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Cat. No. | Product Name | Target | Signaling Pathways |
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T8931L |
ICCB-19 hydrochloride
ICCB-19 HCl(750621-52-4 free base) |
Apoptosis; Others; Autophagy; RIP kinase | Apoptosis; Autophagy; NF-κB; Others |
ICCB-19 hydrochloride (ICCB-19 HCl) 是RIPK1激酶活性的间接抑制剂。它是一种 TRADD 抑制剂,可与 TRADD 的 N 端结构域结合,破坏其与 TRADD-C 和 TRAF2 的结合,诱导自噬和长寿命蛋白质的降解。 | |||
T3726 |
Erdafitinib
厄达替尼,JNJ-42756493 |
Apoptosis; FGFR | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
Erdafitinib (JNJ-42756493) 是一种喹喔啉衍生物,是一种具有口服活性的FGFR 家族抑制剂,抑制FGFR1/2/3/4活性的IC50分别为1.2、 2.5、3.0和5.7 nM。 | |||
T20642 |
Laurdan
6-十二酰基-N,N-二甲基-2-萘胺,6-Dodecanoyl-2-dimethylaminonaphthalene |
Others | Others |
Laurdan (6-Dodecanoyl-2-dimethylaminonaphthalene) 是膜透性荧光探针。它的广义极化 (GP) 定量可用于磷脂相的鉴定,对与之结合的细胞膜磷脂相具有光谱敏感性。 | |||
T17284 |
Zardaverine
BY 290,B 84290 |
PDE | Metabolism |
Zardaverine (BY 290) 是一种可口服且具有选择性和有效性的 PDE3/4 抑制剂 ,具有支气管扩张活性和抗肝癌活性。Zardaverine 在血小板中的作用是通过PDE III同工酶介导,可用于研究急性肾衰竭呵呵慢性气流阻塞。 | |||
T6189 |
Mirdametinib
PD325901,PD0325901 |
Apoptosis; MEK; Autophagy | Apoptosis; Autophagy; MAPK |
Mirdametinib (PD325901) 是一种 MEK 抑制剂 (IC50=0.33 nM),具有选择性、非 ATP 竞争性和口服活性。Mirdametinib 具有抗肿瘤活性,可以抑制 p-ERK1/2 的表达并诱导细胞凋亡。 | |||
T32191 |
Irdabisant
CEP-26401,CEP 26401,CEP26401 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Irdabisant (CEP-26401) 是选择性、口服活性和血脑屏障渗透性的组胺 H3 受体 (histamine H3 receptor, H3R) 拮抗剂/逆激动剂。Irdabisant 显示人 H3R 和大鼠 H3R 的 Ki 分别为 2.0 nM 和 7.2 nM。Irdabisant 抑制 hERG 电流的活性相对较低 (IC50= 13.8 μM)。在大鼠社会认知模型中,Irdabisant 具有认知增强和唤醒作用。Irdabisant 可用于研究精神分裂症或认知障碍。 | |||
T37555 |
Cardanol triene
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Cardanol triene is a phenol found in cashew nut shell liquid that reversibly inhibits tyrosinase with an IC50 value of 40.5 μM in vitro. A mixture of cardanol mono-, di-, and triene is used to synthesize cardanol-metal complexes that inhibit uropathogenic E. coli biofilm formation. | |||
T36477 |
Urdamycin A
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Urdamycin A is a bacterial metabolite originally isolated fromS. fradiaethat has antibacterial and anticancer activities.1,2It is active against a variety of Gram-positive and Gram-negative bacteria, includingB. subtilisand strains ofArthrobacterandStreptomyces, but not the fungusS. cerevisiae, in a disc assay when used at a concentration of 1 mg/ml.2Urdamycin A is cytotoxic to L1210 and HT-29, but not A549, cancer cells (IC50s = 7.5, 5, and >10 μg/ml, respectively).1 | |||
T126318 |
Sordariol
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Sordariol 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 T126318,CAS号为 115873-03-5。 | |||
T26318 |
Verdantiol
Butylphenyl methylpropional methyl anthranilate |
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Verdantiol is a flavanol. | |||
T30669 |
C.I. Mordant Brown 1
NSC-326197,NSC 326197,NSC326197 |
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C.I. Mordant Brown 1 是一种偶氮染料,λmax 为 373 nm、487 nm (2nd)。C.I. Mordant Brown 1 也可以抑制CD40-CD154 共刺激蛋白-蛋白互作。 | |||
T36539 |
Nocardamine
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Nocardamine is a ferrioxamine siderophore that has been found inStreptomycesand has diverse biological activities.1,2,3,4It chelates iron in a chrome azurol S assay (IC50= 9.9 μM).1Nocardamine inhibitsM. smegmatisandM. bovisbiofilm formation (MIC = 10 μM for both), an effect that can be reversed by iron.2It is cytotoxic to T47D, SK-MEL-5, SK-MEL-28, and RPMI-7951 cancer cells (IC50s = 6, 18, 12, and 14 μM, respectively).3Nocardamine also induces morphological changes in BM-N4 insect cells.4 1.Lo... | |||
T36434 |
Sordarin sodium
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Sordarin is an inhibitor of fungal protein synthesis originally isolated from S. araneosa.[1] It binds to elongation factor 2 (EF-2) in the presence of ribosomes and inhibits the uncoupled GTPase activity of equimolar mixtures of EF-2 and ribosomes from C. albicans (IC50 = 0.1 μM). Sordarin inhibits protein synthesis in cell-free lysates of C. albicans, C. glabrata, and C. neoformans (IC50s = 0.01, 0.2, and 0.06 μg/ml, respectively) but not in rabbit reticulocytes (IC50 = >100 μg/ml).[1] [2] It... | |||
T131401 |
Halfordamine
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Halfordamine 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 T131401。 | |||
T125463 |
12-O-Methylsordariol
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12-O-Methylsordariol 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 T125463,CAS号为 1938054-84-2。 | |||
T71813 |
Cardanol diene
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Cardanol diene is a phenol found in cashew nut shell liquid that inhibits tyrosinase with an IC50 value of 52.5 μM in vitro. Cardanol diene is also used to synthesize cardanol-metal complexes that inhibit uropathogenic E. coli biofilm formation. | |||
T69413 |
Primordazine B
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Primordazine B is a selective inhibitor of primordial germ cell (PGC) development which targets poly(A)-tail-independent noncanonical translation (PAINT). | |||
T125499 |
Piperdardine
|
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Piperdardine 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 T125499。 | |||
T34133 |
Primordazine NC-6364997
Primordazine NC 6364997,Primordazine NC6364997 |
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Primordazine NC-6364997 is a negative control for Primordazine A and Primordazine B. | |||
T126401 | Cordatin | ||
Cordatin 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 T126401,CAS号为 110382-43-9。 | |||
T61197 |
Irdabisant hydrochloride
|
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Irdabisant (CEP-26401) hydrochloride 是一种选择性、口服活性的组胺H3受体拮抗剂/逆激动剂,具备良好的血脑屏障渗透性。该化合物对大鼠和人类的H3受体具有高亲和力,其Ki值分别为7.2 nM和2.0 nM。此外,Irdabisant hydrochloride在抑制hERG电流方面表现出较低的活性,IC50为13.8 μM。在大鼠社会认知模型中,它展现了认知增强和唤醒的效果,可作为精神分裂症或认知障碍研究的潜在工具。 | |||
T10795 |
Chlordantoin
Clodantoin,氯登妥因 |
Others | Others |
Chlordantoin is an antifungal agent with the potential for vaginal candidiasis treatment. | |||
T80447 |
Pardaxin P5
|
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Pardaxin P5,一种抗菌肽,其对大肠杆菌的最小抑制浓度(MIC)为13 μM。 | |||
T33483 |
Mordant red 19
NSC-326195,NSC 326195,Acid Chrome Red 5G,Superchrome Red G,NSC326195 |
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Mordant red 19 is an azo dye. | |||
T23399 |
STEARDA
|
Others | Others |
STEARDA potentiates TRPV1-mediated effects of NADA. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TJS0328 |
Nordalbergin
6,7-dihydroxy-4-phenylcoumarin,6,7-Dihydroxy-4-Phenylchromen-2-One,6,7-二羟基-4苯基香豆素 |
Others | Others |
Nordalbergin 是一种香豆素,分离自Dalbergia sissoo 的木皮中。 它能够显著性的诱导 HL-60 细胞的分化。 | |||
TN3594 |
Cardanol (C15:1)
|
Apoptosis; Others | Apoptosis; Others |
Cardanol (C15:1) 存在于腰果壳液中,可诱导人黑色素瘤细胞线粒体相关的细胞凋亡。 | |||
T2994 |
(E)-Cardamonin
Alpinetin chalcone,Cardamomin,小豆蔻明,Cardamonin,(E)-Cardamoni,豆蔻明 |
Apoptosis; TRP/TRPV Channel | Apoptosis; Membrane transporter/Ion channel |
(E)-Cardamonin (Alpinetin chalcone) 是一种新型hTRPA1阳离子通道拮抗剂,IC50值为454 nM。 | |||
T66078 | Cardamonin | ||
Cardamonin, a chalcone extracted from cardamom spice with anti-inflammatory and anti-tumor activities. Cardamonin decreased viability of NPC(Nasopharyngeal carcinoma ) cells in a concentration-dependent manner. The IC50 values were 16.22 μM(CNE-1), 14.34 μM (CNE-2), 16.50 μM (HONE-1), and 68.12 μM (SUNE-1). Moreover, the expression level of the proapoptotic effector protein Bax and Bid was also markedly increased after treatment with cardamonin(15μM) in CNE-2 cells.In vivo, cardamonin (25 mg/kg ... |