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19
Cat. No. | Product Name | Target | Signaling Pathways |
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TP1931L1 |
[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate
[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate(96736-12-8 free base) |
cholecystokinin | GPCR/G Protein |
[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate ([D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate (96736-12-8 free base)) 是广谱神经肽反向激动剂和拮抗剂。 ghrelin 受体的强效完全反向激动剂(EC50 = 5.2 nM);减少组成型生长素释放肽受体信号传导。它也是速激肽、缓激肽、CCK 和铃蟾肽受体的拮抗剂。在体外诱导细胞凋亡并抑制癌细胞生长。 | |||
T37436 |
C12-Ceramide
N-Laurylsphingosine,C12 Ceramide (d18:1/12:0),N-Lauroyl-D-erythro-sphingosine |
||
C12-Ceramide (C12 Ceramide (d18:1/12:0)) 是一种存在于先兆子痫妇女所生婴儿围绕脐带血管的保护膜的神经酰胺,是 C12 鞘磷脂被酸性鞘磷脂酶(ASM)水解后形成的,可用于评估 A 型或 B 型尼曼-皮克病患者血浆中的 ASM 活性水平。 | |||
T9691L |
(D-Trp12,Tyr34)-pTH (7-34) amide (bovine) acetate
|
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
(D-Trp12,Tyr34)-pTH (7-34) amide (bovine) acetate 是一种高效的甲状旁腺激素 (PTH) 拮抗剂,在牛肾皮质膜中的 Ki 值为 69 nM。 | |||
TP2239L |
[D-Phe12]-Bombesin acetate
[D-Phe12]-Bombesin acetate(108437-87-2 free base) |
Bombesin Receptor | GPCR/G Protein |
[D-Phe12]-Bombesin acetate 抑制铃蟾素刺激的分泌。 | |||
TP1916L1 |
[D-Phe12,Leu14]-Bombesin acetate
[D-Phe12,Leu14]-Bombesin acetate(108437-88-3 Free base) |
Bombesin Receptor | GPCR/G Protein |
[D-Phe12,Leu14]-Bombesin acetate 抑制铃蟾素刺激的分泌。 | |||
T10458 |
Banoxantrone (D12)
Banoxantrone D12,AQ4N D12 |
Others | Others |
Banoxantrone D12 (AQ4N D12) is the deuterium-labeled Banoxantrone. Banoxantrone is a bioreductive agent that can be reduced to a stable, DNA-affinity compound AQ4, which is a topoisomerase II inhibitor. | |||
TP2239 |
[D-Phe12]-Bombesin
|
Others | Others |
Bombesin receptor antagonist | |||
TP1916 |
[D-Phe12,Leu14]-Bombesin
|
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Bombesin receptor antagonist that inhibits bombesin binding to rat brain with an IC50 value of 2 μM. Inhibits amylase release in vitro (IC50 = 4 μM) and attenuates bombesin-mediated suppression of food intake in vivo. | |||
T24046 |
WNK-IN-11-d3
WNK inhibitor-12,WNKIN12,WNK IN 12,WNK inhibitor 12,WNK-IN-12 |
||
WNK-IN-12 is an effective, selective, and orally active WNK1 kinase inhibitor. | |||
T9691 |
(D-Trp12,Tyr34)-pTH (7-34) amide (bovine)
|
||
(D-Trp12,Tyr34)-pTH (7-34) amide (bovine) 在生命科学相关研究中具有广泛的应用。 | |||
T13185 |
Topiramate D12
RWJ 17021 D12,McN 4853 D12 |
Others | Others |
Topiramate D12 is a deuterium labeled Topiramate. Topiramate is an agent of broad-spectrum antiepileptic. Topiramate is an antagonist of GluR5 receptor. | |||
T19201 |
Banoxantrone-d12 dihydrochloride
AQ4N D12 dihydrochloride |
Others | Others |
Banoxantrone D12 (AQ4N D12) dihydrochloride is the deuterium-labeled Banoxantrone. Banoxantrone is a bioreductive agent that can be reduced to a stable, DNA-affinity compound AQ4, which is a topoisomerase II inhibitor. | |||
T76612 |
(D-Phe5,Cys6,11,N-Me-D-Trp8)-Somatostatin-14 (5-12) amide
|
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(D-Phe5,Cys6,11,N-Me-D-Trp8)-Somatostatin-14 (5-12) amide (Compound 4) 是一种生长抑素类似物,对 SSTR5、SSTR3、SSTR2、SSTR1和 SSTR4的Kd 分别为 0.61、11.05、23.5、1200 和 >1000 nM。 | |||
T76602 |
(D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat)
|
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(D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat) 作为一种CRF拮抗剂,能有效阻断IL-1a诱发的黄体生成素 (LH) 抑制作用。 | |||
T36648 |
Tucatinib hemiethanolate
|
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Tucatinib (Irbinitinib) hemiethanolate is a potent, orally active and selective HER2 inhibitor with an IC50 of 8 nM. Tucatinib hemiethanolate has nanomolar activity against purified HER2 enzyme and is approximately 500-fold selective for HER2 versus EGFR in cell-based assays. Tucatinib selectively inhibits the receptor tyrosine kinase HER2 relative to EGFR[1].Tucatinib blocks proliferation and the phosphorylation of HER2 and its downstream effector, Akt in HER2 overexpressing cell lines. In the ... | |||
T35689 |
MTP 131 acetate
|
Others | Others |
MTP 131 acetate 是一种小的线粒体靶向四肽。 | |||
T64916 |
D(-)-Norvaline
|
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D(-)-Norvaline 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 T64916,CAS号为 2013-12-9。 | |||
T66872 |
(tert-Butoxycarbonyl)-D-cysteine
|
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(tert-Butoxycarbonyl)-D-cysteine 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 T66872,CAS号为 149270-12-2。 | |||
T65254 |
N2-(tert-Butoxycarbonyl)-Nw-nitro-D-arginine
|
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N2-(tert-Butoxycarbonyl)-Nw-nitro-D-arginine 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 T65254,CAS号为 50913-12-7。 | |||
T66686 |
n-Heptyl β-D-glucopyranoside
|
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n-Heptyl β-D-glucopyranoside 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 T66686,CAS号为 78617-12-6。 | |||
T65722 |
N-Boc-cis-4-Hydroxy-D-proline
|
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N-Boc-cis-4-Hydroxy-D-proline 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 T65722,CAS号为 135042-12-5。 | |||
T66743 | Boc-4-tert-butyl-D-Phe-OH | ||
Boc-4-tert-butyl-D-Phe-OH 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 T66743,CAS号为 250611-12-2。 | |||
TF0087 |
n-Tridecyl-β-D-Maltopyranoside
|
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n-Tridecyl-β-D-Maltopyranoside 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 TF0087,CAS号为 93911-12-7。 | |||
T37010 |
D-threo Sphinganine (d18:0)
D-threo Sphinganine (d18:0) |
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D-threo Sphinganine (d18:0) is a synthetic bioactive sphingolipid and stereoisomer of sphinganine (d18:0) and L-erythro sphinganine (d18:0) . It induces autophagy in HCT116 cells when used at a concentration of 12 μM. D-threo Sphinganine (d18:0) is metabolized via sphinganine N-acyltransferase and sphinganine kinase in vivo in rat liver. | |||
T66382 |
1-((2'-Carboxy-[1,1'-biphenyl]-4-yl)methyl)-4-methyl-2-propyl-1H-benzo[d]imidazole-6-carboxylic acid
|
||
1-((2'-Carboxy-[1,1'-biphenyl]-4-yl)methyl)-4-methyl-2-propyl-1H-benzo[d]imidazole-6-carboxylic 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 T66382,CAS号为 884330-12-5。 | |||
T11269 |
FD-IN-1
|
Others | Others |
FD-IN-1 is a factor D (FD) inhibitor with an IC50 of 12 nM.FD-IN-1 also inhibits factor XIa (FXIa) and Tryptase β2 with IC50s of 7.7 and 6.5μM, respectively. Complement FD, a highly specific S1 serine protease, plays a central role in the alternative complement pathway of the innate immune system. | |||
T37565 |
C6 D-threo Ceramide (d18:1/6:0)
C6 D-threo Ceramide (d18:1/6:0) |
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C6 D-threo Ceramide is a bioactive sphingolipid and cell-permeable analog of naturally occurring ceramides., C6 D-threo Ceramide is cytotoxic to U937 cells in vitro (IC50 = 18 μM). It is metabolically inactive and, unlike C6 L-erythro ceramide , C6 D-threo ceramide cannot be converted to C6 glucosylceramide by ceramide glucosyltransferase. C6 D-threo Ceramide promotes survival of isolated rat spinal neurons when used at concentrations up to 2.5 μM but induces cell death at concentrations greater... | |||
T78508 |
Delmitide acetate
RDP-58 acetate |
IFNAR | Immunology/Inflammation |
Delmitide acetate (RDP58) 是一种 d-异构体十肽,具有抗炎活性和口服活性。该化合物能够抑制 TNF-α、IFN-γ 以及白细胞介素 (IL)-12 的生成,同时提高血红素加氧酶 1 的活性,可用于针对溃疡性结肠炎的研究。 | |||
T81451 |
PKCd (8-17)
|
||
PKCd (8-17) 是源自蛋白激酶 C (PKC)d V1 结构域的生物活性肽。它能抑制由佛波醇 12-肉豆蔻酸酯 13-乙酸酯 (PMA) 诱导的 PKCd 易位和激活。此外,PKCd (8-17) 在降低心脏和脑细胞缺血损伤、促进成纤维细胞增殖、以及抑制小鼠移植冠状动脉疾病方面具有潜在应用。 | |||
T35683 |
2-deoxy-D-Glucose-13C6
2-deoxy-D-Glucose-13C6 |
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2-deoxy-D-Glucose-13C6is intended for use as an internal standard for the quantification of 2-deoxy-D-glucose by GC- or LC-MS. 2-deoxy-D-Glucose is a glucose antimetabolite and an inhibitor of glycolysis.1,2It inhibits hexokinase, the enzyme that converts glucose to glucose-6-phosphate, as well as phosphoglucose isomerase, the enzyme that converts glucose-6-phosphate to fructose-6-phosphate.32-deoxy-D-Glucose (16 mM) induces apoptosis in SK-BR-3 cells, as well as inhibits the growth of 143B oste... | |||
T37540 |
Amycolatopsin B
|
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Amycolatopsin B is a bacterial metabolite originally isolated fromAmycolatopsisthat has anticancer activity.1It is cytotoxic to NCI H460 lung and SW620 colon cancer cells (IC50s = 0.28 and 0.14 μM, respectively). 1.Khalil, Z.G., Salim, A.A., Vuong, D., et al.Amycolatopsins A-C: Antimycobacterial glycosylated polyketide macrolides from the Australian soil Amycolatopsis sp. MST-108494J. Antibiot. (Tokyo)70(12)1097-1103(2017) | |||
T35560 |
SAR502250
|
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SAR502250 is a potent, selective, ATP competitive, orally active and brain-penetrant inhibitor of GSK3, with an IC50 of 12 nM for human GSK-3β. SAR502250 displays antidepressant-like activity. SAR502250 can be used for the research of Alzheimer’s disease (AD)[1][2]. SAR502250 (0.01-1 μM; 36 h) attenuates the Aβ25-35-induced cell death in rat embryonic hippocampal neurons[2]. SAR502250 (1-100 mg/kg; a single p.o,) attenuates tau hyperphosphorylation in the cortex and spinal cord of transgenic mic... | |||
T35840 | 4-Amino-6-chloro-1,3-benzenedisulfonamide | ||
4-Amino-6-chloro-1,3-benzenedisulfonamide is a carbonic anhydrase inhibitor.1 Formulations containing this compound are diuretics.2 4-Amino-6-chloro-1,3-benzenedisulfonamide is detected as a hydrolysis product of chlorothiazide in the urine.2 Diuretics, including chlorothiazide, have been abused as performance-enhancing drugs and masking agents in sports doping.3References1. Nishimori, I., Vullo, D., Minakuchi, T., et al. Carbonic anhydrase inhibitors: Cloning and sulfonamide inhibition studies ... | |||
T37541 |
Amycolatopsin C
|
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Amycolatopsin C is a polyketide macrolide originally isolated fromAmycolatopsisthat has antimycobacterial and anticancer activities.1It is active againstM. bovisandM. tuberculosis(IC50s = 2.7 and 5.7 μM, respectively) but notB. subtilis,S. aureus,E. coli, orP. aeruginosa(IC50s = >30 μM for all). Amycolatopsin C is cytotoxic to SW620 colorectal and NCI H460 lung cancer cells (IC50s = 10 and 5.9 μM, respectively). 1.Khalil, Z.G., Salim, A.A., Vuong, D., et al.Amycolatopsins A-C: Antimycobacterial ... | |||
T37539 |
Amycolatopsin A
|
||
Amycolatopsin A is a macrolide polyketide originally isolated fromAmycolatopsisthat has antimycobacterial and anticancer activities.1It is active againstM. bovisandM. tuberculosis(IC50s = 0.4 and 4.4 μM, respectively) but notB. subtilis,S. aureus,E. coli, orP. aeruginosa(IC50s = >30 μM for all). Amycolatopsin A is cytotoxic to SW620 colorectal and NCI H460 lung cancer cells (IC50s = 0.08 and 1.2 μM, respectively). 1.Khalil, Z.G., Salim, A.A., Vuong, D., et al.Amycolatopsins A-C: Antimycobacteria... | |||
T35519 |
Aflatoxin B2-13C17
Aflatoxin B2-13C17 |
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Aflatoxin B2-13C17(AFB2-13C17) is intended for use as an internal standard for the quantification of AFB2by GC- or LC-MS. AFB2is a mycotoxin that has been found inA. terricola.1It induces hepatic autophagy and apoptosis in broiler chickens when administered at doses of 0.2, 0.4, and 0.8 mg/kg.2AFB2(0.5 and 1 mg/animal) also induces parenchymal cell hyperplasia in rats.3 1.Moubasher, A.H., el-Kady, I.A., and Shoriet, A.Toxigenic Aspergilli isolated from different sources in EgyptAnn. Nutr. Alimen... | |||
T38286 |
C26 Sphingomyelin (d18:1/26:0)
C26 Sphingomyelin (d18:1/26:0) |
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C26 Sphingomyelin is a sphingolipid that has been found in serum and cell or brain extracts.1,2,3C26 sphingomyelin levels are increased in the serum of patients with hemophagocytic lymphohistiocytosis, an inflammatory condition characterized by excessive immune activation.3C26 sphingomyelin has been used a component of monolayers to study the influence of sphingomyelin acyl chain length on sphingomyelin-sterol interactions.4[Matreya, LLC.] 1.Wang, J.-R., Zhang, H., Yau, L.D., et al.Improved sphi... | |||
T36215 |
17R(18S)-EpETE
|
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17R(18S)-EpETE is an oxylipin and a cytochrome P450 metabolite of eicosapentaenoic acid .1,217R(18S)-EpETE is an activator of large-conductance calcium-activated potassium (BKCa) channels, increasing the potassium current amplitude by 15-fold in isolated rat cerebral artery vascular smooth muscle cells (VSMCs) at +60 mV when used at a concentration of 50 nM.2It has negative chronotropic effects in isolated neonatal rat cardiomyocytes (NRCMs; EC50= ~1-2 nM) and prevents calcium-induced increases ... | |||
T37847 |
Zonisamide-13C2,15N
Zonisamide-13C2,15N |
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Zonisamide-13C2,15N is intended for use as an internal standard for the quantification of zonisamide by GC- or LC-MS. Zonisamide is an antiepileptic agent.1 It selectively inhibits the repeated firing of sodium channels (IC50 = 2 μg/ml) in mouse embryo spinal cord neurons and inhibits spontaneous channel firing when used at concentrations greater than 10 μg/ml.2 In rat cerebral cortex neurons, zonisamide (1-1,000 μM) inhibits T-type calcium channels with a maximum reduction of 60% of the calcium... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TN5897 |
12-O-Methylinophyllum D
|
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12-O-Methylinophyllum D 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5897,CAS号为 40883-10-1。 | |||
TN1187 |
12-Hydroxyganoderic acid D
12-羟基灵芝酸 D,12-羟基灵芝酸D |
Others | Others |
12-Hydroxyganoderic acid D is a natural product | |||
TN6719 |
Kaempferol-3-O-β-D-glucosyl(1-2)rhamnoside
|
Others | Others |
Kaempferol-3-O-β-D-glucosyl(1-2)rhamnoside 是一种从阿拉伯茉莉中分离出来的天然产物。 | |||
TN6493 | 19-O-beta-D-carboxyglucopyranosyl-12-O-beta-D-glucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene | ||
19-O-beta-D-carboxyglucopyranosyl-12-O-beta-D-glucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene是一种天然产物,属于松科松属,其产品编号为 TN6493,CAS号为 1011714-20-7。19-O-beta-D-carboxyglucopyranosyl-12-O-beta-D-glucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene可用作对照参考。 | |||
TN6776 |
Cyaonoside B
Cyaonoside B,川牛膝皂苷B |
Others | Others |
Cyaonoside B 是一种皂苷,有一个葡萄糖醛酸连接到碳 C-3,能够从单胞菌中分离。 | |||
TN6734 |
Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnoside
Quercetin 3-O-beta-D-glucosyl-(1->2)-rhamnoside,槲皮素-3-O-葡萄糖基-(1-2)-L-鼠李糖苷,槲皮素 3-O-葡萄糖基 (1→2)鼠李糖苷 |
Others | Others |
Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnoside (Quercetin 3-O-beta-D-glucosyl-(1->2)-rhamnoside) 是 Shuxuenin 中的一种主要抗氧化剂。 | |||
TN4607 |
Myricetin 3-O-beta-D-xylopyranosyl(1-2)-beta-D-glucopyranoside
|
Others | Others |
Myricetin 3-O-beta-D-xylopyranosyl(1-2)-beta-D-glucopyranoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4607,CAS号为 142449-93-2。 | |||
T83579 |
(12β)-20-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-3-one
|
||
(12β)-20-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-3-one为cladosporium微生物[1]中发现的天然化合物。 | |||
T3889 |
Platycodin D
|
Prostaglandin Receptor; AMPK | Chromatin/Epigenetic; GPCR/G Protein; Immunology/Inflammation; PI3K/Akt/mTOR signaling |
Platycodin D 是从桔梗中分离得到的一种皂苷类天然产物,是AMPKα的激活剂,具有抗肥胖活性。它可刺激 TNF-α 合成或抑制 TNF-α mRNA 的降解。 | |||
T36914 |
2-Hydroxyanthraquinone
|
Others | Others |
2-Hydroxyanthraquinone 是一种天然产物,显示出抗肿瘤和免疫抑制活性。 | |||
TN4216 |
Hispidulin 4'-O-β-D-glucopyranoside
Hispidulin 4'-O-beta-D-glucopyranoside |
Others | Others |
Hispidulin 4'-O-β-D-glucopyranoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4216,CAS号为 244285-12-9。 | |||
TN4052 |
Farrerol 7-O-β-D-glucopyranoside
Farrerol 7-O-glucoside |
Others | Others |
Farrerol 7-O-β-D-glucopyranoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4052,CAS号为 885044-12-2。 | |||
TN5753 |
Benzyl β-D-glucopyranoside
苄基-β-D-葡萄糖苷,Benzyl glucoside |
||
Benzyl β-D-glucopyranoside 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN5753,CAS号为 4304-12-5。 | |||
T72172 |
4,6-O-Ethylidene-α-D-glucose
Ethylidene-glucose |
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4,6-O-ethylidene-α-D-glucose (Ethylidene-glucose) 是一种葡萄糖衍生物,是竞争性的葡萄糖转运蛋白 1 (GLUT1) 面部结合部位抑制剂,对野生型 2-脱氧-D-葡萄糖转运的 Ki 值为 12 mM。 | |||
T19329 |
Fructo-oligosaccharide DP12/GF11
蔗果十二糖 |
Others | Others |
Fructo-oligosaccharide DP12/GF11 is a member of fructooligosaccharides (FOS) characterized by a degree of polymerization (DP) of 12. FOS compounds consist of 11 fructose units connected by (2→1)-β-glycosidic bonds, with a lone D-glucosyl unit located at the non-reducing end. | |||
T75567 | Cabenoside D | ||
Cabenoside D(化合物 8)是从苔藓根的甲醇提取物中分离的一种三萜苷,显示出对12-O-十四烷酰基激素-13-乙酸酯(TPA)诱导的小鼠炎症的抗炎活性,并能抑制TPA促使的Epstein-Barr病毒(EBV)早期抗原(EBV-EA)激活。 | |||
TN4683 |
Nyasol
|
ERK; IL Receptor; IκB/IKK; NOS; NF-κB; Akt; Antifection | Cytoskeletal Signaling; Immunology/Inflammation; MAPK; Microbiology/Virology; NF-κB; PI3K/Akt/mTOR signaling |
Nyasol may have potential to be developed as medicines for the treatment of allergies by inhibiting the activation of mast cells. Nyasol shows anti-inflammatory properties by inhibiting iNOS expression; it also has antifungal activity, it is significantly | |||
T37272 |
9(S),12(S),13(S)-TriHOME
|
||
9(S),12(S),13(S)-TriHOME is a linoleic acid-derived oxylipin that has diverse biological activities.1,2,3,4It has been found in various plants and is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble epoxide hydrolase-independent manner.1,59(S),12(S)13(S)-TriHOME inhibits antigen-induced β-hexosaminidase release from RBL-2H3 mast cells (IC50= 28.7 μg/ml).2It inhibits LPS-induced nitric oxide (NO) production in BV-2 microglia (IC50= 40.95 μM).3In vivo, 9(S),12(S),13(S)-TriHOME... | |||
T36954 |
Nemorosone
|
||
Nemorosone is a polycyclic polyprenylated acylphloroglucinol (PPAP) originally isolated from C. rosea that has antiproliferative properties.1 Nemorosone inhibits growth of NB69, Kelly, SK-N-AS, and LAN-1 neuroblastoma cells (IC50s = 3.1-6.3 μM), including several drug-resistant clones, but not MRC-5 human embryonic fibroblasts (IC50 = >40 μM).2 It increases DNA fragmentation in LAN-1 cells in a dose-dependent manner, and decreases N-Myc protein levels and phosphorylation of ERK1/2 by MEK1/2. Nem... |