Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T30450 |
Biguanide
AI352571,AI3-52571,AI3 52571 |
||
Biguanide can reduce oxidative stress in rats with hyperglycemia. | |||
T65926 | Poly (hexamethylene biguanide) hydrochloride | ||
Poly (hexamethylene biguanide) hydrochloride 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 T65926。 | |||
T67045 |
1-(4-Chlorophenyl)biguanide hydrochloride
|
||
1-(4-Chlorophenyl)biguanide hydrochloride 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 T67045,CAS号为 4022-81-5。 | |||
T4382 |
Proguanil hydrochloride
Paludrine hydrochloride,盐酸氯胍,Chlorguanide hydrochloride,Chloroquanil |
Others; Dehydrogenase; DNA/RNA Synthesis; Antifolate; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; Others |
Proguanil hydrochloride (Chloroquanil) 是一种双胍类抗疟疾剂,在体内代谢形成环胍。它还是一种二氢叶酸还原酶抑制剂。 | |||
T1000L |
Chlorhexidine diacetate
醋酸氯己定,Hibitane diacetate,Chlorhexidine Acetate,Bactigras |
CAT; Antibacterial; Antibiotic; Antifection | Microbiology/Virology; oxidation-reduction |
Chlorhexidine diacetate (Bactigras) 是一种双胍类杀菌剂,能快速消灭革兰氏阳性菌和革兰氏阴性菌。它也用作漱口水以防止口腔菌斑。 | |||
T20029 |
Buformin hydrochloride
NSC528218,NSC-528218,盐酸丁双胍,NSC 528218 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Buformin hydrochloride (NSC-528218) 是一种有效的 AMPK 激活剂,是一种双胍类的口服抗糖尿病药物。Buformin 延缓胃肠道对葡萄糖的吸收,增加胰岛素敏感性和葡萄糖对细胞的吸收,并抑制肝脏对葡萄糖的合成。Buformin 也具有抗癌活性,可用于各种癌症研究。 | |||
T22959 |
m-Chlorophenylbiguanide hydrochloride
1-(3-Chlorophenyl)biguanidehydrochloride,1-(3-氯苯基)双胍 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
m-Chlorophenylbiguanide hydrochloride 是一种 5-HT3 受体激动剂。它选择性结合 5-HT3(Ki: 0.002 µM) 超过 5-HT1A(Ki: 10 µM) 和 5-HT2(Ki: 10 µM) 受体,但也结合多巴胺转运蛋白上的高亲和力和低亲和力位点( DAT;IC50:在大鼠尾状壳核突触体膜中分别为 0.4 和 34.8 µM)。 | |||
T7135 |
Phenylbiguanide
PBG,N-Phenylbiguanide,1-苯基双胍,1-Phenylbiguanide |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Phenylbiguanide (N-Phenylbiguanide) 是一种 5-HT3 受体选择性激动剂,EC50为 3.0±0.1 μM。 | |||
T77210 | Poly(hexamethylenebiguanide) hydrochloride | ||
Poly(hexamethylenebiguanide) hydrochloride 是一款用于医疗、服装和家用纺织品的抗菌剂。 | |||
PDK0269 |
1-Phenylbiguanide HCl
Phenylbiguanide hydrochloride |
||
Compound PDK0269作为5-HT3受体激动剂(3-100 μM, pEC50 5.05±0.06),可急性增加XII(舌下)发作频率和规律性,并降低发作/次。Phenylbiguanide 产生剂量依赖性(10-500 μM)的多巴胺释放增加(280-2000%)。当Ringer 溶液中加入5 μM 的 nomifensine 时,Compound PDK0269对多巴胺释放的影响得到改善或抑制。 | |||
T1453 |
Phenformin hydrochloride
Phenformin HCl,Phenethylbiguanide hydrochloride,盐酸苯乙福明 |
Potassium Channel; AMPK; Autophagy | Autophagy; Chromatin/Epigenetic; Membrane transporter/Ion channel; PI3K/Akt/mTOR signaling |
Phenformin hydrochloride (Phenformin HCl) 是一种具有抗高血糖活性的双胍类抗糖尿病药物,能够使 AMPK 活化。 | |||
T20158 |
Phenformin
Debeone,N-Phenethylbiguanide,Insoral,BRN 1977317,Azucaps |
Apoptosis | Apoptosis |
Phenformin (BRN 1977317) 是一种双胍化合物,具有抗癌和抗血糖活性,抑制皮肤肿瘤生长并促进角质形成细胞分化,促进细胞凋亡。 | |||
T1000 |
Chlorhexidine
氯己定,Chlorhexidinum,Nolvasan,Rotersept |
CAT; Antibacterial; Antibiotic; Antifection | Microbiology/Virology; oxidation-reduction |
Chlorhexidine (Rotersept) 是一种抗菌剂和防腐剂。它可用于注射前、手术前或外伤后清洁皮肤。 | |||
T12470 |
Picloxydine
|
Antibacterial | Microbiology/Virology |
Picloxydine 是一种杂环双胍,有抗细菌和牙菌斑活性。 | |||
T23837 |
Buformin
丁双胍,W37,W 37,H 224,W-37 |
||
Buformin (1-butylbiguanide) is an oral antidiabetic drug of the biguanide class. It also inhibits the synthesis of glucose by the liver. Buformin delays absorption of glucose from the gastrointestinal tract increases insulin sensitivity and glucose uptake | |||
T69995 |
Chlorhexidine-d8 HCl
|
||
Chlorhexidine-d8 is intended for use as an internal standard for the quantification of chlorhexidine by GC- or LC-MS. Chlorhexidine is a bis(biguanide) antimicrobial disinfectant and antiseptic agent. It inhibits growth of clinical methicillin-resistant S. aureus (MRSA) isolates (MIC90 = 4 μg/ml). It is also active against canine isolates of MRSA, methicillin-susceptible S. aureus (MSSA), methicillin-resistant S. pseudintermedius (MRSP), and methicillin-susceptible S. pseudintermedius (MSSP; MIC... | |||
T83866 | LCC-12 formate | ||
LCC-12是一种铜(II)螯合剂,为二甲双胍的衍生物。作为单体,它能结合铜(II)并在20 µM的浓度下减少氢过氧化物依赖的NADH向NAD+的氧化。在10 µM的浓度下,LCC-12降低一次性人类细胞因子激活的单核衍生的巨噬细胞(MDMs)中IL-1β、IL-2、IL-6、IL-8和TNF-α的细胞因子水平,以及JAK2、STAT2和IL-1受体相关激酶4(IRAK4)的水平。此外,同样浓度的LCC-12减少了细胞因子激活的MDMs中CD80+和CD86+的数量。每日0.3 mg/kg的剂量可提高LPS或盲肠结扎穿孔模型小鼠的存活率。 |