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35
Cat. No. | Product Name | Target | Signaling Pathways |
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T125940 | Penicilliumin A | ||
Penicilliumin A 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 T125940,CAS号为 1393131-81-1。 | |||
T124797 |
Ochratoxin B
|
Endogenous Metabolite | Metabolism |
Ochratoxin B 由多种曲霉和青霉菌产生的,是霉菌毒素 Ochratoxin A 的类似物,会对农产品造成污染。 | |||
T27300 |
Olorofim
Olorofim,F901318,F-901318 |
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Olorofim 是一种新型的选择性抗真菌化合物,对烟曲霉DHODH 具有抑制作用(IC50:44 nM),对人类DHODH 几乎没有抑制作用(>100 uM)。Olorofim 对青霉菌属、皮炎杆菌属、镰刀菌属等各种致病性丝状和二形真菌有很好的疗效。 | |||
T29345 |
2-Ethyl-5-methylphenol
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Others | Others |
2-Ethyl-5-methylphenol 是一种烷基苯酚,可从金黄色青霉、疣状假单胞菌和绿色青霉中分离或鉴定的化合物。 | |||
T32262 | Janthitrem G | ||
Janthitrem G is a type of naphthopyran. Janthitrem G is obtained from Penicillium janthinellum. Tremorgenic mycotoxi. | |||
T31761 |
Fellutamide A
|
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Fellutamide A as a tripeptide derivative from Penicillium fellutanum can enhance nerve growth factor (NGF) synthesis and secretion in vitro. | |||
T34444 | Rubroskyrin | ||
Rubroskyrin is a modified bis-anthraquinone pigment that comes from Penicillium islandicum Sopp. | |||
T32982 |
Luteoskyrin
Flavomycelin |
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Luteoskyrin is a hepatotoxic and hepatocarcinogenic bisdihydroanthraquinone produced by Penicillium islandicum Sopp. | |||
T34717 |
Stevastelin B3
NK374186B3,NK 374186B3,Antibiotic NK 374186B3,NK-374186B3 |
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Stevastelin B3 is a depsipeptide isolated from Penicillium. | |||
T34447 |
Rugulin
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Rugulin is a minor metabolite from Penicillium rugulosum and a naturally occurring bisanthraquinone. | |||
T38315 |
Penigequinolone A
|
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Penigequinolone A 可由 Penicillium sp., No. 410 产生,具有花粉生长抑制剂作用。 | |||
T34190 |
Puberuline
Fructigenine A,Rugulosuvine-B,Fructigenine-A,Rugulosuvine B,Puberulin |
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Puberuline is a diketopiperazine alkaloid isolated from Penicillium piscarium. | |||
T32258 |
Janthitrem B
|
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Janthitrem B is a trematoxin produced by certain isolates of Penicillium violaceum. | |||
T80312 |
PAF26
|
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PAF26为针对植物病原真菌Penicillium digitatum、Penicillium italicum及Botrytis cinerea具有活性的抗菌肽。 | |||
T33551 |
N(alpha)-Acetylfusarinines
Nalpha-Acetylfusarinines |
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N(alpha)-Acetylfusarinines is a group of naturally occurring hydroxamic acids produced by unidentified species of Penicillium when grown on iron-deficient media. | |||
T32260 |
Janthitrem E
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Janthitrem E is a type of naphthopyran. Janthitrem E is obtained from Penicillium janthinellum. Tremorgenic mycotoxi. | |||
T32259 |
Janthitrem C
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Janthitrem c is a type of naphthopyran. Janthitrem C is obtained form Penicillium janthinellum. Tremorgenic mycotoxin. | |||
T32261 |
Janthitrem F
Janthitrem E monoacetate |
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Janthitrem f, as a 10-0-acetyljanthitrem e or janthitrem e monoacetate, is a type ofnaphthopyran. Janthitrem F is prepared by Penicillium janthinellum. Tremorgenic mycotoxi. | |||
T37254 |
Rugulotrosin A
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Rugulotrosin A is an antibiotic originally isolated from Penicillium. It is active against the Gram-positive bacteria E. faecalis, B. cereus, B. subtilis, and S. aureus with 99% lethal dose (LD99) values of 1.6, 3.1, 5.5, and 200 μg/ml, respectively. Rugulotrosin A is inactive against Gram-negative bacteria. | |||
T25170 |
Botryodiplodin
Cytostipin,Antibiotic PSX 1 |
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Botryodiplodin, an antibiotic, has antileukemic activity from Botryodiplodia theobromae. It has the property of turning the skin of the individual in various shades of pink 2-3 hrs after application. It is a toxic metabolite of Penicillium carneo-lutescen | |||
T36878 |
Sclerotiorin
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Sclerotiorin is a natural product isolated primarily from Penicillium species. It inhibits soybean lipoxygenase-1 with an IC50 value of 4.2 μM. Sclerotiorin also exhibits a number of other activities including inhibition of cholesterol ester transfer protein (IC50 = 19.4 μM),, inhibition of Grb2-Shc interaction (IC50 = 22 μM),, and antagonism of endothelin receptors (IC50 = 114 and 152 μM for human ETA and ETB, respectively). | |||
T38255 |
Penipurdin A
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Penipurdin A is an anthraquinone fungal metabolite originally isolated fromP. purpurogenumthat has antibacterial activity.1,2It is active againstM. tuberculosiswith a MIC value of 25 μg/ml.2 1.Xue, J., Fu, Y., Wu, P., et al.Two new anthraquinones from the soil fungus Penicillium purpurogenum SC0070J. Antibiot. (Tokyo)68(9)598-599(2015) 2.Daengrot, C., Rukachaisirikul, V., Tadpetch, K., et al.Penicillanthone and penicillidic acids A-C from the soil-derived fungus Penicillium aculeatum PSU-RSPG105... | |||
T35909 |
Penicinoline
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Penicinoline is an alkaloid that has been found in Penicillium and has antimalarial, insecticidal, and anticancer activities.1,2 It is active against chloroquine-sensitive and -resistant strains of P. falciparum (IC50 = 25 μM for both).1 Penicinoline (1,000 ppm) is also active against the aphid A. gossypii.2 It inhibits proliferation of 95-D and HepG2 cancer cells (IC50s = 0.57 and 6.5 μg/ml, respectively) but not HeLa, KB, KBv200, or Hep-2 cells (IC50s = >100 μg/ml). |1. Naveen, B., Ommi, N.B.,... | |||
T38276 |
Benzomalvin C
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Benzomalvin C is a weak antagonist of the neurokinin-1 (NK1) receptor inhibiting binding of substance P by 46% when used at 100 μg/ml in vitro. It is also a weak inhibitor of indolamine 2,3-dioxygenase (IDO) with an IC50 value of 130 μM for recombinant IDO. It was isolated from Penicillium and contains an epoxide group at C-19 and C-20, which is not present in benzomalvins A, B, or E. | |||
T75444 | Peniterphenyl A | ||
Peniterphenyl A,一种源于深海青霉属植物的天然产物,能够抑制HSV-1/2病毒的细胞内入侵。它可能通过与HSV-1/2病毒的糖蛋白D直接相互作用,干扰病毒的吸附和膜融合过程,进而有效阻断病毒感染。因此,Peniterphenyl A是抗HSV-1/2研究领域中一个极具潜力的先导化合物。 | |||
T35776 | Janthitrem A | ||
Janthitrem A is a mycotoxin that has been found inP. janthinellum.1It induces tremors in mice and decreases the time to fall from the rotarod when administered at a dose of 4 mg/kg.2Janthitrem A (20 μg/g) also reducesW. cervinatalarvae weight gain and food consumption. 1.Gallagher, R.T., Latch, G.C., and Keogh, R.G.The janthitrems: Fluorescent tremorgenic toxins produced by Penicillium janthinellum isolates from ryegrass pasturesAppl. Environ. Microbiol.39(1)272-273(1980) 2.Babu, J.V., Popay, A.... | |||
T37288 |
Remisporine B
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Remisporine B is a polyketide and derivative of remisporine A that has been found inPenicilliumand has immunosuppressant activity.1,2It inhibits LPS- or concanavalin A-induced proliferation of isolated mouse splenic lymphocytes (IC50s = 30.1 and 32.4 μg/ml, respectively).1 1.Liu, H., Chen, S., Liu, W., et al.Polyketides with immunosuppressive activities from mangrove endophytic fungus Penicillium sp. ZJ-SY2Mar. Drugs14(12)217(2016) 2.Kong, F., and Carter, G.T.Remisporine B, a novel dimeric chrom... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T8693 |
Diallyl Trisulfide
二烯丙基三硫化物,二烯丙基三硫醚 |
Apoptosis; Reactive Oxygen Species; Antifungal | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Diallyl Trisulfide 是一种在大蒜中发现的有机多硫化物,可作为 H2S 供体。它抑制扩张性青霉的生长,有抗癌能力。 | |||
T3936 |
PATULIN
Expansin,Claviform,散毒素,Clavacin,棒曲霉素 |
Apoptosis; Others; Antibacterial; Antibiotic; Autophagy | Apoptosis; Autophagy; Microbiology/Virology; Others |
Patulin (Claviform) 是由 Aspergillus、Penicillium 和 Byssochlamys 几种真菌属产生的霉菌毒素,有致染色体断裂、突变,致畸和细胞毒性作用。它通过溶酶体-线粒体轴诱导自噬依赖性细胞凋亡,能造成 DNA 损伤。 | |||
T8335 |
Lycobetaine acetate
氧化石蒜碱乙酸盐,Oxylycorine |
Others | Others |
Lycobetaine acetate (Oxylycorine) 是一种潜在的抗罗克福提青霉和黑曲霉的生物杀菌剂。 | |||
T13305 |
Viridicatol
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Anti-infection; Antifungal | Microbiology/Virology |
Viridicatol 是从夹竹桃的内生真菌青霉菌属的发酵中分离出的一种喹诺酮类生物碱,对金黄色葡萄球菌有抗菌活性,MIC 值为 15.6 μg/mL。 | |||
T70955 |
Vinaxanthone
SM-345431 |
Phospholipase; Antibacterial | Metabolism; Microbiology/Virology |
Vinaxanthone (SM-345431) 是一种从青霉菌中提取的小分子化合物,是一种具有选择性和有效性的 semaphorin3A、phospholipase C (PLC) 和 FabI 抑制剂,抑制semaphorin3A 和 FabI。Vinaxanthone 具有抗菌活性,阻止细胞内脂肪酸合成,抑制金黄色葡萄球菌的生长。 | |||
TN3861 |
Dihydropinosylvin
山药 |
Anti-infection | Microbiology/Virology |
Dihydropinosylvin 是一种植物抗毒素,对枝孢枝孢菌、Botryodiplodia theobromae、黑曲霉和石化青霉具有抗真菌活性,对蜡状芽孢杆菌、金黄色葡萄球菌、铜绿假单胞菌和大肠杆菌也有很强的抗菌活性。双色高粱幼苗的种子和根伸长。 | |||
T2S1792 |
Lycobetaine
石蒜内胺,Ungeremine,石蒜醋胺,石蒜碱内铵盐 |
Antibacterial | Microbiology/Virology |
Lycobetaine (Ungeremine) 是一种潜在的抗罗克福尔青霉和黑曲霉的生物杀菌剂。它对柱状黄杆菌有很强的抗菌活性。它有效地靶向哺乳动物以及细菌I 型和II 型拓扑异构酶。它显示出强烈的乙酰胆碱酯酶抑制活性(IC(50) 值为 0.35 microM)。 它具有抗原生动物活性,在体外试验中对Trypanosoma brucei rhodesiense、T. cruzi 表现出良好的活性。 | |||
T82955 |
Asperazine
(+)-Asperazine |
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Asperazine (Compound 5),一种Penicillium oxalicum产生的生物碱,在HepG2和CaSki细胞系上展现了适度的活性(IC50>50 μM)。 | |||
T73887 | Cycloaspeptide A | ||
Cycloaspeptide A 是从内生真菌Penicillium janczewskii 中分离出来的,具有抗寄生虫活性。 | |||
T82448 |
Eremofortin B
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Eremofortin B是倍半萜类化合物,由Penicillium roqueforti PR毒素(PRT)合成。 | |||
T13297 |
Verruculogen
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Others | Others |
Verruculogen is a toxin produced mainly by Penicillium and Aspergillus spp. Verruculogen inhibits Ca2+-activated K+ channels, and is an M phase inhibitor of the mammalian cell cycle. | |||
T81676 |
NG-012
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NG-012为一种神经生长因子(NGF)增强剂,来源于Penicillium verruculosum F-4542的培养液。该化合物能在大鼠嗜铬细胞瘤细胞系(PC12)中提升NGF引导的神经突生长效应。 | |||
TN3373 | Albrassitriol | Others | Others |
Albrassitriol is a natural product from the cultures of the fungus Penicillium sp. | |||
T75459 | Canadensolide | ||
Canadensolide 是一种 Penicillium canadense 的抗真菌代谢产物。 | |||
T13629 | Cyclo(Ala-Gly) | Others | Others |
Cyclo (Ala-Gly) is a mangrove endophytic fungus, a metabolite of Penicillium thomi, which is cytotoxic to A549, HepG2 and HT29 cells. The IC50 value is in the range of 9.5-18.1 μM. | |||
T13608 |
Chaetoglobosin A
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Others | Others |
Chaetoglobosin A, the active compound extracted of Penicillium aquamarinium, is a member of the cytochalasan family. It preferentially induces apoptosis. | |||
T73914 |
Eremofortin A
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Eremofortin A 是一种代谢产物,可以从罗氏青霉的培养物中分离出来。 | |||
T71750 | Quinolactacin A1 | ||
Quinolactacin A1 是一种有效的乙酰胆碱酯酶 (AChE) 抑制剂,可从Penicillium citrinum 中得到。Quinolactacin A1 可用于阿尔茨海默病的研究。 | |||
T31134 |
Cyclochlorotine
CCRIS 1316 |
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Cyclochlorotine is a mycotoxin produced by Penicillium insularum, which can cause liver injury and has carcinogenic properties. | |||
T25211 |
CC 1014
CC1014,CC-1014,NSC-356885,NSC356885,NSC 356885 |
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CC 1014 is a polypeptide antibiotic isolated from Penicillium lilacinum that inhibits phosphorylation of ADP, Mg ATPase. | |||
T82210 |
Herqueilenone A
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Herqueilenone A,一种苯醌-色满酮类化合物,源自夏威夷火山土壤中的真菌Penicillium herquei FT729。 | |||
T28379 |
PF-1163B
PF1163B,(-)-PF1163B,PF 1163B |
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PF-1163B is an antifungal agent form Penicillium sp. II. PF-1163B inhibits ergosterol (ERG) synthesis with IC50 value of 34 ng/ml. PF-1163B showed potent growth inhibitory activity against pathogenic fungal strain Candida albicans but did not show cytotox | |||
T12373 |
Paxilline
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Others | Others |
Paxilline is an indole alkaloid mycotoxin from Penicillium paxilli, acts as a potent BK channels inhibitor by an almost exclusively closed-channel block mechanism. Paxilline possesses significant anticonvulsant activity. | |||
T13618 |
Citreoviridin
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Others | Others |
Citreoviridin, a toxin from Penicillium citreoviride NRRL 2579, inhibits brain synaptosomal Na+/K+-ATPase whereas, in microsomes, both Na+/K+-ATPase and Mg2+-ATPase activities are significantly stimulated in a dose-dependent manner. | |||
T13872 |
Roquefortine C
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Others | Others |
Roquefortine C is a fungal cyclopeptide isolated from Penicillium roquefortii, activates P-gp and also inhibits P450-3A and other haemoproteins | |||
T38338 |
Quinolactacin A
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Quinolactactin A is a quinolone fungal metabolite originally isolated from Penicillium. It inhibits TNF production induced by LPS in murine peritoneal macrophages (IC50 = 12.2 μg/ml). It is not active against a variety of bacteria, fungi, and yeasts. Quinolactacin A is a mixture of quinolactacin A1 and A2. | |||
T38033 |
Benzomalvin B
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Benzomalvin B is a fungal metabolite originally isolated from Penicillium. It acts as an antagonist of neurokinin-1 (NK1) receptors, inhibiting binding of substance P by 24% in vitro when used at a concentration of 100 μg/ml. | |||
T16035 |
Meleagrin
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Others | Others |
Meleagrin, a roquefortine C-derived alkaloid produced by Penicillium fungi, serves as both a class of FabI inhibitors and a lead c-Met inhibitory entity for controlling c-Met-dependent metastatic and invasive breast malignancies. It exhibits antimicrobial and anti-proliferative activities. | |||
T13815 |
Penicillic acid
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Apoptosis; Caspase; Antibacterial; Antibiotic | Apoptosis; Microbiology/Virology; Proteases/Proteasome |
Penicillic acid,一种由多种Aspergillus和Penicillium物种合成的polyketide mycotoxin,通过阻碍caspase-8的自我处理作用,抑制Fas ligand引发的apoptosis。此外,体外研究表明,Penicillic acid在rat alveolar macrophages中显示出cytotoxic特性。 | |||
T83475 |
1,3,5,6-Tetrahydroxy-8-methylxanthone
|
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1,3,5,6-四羟基-8-甲基黄酮 (compound 8) 是从海洋真菌青霉属中分离的一种二聚1,4-苯醌衍生物。 | |||
T36931 |
Penicillide
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Penicillide is a fungal metabolite originally isolated from Penicillium that has diverse biological activities. It is an inhibitor of calpain 2/m-calpain (IC50 = 7.1 μM) and acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 22.9 μM). It is also an antagonist of oxytocin receptors (IC50 = 67 μM). Penicillide inhibits RNA synthesis in P388 murine leukemia cells. | |||
T36438 |
Sporogen-AO 1
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Sporogen-AO 1 is a fungal metabolite originally isolated fromA. oryzaethat has diverse biological activities.1,2,3,4,5It inhibits HIV-1 Tat transactivation in a cell-based assay with an IC50value of 15.8 μM.4Sporogen-AO 1 is cytotoxic to HeLa, KB, and NCI H187 cancer cells (IC50s = 8.3, 9, and 5.1 μM, respectively).2,5It is active againstC. albicans(MIC = 4 mM).3 1.Tanaka, S., Wada, K., Marumo, S., et al.Structure of sporogen-ao 1, a sporogenic substance of Aspergillus oryzaeTetrahedron Lett.25(... | |||
T37690 |
Phenylpyropene A
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Phenylpyropene A is a fungal metabolite originally isolated from P. griseofulvum that has enzyme inhibitory and insecticidal activities.1,2,3 It inhibits acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 0.8 μM).1 Phenylpyropene A inhibits diacylglycerol acyltransferase (DGAT) in rat liver microsomes (IC50 = 78.7 μM). It induces mortality in 100% of M. persicae when used at a concentration of 5 ppm.3 |1. Kwon, O.E., Rho, M.C., Song, H.Y., et al. Phenylpyropene A and B, new inhibitors of ... | |||
T38108 |
Fulvic Acid
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Antioxidant; PDE | Metabolism; oxidation-reduction |
Fulvic Acid 是一种来自土壤、沉积物或水生环境中微生物产生的腐殖质的天然产物,是一种首次青霉菌中分离出的酚酸和真菌代谢产物。Fulvic Acid 抑制淀粉样蛋白b (17-42) (AB17-42)二聚化,破坏预先形成的AB17-42三聚体,并结合到磷酸二酯酶5A (PDE5A)的催化位点,可以调节机体免疫系统,影响细胞的氧化状态,改善胃肠功能。Fulvic Acid 可作为氧化剂或还原剂, 具有研究糖尿病等慢性炎症性疾病的潜力。 | |||
T35761 |
Carviolin
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Carviolin is an anthraquinone fungal metabolite that has been found inZ. longicaudatawith immunosuppressive and antitrypanosomal activities.1,2It inhibits LPS- or concanavalin A-induced proliferation of mouse splenocytes (IC50s = 4 and 4.5 μg/ml, respectively).1Carviolin is active againstT. b. brucei(MIC = 41.66 μM).2 1.Fujimoto, H., Nakamura, E., Okuyama, E., et al.Six immunosuppressive features from an ascomycete, Zopfiella longicaudata, found in a screening study monitored by immunomodulatory... |