Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7549 |
Talnetant
SB 223412 |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Talnetant (SB 223412) 是一种选择性、竞争性、脑渗透性 NK3 受体拮抗剂,Ki 为1.4 nM。它比对hNK-2受体的抑制性高100倍,具有调节中脑边缘和中脑皮质多巴胺能神经传递的能力。 | |||
T7633 |
Senktide
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Senktide 是速激肽NK3受体激动剂。 | |||
TP1851L |
Scyliorhinin II acetate
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Scyliorhinin II acetate 是大鼠大脑皮层神经激肽 3 (NK3) 受体 (Ki = 2.5 nM) 的选择性激动剂。 | |||
T16114 |
Pavinetant
AZD4901,MLE-4901,AZD2624 |
MEK | MAPK |
Pavinetant 是一种小分子具有口服活性的和选择性的神经激肽-3 (NK3)受体拮抗剂,可用于治疗潮热和多囊卵巢综合征(PCOS),是治疗精神分裂症的潜在化合物。 | |||
TP1899L1 |
Hemokinin 1 (human) acetate(491851-53-7 free base)
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Hemokinin 1 (human) acetate(491851-53-7 free base) 是一种内源性 P 物质同系物,是速激肽 NK1 受体的选择性激动剂(NK1、NK3 和 NK2 受体的 IC50 值分别为 1.8、370 和 480 nM)。在体外对 B 细胞具有增殖和抗凋亡作用,在体内具有抗高血压作用。 | |||
T68623 |
RO4583298
|
||
RO4583298 is a highly potent dual NK1/NK3 receptor antagonist with in vivo activity. | |||
T23395 |
SSR 146977 hydrochloride
|
Others | Others |
NK3 receptor antagonist | |||
T32004 |
GSK172981
GSK 172981,GSK-172981 |
||
GSK172981 is a non-peptide tachykinin NK3 receptor antagonist with a high affinity for the recombinant human (PK (I) value 7.7) and native guinea pig (PK (I) value 7.8) tachykinin NK3 receptor. In vitro, the functional evaluation showed that GSK172981 was | |||
TP1851 |
Scyliorhinin II
|
||
Scyliorhinin II, a cyclic Tachykinin peptide, is a potent NK3 receptor agonist. | |||
T16408 |
Osanetant
SR142801 |
Others | Others |
Osanetant produces anxiolytic- and antidepressant-like effects. Osanetant is a selective NK3 receptor antagonist. It is researched for schizophrenia. | |||
T7633L |
Senktide acetate
Senktide acetate(106128-89-6 free base) |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Senktide acetate 是一种选择性速激肽 NK3 受体激动剂,促进 ELM 的巩固或表达,可用于研究阿尔茨海默症。 | |||
T74413 | (S)-Osanetant | ||
(S)-Osanetant 是 Osanetant 的S 对映体。Osanetant (SR142801) 是一种选择性的NK3受体拮抗剂。Osanetant 有抗焦虑和抗抑郁的作用,并被研究用于精神分裂症。 | |||
T75881 |
GR 64349 TFA
|
||
GR 64349为一种有效且高度选择性的神经激肽 2(NK2)受体肽类拮抗剂,具有在大鼠结肠中的EC50值仅为3.7 nM。相较于NK1和NK3受体,GR 64349展现出超过1000倍与300倍的选择性差异。 | |||
TP2023 |
GR 64349
|
||
Potent and selective tachykinin NK2 receptor agonist (EC50 = 3.7 nM in rat colon). Displays > 1000- and > 300-fold selectivity over NK1 and NK3 receptors respectively. Active in vivo. | |||
T10892 |
CS-003 Free base
|
Neurokinin receptor | GPCR/G Protein; Neuroscience |
CS-003 free base (CS-003) is a triple tachykinin receptor antagonist with high affinity for human (neurokinin) NK1, NK2 and NK3 receptors, with Ki values of 2.3 nM and 0.54 nM, respectively And 0.74 nM. CS-003 free base (CS-003) has therapeutic effects on | |||
T78104 |
Fosnetupitant chloride monohydrochloride
Pronetupitant chloride monohydrochloride |
Neurokinin receptor | GPCR/G Protein; Neuroscience |
Fosnetupitant chloride monohydrochloride(Pronetupitant chloride monohydrochloride)为NK1受体拮抗剂,对人NK1受体和NK3受体的pKi分别为9.5和6.1。它是奈妥匹坦的亚甲基磷酸酯前体。 | |||
TP1899 |
Hemokinin 1, human
Hemokinin 1 (human) |
||
Endogenous substance P homolog that is a selective agonist at the tachykinin NK1 receptor (IC50 values are 1.8, 370 and 480 nM for NK1, NK3 and NK2 receptors respectively). Has proliferative and antiapoptotic actions on B-cells in vitro and is antihyperte | |||
T62199 | Talnetant hydrochloride | ||
Talnetant (SB 223412) hydrochloride 是一种选择性的 NK3 受体拮抗剂,能够作用于 hNK-3-CHO 细胞中 (Ki: 1.4 nM)。Talnetant hydrochloride 对 hNK-3 受体的选择性是 hNK-2 受体的 100 倍,同时在 100 μM 的浓度下对 hNK-1 也没有亲和力。 | |||
T75840 |
Hemokinin 1, human TFA
|
||
Hemokinin 1, human TFA 是选择性的速激肽神经激肽 1 (NK1) 受体完全激动剂。Hemokinin 1, human TFA 也是 NK2和 NK3受体的完全激动剂。Hemokinin 1, human TFA 可以产生非阿片样物质的缓解疼痛作用。 | |||
T75880 |
GR 94800 TFA
|
||
GR 94800 TFA 是有效的、选择性的神经激肽 2(NK2)受体的肽类拮抗剂,其对 NK2、NK1和 NK3受体的 pKB 值分别为 9.6、6.4 和 6.0。 | |||
T70456 |
Nolpitantium Free Base
|
||
Nolpitantium Free Base is a highly selective nonpeptide antagonist of neurokinin-1 (NK1) receptor. Nolpitantium potently, selectively and competitively inhibited substance P binding to NK1 receptors from various animal species, including humans. In vitro, it was a potent antagonist in functional assays for NK1 receptors such as [Sar9, Met(O2)11]substance P-induced endothelium-dependent relaxation of rabbit pulmonary artery and contraction of guinea-pig ileum. Up to 1 mkM, Nolpitantium had no eff... |