状旁腺激素 (PTH) 分泌,从而降低血液中的 PTH 水平。 3 Upacicalcet 是钙敏感受体的正变构调节剂,可预防大鼠腺嘌呤诱导的继发性甲状旁腺功能亢进模型中的血管钙化和骨骼疾病。 | |||
T21907 |
PACOCF3
1,1,1-trifluoroheptadecan-2-one,Palmityltrifluoromethylketone |
Phospholipase | Metabolism |
PACOCF3 (Palmityltrifluoromethylketone) (Palmityltrifluoromethylketone) 是一种钙非依赖性的磷脂酶 A2 (phospholipase A2) 抑制剂,IC50为 3.8 μM。PACOCF3 改变肾小管细胞中的 Ca2+信号传导。 | |||
T20864 |
7-Troc-paclitaxel
|
Others | Others |
7-Troc-paclitaxel 是紫杉醇的前体,紫杉醇具有抗肿瘤活性。 | |||
T37435 | PACAP-related Peptide (rat) (trifluoroacetate salt) | PACAP | GPCR/G Protein |
PACAP-related peptide (PRP) is an endogenous 29-amino acid peptide that belongs to the secretin/glucagon superfamily of peptides, which includes secretin , glucagon , glucagon-like peptide-1 , GLP-2 , and pituitary adenylate cyclase-activating polypeptide . It is expressed in rat hypothalamus as well as within the nerves of the median eminence, the anterior pituitary, bed nucleus of the stria terminalis, cerebellum, cerebral cortex, and amygdala. PRP is also expressed in vaginal, uterine cervica... | |||
T124630 | Carpachromene | ||
Carpachromene 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T124630。 | |||
T33861 | Paclitaxel-MVCP | ||
Paclitaxel-MVCP ( MC-val-cit-pab-paclitaxel )is a paclitaxel derivative with an MC-Val-Cit-PAB linker, which can be used for the preparation of Paclitaxel conjugates for drug delivery and nanomedicine research. | |||
T77128 | Pacmilimab | ||
Pacmilimab (CX-072) 是一种有效的PD-L1抑制剂。 Pacmilimab 显示出抗肿瘤活性。 | |||
T126370 | Dopacetamide | ||
Dopacetamide 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T126370,CAS号为 1129-53-9。 | |||
T73863 | PPACK II | ||
PPACK II 是一种不可逆的特异性腺体和血浆激肽释放酶 (kallikreins) 抑制剂。 | |||
T77127 | Pacanalotamab | ||
Pacanalotamab (AMG 420;BI-836909) 是一种双特异性 T 细胞接合剂 (BiTE),靶向 BCMA 和 CD3ɛ。BCMA 是指 B 细胞成熟抗原,而 Pacanalotamab 会将 T 细胞重定向到细胞表面的 BCMA 表达细胞。Pacanalotamab 可对人多发性骨髓瘤 (MM) 细胞系进行 T 细胞重定向裂解。 | |||
T75594 | Harpactira Baviana Venom | ||
Harpactira Baviana Venom (Baboon Tarantula Venom) 是一种蜘蛛毒液,能够从皇帝巴布蜘蛛蜘蛛中获得。Harpactira Baviana Venom 可以调节 NaV1.8和诱导痛觉过敏。 | |||
TP1414 |
PACAP-38 (31-38), human, mouse, rat TFA
|
||
PACAP-38 (31-38), human, mouse, rat (TFA) demonstrates potent, efficacious, and sustained stimulatory effects on sympathetic neuronal. | |||
T83510 |
[Arg-15,20,21,Leu17]-PACAP-Gly-Lys-Arg-NH2
BM-PACAP |
||
[Arg-15,-20,-21,Leu17]-PACAP-Gly-Lys-Arg-NH2 (BM-PACAP) 为合成PACAP 1-27 类似物,展现出明显的松弛效应。 | |||
T81571 |
PACAP (1-38) free acid TFA
|
||
PACAP (1-38) free acid TFA,一种内源性神经肽,能有效促进胃窦运动,增强体液蛋白分泌,同时抑制胃泌素释放。此外,它刺激血管活性肠肽、胃泌素释放肽和P物质的释放,并通过RACK1增强N-甲基-D-天门冬氨酸受体功能及脑源性神经营养因子表达。 | |||
T81572 |
PACAP (1-38) free acid
|
||
PACAP (1-38) free acid 是一种具有多重生物功能的内源性神经肽,主要作用包括刺激胃窦运动、增进体液蛋白分泌、抑制胃泌素分泌,以及促进血管活性肠肽、胃泌素释放肽和P 物质的释放。此外,PACAP (1-38) free acid 通过与RACK1互作,可以增强N-甲基-D-天门冬氨酸受体的功能并促进脑源性神经营养因子的表达。 | |||
T70114 |
Paclitaxel Ceribate
|
||
Paclitaxel Ceribate is a mitotic inhibitor used in cancer chemotherapy. | |||
T70006 |
DHA-paclitaxel
|
||
DHA-paclitaxel, also know as Taxoprexin, is prodrug comprised of the naturally occurring omega-3 fatty acid docosahexaenoic acid (DHA) covalently conjugated to the anti-microtubule agent paclitaxel. Because tumor cells take up DHA, DHA-paclitaxel is delivered directly to tumor tissue, where the paclitaxel moiety binds to tubulin and inhibits the disassembly of microtubules, thereby resulting in the inhibition of cell division. Paclitaxel also induces apoptosis by binding to and blocking the func... | |||
T25977 |
Ppack trifluoroacetate
Ppack trifluoroacetate salt |
||
Ppack trifluoroacetate is a peptide derivative that irreversibly and specifically suppresses thrombin-mediated platelet activation by binding with high affinity to the active site of thrombin (Ki: 0.24 nM). It has been utilized as an anticoagulant (100 μM | |||
T69421 |
Hydrolapachol
|
||
Hydrolapachol is a novel potent and selective inhibitor of schistosoma mansoni dihydroorotate dehydrogenase (smdhodh) | |||
T66146 |
(SP-4-4)-2-[2-(Amino-KappaN)ethyl]phenyl-KappaC]chloro[dicyclohexyl[2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]phosphine]-Palladium
|
||
(SP-4-4)-2-[2-(Amino-KappaN)ethyl]phenyl-KappaC]chloro[dicyclohexyl[2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]phosphine]-Palladium 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66146,CAS号为 1028206-56-5。 | |||
T36896 |
6α-hydroxy Paclitaxel
6alpha-hydroxypaclitaxel |
Drug Metabolite | Metabolism |
6α-hydroxy Paclitaxel (6α-OH-PTX) 是抗癌化合物紫杉醇的主要代谢产物,具有部分细胞毒性。 | |||
T33860 | Pacifenol | ||
Pacifenol is a sesquiterpene isolated from sea weeds and marine alga Laurencia claviformis. | |||
T28289 |
Paclitaxel-SMCC
SMCC taxol, Taxol-SMCC, Taxol SMCC,Paclitaxel with SMCC linker,SMCC-Taxol,Paclitaxel ADC conjugate. |
||
Paclitaxel-SMCC is a paclitaxel derivative with a SMCC linker. (Succinimidyl-4-( N -maleimidomethyl)cyclohexane-1-carboxylate). Paclitaxel-SMCC can be used to synthesize Paclitaxel bioconjugates with enzymes, antobodies, antigens and other biopolymers. Pa | |||
T28290 |
Pactimibe
CS 505,CS-505,CS505,Pactimibe free base,帕替麦布 |
||
Pactimibe is a ACAT inhibitor. It has anti-atherosclerotic activity. | |||
TP1069 |
PACAP (1-27), human, ovine, rat TFA
PACAP 1-27 TFA |
||
PACAP (1-27), human, ovine, rat TFA (PACAP 1-27 TFA) is an N-terminal fragment of pacap-38 and an effective PACAP receptor antagonist. The IC50s for rat PAC1, rat VPAC1 and human VPAC2 are 3nm, 2nm and 5nm respectively. | |||
T80069 |
PACAP (6-27) (human, ovine, rat)
Pituitary adenylate cyclase-activating peptide (6-27) |
||
PACAP (6-27) (human, ovine, rat) 是一种对PACAP受体具有拮抗作用的化合物,可以抑制犬肾上腺对外源性VIP的反应。此化合物在心血管疾病和神经系统疾病研究中展现出应用潜力。 | |||
T20505 |
PPACK
D-Phe-pro-arg CH2Cl |
||
PPACK is a synthetic peptide derivative. It also irreversibly and specifically inhibits thrombin-mediated platelet activation by binding with high affinity to the active site of thrombin (Ki = 0.24 nM). | |||
T36427 |
PACAP (6-27) (human, chicken, mouse, ovine, porcine, rat) (trifluoroacetate salt)
|
PACAP | GPCR/G Protein |
Pituitary adenylate cyclase-activating peptide (PACAP) (6-27) is a PACAP receptor antagonist with IC50 values of 1,500, 600, and 300 nM, respectively, for rat PAC1, rat VPAC1, and human VPAC2 recombinant receptors expressed in CHO cells. It binds to PACAP receptors on SH-SY5Y and SK-N-MC human neuroblastoma and T47D human breast cancer cells (IC50s = 24.5, 106, and 105 nM, respectively) and inhibits cAMP accumulation induced by PACAP (1-38) (Kis = 457, 102, and 283 nM, respectively, in SH-SY5Y, ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S1884 |
Benzoylhypaconine
苯甲酰次乌头碱,Benzoylhypacoitine,苯甲酰次乌头原碱 |
Others | Others |
Benzoylhypaconine (Benzoylhypacoitine) 是来自 Aconitum 中的一种单酯生物碱,也是Aconitum 的主要药理和毒性成分。 | |||
T6S0619 |
Pachymic acid
3-O-Acetyltumulosic acid,茯苓酸 |
ERK; Akt | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
Pachymic acid (3-O-Acetyltumulosic acid) 是来自茯苓的一种三萜,可抑制Akt 和ERK 信号传导途径。 | |||
TN1563 |
Dehydropachymic acid
|
Autophagy; Immunology/Inflammation related | Autophagy; Immunology/Inflammation |
Dehydropachymic acid 是从茯苓中分离出的一种三萜类天然产物,有抗炎活性。 | |||
T5749 |
10-Deacetyl-7-xylosyl paclitaxel
10-Deacetyl-7-xylosyltaxol,10-Deacetyltaxol 7-Xyloside,7-Xylosyl-10-deacetyltaxol,7-木糖甙-10-脱乙酰基紫杉醇,10-Deacetylpaclitaxel 7-Xyloside |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
10-Deacetyl-7-xylosyl paclitaxel (7-Xylosyl-10-deacetyltaxol) 是一种紫杉醇衍生物,具有改进的药理特性和更高的水溶性,用于治疗癌症。 | |||
T32570 |
Lappaconine
20-ethyl-1,14,16-trimethoxyaconitane-4,6,8-triol,O(sup 1)-Methyllappaconidine |
Others | Others |
Lappaconine (20-ethyl-1,14,16-trimethoxyaconitane-4,6,8-triol) 衍生自去甲二萜生物碱。 | |||
T4136 |
Lapachol
Bethabarra wood,CI75490,黄钟花醌,Greenhartin,Tecomin |
Others; Influenza Virus; Antibacterial; Parasite; Antifungal | Microbiology/Virology; Others |
Lapachol (CI75490) 是从Tabebuia avellanedae 中分离得到的一种萘醌。它具有具有抗菌、抗炎、镇痛、抗肿瘤和抗生素特性。 | |||
TN7058 |
Dihydrolapachenole
6-methoxy-2,2-dimethyl-3,4-dihydro-2H-benzo[h]chromene |
Others | Others |
Dihydrolapachenole (6-methoxy-2,2-dimethyl-3,4-dihydro-2H-benzo[h]chromene) 可分离自T. chrysantha。 | |||
T6560 |
Lappaconitine hydrobromide
氢溴酸高乌甲素,Lappaconite HBr,Allapinine |
Others | Others |
Lappaconitine hydrobromide (Allapinine) 是天然生物碱类化合物,具有抗心律失常作用。 | |||
T5738 |
7-Epi 10-desacetyl paclitaxel
10-Deacetyl-7-epipaclitaxel,7-Epi-10-deacetyltaxol,7-表-10-去乙酰基云南紫杉宁A |
Others | Others |
7-Epi 10-desacetyl paclitaxel (10-Deacetyl-7-epipaclitaxel) 是紫杉醇衍生物,对 HeLa 细胞具有细胞毒性(IC50:85 μM)。 | |||
T37267 |
Pachybasin
|
Antibacterial | Microbiology/Virology |
Pachybasin 是一种蒽醌真菌代谢物。 Pachybasin 对大肠杆菌、枯草芽孢杆菌、M. luteus、S. cerevisiae、C. albicans、A. niger 和 A. flavus 具有抗菌活性,MIC 值为 64.0 μg/mL,对金黄色葡萄球菌具有抗菌活性 和尖孢镰刀菌,MIC 值分别为 32.0 和 16.0 μg/mL。 | |||
TN1375 |
α-Lapachone
ALPHA-拉杷醌,alpha-Lapachone |
Topoisomerase; Antifection | DNA Damage/DNA Repair; Microbiology/Virology |
α-Lapachone 具有杀锥虫作用。 | |||
T6S0630 |
Hypaconitine
|
P450; TNF | Apoptosis; Metabolism |
Hypaconitine 是从乌头属种分离的一种高毒性成分,可研究风湿病。 | |||
T6407 |
β-Lapachone
3,4-二氢-2,2-二甲基-2H-萘并[1,2-B]吡喃-5,6-二酮,Beta-Lapachone,NSC-26326,SL-11001,ARQ-501 |
IDO; Apoptosis; Topoisomerase; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism |
β-Lapachone (ARQ-501) 是一种萘醌类天然产物,是拓扑异构酶 I 抑制剂,通过抑制细胞周期进程来诱导细胞凋亡。 | |||
T2806 |
Lappaconitine
高乌甲素,(+)-Lappaconitine |
P2X Receptor; Sodium Channel | Membrane transporter/Ion channel; Neuroscience |
Lappaconitine ((+)-Lappaconitine) 是从高乌头中分离得到的一种天然产物,可用于缓解疼痛的研究。 | |||
TN1754 |
Hypaconine
|
Others | Others |
Hypaconine 是一种 C19-二萜生物碱,从乌头和飞燕草属中分离出来得到。 它表现出强烈的心脏活性。 | |||
T38815 |
Millepachine
|
Apoptosis | Apoptosis |
Millepachine 是分离自中草药Millettia pachycarpaBenth 的查尔酮,在体内外对多种人类癌细胞均显示出强大的抗增殖作用。 | |||
T0968 |
Paclitaxel
Taxol,紫杉醇,NSC 125973 |
Apoptosis; Microtubule Associated; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling |
Paclitaxel (Taxol) 属于天然产物,是一种微管聚合物稳定剂。Paclitaxel 具有抗肿瘤活性;通过诱导有丝分裂停滞、细胞凋亡、细胞自噬等,导致细胞死亡。 | |||
TN1569 |
Deoxylapachol
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Antifection; Antifungal | Microbiology/Virology |
Deoxylapachol 是新西兰褐藻Landsburgia quercifolia 的主要细胞毒性成分,有抗真菌和抗癌活性。 | |||
TN4731 |
Pachyaximine A
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Antifection | Microbiology/Virology |
Pachyaximine A possesses significant antibacterial activity against Escherichia coli, Staphylococcus aureus, Corynebacterium diphtheriae and Corynebacterium pyrogenes. (-)-Pachyaximine A demonstrates significant activity as antiestrogen binding site (AEBS | |||
TN3318 | 9-Hydroxy-alpha-lapachone | Antifection | Microbiology/Virology |
9-Hydroxy-alpha-lapachone can highly inhibit the growth of H. pylori, it exhibits potent inhibitory activity against H. pylori Cystathionine gamma-synthase, with IC(50) values of 4.64 microM. It may have anti-inflammatory activity, it exhibits potent inhi | |||
T35750 |
Trypacidin
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Trypacidin is a fungal metabolite originally isolated fromA. fumigatus.1It is active againstB. subtilisandM. bovis(MICs = 12.5 and 1.25 μg/ml, respectively), as well asT. cruziandT. gondii(MICs = 5-10 and 10-20 μg/ml, respectively).1,2It reduces viability and induces lysis of A549 human lung cancer cells (IC50s = 7.4 μM for both).3Trypacidin increases survival in a mouse model ofT. gondiiinfection when administered in six doses of 12.5 mg/kg each.1 1.Balan, J., Ebringer, L., Nemec, P., et al.Ant... | |||
TN4732 |
Pachysamine M
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Others | Others |
Pachysamine M shows inhibitory activities against multiple types of cancer cells. | |||
TN3321 |
9-Methoxy-alpha-lapachone
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Others | Others |
9-Methoxy-alpha-lapachone has antitumor-promoting effect, it exhibits significant inhibitory activity against 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced Epstein- Barr virus early antigen (EBV-EA) activation in Raji cells. | |||
TN3899 |
Drupacine
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Others | Others |
Drupacine and a crude alkaloid extract suppress nematode hatch, activity of mixed life stages, and population numbers on plant roots. | |||
TN2032 |
Pachypodol
霍香黃酮醇 |
Antifection | Microbiology/Virology |
Pachypodol has antibacterial and antifungal activities against Bacillus subtilis, Staphylococcus aureus, Staphylococcus faecalis, Echerichia coli, Pseudomonas aeruginosa, Candida albicans, Candida krusei and Candida galabrata. | |||
TN3019 |
4,9-Dihydroxy-alpha-lapachone
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Others | Others |
4,9-Dihydroxy-alpha-lapachone has antitumor-promoting effects, it exhibits significant inhibitory activity against 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced Epstein-Barr virus early antigen (EBV-EA) activation in Raji cells. 4,9-Dihydroxy-alpha-l | |||
TN1247 |
3-Epidehydropachymic acid
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Others | Others |
3-Epidehydropachymic acid is a natural product | |||
TN6657 |
4-(Dimethylamino)cinnamaldehyde
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4-Dimethylaminocinnamaldehyde is a photometric reagent for primary aromatic amines. The 4-(dimethylamino)cinnamaldehyde assay is currently used to quantify proanthocyanidin (PAC) content in cranberry products. |