346
70
Cat. No. | Product Name | Target | Signaling Pathways |
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T36983 |
Cyclic-di-GMP disodium
Cyclic diguanylate,5GP-5GP disodium,3',5'-Cyclic diguanylic acid,Cyclic di-GMP (sodium salt),cyclic diguanylate disodium,c-di-GMP,c-di-GMP disodium |
STING; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
Cyclic-di-GMP disodium (5GP-5GP disodium) 是细菌的第二信使,也是一种 STING 激动剂,参与原核生物的多种过程,包括生物膜的形成、运动、和细胞周期的进展。Cyclic-di-GMP disodium 对癌细胞显示出抗增殖活性,可诱导 CD4 受体表达升高和细胞周期停滞。Cyclic-di-GMP disodium 可用于癌研究癌症。 | |||
T12472 |
Pifithrin-α, p-Nitro, Cyclic
PFN-α |
p53 | Apoptosis |
Pifithrin-α, p-Nitro, Cyclic (PFN-α) 是 p53 的细胞渗透性和活性形式抑制剂。它对暴露于 Etoposide 的皮层神经元的保护作用比 Pifithrin-α 强一个数量级,ED50为30 nM。它也作为 p53 转录后的活性抑制剂。 | |||
TP1035 |
Cyclic somatostatin
SRIF-14,合成生长抑素,环状生长激素抑制素,Somatostatin-14 |
Others | Others |
Cyclic somatostatin (SRIF-14) 是生长激素释放抑制因子,可用于研究胃十二指肠溃疡出血。 | |||
TP1501L |
CTTHWGFTLC, CYCLIC acetate(244082-19-7 free base)
|
MMP | Proteases/Proteasome |
CTTHWGFTLC, CYCLIC acetate(244082-19-7 free base) 是基质金属蛋白酶 (MMP)-2 和 MMP-9 的抑制剂。它也被称为IV 型胶原酶或明胶酶。明胶酶是癌症治疗干预的潜在靶点,这些酶的抑制剂可以防止肿瘤进展。 | |||
TP1035L |
Cyclic somatostatin Acetate(38916-34-6(free base))
Somatostatin (sheep), monoacetate (salt),Somatostatin-14,SRIF-14,monoacetate (salt) |
Others | Others |
Cyclic somatostatin Acetate(38916-34-6(free base)) (Somatostatin-14) 是一种环状十四肽,可调节许多内分泌和神经系统功能。 | |||
T3637 |
Pifithrin-β hydrobromide
Cyclic PFT-α,PFT-β,Cyclic Pifithrin-α hydrobromide,Pifithrin-β,PFT β (hydrobromide) |
Ferroptosis; p53 | Apoptosis |
Pifithrin-β hydrobromide (Cyclic PFT-α) 是一种 p53 的抑制剂,可逆地阻断 p53 依赖性转录激活和细胞凋亡。IC50值为23 μM。 | |||
T37475 |
Cyclic ADP-Ribose (ammonium salt)
cADP-Ribose,cADPR,Cyclic ADP-Ribose (ammonium salt) |
||
Cyclic ADP-ribose (cADP-ribose) is an endogenous metabolite of NAD+ that mobilizes the release of stored Ca2+ in the endoplasmic reticulum via ryanodine receptors in various cell types.[1],[2],[3],[4],[5] This second messenger is generated via the cADP-ribose synthases CD38 and CD157.[6],[5],[7] cADP-Ribose may also trigger the cell surface Ca2+ influx channel TRPM2 in a temperature-dependent manner.[8] In vitro, cADP-ribose modulates Ca2+ signaling in rat and mouse cardiomyocytes treated with i... | |||
T33516 |
Msh (5-10), cyclic
Cyclic H-asp-his-phe-arg-trp-lys-NH2 |
||
Msh (5-10), cyclic, as a synthetic peptide, can conjugate with fatty acids for enhanced potency. | |||
TP1620 |
Cyclic MKEY
|
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MKEY, a synthetic cyclic peptide inhibitor of CXCL4-CCL5 heterodimer formation, has been shown to protect against atherosclerosis and aortic aneurysm formation by mediating inflammation, but whether it modulates neuroinflammation and brain injury has not | |||
TP1501 |
CTTHWGFTLC, CYCLIC
|
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This cyclic CTT Gelatinase Inhibitor peptide is an inhibitor for matrix metalloproteinases (MMP)-2 and MMP-9. It is also called type IV collagenase or gelatinase. Gelatinases are potential targets of therapeutic intervention in cancer, and inhibitors of t | |||
T36985 |
Cyclic di-UMP (sodium salt)
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Cyclic di-UMP is a pyrimidine-containing cyclic dinucleotide (CDN).1It is produced by bacterial cGAS/DncV-like nucleotidyltransferases (CD-NTases), such as LpCdnE02 fromL. pneumophila, and binds to cGAS, in the apo or dsDNA-bound forms, with reduced affinity compared to 2'3'-cGAMP or 3'3'-cGAMP .1,2Cyclic di-UMP is intended for use as a negative control for cyclic di-GMP signaling. 1.Whiteley, A.T., Eaglesham, J.B., de Oliveira Mann, C.C., et al.Bacterial cGAS-like enzymes synthesize diverse nuc... | |||
T36984 |
Cyclic di-IMP (sodium salt)
|
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Cyclic di-IMP (sodium salt) (c-di-IMP) is a synthetic second messenger structurally related to the bacterial second messengers cyclic di-GMP and cyclic di-AMP . C-di-IMP has adjuvant properties when co-administered with antigens in vitro and by mucosal routes in vivo. C-di-IMP enriches the population of MHC class I and II, CD80, CD86, CD40, and CD54 positive dendritic cells derived from murine bone marrow. It also stimulates macrophages at 500 ng/ml. Mice immunized with β-galactosidase (β-gal) p... | |||
T35424 |
8-bromo-Cyclic AMP
|
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8-bromo-Cyclic AMP is a brominated derivative of cAMP that remains long-acting due to its resistance to degradation by cAMP phosphodiesterase. It can activate cAMP-dependent protein kinase, inhibiting growth, decreasing proliferation, increasing differentiation, and inducing apoptosis of cancer cells. | |||
T35595 | Cyclic di-AMP (sodium salt) | ||
Cyclic di-AMP (c-di-AMP) is a second messenger produced by bacteria but not by mammals. Generated by a family of diadenylate cyclases, c-di-AMP can impact bacterial cell growth, cell wall homeostasis, pathogenicity, and other cellular functions. Bacteria-derived cyclic dinucleotides, including c-di-AMP, trigger the expression of interferon genes in mammalian cells. | |||
T64318 |
Capecitabine-2',3'-cyclic Carbonate
|
Others | Others |
Capecitabine-2',3'-cyclic Carbonate 是一种抗增殖化合物。 | |||
T37803 | 8-bromo-Cyclic ADP-Ribose (sodium salt) | ||
Cyclic ADP-ribose (cADP-ribose) is a calcium mobilizing nucleotide that is biosynthesized from NAD+ by cADP-ribose synthases, including CD38. cADP-Ribose appears to activate calcium channels in intracellular membranes, which in turn activate ryanodine receptors. 8-bromo-cADP-Ribose is a stable, cell-permeable analog that blocks calcium release evoked by cADP-ribose in sea urchin egg homogenates with an IC50 value of 1.7 μM. It is commonly used to investigate intracellular signaling through cADP-... | |||
T21697 |
Sp-Cyclic AMPS (sodium salt)
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Sp-cAMPS sodium salt 作为 cAMP 类似物,是一种依赖 cAMP 的PKA I 和PKA II 的有效激活剂。Sp-cAMPS sodium salt 还是一种有效的竞争性磷酸二酯酶 (PDE3A) 抑制剂,Ki 为 47.6 μM。Sp-cAMPS sodium salt 结合PDE10 GAF 结构域,EC50为 40 μM 。 | |||
T36677 |
Rp-8-bromo-Cyclic AMPS (sodium salt)
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Rp-8-bromo-Cyclic AMPS (Rp-8-bromo-cAMPS) is a cell-permeable cAMP analog that combines an exocyclic sulfur substitution in the equatorial position of the cyclophosphate ring with a bromine substitution in the adenine base of cAMP. It acts as an antagonist of cAMP-dependent protein kinases (PKAs) and is resistant to hydrolysis by cyclic nucleotide phosphodiesterases. Rp-8-bromo-cAMPS more effectively antagonizes cAMP-dependent activation of purified PKA type I from rabbit muscle than PKA type II... | |||
T60419 | Cyclic HPMPC | ||
Cyclic HPMPC 是有效的抗病毒剂,可以增加感染致死性牛痘苗病毒 (IHD 株) 小鼠的动脉氧饱和度水平。用 Cyclic HPMPC 治疗可改善先天性豚鼠巨细胞病毒 (GPCMV) 感染的结果并减少豚鼠模型中的病毒复制。 | |||
T21705 |
8-CPT-Cyclic AMP (sodium salt)
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8-CPT-Cyclic AMP (8-CPT-cAMP) sodium 是环 AMP 依赖性蛋白激酶的选择性激活剂。 8-CPT-Cyclic AMP sodium 也是有效的环 GMP 特异性磷酸二酯酶(PDE VA)抑制剂,IC50为 0.9 μM。 8-CPT-Cyclic AMP sodium 还抑制 PDE III 和 PDE IV,IC50分别为 24 和 25 μM。8-CPT-Cyclic AMP sodium 对 Epac 具有非常高的亲和力,是一种有效的Epac 活化剂。 | |||
T73362 |
C-di-IMP
Cyclic-di-IMP |
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C-di-IMP (Cyclic-di-IMP) 是一种STING 激动剂。C-di-IMP 可用于肿瘤的研究。 | |||
T10642 |
c-di-AMP
环二腺苷酸,Cyclic diadenylate,Cyclic-di-AMP |
Others | Others |
c-di-AMP (Cyclic diadenylate) is a STING agonist. It binds to the transmembrane protein STING thereby activating the TBK3-IRF3 signaling pathway. | |||
T78011 |
Cyclic MKEY TFA
|
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Cyclic MKEY TFA为CXCL4-CCL5异二聚体的合成环肽抑制剂,可通过调控炎症反应预防动脉粥样硬化和主动脉瘤。此外,该化合物亦能阻止小鼠中风后脑损伤的发生。 | |||
T76017 |
CTTHWGFTLC, CYCLIC TFA
|
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CTTHWGFTLC, CYCLIC TFA 是一种基质金属蛋白酶 MMP-2和MMP-9的环肽抑制剂。对MMP-9的IC50约为 8 μM。 | |||
T82645 |
Cyclic PSAP peptide
|
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Cyclic PSAP peptide(DWLPK)是一种环五肽,具有活性分子特性,在体内能够抑制肿瘤转移扩散和发展。 | |||
T76544 |
Cyclic SSTR agonist octreotide
|
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Cyclic SSTR agonist octreotide 是一种 Octreotide ,可作为生长抑素受体 (SSTR) 的激动剂。 | |||
T82760 |
C-di-IMP disodium
Cyclic-di-IMP disodium |
STING | Immunology/Inflammation |
C-di-IMP二钠是一种效果显著的STING激动剂,主要在肿瘤领域的研究中应用。 | |||
T13606 |
cGAMP
3',3'-cGAMP,Cyclic GMP-AMP |
Others | Others |
cGAMP is an endogenous second messenger in metazoans and triggers interferon production in response to cytosolic DNA. It also is a STING ligand. | |||
T10065 |
2',3'-cGAMP
2'-3'-cyclic GMP-AMP |
STING; cGAS | Immunology/Inflammation |
2',3'-cGAMP (2'-3'-cyclic GMP-AMP) 是细胞天然免疫中第二信使,在DNA结合条件下由 cGAMP 合成酶 (cGAS) 催化形成。2',3'-cGAMP 可与 STING 结合形成二聚体,诱导干扰素-β(IFN-β)及其他细胞因子的产生和表达。 | |||
T9213 |
G140
|
cGAS | Immunology/Inflammation |
G140 是选择性环状GMP-AMP 合酶抑制剂,具有抗炎活性,对 h-cGAS 和 m-cGAS 的IC50值分别为 14.0 和 442 nM。 | |||
T83402 |
2′,3′-cGMP triethylamine
Guanosine 2',3'-cyclic phosphate triethylamine |
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2',3'-cGMP triethylamine(Guanosine 2',3'-cyclic phosphate triethylamine)是一种活性化合物,常被用于多种科学研究领域。 | |||
T12432 |
PF-06928215
|
cGAS | Immunology/Inflammation |
PF-06928215 是高亲和力 cGAS 抑制剂,IC50为 4.9 μΜ,亲和力 Kd 值为 0.2 μΜ。 | |||
T5486 |
RU.521
RU320521 |
DNA; cGAS | DNA Damage/DNA Repair; Immunology/Inflammation |
RU.521 (RU3205217) 是选择性的环状 GMP-AMP 合成酶 (cGAS) 抑制剂,抑制 cGAS 介导的干扰素上调。它也抑制dsDNA 激活受体的活性,IC50为 700 nM。它可降低来自 Aicardi-Goutières 综合征小鼠模型的巨噬细胞中干扰素的组成型表达。 | |||
T11673 |
IRAK4-IN-4
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IRAK; cGAS | Immunology/Inflammation; NF-κB |
IRAK4-IN-4 (化合物 15) 是白介素-1 受体相关激酶抑制剂,IC50为 2.8 nM。它还抑制环 GMP-AM 合酶 ,IC50为 2.1 nM。 | |||
T11344 |
G150
|
DNA; cGAS | DNA Damage/DNA Repair; Immunology/Inflammation |
G150 是高选择性h-cGAS 抑制剂,IC50值为 10.2 nM,用于抑制 dsDNA 引发的干扰素表达。 | |||
T83671 |
CCP-biotin Peptide (non-cyclized)
Citrullinated Filaggrin (Q447H, S449C, G459R, E460G, S462C) (R455) (447-467)-biotin Peptide (non-cyclized),Cyclic Citrullinated Peptide-biotin Peptide (non-cyclized) |
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CCP-biotin Peptide(非环化)是一种生物素化且非环化的圆形瓜氨酸化肽(CCP)版本。该序列对应于人类filaggrin的447-467氨基酸,但包含Q447H、S449C、G459R、E460G和S462C的替换,并在455位的精氨酸处发生了瓜氨酸化。CCP-biotin Peptide(非环化)旨在用于检测可能与线性肽结合的抗瓜氨酸自身抗体。 | |||
T7511 |
Cyclo(his-pro)
|
NF-κB; Endogenous Metabolite | Metabolism; NF-κB |
Cyclo(his-pro) 是一种口服具有活力的,结构上与促甲状腺激素释放激素相关的环状二肽。它能够抑制NF-κB 核积累,也能够穿越脑血屏障并影响多种炎症和应激反应。 | |||
T2923 |
Apremilast
阿普斯特,CC-10004,阿普司特 |
Apoptosis; TNF; PDE | Apoptosis; Metabolism |
Apremilast (CC-10004) 是一种口服有效的磷酸二酯酶 4 抑制剂,IC50为 74 nM。它抑制脂多糖释放TNF-α,IC50为 104 nM。 | |||
T2535 |
Ivabradine hydrochloride
盐酸伊伐布雷定,S 16257-2,Ivabradine HCl |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Ivabradine hydrochloride (S 16257-2) 是一种可口服的,超极化激活的环核苷酸门控离子通道通道阻滞剂。 | |||
T2137 |
Ibudilast
AV-411,KC-404,MN-166,异丁司特 |
PDE | Metabolism |
Ibudilast (MN-166) 是一种环腺苷酸磷酸二酯酶 (PDE) 抑制剂,具有抗血小板聚集作用。它能够抑制气管平滑肌收缩性,可用于研究哮喘。它可对抗活化小胶质细胞的神经毒性,可能是一种有效的神经保护和抗痴呆药物。 | |||
T36678 |
Rp-8-CPT-cAMPS sodium
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Rp-8-CPT-cAMP is a structural combination of the lipophilic and non-hydrolyzable cAMP analogs, 8-CPT-cyclic AMP and Rp-cyclic AMPS .[1] It functions as a site-selective inhibitor of protein kinase A (PKA) type I and II, with preference towards site A of type I and site B of type II.2 By occupying cAMP binding sites at the regulatory subunit of PKA, Rp-8-CPT-cAMP prevents the kinase holoenzyme from dissociative activation.[2],[3] | |||
T9137 |
SN-011
[1,1'-Biphenyl]-4-carboxamide, N-[3-[[(4-fluorophenyl)sulfonyl]amino]-4-hydroxyphenyl]-,GUN35901 |
STING | Immunology/Inflammation |
SN-011 (GUN35901) 是选择性 STING 抑制剂,可与环状二核苷酸 (CDN) 竞争 STING 二聚体的结合口袋,从而阻断 CDN 结合和 STING 激活。它用于 STING 驱动的自身免疫和炎症性疾病的研究,抑制 STING 信号传导的 IC50值为 76 nM。 | |||
T35421 |
2'-O-Succinyl-cAMP
|
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2'-O-Monosuccinyladenosine-3',5'-cyclic monophosphate is an immunogenic derivative of cAMP that has been used to generate anti-cAMP antisera and antibodies.1,2 | |||
T7516 |
ZD7288
N-乙基-1,6-二氢-1,2-二甲基-6-(甲基亚氨基)-N-苯基-4-嘧啶胺盐酸盐,ICI D7288 |
HCN Channel | Membrane transporter/Ion channel |
ZD7288 (ICI D7288) 是一种选择性超极化激活的环核苷酸门控通道阻滞剂,可抑制海马突触可塑性。 | |||
T83937 |
Tricyclic cytosine tC
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Tricyclic cytosine tC 是一种用于在活细胞中成像 RNA 的荧光胞嘧啶类似物。当与共聚焦成像技术结合使用时,可用于研究单细胞分辨率下的 RNA 合成、降解和运输。激发/发射最大值 (λ) = 375/505 nm;消光系数 = 4000 M-1cm-1;量子产率 = 0.2。 | |||
T36330 |
Terrecyclic Acid
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Terrecyclic acid is a sesquiterpene originally isolated from A. terreus with antibiotic and anticancer activity. It is active against S. aureus, B. subtilis, and M. roseus (MICs = 25, 50, and 25 μg/ml, respectively). Terrecyclic acid induces a heat shock response, increases levels of reactive oxygen species (ROS), and inhibits NF-κB activity and cell growth in 3T3-Y9-B12 cells. In vivo, terrecyclic acid (0.1, 1, and 10 mg/ml) reduces the number of ascitic fluid tumor cells in a mouse model of P3... | |||
T36548 |
Carbocyclic Thromboxane A2
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Carbocyclic Thromboxane A2 可用于生命科学领域的相关研究。其产品编号为 T36548,CAS号为 74034-56-3。 | |||
T130205 | Dihydroterrecyclic acid | ||
Dihydroterrecyclic acid 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 T130205。 | |||
T6747 |
8-Bromo-cAMP sodium salt
8-Br-Camp sodium salt,8-溴腺苷-3',5'-环单磷酸钠,8-Bromo-cAMP(sodium salt),8-Bromo-cAMP |
PKA | Tyrosine Kinase/Adaptors |
8-Bromo-cAMP sodium salt (8-Br-Camp sodium salt) 是一种环 AMP 依赖性蛋白激酶 (PKA) 激活剂,是一种环 AMP 类似物。 | |||
T29038 |
KL8604166
UCB11056,UCB-11056,UCB 11056 |
Others | Others |
KL8604166(UCB-11056) 是一种潜在的益智化合物。UCB-11056 能扩大大鼠脑组织中诱导环 AMP 的形成。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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TCO2745 |
Cyclic AMP
Adenosine 3',5'-cyclophosphate,cAMP,腺苷环磷酸酯,环磷腺苷,Cyclic 3',5'-monophosphate adenosine,3',5'-AMP,Adenosine Cyclophosphate |
Others; Endogenous Metabolite | Metabolism; Others |
Cyclic AMP (cAMP)(Adenosine 3',5'-cyclophosphate) 是有丝分裂信使,可以促进 G1期到 S 期的细胞周期进程。 | |||
T5065 |
GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD
Monosodium-GMP,cGMP sodium salt,鸟苷-3',5'-环磷酸一钠盐,Cyclic GMP |
PKA | Tyrosine Kinase/Adaptors |
GUANOSINE 3':5'-CYCLIC MONOPHOSPHATE SOD (cGMP sodium salt) 也称为 cGMP,是一种细胞调节剂,被描述为第二信使。它的水平随着各种激素的增加而增加,包括乙酰胆碱、胰岛素和催产素。 cGMP 激活蛋白激酶 G(PKG) 并调节离子通道电导,信号传导影响多种过程,包括平滑肌松弛和增殖、光转导和能量稳态。 | |||
T10065L |
2',3'-cGAMP sodium
2'-3'-cyclic GMP-AMP sodium |
STING; cGAS | Immunology/Inflammation |
2',3'-cGAMP sodium (2'-3'-cyclic GMP-AMP sodium) 是一种cGAMP 合成酶(cGAS)影响细胞质DNA 产生的第二信使,是一种跨膜衔接蛋白,是细胞对致病性细胞质DNA 的先天免疫反应的关键组成部分。 | |||
T10909 |
Cyclic-di-GMP
c-di-GMP,cyclic diguanylate,5GP-5GP |
Others | Others |
Cyclic-di-GMP is a STING agonist and ubiquitous second messenger, which regulates the formation, motility and virulence of biofilms in various bacterial species. | |||
T72243 |
Cyclic-di-GMP diammonium
5GP-5GP diammonium,c-di-GMP diammonium ; cyclic diguanylate diammonium ; 5GP-5GP diammonium,c-di-GMP diammonium,cyclic diguanylate diammonium |
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Cyclic di-GMP (c-di-GMP) diammonium 是一种STING 激活剂和无处不在的第二信使,调节生物膜的形成、运动和各种细菌的毒力。 | |||
T37687 | Cyclic ADP-ribose ammonium | ||
Cyclic ADP-ribose ammonium (cADPR ammonium) is a powerful calcium mobilization second messenger synthesized from NAD+ by an ADP-ribosyl cyclase. It primarily raises cytosolic calcium levels through Ryanodine receptor-mediated release from the endoplasmic reticulum, while also facilitating extracellular influx through the opening of TRPM2 channels [1][2][3]. | |||
T19253 |
Cyclic ADP-ribose
cADPR |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Cyclic ADP-ribose (cADPR) is an effective calcium mobilization second messenger, which is synthesized from NAD + by ADP-ribosyl cyclase. Cyclic ADP-ribose mainly increases cytosolic calcium through Ryanodine receptor-mediated endoplasmic reticulum release | |||
T64248 | Cyclic-di-GMP sodium | ||
Cyclic di-GMP sodium (c-di-GMP sodium) 是一种 STING 激活剂,也是一种无处不在的第二信使,具有调节生物膜的形成、运动和各种细菌的毒力的作用。 | |||
T5671 |
Isophorone
|
Others | Others |
Isophorone 是一种可用作聚合物前体的 α,β-不饱和环状酮。 | |||
T4725 |
N-Acetyl-D-mannosamine
N-乙酰-D-甘露糖胺,2-ACETAMIDO-2-DEOXY-D-MANNOPYRANOSE HYDRATE |
Others; Endogenous Metabolite | Metabolism; Others |
N-Acetyl-D-mannosamine (2-ACETAMIDO-2-DEOXY-D-MANNOPYRANOSE HYDRATE) 是一种单糖,在糖脂和糖蛋白中发现的神经氨酸的化学或酶合成中用作前体。N-Acetyl-D-mannosamine 是合成细菌荚膜聚唾液酸(PA)必需前体n -乙酰神经氨酸的特异性底物。N-Acetyl-D-mannosamine 用于合成唾液酸。它也是许多碳水化合物衍生的生物活性化合物家族和候选药物的合成中间体。 | |||
T1083 |
Theophylline
Theo-24,1,3-Dimethylxanthine,茶碱 |
Endogenous Metabolite; HDAC; PDE; Adenosine Receptor; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; GPCR/G Protein; Metabolism; Neuroscience |
Theophylline (1,3-Dimethylxanthine) 是茶中的甲基黄嘌呤衍生物,具有利尿、平滑肌松弛、支气管扩张、心脏和中枢神经系统兴奋作用。 | |||
TN4510 |
(+)-Medioresinol Di-O-β-D-glucopyranoside
(+)-Mediresinol Di-O-beta-D-glucopyranoside,(+)-Medioresinol Di-O-β-D-glucopyranoside |
PDE | Metabolism |
(+)-Medioresinol Di-O-β-D-glucopyranoside 对环 AMP 磷酸二酯酶具有很强的抑制活性。 | |||
T1665 |
Daptomycin
达托霉素,LY146032 |
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Daptomycin (LY146032) 是脂肽类抗生素,在体外快速灭活革兰氏阳性细菌。 | |||
T13495 |
3-Amino-2-piperidinone
Cyclo-ornithine |
Endogenous Metabolite | Metabolism |
3-Amino-2-piperidinone 是来自生物体的代谢物,可用作环状鸟氨酸类似物。 | |||
TN7068 |
Sinomenine N-oxide
|
Others | Others |
Sinomenine N-oxide 是青藤碱循环代谢机制的主要代谢产物之一。 | |||
TN6444 |
Cyclo(Tyr-Leu)
|
Antifungal | Microbiology/Virology |
Cyclo(Tyr-Leu) 是一种来自马齿苋 Portulaca oleracea Linn 的环状二肽,具有细胞毒性、抗真菌和抗凝血活性。 | |||
T21518 |
Colistin methanesulfonate sodium salt
粘杆菌素甲基磺酸钠,Colistin Methanesulfonate (sodium salt) |
Cell wall; Antibacterial | Immunology/Inflammation; Microbiology/Virology |
Colistin methanesulfonate sodium salt (Colistimethate Sodium) 是一种来自 Bacillus colistinus 的环状多肽抗生素,由多粘菌素 E1 和 E2 组成。 | |||
T4805 |
α-Pyridone
2-Hydroxypyridine,2-羟基吡啶 |
Others; Endogenous Metabolite | Metabolism; Others |
α-Pyridone (2-Hydroxypyridine) 是内源性代谢产物的一种。 | |||
T1226 |
Bacitracin
Albac,Ziba-RX,杆菌肽 |
Antibacterial; Antibiotic | Microbiology/Virology |
Bacitracin (Ziba-RX) 是一种用于葡萄球菌感染的多肽抗生素。它通过与焦磷酸十一癸烯基结合,起抑制细胞壁生物合成作用。 | |||
T1441 |
Capreomycin sulfate
Capastat sulfate,硫酸卷曲霉素 |
ribosome; Antibacterial; Antibiotic | Microbiology/Virology |
Capreomycin sulfate (Capastat sulfate) 是一种多肽类抗生素,与其它抗生素结合用于MDR-肺结核。 | |||
T9267 |
Aureobasidin A
|
Others; Antifungal | Microbiology/Virology; Others |
Aureobasidin A 是一种环肽和抗真菌抗生素。它是肌醇磷酸神经酰胺合酶 AUR1 的抑制剂。 | |||
T1245 |
Colistin sulfate
Colistin sulfate (1066-17-7 free base),Polymixin E Sulfate,Polymyxin E Sulfate,硫酸粘杆菌素 |
Cell wall; Antibacterial; Antibiotic; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology |
Colistin sulfate (Colistin sulfate (1066-17-7 free base)) 是抑制革兰氏阴性细菌的一种多肽抗生素,与革兰氏阴性细菌的外细胞膜中的脂多糖和磷脂结合起作用。 | |||
T1679 |
Thiostrepton
Thiactin,Bryamycin,Alaninamide,硫链丝菌素 |
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Thiostrepton (Alaninamide) 是一种选择性抑制FOXM1的抗生素。FOXM1会与 YAP/TEAD 复合物结合,形成YAP/TEAD/FOXM1 复合物。 | |||
T6S0627 |
Mesaconitine
新乌碱,新乌头碱;中乌头碱 |
TNF | Apoptosis |
Mesaconitine 是乌头属植物的一种主要活性成分,通过循环 AMP 和刺激中枢 β-肾上腺素能系统具有镇痛活性,还有抗炎活性。 | |||
T4S0792 |
Pinoresinol 4-O-β-D-glucopyranoside
(+)-pinor,(+)-pinoresinol-β-D-glucoside; (+)-pinor,(+)-pinoresinol-β-D-glucoside |
Others | Others |
(+)-pinoresinol-β-D-glucoside; (+)-pinor 是连翘中主要的活性呋喃类木脂素。它显示出抗氧化、降血压和环磷酸腺苷 (cAMP) 磷酸二酯酶抑制活性。 | |||
T7933 |
D(+)-LACTIDE
|
Others | Others |
D(+)-LACTIDE 是丙酮的环状二聚体,用于合成各种药物和其他化合物,也可用于生物化学和生理学研究。 | |||
T0167 |
Vinpocetine
长春西丁,RGH-4405,长春西汀,Ethyl apovincaminate |
IκB/IKK; NF-κB; Sodium Channel; PDE | Membrane transporter/Ion channel; Metabolism; NF-κB |
Vinpocetine (RGH-4405) 是一种长春花生物碱衍生物,是阻断 Na+通道的阻断剂。Vinpocetine 抑制IKK 的IC50为 17.17 μM。Vinpocetine 也是PDE 抑制剂,并通过直接靶向IKK 抑制NF-κB 依赖性炎症反应,已被广泛用于研究脑血管疾病。 | |||
T2723 |
Ketoisophorone
茶香酮,4-Oxoisophorone,2,6,6-Trimethyl-2-cyclohexene-1,4-dione |
Others | Others |
Ketoisophorone (2,6,6-Trimethyl-2-cyclohexene-1,4-dione) 是工业上重要的环状内酯,是合成类胡萝卜素和调味剂的关键中间体。 | |||
T1130 |
Gramicidin
短杆菌肽,Gramicidinum,Gramicidine,Gramicidina |
MRP; Antibacterial; Antibiotic | Immunology/Inflammation; Microbiology/Virology |
Gramicidin (Gramicidine) 是一种抗菌肽。它通过组装成膜中的通道,增加其对阳离子的渗透性。 | |||
TN6900 |
Reptoside
|
Others | Others |
Reptoside 可从杜仲和 Ajuga chamaepitys (L.) Schreb 根部和地上部分中提取,是杜仲治疗骨质疏松症的活性环烯醚萜苷之一。 | |||
PDK0014 |
3-Methylxanthine
|
Endogenous Metabolite | Metabolism |
3-Methylxanthine 是一种黄嘌呤衍生物和环磷酸鸟苷(GMP)抑制剂,在豚鼠分离的气管肌肉中测得其IC50值为 920 μM。 | |||
T0945 |
Cyclosporin A
环孢素,Cyclosporine A,Ciclosporin,Cyclosporine,环孢菌素 |
Phosphatase; Antibiotic; Complement System | Immunology/Inflammation; Metabolism; Microbiology/Virology |
Cyclosporin A 属于天然产物,是一种真菌的活性代谢产物,一种环状多肽。Cyclosporin A 是一种能与亲环素结合的免疫抑制剂,可以抑制 calcineurin (IC50=7 nM)。 | |||
TP1072 |
Valinomycin
缬氨霉素,NSC 122023 |
Apoptosis; PTEN; Antibacterial; Antibiotic; Autophagy | Apoptosis; Autophagy; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Valinomycin (NSC-122023) 是钾离子选择性运输载体,是一种环状缩酚肽类抗生素。它通过影响生物膜抑制淋巴细胞的扩增,能诱导 CHO 细胞凋亡,也可诱导 PINK1 激活,促进 Parkin 在 Ser65 位点磷酸化。 | |||
T8787 |
Drotaverine hydrochloride
|
PDE | Metabolism |
Drotaverine hydrochloride 是磷酸二酯酶 4 (PDE4)的抑制剂,也是 L 型电压依赖钙通道(L-VDCC)的阻滞剂,可阻断3',5'-环腺苷单磷酸的降解。它在体内有抗痉挛效果,但无抗胆碱能的效果。 | |||
T0933 |
D-(+)-Glucono-1,5-lactone
Gluconic acid lactone,Delta-Gluconolactone,Gluconolactone,葡萄糖酸内酯 |
Others; Reactive Oxygen Species; Endogenous Metabolite | Immunology/Inflammation; Metabolism; NF-κB; Others |
D-(+)-Glucono-1,5-lactone (Gluconolactone) 是聚羟基酸,可螯合金属离子,具有保湿、抗氧化特性。 | |||
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。 | |||
T1009 |
Estrone
Oestrone,雌酮,Fluoroethyl,Aquacrine |
Estrogen Receptor/ERR; Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Estrone (Aquacrine) 是内源性雌激素的主要代表,由多种组织产生,尤其是脂肪组织。它是脂肪细胞中雄烯二酮芳构化过程的结果。 | |||
T3929 |
Kaurenoic acid
Kauren-19-Oic Acid,异贝壳杉烯酸,kaurenoate,kaur-16-en-18-oic acid |
Others | Others |
Kaurenoic acid (kaurenoate) 是一种二萜,来源于 Sphagneticola trilobata 中,可以抑制细胞因子的产生和激活 NO–cyclic GMP–PKG–ATP- 敏感型钾通道信号通路,并抑制炎症疼痛。 | |||
TN3013 |
4,5-Dimethoxycanthin-6-one
Methylnigakinone |
P450; Antibacterial; PDE | Metabolism; Microbiology/Virology |
4,5-Dimethoxycanthin-6-one 从 Picrasma quassioides BENNET (Simaroubaceae)是一种从 Picrasma quassioides BENNET (Simaroubaceae) 中分离得到生物碱。4,5-Dimethoxycanthin-6-one 是一种有效的、非竞争性的 CYP1A2 介导的 phenacetin O-deethylation 抑制剂(IC50 : 1.7 μM, Ki : 2.6 μM),对环磷酸腺苷(cAMP)磷酸二酯酶有很强的抑制作用。4,5-Dimethoxycanthin-6-one 具有抗菌活性,对金黄色葡萄球菌及其耐药菌株有抑制作用。4,5-Dimethoxycanthin-6-one 对肿瘤细胞株 U937 和 HepG2 具有细胞毒性。 | |||
T16397 |
Ophiobolin A
|
Others | Others |
Ophiobolin A is a fungal metabolite and a phytotoxin and is an effective and irreversibly inhibitor of calmodulin-activated cyclic nucleotide phosphodiesterase (IC50: 9 μM). Ophiobolin A also has antimicrobial and anticancer activity. | |||
T38650 |
Lyciumin B
|
||
Lyciumin B is a cyclic peptide isolated from Lysium chinense. | |||
T31141 | Cyclotheonamide A | ||
Cyclotheonamide A is a cyclic peptide isolated from the marine sponge Theonella. | |||
T21098 |
Decamethylcyclopentasiloxane
Dekamethylcyklopentasiloxan,Cyclopentasiloxane, decamethyl- |
||
Decamethylcyclopentasiloxane is a cyclic methylsiloxane with volatile properties. | |||
TN6447 | Cyclo(Leu-Val) | ||
Cyclo(Leu-Val) is a cyclic dipeptide from the fermentation broth of F8712 strain. | |||
T39649 | ε-Amanitin | ||
ε-Amanitin is a cyclic peptide obtained from various mushroom species. It exhibits a strong affinity for RNA polymerase II and effectively inhibits its activity. | |||
T37876 | Fengycin | ||
Fengycin is a cyclic lipopeptide used as an agricultural fungicide. Fengmycin has an anti-fungal infection effect by damaging the target’s cell membrane[1]. [1]. Sreyoshi Sur, et al. Selectivity and Mechanism of Fengycin, an Antimicrobial Lipopeptide, from Molecular Dynamics. J Phys Chem B. 2018 Mar 1;122(8):2219-2226. | |||
T68351 | Homodestcardin | ||
Homodestcardin is a cyclic depsipeptide fungal metabolite that has been found in T. roseum and has immunosuppressant activity. It inhibits concanavalin A-induced proliferation of isolated mouse T cells. | |||
T38649 | Lyciumin A | ||
Lyciumin A, a cyclic octapeptide, possesses inhibitory properties against proteases, renin, and angiotensin-converting enzyme. It holds potential for hypertension research. | |||
T38415 | Adenosine 5′-monophosphoramidate sodium | ||
Adenosine 5′-monophosphoramidate sodium is a derivative of adenosine used as an intermediate for nucleotide synthesis. It significantly influences the accumulation of cyclic AMP. | |||
T12448 |
Phomopsin A
|
Others | Others |
Phomopsin A is a cyclic hexapeptide mycotoxin isolated from the fungus Phomopsis leptostomiformis. | |||
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