Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP1179L |
Porcine dynorphin A(1-13) acetate
Dynorphin A Porcine Fragment 1-13 acetate,Porcine dynorphin A(1-13) acetate(72957-38-1 free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Porcine dynorphin A(1-13) acetate (Dynorphin A Porcine Fragment 1-13 acetate)(72957-38-1 free base) 是一种有效的内源性 κ opioid 受体激动剂,在生理浓度下具有镇痛作用。暴露于强啡肽 A (1-13) 会导致单个神经元中 [Ca2+]i 的急剧增加,类似于急性 NMDA 治疗所见的增加。 | |||
T76341L |
[DPro10] Dynorphin A (1-11)acetate,porcine
[DPro10] Dynorphin A (1-11)acetate,porcine(94596-26-6 Free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
[DPro10] Dynorphin A (1-11)acetate,porcine 是一种高效的 κ-阿片受体激动剂,其 Ki 值为 0.13 nM。[DPro10] Dynorphin A (1-11), porcine 是一种 N-烷基化衍生物,具有镇痛活性。 | |||
TP2040L |
Dynorphin A acetate(80448-90-4 free base)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Dynorphin A acetate(80448-90-4 free base) 是一种内源性 kappa 受体激动剂。 | |||
TP1813L |
Dynorphin A 1-10 acetate(79994-24-4 free base)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Dynorphin A 1-10 acetate(79994-24-4 free base) 是一种内源性 opioid 样物质神经肽,与 κ-opioid 样物质受体的细胞外环 2 结合。 Dynorphin A (1-10) 还阻断 NMDA 激活的电流,IC50 为 42.0 μM。 | |||
TP1826L |
Dynorphin B (1-13) acetate(83335-41-5 free base)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Dynorphin B (1-13) acetate(83335-41-5 free base) 作为 opioid κ 受体的激动剂。 | |||
T20403 |
Dynorphin A (1-8)
PH-8P,Dynorphin (1-8) |
||
Dynorphin (1-8) is an opioid octapeptide from the porcine hypothalamus. It comprises the N-terminal eight residues of dynorphin. | |||
TP1813 |
Dynorphin A (1-10)
Dynorphin A 1-10 |
||
Dynorphin A (1-10), an endogenous opioid neuropeptide, binds to extracellular loop 2 of the κ-opioid receptor. Dynorphin A (1-10) also blocks NMDA-activated current with an IC50 of 42.0 μM. | |||
TP2040 |
Dynorphin A
|
||
Endogenous kappa receptor agonist. | |||
TP1179 |
Porcine dynorphin A(1-13)
Dynorphin A Porcine Fragment 1-13 |
||
Porcine dynorphin A (1-13) is a potent, endogenous κ opioid receptor agonist and is antinociceptive at physiological concentrations. Exposure to dynorphin A (1-13) causes acute increases in [Ca2+]i in individual neurons similar to increases seen with acut | |||
TP1423 |
Dynorphin A (1-10) TFA(79994-24-4,free)
Dynorphin A (1-10) TFA |
||
Dynorphin A (1-10) (TFA), an endogenous opioid neuropeptide, binds in the transmembrane domain of the κ-receptor. | |||
TP1372 |
Dynorphin B (1-13) (TFA)(83335-41-5,free)
Dynorphin B (1-13) (TFA) |
||
Dynorphin B (1-13), a 13 amino acid, is an extraordinarily potent opioid peptide. | |||
TP1826 |
Dynorphin B (1-13)
|
||
Dynorphin B (1-13) acts as an agonist on opioid κ-receptor. | |||
TP2243 |
Dynorphin (2-17), amide, porcine
|
Others | Others |
Dynorphins are a class of opioid peptides that arise from the precursor protein prodynorphin. When prodynorphin is cleaved during processing by proprotein convertase 2 (PC2), multiple active peptides are released: dynorphin A, dynorphin B, and α/β-neo-end | |||
T75916 |
Dynorphin A TFA
|
||
Dynorphin A TFA, 作为一种内源性阿片肽,主要在中枢神经系统(CNS)中发挥抑制性神经传导的作用。该化合物不仅是kappa阿片受体(KOR)的高效激动剂,还能激活其他阿片受体,包括mu(MOR)和delta(DOR)。Dynorphin A TFA具有诱导神经元死亡的能力,因此在神经系统疾病的研究中具有应用价值。 | |||
T82518 |
Dynorphin B 29 (pig)
Leumorphin (pig) |
||
Dynorphin B 29 (Leumorphin) (pig) 是一种可与大脑及孤立组织系统中的多种受体交互作用的肽,并可被用于研究免疫反应。 | |||
T80463 |
Dynorphin B (1-9)
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Dynorphin B (1-9)为Dynorphin B的N-端裂解产物,属于神经肽类。其形成受到半胱氨酸肽酶非选择性抑制剂N-ethylmaleimide的阻断。 | |||
T75988 |
Dynorphin A (1-10) (TFA)
|
||
Dynorphin A (1-10) (TFA) 是一种内源性的阿片样神经肽,与 κ 阿片受体 (κ-opioid receptor) 结合。Dynorphin A (1-10) (TFA) 也阻断 NMDA 激活的电流,IC50为 42.0 μM。 | |||
T76335 |
Dynorphin (2-17), amide (porcine)
|
||
Dynorphin (2-17), amide (porcine) 为 dynorphin 衍生物,展现镇痛效果。该化合物源自前体蛋白强啡肽原,涉及阿片肽类,参与疼痛调控、成瘾及情绪调节等生理过程。 | |||
T31173 |
Daaccal
2-Cys-5-cys-7-mearg-8-leu-dynorphin A (1-9)-NH2 |
||
Daaccal 可用于生命科学领域的相关研究。其产品编号为 T31173,CAS号为 103614-06-8。 | |||
T82520 |
Dynorphin (2-17) (porcine)
|
||
Dynorphin (2-17) (porcine),一种源自Prodynorphin的肽类化合物,具有缓解Morphine依赖性戒断症状的功能。 | |||
T83505 |
[DAla2] Dynorphin A (1-9) (porcine)
|
||
"[DAla2] Dynorphin A (1-9) (porcine)" 是一种强效的肽类化合物,常用于疼痛、成瘾和抑郁研究。 | |||
T82519 |
Dynorphin A (1-13) amide
|
||
Dynorphin A (1-13) amide 为一种内源性阿片肽,能够拮抗吗啡引发的镇痛效应。 | |||
T76341 |
[DPro10] Dynorphin A (1-11), porcine
|
||
[DPro10] Dynorphin A (1-11), porcine 是一种 N-烷基化衍生物,是一种有效的 κ-阿片受体激动剂,其Ki 值为 0.13 nM。[DPro10] Dynorphin A (1-11), porcine 具有镇痛作用。 | |||
T75918 |
Dynorphin B (1-13) (TFA)
|
||
Dynorphin B (1-13) TFA 是一种阿片样 κ 受体 (κ-opioid receptor) 激动剂。 | |||
T76338 |
[DAla2] Dynorphin A (1-13), amide (porcine)
|
||
[DAla2] Dynorphin A (1-13), amide (porcine) 是一种肽,其可能作为κ阿片受体激动剂,适用于神经系统研究。 | |||
T80085 |
[DPro10] Dynorphin A (1-11), porcine hydrochloride
|
||
[DPro10] Dynorphin A (1-11), porcine hydrochloride,为N-烷基化衍生物,作为κ-阿片受体激动剂,具有显著活性,Ki值达0.13 nM,且表现出镇痛效果。 | |||
T76337 |
[DAla2, DArg6] Dynorphin A, (1-13) (porcine)
|
||
[DAla2, DArg6] Dynorphin A, (1-13) (porcine) (DADAD) 是猪脑垂体提取物中发现的阿片肽(dynorphinl-13, DYN)的一个衍生物。该化合物对GPI和MVD的外周阿片受体有高效力,但在体内易被快速分解。与原始肽相比,[DAla2, DArg6] Dynorphin A, (1-13) (porcine) 更具酶解稳定性,能有效抵抗酶的裂解作用。 | |||
T76631 |
(N-Me-Tyr1,N-Me-Arg7,D-Leu-NHEt8)-Dynorphin A (1-8)
|
||
(N-Me-Tyr1,N-Me-Arg7,D-Leu-NHEt8)-Dynorphin A (1-8) (E-2078) 是一种稳定的 Dynorphin A (1-8) 类似物,是 kappa 阿片受体 (KOR) 激动剂。 | |||
TP1071 |
Nociceptin
Orphanin FQ,孤菲肽 |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Nociceptin (Orphanin FQ) 是一种 17 个氨基酸的多肽,是 nociceptin 受体的内源性配体,具有缓解疼痛的作用。 | |||
T23963 |
Daeatal
|
||
Dynorphin A ethylamide (1-9), the opioid activities were examined in the bioassays. | |||
T31190 |
Dafphedyn
|
||
Dafphedyn, [D-Ala2, (F5) Phe4]-dynorphin 1-13-NH2 (DAFPHEDYN) is an effective analog of strong endorphin 1-13 and produces diuretic and deep analgesia when administered intravenously in rats. | |||
T83709 |
LIH383 TFA
Phe-Gly-Gly-Phe-Met-Arg-Arg-Lys-NH2 |
||
LIH383是一种趋化因子(C-X-C motif) 受体7 (CXCR7)的多肽激动剂,属于趋化因子和阿片肽清除受体。它专一性激活CXCR7 (EC50 = 0.61 nM),在3 µM浓度时,相比μ-、δ-、κ-阿片受体以及诺氨酸阿片肽(NOP)受体的β-arrestin招募实验中表现出高选择性。LIH383(3 µM)通过阻止U87-ACKR3细胞中,由非选择性阿片受体激动剂dynorphin A诱导的CXCR7对阿片肽的摄取,发挥作用。 |