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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T13210 |
Trombodipine
PCA-4230 |
Others | Others |
Trombodipine is an agent of antithrombotic. | |||
T68644 | Pca 4233 | ||
Pca 4233 belongs to a class of selective PAF-receptor antagonists. | |||
T33356 |
Methylsilanol PCA
|
||
Methylsilanol PCA is a bioactive chemical. | |||
T23123 |
PCA 4248
|
Others | Others |
PAF antagonist | |||
T33060 |
Lysine PCA
|
||
Lysine PCA is a bioactive chemical. | |||
TP1037 |
D-Lys(Z)-Pro-Arg-pNA diacetate
Spectrozyme PCa,Chromozym Pca diacetate |
||
D-Lys(Z)-Pro-Arg-pNA (diacetate) diacetate is a chromogenic substrate. | |||
TP1196 |
D-Lys(Z)-Pro-Arg-pNA
Chromozym Pca |
||
D-Lys(Z)-Pro-Arg-pNA is a luminescent substrate of activated protein C (APC). | |||
T9593 |
Senaparib
IMP4297 |
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Senaparib (IMP4297) 是一种选择性和口服有效的PARP1/2抑制剂,具有强效的抗肿瘤活性。 | |||
T3160 |
HUHS015
|
Others | Others |
HUHS015 是高效的PCA-1/ALKBH3抑制剂。它对 PCA-1 作用的IC50值为 0.67 μM。 | |||
T13812 |
PCA50941
|
Others | Others |
PCA50941 is a 1,4-dihydropyridine derivative, treatment for cardiovascular disease. | |||
T0860L |
Mefloquine
Ro215998,WR 142490,Ro-215998,氟甲喹羟哌啶,Lariam,Ro 215998 |
Others | Others |
Mefloquine (Ro 215998) 是一种喹啉抗疟药,是一种抗 SARS-CoV-2 进入抑制剂。 Mefloquine 也是一种 K+ 通道 (KvQT1/minK) 拮抗剂,IC50 为 ~1 μM。它可用于疟疾、系统性红斑狼疮和癌症研究。 | |||
T21653 |
1,4-DPCA
|
HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism |
1,4-DPCA 是一种脯氨酰羟化酶抑制剂,对人源包皮成纤维细胞中胶原羟基化的 IC50 为 2.4 μM,对因子抑制 HIF (FIH) 的 IC50 为 60 μM。 | |||
T3049 |
TPCA-1
GW683965,IKK2 Inhibitor IV,TPCA1 |
Apoptosis; IκB/IKK; STAT | Apoptosis; JAK/STAT signaling; NF-κB; Stem Cells |
TPCA-1 (TPCA1) 是一种选择性IKK-2抑制剂,IC50值为 17.9 nM。它也是反式激活、DNA 结合以及STAT3磷酸化的一种抑制剂。 | |||
T60452 | PCAF-IN-2 | ||
PCAF-IN-2 (compound 17) 是一种有效的 PCAF 抑制剂(IC50 = 5.31 µM)。PCAF-IN-2 具有抗肿瘤活性。PCAF-IN-2 诱导细胞凋亡并且阻滞细胞周期在 G2/M 期。 | |||
T80282 |
cPcAMP1/26
|
||
cPcAMP1/26 是一款抗菌肽,能高效清除A.Hydrophila及金黄色葡萄球菌 (S. aureus)。该化合物通过诱导细菌质膜去极化作用并提升细胞内ROS水平,展示其抗菌机制。 | |||
T24146 | HOCPCA | ||
HOCPCA is an effective and selective ligand for the GHB binding sites that acts by binding with 27 times better affinity than GHB itself and crossing the blood-brain barrier in vitro and in vivo. | |||
T60762 |
PCAF-IN-1
|
||
PCAF-IN-1 是用于肿瘤治疗研究的抗肿瘤剂。PCAF-IN-1 是高度选择性的PCAF 抑制剂。 | |||
T36796 |
1,4-DPCA ethyl ester
|
||
1,4-DPCA ethyl ester, the ethyl ester derivative of 1,4-DPCA, acts as an inhibitor of the enzyme factor inhibiting HIF (FIH)[1]. | |||
T77552 |
SLU-PP-1072
|
Apoptosis; Estrogen/progestogen Receptor | Apoptosis; Endocrinology/Hormones |
SLU-PP-1072 是一种 ERRα和ERRγ 反向双重激动剂,破坏 PCa 细胞代谢,通过细胞周期失调诱导凋亡 (apoptosis)。SLU-PP-1072 用于研究前列腺癌 (PCa) 。 | |||
T69564 |
YK-2-69
|
||
YK-2-69 is a highly selective DYRK2 inhibitor which specifically interacts with Lys-231 and Lys-234 in the co-crystal structure. Especially, YK-2-69 exhibits more potent anti-PCa efficacy than the first-line drug enzalutamide in vivo. | |||
T15594 |
MKC8866
|
IRE1 | Cell Cycle/Checkpoint |
MKC8866 是一种选择性IRE1 RNase 抑制剂,在体外的IC50为 0.29 μM,是水杨醛类似物。 它抑制乳腺癌细胞中的 IRE1 RNase,导致促肿瘤因子的产生减少,并且可以抑制前列腺癌 (PCa) 肿瘤的生长。它强烈抑制二硫苏糖醇诱导的 XBP1s 表达,EC50为 0.52 μM。 | |||
T11581 |
HSR6071
|
Others | Others |
HSR6071 是一种新型具有口服活性和有效性的抗过敏制剂,能抑制被动皮肤过敏反应 (PCA)。HSR6071 在大鼠实验性哮喘模型中显示出抗哮喘活性。 | |||
T40687 |
1,1,1,3,10,11-Hexachloroundecane
|
||
1,1,1,3,10,11-Hexachloroundecane is a polychlorinated alkane (PCA) characterized by a lengthy carbon chain. | |||
T26832 |
BKM1740
BKM-1740,BKM 1740 |
||
BKM1740 induced apoptosis in prostate cancer (PCa) cells by repressing survivin at both the mRNA and protein levels in vitro. | |||
T26831 |
BKM1644
BKM 1644,BKM-1644 |
||
BKM1644 is an effective inhibition of the proliferation of metastatic, castration-resistant PCa (mCRPC) cells. | |||
T78153 |
PSMA I&T
|
Others | Others |
PSMAI&T为高效的前列腺特异性膜抗原(PSMA)抑制剂,适用于前列腺癌(PCa)的单光子发射计算机断层扫描(SPECT)/计算机断层扫描(CT)显像及放射性核素研究。 | |||
T41175 |
OB 24 hydrochloride
|
||
OB 24 hydrochloride is a potent and selective heme oxygenase 1 (HO-1) inhibitor (IC50 values are 1.9 and >100 μM for HO-1 and HO-2 respectively), reduces protein carbonylation and reactive oxygen species formation in advanced prostate cancer cells (PCA). Inhibits cell proliferationin vitroand PCA tumor growth and lymph node/lung metastasesin vivo. Synergizes with Taxol. | |||
T38127 |
pNPS-DHA
|
||
pNPS-DHA is an arylamide derivative of docosahexaenoyl ethanolamide that has anti-allergic activity.1It inhibits degranulation of RBL-2H3 mast cells (IC50= 15 μM).pNPS-DHA (1,000 mg/kg) inhibits IgE-dependent passive cutaneous anaphylaxis (PCA) in mice. 1.Kim, I.-H., Kanayama, Y., Nishiwaki, H., et al.Structure-activity relationships of fish oil derivatives with anti-allergic activity in vitro and in vivoJ. Med. Chem.62(21)9576-9592(2019) | |||
T79674 |
HDAC-IN-64
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
HDAC-IN-64 (Compound 13) 为HDAC抑制剂,对HDAC4/6的IC50值为24 nM及85 nM。其对前列腺癌(PCA)细胞表现出抗增殖与抗迁移效果,并能抑制LNCaP和RWPE-1细胞的生长,GI50值分别达到0.32 μM与1.1 μM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3324 |
Lycorine
Galanthidine,Narcissine,石蒜碱,Amarylline,Belamarine,Licorine,番石榴碱 |
Apoptosis; Virus Protease; Antibacterial; AChR; Fatty Acid Synthase | Apoptosis; Metabolism; Microbiology/Virology; Neuroscience |
Lycorine (Narcissine) 是从金眼科植物科中提取的一种天然生物碱。它是一种具有口服活性的SCAP 抑制剂,Kd 值 15.24 nM。它也是黑色素瘤血管生成抑制剂,有用于前列腺癌和代谢疾病的研究潜力。 | |||
T4814 |
(R)-5-Oxopyrrolidine-2-carboxylic acid
D-Pyroglutamic acid,(R)-(+)-2-Pyrrolidone-5-carboxylic acid,D-焦谷氨酸 |
Others; Endogenous Metabolite | Metabolism; Others |
(R)-5-Oxopyrrolidine-2-carboxylic acid (D-Pyroglutamic acid) 是内源性代谢产物的一种。 | |||
TN1805 |
Isosilybin B
|
Apoptosis; Androgen Receptor | Apoptosis; Endocrinology/Hormones |
Isosilybin B 是一种从水飞蓟中提取的黄酮木脂素,具有抗前列腺癌 (PCA) 活性,对癌细胞增殖有抑制作用,促使 G1 期阻滞和凋亡。Isosilybin B 诱导雄激素受体降解。 | |||
TN1804 |
Isosilybin A
异水飞蓟素 A,异水飞蓟宾A,水飞蓟素 B2 |
Apoptosis; Tyrosinase; PPAR; ABC | Apoptosis; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism; Proteases/Proteasome |
Isosilybin A 是从水飞蓟中分离出来的一种黄酮木脂素,可抑制癌细胞增殖并诱导 G1 期停滞和凋亡,通过靶向 Akt-NF-κB-雄激素受体轴激活前列腺癌细胞的凋亡机制,具有抗前列腺癌活性。 | |||
T4716 |
Pyrrole-2-carboxylic acid
吡咯-2-羧酸,2-Pyrrolecarboxylic acid,Minaline |
Endogenous Metabolite | Metabolism |
Pyrrole-2-carboxylic acid (Minaline) 是一种天然生物碱类,从海洋细菌Pelomonas puraquaesp. Nov 中分离得到。 | |||
TN2155 |
Rhodiocyanoside A
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Rhodiocyanoside A has antiallergic activity, it exhibits inhibitory activity on the histamine release from rat peritoneal exudate cells sensitized with anti-DNP IgE and inhibits the PCA reaction in rats. | |||
T82248 |
Gymnoside I
|
||
Gymnoside I(化合物1)是糖苷氧基苄基2-异丁基苹果酸,其在小鼠被动皮肤过敏反应(PCA)实验中展现出抗过敏效能。该化合物有望在哮喘、神经衰弱和慢性肝炎治疗研究中应用。 |