80
20
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP2036L |
DPDPE TFA (88373-73-3 free base)
DPDPE TFA |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
DPDPE TFA 是选择性 δ-阿片受体激动剂肽,在体内具有镇痛作用。 | |||
T6277 |
Doramapimod
BIRB 796,达马莫德,度马莫德 |
Raf; p38 MAPK; Autophagy | Autophagy; MAPK |
Doramapimod (BIRB 796) 是一种具有口服活性的p38 MAPK 抑制剂,Kd 值为0.1nM。它也抑制B-Raf 和 Abl,IC50分别为 83 nM 和 14.6 μM。 | |||
T22314 |
Doripenem
|
Antibacterial; Antibiotic | Microbiology/Virology |
Doripenem 是对革兰氏阳性菌、阴性菌和厌氧菌有效的β-内酰胺广谱抗生素。 | |||
T26760 |
Bedoradrine sulfate
KUR1246,MN 221 sulfate,KUR1246 sulfate,MN221 sulfate,KUR 1246 sulfate,MN-221 sulfate,KUR 1246,KUR-1246 sulfate,MN-221,MN 221,MN221,KUR-1246 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bedoradrine sulfate(MN-221 sulfate) 是一种超选择性β2激动剂,可用于治疗哮喘加重和慢性阻塞性肺病。 | |||
T72166 |
Xanthine oxidoreductase-IN-5
|
Xanthine Oxidase | Metabolism |
Xanthine oxidoreductase-IN-5 是一种具有口服活性的黄氨酸氧化还原酶 (XOR) 抑制剂(IC50 : 55 nM)。Xanthine oxidoreductase-IN-5 可用于急性高尿酸血症的研究。 | |||
T38193L |
β-Endorphin (1-27) (human) acetate
β-Endorphin (1-27) (human) acetate(76622-84-9 Free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
β-Endorphin (1-27) (human) acetate 存在于大脑垂体和下丘脑中,具有镇痛活性。 β-Endorphin (1-27) (human) acetate 是一种阿片受体激动剂,对 μ-阿片受体和 δ-阿片受体具有较好的亲和力。 | |||
T21511L |
alpha-Endorphin acetate
α-内啡肽,alpha-Endorphin acetate (59004-96-5 Free base) |
Others | Others |
alpha-Endorphin acetate 是具有特征生物活性的原阿片黑皮质素家族的相关肽,从单个人类垂体中纯化至同质。 | |||
T1037 |
Doripenem monohydrate
多尼培南(一水合物),S 4661 monohydrate,Doripenem Hydrate,S-4661 |
Antibacterial; Antibiotic | Microbiology/Virology |
Doripenem monohydrate (S 4661 monohydrate) 是广谱β-内酰胺抗生素,它对革兰氏阳性,阴性和厌氧菌有抗菌作用。 | |||
T15756 |
Lidorestat
IDD-676 |
Reductase | Endocrinology/Hormones; Metabolism |
Lidorestat (IDD-676) 是一种醛糖还原酶抑制剂(IC50: 5 nM),具有有效性,选择性和口服活性。Lidorestat 改善神经传导,减少白内障的形成。Lidorestat 可用于治疗慢性糖尿病并发症。 | |||
T70047 |
Bedoradrine
Bedoradrine free base |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bedoradrine free base 是一种新型高选择性 β2-肾上腺素受体激动剂,可用于治疗哮喘和慢性阻塞性肺疾病。 | |||
T62839 |
Dalzanemdor
SAGE-718 |
NMDAR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Dalzanemdor (SAGE-718) 是 NMDA 受体阳性变构调节剂,可用于研究亨廷顿舞蹈病、阿尔茨海默病和认知功能障碍。 | |||
T30098 |
Aplindore Fumarate
Aplindore,DAB-452 Fumarate,DAB-452 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Aplindore Fumarate (DAB-452)是一种小分子多巴胺 D2 受体部分激动剂,Aplindore Fumarate 对多巴胺D2 和D3 受体表现出高亲和力,对多巴胺D4、5-羟色胺(5-HT2)和α1-肾上腺素受体表现出低亲和力。Aplindore Fumarate 可用于研究帕金森和精神分裂症。 | |||
TP1508L |
N-Acetyl-α-Endorphin acetate(88264-63-5 free base)
|
Others | Others |
N-Acetyl-α-Endorphin acetate(88264-63-5 free base) 是 N 末端乙酰化的 α-Endorphin。 α-内啡肽是一种内源性 opioid 肽。 | |||
TP2322L |
beta-Neoendorphin acetate(77739-21-0 free base)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
beta-Neoendorphin acetate(77739-21-0 free base) 是 κ-opioid 受体的激动剂 | |||
T5500 |
DORA-22
|
OX Receptor | GPCR/G Protein; Neuroscience |
DORA-22 是一种双食欲素受体拮抗剂,可改善轻度压力引起的失眠,对记忆的影响很小。 | |||
T67888L |
Samidorphan HCl
Samidorphan HCl(852626-89-2 free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Samidorphan HCl 是一种具有口服活性和高效性的 opioid 系统调节剂,可与 μ‐opioid、 κ‐opioid 和 δ‐opioid 受体结合。Samidorphan HCl 是一种新型 μ‐opioid 受体拮抗剂,是 k-opioid 受体和 δ‐opioid 受体的部分激动剂。Samidorphan HCl 可用于预防和治疗精神分裂。 | |||
T1977 |
Dorsomorphin
Compound C,BML-275 |
AMPK; Autophagy; TGF-beta/Smad | Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling; Stem Cells |
Dorsomorphin (BML-275) 是一种 AMPK 抑制剂 (Ki=109 nM),具有选择性和 ATP 竞争性。Dorsomorphin 可以抑制 BMP I 型受体 ALK2、ALK3 和 ALK6。Dorsomorphin 可诱导自噬,具有抗肿瘤活性。 | |||
T15159 |
Dorzagliatin
HMS5552 |
Glucokinase | Metabolism |
Dorzagliatin (HMS5552) 是双重作用的葡萄糖激酶 (glucokinase;GK) 激活剂,可改善 2 型糖尿病的血糖控制,提高胰腺 β 细胞功能。 | |||
T2134 |
Dorzolamide hydrochloride
MK507 hydrochloride,L671152 hydrochloride,MK-507 (L-671152) HCl,盐酸多佐胺,Dorzolamide HCl |
Carbonic Anhydrase | Metabolism |
Dorzolamide hydrochloride (MK507 hydrochloride) 是一种碳酸酐酶carbonic anhydrase II 抑制剂,能够抑制红细胞CA-II(IC50:0.18 nM) 和CA-I(IC50:600 nM) 。 | |||
T69146 |
Suksdorfin
|
PPAR | DNA Damage/DNA Repair; Metabolism |
Suksdorfin 具有降血糖作用,可促进脂肪细胞分化并增强脂联素的产生,可激活过氧化物酶体增殖物激活受体 γ (PPARγ),可促进脂肪细胞对胰岛素依赖性葡萄糖的摄取,可用于肥胖相关研究。 | |||
T72165 |
Xanthine oxidoreductase-IN-3
|
Xanthine Oxidase | Metabolism |
Xanthine oxidoreductase-IN-3 是一种具有口服活性的黄氨酸氧化还原酶 (XOR) 抑制剂(IC50 : 26.3 nM)。Xanthine oxidoreductase-IN-3 可用急性高尿酸血症的研究。 | |||
T5015 |
Gonadorelin Acetate (33515-09-2 free base)
醋酸戈那瑞林,Luteinizing Hormone Releasing Hormone (LH-RH),Luteinizing Hormone Releasing Hormone (LH-RH), human,Gonadorelin Acetate |
Reductase | Endocrinology/Hormones; Metabolism |
Gonadorelin Acetate (33515-09-2 free base) (Luteinizing Hormone Releasing Hormone (LH-RH)) 是下丘脑神经肽,在控制生殖功能中起关键作用。 | |||
T3632 |
Doravirine
多拉维林,多拉韦林,MK-1439 |
HIV Protease; Reverse Transcriptase | Microbiology/Virology; Proteases/Proteasome |
Doravirine (MK-1439) 是一种高度特异性的HIV-1非核苷逆转录酶抑制剂,对野生型以及K103N 和Y181C 逆转录酶突变体的IC50值分别为 4.5 nM,5.5 nM 和 6.1 nM。 | |||
T7830 |
Windorphen
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
Windorphen 是一种 Wnt 抑制剂,可选择性地消除 Wnt 信号传导。 | |||
T72078 |
Xanthine oxidoreductase-IN-4
|
Xanthine Oxidase | Metabolism |
Xanthine oxidoreductase-IN-4 是一种具有有口服活性黄嘌呤氧化还原酶 (XOR) 抑制剂,对 XOR 具有抑制作用,IC50 值为 29.3 nM。Xanthine oxidoreductase-IN-4 可用于研究高尿酸血症。 | |||
T67782 |
Daridorexant hydrochloride
Nemorexant hydrochloride,Quviviq |
OX Receptor | GPCR/G Protein; Neuroscience |
Daridorexant hydrochloride (Nemorexant hydrochloride) 是一种新型的双Orexin 受体拮抗剂。Daridorexant hydrochloride 可用于失眠研究。 | |||
T6146 |
Dorsomorphin dihydrochloride
BML-275 2HCl,Compound C dihydrochloride,6-[4-[2-(1-哌啶基)乙氧基]苯基]-3-(4-吡啶基)吡唑并[1,5-A]嘧啶,Dorsomorphin (Compound C) 2HCl,Compound C 2HCl,BML-275 dihydrochloride |
AMPK; Autophagy; TGF-beta/Smad | Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling; Stem Cells |
Dorsomorphin dihydrochloride (BML-275 2HCl) 是一种选择性和 ATP 竞争性的AMPK 抑制剂,Ki 为 109 nM。它诱导自噬,通过靶向抑制 I 型受体ALK2,ALK3和ALK6来抑制 BMP 途径。 | |||
T70072 | Aplindore | ||
Aplindore is a dopamine receptor agonist used in the therapeutic treatment of Parkinson's Disease. | |||
T29818 | Aladorian sodium | ||
Aladorian sodium is used for Treatment of Cardiovascular Diseases. | |||
T14153 |
Aladorian
ARM036 |
Others | Others |
Aladorian (ARM036) is a benzothiazepine derivative and it has anti-arrhythmia effect. Aladorian is used for the research of heart failure and catecholaminergic polymorphic ventricular tachycardia[1][2]. | |||
T80515 |
β-Endorphin (1-27) (human)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
β-Endorphin (1-27) (human) 是一种 opioid 拮抗剂,与 μ-、δ- 及 κ-阿片受体结合,其 Kis 分别为 5.31、6.17 及 39.82 nM。该化合物还能够抑制由 β-Endorphin 及 etorphine 引起的痛觉消失。 | |||
T35460 |
β-Endorphin (rat)
|
||
β-Endorphin (β-EP) is an endogenous opioid neuropeptide with diverse biological activities. It is produced via piomelanocortin cleavage in the pituitary gland, hypothalamus, and in lymphocytes, then migrates to its sites of action which include plasma, gut, skin, placenta, cerebrospinal fluid, and cardiac tissues. β-EP induces concentration-dependent decreases in electrically stimulated contraction of the mouse vas deferens that can be reversed by the μ-opioid antagonist CTP and δ-opioid antagon... | |||
T25034 |
Alcindoromycin
|
||
Alcindoromycin 是从bohemic acid complex 中分离得到,具有抗肿瘤活性。 | |||
T11656 |
Indoramin D5
Indoramine D5,Wy-21901 D5 |
CDK | Cell Cycle/Checkpoint |
Indoramin D5 is a piperidine antiadrenergic agent. Indoramin D5 is deuterium labeled Indoramin. | |||
T32584 |
Lathodoratin
|
||
Lathodoratin is a bioactive chemical. | |||
T61165 |
Indoramin
|
||
Indoramin, an orally active antihypertensive agent, exhibits selectivity for the α 1A -adrenoceptor [1]. | |||
T82072 |
Indoramin hydrochloride
Indoramine hydrochloride,Wy 21901 hydrochloride |
||
Indoramin (hydrochloride) is a novel antihypertensive agent that exhibits selectivity for the α1A-adrenergic receptor. | |||
T124290 | Doronenine | ||
Doronenine 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 T124290。 | |||
T125713 | Dorrigocin B | ||
T24013 |
DORA 42
DORA42,DORA-42 |
||
DORA 42 is a dual antagonist of the orexin receptor OX1R and OX2R. | |||
T82532 |
Dorlimomab aritox
4197X-RA,MDX-RA (ricin A chain) immunotoxin |
||
Dorlimomab aritox(4197X-RA; MDX-RA (ricin A chain) immunotoxin)是一种偶联了蓖麻毒素Ricinus communis ricin A的小鼠源单克隆抗体。 | |||
T35733 |
Doramectin aglycone
|
||
Doramectin aglycone is an acid degradation product of doramectin , a disaccharide-containing anthelmintic that potentiates glutamate- and GABA-gated chloride channel opening in nematodes, and its acid-catalyzed hydrolysis product doramectin monosaccharide . Doramectin undergoes one round of acid-catalyzed hydrolysis to form doramectin monosaccharide which is then hydrolyzed again to remove the remaining saccharide unit and form doramectin aglycone. | |||
T126476 |
Moellendorffilin
|
||
Moellendorffilin 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 T126476。 | |||
T68929 |
Lidorestat monohydrate
|
||
Lidorestat monohydrate is an aldose reductase inhibitor potentially for the treatment of diabetic neuropathy and diabetic complications. | |||
T22515 |
5'-Iodoresiniferatoxin
|
Others | Others |
TRPV1 (VR1) receptor antagonist | |||
T22527 | 6'-Iodoresiniferatoxin | Others | Others |
TRPV1 (VR1) vanilloid receptor partial agonist | |||
T32175 | Iodorivanol | ||
Iodorivanol is a cytotoxic agent. | |||
T76913 | Avdoralimab | ||
Avdoralimab (IPH 5401),一种全人IgGκ单克隆抗体,针对补体C5a受体1 (C5aR1),阻碍其与C5a结合。该药物适用于研究补体驱动的炎症性疾病及实体瘤。 | |||
T75592 | Odonthobuthus Doriae Venom | ||
Odonthobuthus Doriae Venom,一种从Odonthobuthus Doriae获得的蝎子毒液,通过调节离子通道产生神经毒性。 | |||
TP1391 |
β-Endorphin, equine (TFA)
|
||
β-Endorphin, equine (TFA) is an endogenous opioid peptide, which binds at high affinity to both μ/δ opioid receptors. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0969 |
Doramectin
Dectomax,Cyclohexylavermectin B1,多拉菌素 |
Others; Antibiotic; Parasite | Microbiology/Virology; Others |
Doramectin (Dectomax) 是 Ivermectin 的衍生物。它是一种抗寄生虫抗生素。它具有在 NMRI 小鼠感染模型中抗曼氏链球菌作用。 | |||
T81621 |
Odoratisol B
|
||
Odoratisol B为从Machilus odoratissimaNEES分离获得的天然化合物。 | |||
TN4695 |
Odorine
|
Others | Others |
Odorine has potent anti-carcinogenic effect by inhibiting both the initiation and promotion stages of two-stage skin carcinogenesis. It was found to inhibit the growth of the vinblastine-resistant KB cells by enhancing the anticancer activity of vinblastine. | |||
TN4285 | Isodorsmanin A | Others | Others |
Isodorsmanin A 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 TN4285,CAS号为 118266-99-2。 | |||
T13433 |
β-Endorphin, human
|
Others | Others |
β-Endorphin, human, a prominent endogenous peptide, existing in the hypophysis cerebri and hypothalamus,and is an agonist of opioid receptor. | |||
TN3284 |
8-Hydroxyodoroside A
|
Others | Others |
An antitumor agent containing at least one compound selected from the group consisting of nerigoside, oleandrigenin, sarmentoside, oleaside A, oleandrin, 8β-hydroxy odoroside A, narciclasine, trans-dihydronarciclasine and bisdeoxynarciclasine is provided, this antitumor agent has an advantage of having an excellent therapeutic effect of tumor and less side effects. | |||
TN4697 |
Odoroside H
|
ATPase; Potassium Channel; Sodium Channel | Membrane transporter/Ion channel |
Odoroside H has anticancer activities, the cytotoxic effects are induced by the inhibition of the plasma membrane bound Na(+)/K(+)-ATPase. | |||
TN4694 | Odoratone | Others | Others |
Odoratone shows insecticidal activities, it shows mortality on fourth instar larvae of mosquitoes (Anopheles stephensi) with LC(50) values of 154 ppm. Odoratone exhibits strong antifeedant activity against Pieris brassicae. | |||
T76027 |
β-Endorphin, equine TFA
|
||
β-Endorphin, equine TFA,是具备强效亲和力于μ和δ阿片受体(μ/δ opioid receptors)的内源性阿片类多肽,主要功能包括止痛。 | |||
TN2006 |
Odoriflavene
|
Others | Others |
Odoriflavene has antioxidant activity, and it also shows inhibition effects on the decrease of glutathione level of rat lens induced by UV irradiation. Odoriflavene shows cytotoxic activity against a SH-SY5Y cell line in vitro. | |||
TN3888 |
Dorsmanin A
|
Others | Others |
Dorsmanin A is a natural product from Psoralea corylifolia. | |||
TN5234 |
Vindorosine
|
Calcium Channel; Sodium Channel | Membrane transporter/Ion channel; Metabolism |
Vindorosine has blood vessel relaxation effect, possible underlying mechanisms involving the inhibition of Ca(2+) entry via L-type Ca(2+) channels in vascular smooth muscles. | |||
TN3835 |
Desacetyldoronine
|
Others | Others |
Desacetyldoronine is a hepatotoxic pyrrolizidine alkaloid. | |||
TN4696 | Odorinol | Antifection | Microbiology/Virology |
Odorine and odorinol inhibit both the initiation and promotion stages of two-stage skin carcinogenesis. (+)-Odorinol exhibits strong antiviral activity against Ranikhet disease virus (RVD) in chick embryo. | |||
TN5589 | 6α-Hydroxynidorellol | ||
6alpha-Hydroxynidorellol is a natural product from Callicarpa macrophylla. | |||
T75669 | Odoroside A | ||
Odoroside A,一种自夹竹桃叶中提取的有效成分,具抗癌活性。它通过ROS/p53信号通路诱导细胞凋亡及细胞周期阻滞,进而引发肿瘤细胞死亡。 | |||
TN6351 |
Dorsmanin I
|
||
Dorsmanin I 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 TN6351,CAS号为 329703-46-0。 | |||
TN3159 |
6-Deoxy-9alpha-hydroxycedrodorin
|
Others | Others |
6-Deoxy-9alpha-hydroxycedrodorin shows potential value in the selection of insect-resistant clones for timber plantations. | |||
TN2005 |
Odoratisol A
|
Others | Others |
Odoratisol A is a natural product from Myristica fragrans Houtt. | |||
T83913 |
Mitraciliatine
|
||
Mitraciliatine是一种在M. speciosa(泰国称为Kratom)中发现的生物碱,是μ-阿片受体(MOR)部分激动剂和κ-阿片受体(KOR)激动剂。该化合物对MOR和KOR具有选择性,与δ-阿片受体(DOR; EC50s分别为228, 218, 和 >1,000 nM,针对小鼠受体在GTPγS结合实验中的表现)。Mitraciliatine(100 nmol/动物,脑室内注射)在小鼠的热水尾部缩回实验中延长了撤回潜伏期,这一效果可以通过敲除MOR而非KOR来逆转。与吗啡不同,Mitraciliatine不会诱发过度活动或呼吸抑制。 |