129
24
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37704 |
Olanzapine Lactam Impurity
|
||
Olanzapine lactam impurity is a potential impurity found in commercial preparations of olanzapine.1It is a degradation product formed by exposure to thermal or oxidative stress. 1.Baertschi, S.W., Brunner, H., Bunnell, C.A., et al.Isolation, identification, and synthesis of two oxidative degradation products of olanzapine (LY170053) in solid oral formulationsJ. Pharm. Sci.97(2)883-892(2008) | |||
T36053 |
D-Lysine lactam
|
||
D-Lysine lactam is a chiral building block.1,2It has been used in the synthesis of a chiral antibiotic synthetic intermediate, as well as in the stereoselective synthesis of neurokinin (NK) receptor antagonists. 1.Kumar, A., Bhashkar, B., Bhavsar, J., et al.Catalytic reduction: Efficient synthesis of chiral key intermediate of besifloxacin hydrochlorideDer Pharma Chemica7(9)297-3000(2015) 2.Gerspacher, M., Lewis, C., Ball, H.A., et al.Stereoselective preparation of N-[(R,R)-(E)-1-(3,4-dichlorobe... | |||
T36422 |
L-Lysine lactam (hydrochloride)
|
||
L-lysine lactam is a building block.1,2It has been used in the synthesis of lysine sulfonamide HIV protease inhibitors, as well as bengamide derivatives within vitroanticancer activity. | |||
T34138 |
Prolyldiketopiperazine B
Homoleucyl-D-proline lactam, L-,L-Homoleucyl-D-proline lactam |
||
Prolyldiketopiperazine B is a proline-based diketopiperazine. | |||
T68462 |
D-Ornithine lactam
|
||
D-Ornithine lactam is a building block. It has been used in the synthesis of hepatitis C virus non-structural protein 5B inhibitors, as well as αVβ3 integrin receptor antagonists. | |||
T71831 |
L-Ornithine lactam hydrochloride
|
||
L-Ornithine lactam is a synthetic intermediate. It has been used in the synthesis of dipeptidyl peptidase 4 (DPP-4) inhibitors, as well as signaling peptides. | |||
T8866 |
GW779439X
|
Apoptosis; Antibacterial; CDK; Aurora Kinase | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Microbiology/Virology |
GW779439X 属于吡唑并吡啶类,是一种金黄色葡萄球菌 PASTA 激酶 Stk1抑制剂。它是一种AURKA 抑制剂,可通过 caspases 3/7 诱导细胞凋亡。 | |||
T8507 |
MAC-545496
|
Antibacterial | Microbiology/Virology |
MAC-545496 是一种抗毒剂,可逆转耐甲氧西林的菌株中的 β-内酰胺耐药性。它是糖肽抗性相关蛋白 R 的纳摩尔抑制剂,对全长 GraR 蛋白具有很强的结合亲和力。 | |||
T60050 |
ANT3310
|
Antibacterial | Microbiology/Virology |
ANT3310 是一种广谱共价丝氨酸 β-内酰胺酶抑制剂,对 AmpC、CTX-M-15、TEM-1、OXA-48、OXA-23 和 KPC-2 的 IC50 范围为 1 nM 至 175 nM。 ANT3310 可用于细菌感染研究。 | |||
T14979 |
Clavulanate lithium
Clavulanic acid lithium,克拉维酸锂 |
Antibacterial | Microbiology/Virology |
Clavulanate lithium (Clavulanic acid lithium) 是一种β-lactamase 的高效抑制剂,可作抗生素。 | |||
T4405 |
Ceftibuten dihydrate
头孢布烯二水合物,Sch-39720 dihydrate |
Antibacterial; Antibiotic | Microbiology/Virology |
Ceftibuten dihydrate (Sch-39720 dihydrate) 是一种具有口服活性的头孢菌素,在体外对多种革兰氏阴性和某些革兰氏阳性病原体有抗菌活性。 | |||
T0234 |
Methicillin sodium salt
Methicillin sodium,Meticillin sodium,甲氧西林钠 |
Antibacterial; Antibiotic | Microbiology/Virology |
Methicillin sodium salt 是β-内酰胺抗生素,抑制参与肽聚糖合成的青霉素结合蛋白。 | |||
T6438 |
Cefoselis Sulfate
FK 037 Sulfate,FK-037,硫酸头孢噻利 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefoselis Sulfate (FK 037 Sulfate) 是一种头孢菌素 β-内酰胺抗生素。它对多种革兰氏阳性和革兰氏阴性生物均表现出良好的活性。它可以透过血脑屏障。 | |||
T6471 |
Dicloxacillin Sodium
Veracillin,双氯西林,BRL1702 Sodium,BRL1702,Sodium dicloxacillin,双氯西林钠 |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Dicloxacillin Sodium (BRL1702 Sodium) 是一种青霉素类窄谱β内酰胺抗生素, 用于革兰氏阳性菌感染的研究。它对β-内酰胺酶产生的微生物有抗菌作用。 | |||
T38476 |
Metallo β-lactamase ligand 1
|
Antibacterial | Microbiology/Virology |
Metallo β-lactamase ligand 1 是B 类β-内酰胺酶的抑制剂,具有抗菌活性。 | |||
T35427 |
β-Lactamase-IN-2
|
Antibacterial | Microbiology/Virology |
β-Lactamase-IN-2 是 β-内酰胺酶的有效抑制剂。β-Lactamase-IN-2显示出抗菌活性。 | |||
T6179 |
Moxalactam sodium salt
Latamoxef sodium,6059 S,拉氧头孢钠,Moxalactam Disodium,LY-127935,Antibiotic 6059S,Shiomarin,FestamoxinLy |
Antibacterial; Antibiotic | Microbiology/Virology |
Moxalactam sodium salt (LY-127935) 是一种抗生素, 对大肠杆菌和绿脓杆菌有作用。 | |||
T20386 |
Caprolactam
|
Others | Others |
Caprolactam 是一种用于制造聚酰胺类合成纤维的天然产物。 | |||
T19206 |
β-Lactamase-IN-1
4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one,beta-lactamase-IN-1 |
Antibacterial | Microbiology/Virology |
β-Lactamase-IN-1 (4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one) 是一种 β-Lactamase 抑制剂,针对淋病奈瑟菌的感染。 | |||
T60282 |
Metallo-β-lactamase-IN-3
|
||
Metallo-β-lactamase-IN-3 (compound 35) 是一种有效的金属 -β- 内酰胺酶 (MBL) 抑制剂,具有恢复现有 β-内酰胺类抗生素活性的潜力并为新抗生素的发现提供正交策略。Metallo-β-lactamase-IN-3 对 VIM-1和 NDM-1的活性较高,其 IC50值分别为 0.6 和 1.0 μM。Metallo-β-lactamase-IN-3 对 IMP-7 无抑制作用。 | |||
T60239 | Metallo-β-lactamase-IN-6 | ||
Metallo-β-lactamase-IN-6 is a highly effective inhibitor of VIM-Type metallo-β-lactamase, demonstrating IC 50 values of 0.56 μM, 29.50 μM, and 5.78 μM for VIM-2, VIM-1, and VIM-5, respectively. In addition, Metallo-β-lactamase-IN-6 exhibits potent synergistic antibacterial properties when combined with Meropenem, particularly against engineered Escherichia coli strains and clinically isolated Pseudomonas aeruginosa carrying the VIM-2 MBL gene [1]. | |||
T79435 |
Metallo-β-lactamase-IN-11
|
||
Metallo-β-lactamase-IN-11(化合物5f)是一种针对Metallo-β-lactamases(MBLs)的抑制剂,对CphA表现出较强的抑制活性(IC50=45 µM)。在10 µM浓度下,能分别抑制49%的NDM-1和61%的AIM-1。此化合物对于研究针对抗生素耐药性的策略具有潜在应用价值。 | |||
T125605 |
Aburatubolactam A
|
||
Aburatubolactam 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 T125605。 | |||
T38955 |
β-Lactamase-IN-4
|
||
β-Lactamase-IN-4 (WO2013149121A1, compound 708) is a potent β-lactamase inhibitor. It serves as a valuable tool in the investigation of bacterial infections. | |||
T125587 |
Spirodihydrobenzofuranlactam IV
|
||
Spirodihydrobenzofuranlactam IV 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 T125587,CAS号为 173220-03-6。 | |||
T60387 | β-Lactamase-IN-8 | ||
β-Lactamase-IN-8 (compound 20) 是一种有效的、口服生物可利用的广谱环硼酸β- 内酰胺酶 (β-lactamase)抑制剂,可用于抗菌研究。 | |||
T60370 | Metallo-β-lactamase-IN-2 | ||
Metallo-β-lactamase-IN-4 (compound 40) 是一种有效的金属 -β- 内酰胺酶 (MBL) 抑制剂,其对于 VIM-1、NDM-1和 IMP-7的 IC50值分别为 0.1 μM, 1.3 μM 和 5.0 μM。 | |||
T38956 |
β-Lactamase-IN-5
|
||
β-Lactamase-IN-5, a β-lactamase inhibitor isolated from compound 720, holds significant potential for studying bacterial infections. | |||
T126315 |
Piperolactam D
|
||
Piperolactam D 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 T126315,CAS号为 116084-93-6。 | |||
T61173 |
Metallo-β-lactamase-IN-5
|
||
Metallo-β-lactamase-IN-5 (compound 5c) is a powerful inhibitor of metallo-β-lactamases (MBLs). Its inhibitory activity against MBLs NDM-1 and VIM-1 has been demonstrated. With an IC50 value of 45 μg/mL, Metallo-β-lactamase-IN-5 effectively inhibits HUVECs. Additionally, when combined with Imipenem, Metallo-β-lactamase-IN-5 exhibits synergistic antimicrobial activity [1]. | |||
T67386 | Olanzapine Thiolactam Impurity | ||
(Z)-1-(4-(4-Methylpiperazin-1-yl)-2-thioxo-1H-benzo[b][1,4]diazepin-3(2H)-ylidene)propan-2-one 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 T67386。 | |||
T60914 | Metallo-β-lactamase-IN-8 | ||
Metallo-β-lactamase-IN-8 (化合物 17) 是有效,可逆和竞争性的广谱金属-β-内酰胺酶 (MβLs)抑制剂,具有抗菌活性。Metallo-β-lactamase-IN-8 对L1,ImiS,IMP-1和VIM-2的IC50值分别为 1.3 μM,5.7 μM,9.8 μM。 | |||
T60797 |
β-Lactamase-IN-7
|
||
β-Lactamase-IN-7 (compound 14) 能够有效抑制肺炎克雷伯菌,它是 VIM 型金属 β 内酰胺酶的有效抑制剂,对VIM-1和VIM-4的Ki 值分别为 1.26 μM 和 0.54 μM。 | |||
T60694 |
Metallo-β-lactamase-IN-4
|
||
Metallo-β-lactamase-IN-4 (compound 40) 是金属 -β- 内酰胺酶 (MBL) 的有效抑制剂,对VIM-1、NDM-1 和 IMP 的IC50值分别为 0.5 μM, 2.1 μM 和 3.3 μM。 | |||
T25117 | Atrolactamide | ||
Atrolactamide is an anticonvulsant. | |||
T72261 | Metallo-β-lactamase-IN-9 | ||
Metallo-β-lactamase-IN-9 (Compound 23) 是一种高效的泛金属-β-内酰胺酶 (MBL) 抑制剂,其对 NDM-1、VIM-1 和 IMP-1 的抑制活性表现在 IC50 值上,分别为 35 nM、269 nM 和 369 nM。 | |||
T17299 |
(-)-Indolactam V
Indolactam V |
PKC | Chromatin/Epigenetic; Cytoskeletal Signaling |
(-)-Indolactam V is a PKC activator (Kis: 3.36 nM, 1.03 μM for η-CRD2 , γ-CRD2). (-)-Indolactam V also has the Kds are 5.5 nM (η-C1B), 7.7 nM (ε-C1B), 8.3 nM (δ-C1B), 18.9 nM (β-C1A-long), 20.8 nM (α-C1A-long), 137 nM (β-C1B), 138 nM (γ-C1A), 213 nM (γ-C1 | |||
T60494 |
Metallo-β-lactamase-IN-7
|
||
Metallo-β-lactamase-IN-7 是VIM 型金属 β-内酰胺酶的有效抑制剂,其对VIM-2、VIM-1和VIM-5 的IC50值分别为 0.019 μM、13.64 μM 和 0.38 μM。它还可以增强 Meropenem 对革兰氏阴性菌的抗菌活性。 | |||
T125112 | Stigmalactam | ||
Stigmalactam 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 T125112。 | |||
T124662 |
Aristololactam II
|
||
Aristololactam II 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 T124662。 | |||
T39865 |
β-Lactamase-IN-6
|
||
β-Lactamase-IN-6 is a β-Lactamase inhibitor that shows high antibacetrial activity. | |||
T6622 |
Oxacillin sodium monohydrate
苯唑西林钠一水合物,Stapenor monohydrate,苯唑青霉素钠,Sodium oxacillin monohydrate,Methicillin,Bactocill monohydrate |
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Oxacillin sodium monohydrate (Stapenor monohydrate) 是一种抗生素,可研究耐药性葡萄球菌感染,类似 Flucloxacillin。 | |||
T0827 |
Cefsulodin sodium
Cefsulodine sodium,Sulcephalosporin,头孢磺啶钠 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefsulodin sodium (Sulcephalosporin) 是β内酰胺抗生素,对缘脓杆菌和肠杆菌有活性。 | |||
T1495 |
Cefaclor monohydrate
Cefaclor,头孢克洛一水物,头孢克洛一水合物,Cefaclorum,Cefachlor |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefaclor monohydrate (Cefaclorum) 是一种抗生素,可特异性地结合青霉素结合蛋白。 | |||
T5570 |
Cephalothin
头孢噻吩,Cephalotin acid |
Antibacterial; Antibiotic | Microbiology/Virology |
Cephalothin 是一种 β-内酰胺抗生素,抑制 C 类 β-内酰胺酶活性的 Ki 值为 0.32 µM。 | |||
T6385 |
Amoxicillin Sodium
阿莫西林钠,Clavulanate |
Antibacterial; Antibiotic | Microbiology/Virology |
Amoxicillin Sodium (Clavulanate) 是一种有广谱抗菌活性,口服吸收好的抗生素。它能抑制细胞壁中多肽的生物合成,可抑制细胞生长。 | |||
T5024 |
Cefotiam Hexetil Hydrochloride
盐酸头孢替安酯,头孢替安海替酯盐酸盐 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefotiam hexetil hydrochloride 是一种可口服头孢菌素,是抗生素 cefotiam 的前药,但无抗菌作用。 | |||
T1001 |
Dicloxacillin Sodium hydrate
Dicloxacillin sodium salt monohydrate,双氯西林钠,Dicloxacillin sodium monohydrate |
Antibacterial; Antibiotic | Microbiology/Virology |
Dicloxacillin Sodium hydrate 是一种青霉素类窄谱β内酰胺抗生素,可研究革兰氏阳性菌感染。 | |||
T6582 |
Mezlocillin Sodium
美洛西林钠,Baycipen |
Antibacterial; Antibiotic | Microbiology/Virology |
Mezlocillin Sodium (Baycipen) 是一种青霉素 β-内酰胺类抗生素,用于治疗由易感染微生物引起的细菌感染。 | |||
T1305 |
Ceftazidime
GR20263,头孢他啶 |
Antibacterial; Antibiotic | Microbiology/Virology |
Ceftazidime (GR20263) 是可静脉内或肌肉给药的第头孢菌素。它对革兰氏阳性和革兰氏阴性需氧细菌有体外活性。它对肠杆菌科特别有效,对大多数 β-内酰胺酶具有抗水解作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3S1227 |
Aristolactam I
Aristolactam,Aristololactam I,马兜铃内酰胺I,Aristololactum |
Apoptosis; Caspase | Apoptosis; Proteases/Proteasome |
Aristolactam I (Aristololactum) 是马兜铃酸 I (AA-I) 的主要代谢产物,参与导致肾损伤的过程。它具有细胞毒性,通过诱导半胱天冬酶 3 依赖性途径中的细胞凋亡介导。 | |||
T83229 |
9-Methoxyaristolactam I
|
||
9-Methoxyaristolactam I为一自Asarum sieboldii Miq. var. Seoulense Nakai根部提取的天然化合物。 | |||
TN5251 |
Walsuralactam A
|
Others | Others |
Walsuralactam A in the formula I, which is used as an active ingredient, and is used for treating and preventing the tumour. | |||
TN6118 |
Aristolactam IIIa N-β-glucoside
|
||
Aristolactam IIIa N-β-glucoside 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 TN6118,CAS号为 80311-26-8。 | |||
TL0017 |
Aristolactam AIIIa
|
MAPK; CDK | Cell Cycle/Checkpoint; MAPK |
Aristolactam AIIIa is a new type of Plk1 inhibitors, targeting the Polo Box domain (PBD), it has anti-tumor activity. Aristolactam IIIa shows inhibition of platelet aggregation induced by collagen or arachidonic acid. | |||
T81456 | Piperlactam S | ||
Piperlactam S, 分离自Piper kadsura,是一种用于慢性炎症研究的活性化合物。 | |||
TN4855 | Pterolactam | Others | Others |
Pterolactam是一种天然产物,属于蚌壳蕨科金毛狗蕨属,其产品编号为 TN4855,CAS号为 38072-88-7。Pterolactam可用作对照参考。 | |||
TJS1226 |
7-(deoxyadenosin-N(6)-yl)aristolactam I
|
Others | Others |
7-(deoxyadenosin-N(6)-yl)aristolactam I是一种来自马兜铃草药的天然化合物。 | |||
TN3630 |
Chartarlactam A
|
Others | Others |
Chartarlactam A shows antihyperlipidemic effects in HepG2 cells. | |||
TN6034 |
Aristolactam AIa
|
||
Aristolactam AIa 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 TN6034,CAS号为 97399-90-1。 | |||
TN3444 |
Aristolactam BII
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Aristolactam BII exhibits antimicrobial and antiinflammatory activity, it shows significant activity towards DPPH radical scavenging and potent inhibitory effects against tyrosinase mushroom. Aristolactam BII also exerts its significant neuroprotective ef | |||
T82970 |
Aristolactam A III
Aristololactam A III |
||
Aristolactam A III (Aristololactam A III) 为一生物碱,具潜在细胞毒性,并可从鱼腥草中分离。 | |||
TN4797 | Piperolactam C | PAFR; Antifection | GPCR/G Protein; Microbiology/Virology |
Piperolactam C possesses anti-platelet aggregation activity in vitro. It can inhibit the growth of the fungi Cladosporium sphaerospermum and C. cladosporioides. | |||
T75619 | Aristololactam IIIa | ||
Aristololactam IIIa 对超氧阴离子生成和弹性蛋白酶的释放有显著抑制作用,其 IC50值分别为 0.12 和 0.20 μg/mL。 | |||
TN3443 |
Aristolactam AII
|
PAFR | GPCR/G Protein |
Aristolactam AII has cytotoxic activity, it also shows platelet aggregation inhibitory activity. | |||
TN5059 |
Stachybotrylactam
|
Others | Others |
Stachybotrylactam has toxicity. | |||
T16846 |
Sauristolactam
Saurolactam |
Others | Others |
Sauristolactam inhibits the receptor activator of nuclear factor-κB ligand (RANKL)-induced osteoclastogenesis and has the potential to inhibit osteoclast differentiation. Sauristolactam, a natural aristolactam isolated from aerial portions of Saururus Chi | |||
TN3445 |
Aristolactam BIII
|
PAFR | GPCR/G Protein |
Aristolactam BIII possesses anti-platelet aggregation activity in vitro, it also shows significant cytotoxic activity (IC50 values < 4 microg/mL) against P-388, HT-29 and A549 cell lines in vitro. | |||
TN3446 |
Aristolactam FI
|
Others | Others |
Aristolactam FI shows platelet aggregation inhibitory activity.It is a potential cancer chemotherapeutic and chemopreventive agent. | |||
T1029 |
Aztreonam
SQ-26,776,氨曲南 |
Antibacterial; Antibiotic | Microbiology/Virology |
Aztreonam (SQ-26,776) 是单环β-内酰胺抗生素,与青霉素结合蛋白3有较高亲和力。 | |||
T0814 |
Ampicillin Trihydrate
NCI-C56086,氨苄青霉素三水合物 |
Antibacterial; Antibiotic | Microbiology/Virology |
Ampicillin Trihydrate (NCI-C56086) 是一种 β-内酰胺类广谱抗生素,可对抗多种革兰氏阳性和革兰氏阴性细菌。 | |||
T1505 |
Imipenem monohydrate
N-Formimidoyl thienamycin monohydrate,亚胺培南,Imipenem,亚胺培南一水物 |
Antibacterial; Antibiotic | Microbiology/Virology |
Imipenem monohydrate (Imipenem) 是从微生物 Streptomyces cattleya 分离得到的碳青霉烯类抗生素,是一种用于静脉注射的β 内酰胺类抗生素,作用于细菌细胞壁,能广泛有效抑制多种革兰氏阳性和阴性菌。 | |||
T0814L |
Ampicillin
Amcill,D-(-)-α-Aminobenzylpenicillin,Aminobenzylpenicillin,氨苄青霉素,Ampicillin acid |
Antibacterial; Antibiotic | Microbiology/Virology |
Ampicillin (Aminobenzylpenicillin) 属于 β-内酰胺类抗生素,是一种半合成的青霉素。Ampicillin 具有杀菌活性,对各种革兰氏阳性细菌和革兰氏阴性细菌均有抑制活性。 | |||
T8261 |
Ceftazidime Pentahydrate
头孢他啶五水合物,头孢他啶 |
Antibacterial; Antibiotic | Microbiology/Virology |
Ceftazidime pentahydrate 是一种β-内酰胺类抗菌剂,对革兰氏阳性和革兰氏阴性需氧细菌有广谱活性,可静脉内或肌肉给药。它对肠杆菌科特别有效,对大多数 β-内酰胺酶具有抗水解作用。 |