| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V70811 | (D-Pro2,D-Trp6,8,Nle10)-Neurokinin B | 109212-72-8 | (D-Pro2,D-Trp6,8,Nle10)-Neurokinin B is a competitive antagonist of Neurokinin B (Neurokinin Receptor) with a pA2 of 5.5 and has no effect on Substance P or Neurokinin A. |
|
V70795 | (R)-Casopitant ((R)-GW679769) | 414910-26-2 | (R)-Casopitant ((R)-GW679769) is an isomer of Casopitant. |
|
V70807 | (Trp7,β-Ala8)-Neurokinin A (4-10) | 132041-95-3 | (Trp7,β-Ala8)-Neurokinin A (4-10) is a potent neurokinin-3 (NK3) antagonist. |
|
V70819 | (β-Ala8)-Neurokinin A (4-10) | 127633-71-0 | (β-Ala8)-Neurokinin A (4-10) is a neuropeptide and a potent and specific NK-2 (Neurokinin Receptor) tachykinin receptor agonist (activator). |
|
V77477 | [D-Pro2] Spantide I TFA | [D-Pro2] Spantide I TFA is a Spantide analog. | |
|
V70798 | [D-Trp2,7,9] Substance P | 100930-11-8 | [D-Trp2,7,9] Substance P is a tachykinin (Neurokinin Receptor) antagonist (inhibitor) with Kis of 1 μM, 1.3 μM and ~ for NK-1, NK-2 and NK-3 receptors respectively. |
|
V70800 | [DAla4] Substance P (4-11) | 81381-50-2 | [DAla4] Substance P (4-11) is an analogue of Substance P (Substance P ) and inhibits 125I-Bolton Hunter conjugated Eledoisin (IC50 of 0.5 μM) and 125I-Bolton Hunter conjugated Substance P (IC50 of 0.15 μM) to rat cerebral cortical membranes. |
|
V70809 | [Glp5,Sar9] Substance P (5-11) | 77128-78-0 | [Glp5,Sar9] Substance P (5-11) is an analog of Substance P. |
|
V77480 | [His11]Substance P | [His11]Substance P is the analog of Substance P. | |
|
V70813 | [Lys5,MeLeu9,Nle10]-NKA(4-10) | 137565-28-7 | [Lys5,MeLeu9,Nle10]-NKA(4-10) is a selective NK2 receptor agonist (activator) with IC50 of 6.1 nM. |
|
V77481 | [Lys5,MeLeu9,Nle10]-NKA(4-10) TFA | [Lys5,MeLeu9,Nle10]-NKA(4-10) TFA is a selective NK2 receptor agonist (activator) with IC50 of 6.1 nM. | |
|
V70791 | [Lys5,MeLeu9,Nle10]Neurokinin A(4-10) (LMN-NKA) | 149270-28-0 | [Lys5,MeLeu9,Nle10]Neurokinin A(4-10) (LMN-NKA), an analog of Neurokinin A, is a selective NK2R agonist. |
|
V70818 | [MePhe7]-Neurokinin B | 110880-53-0 | [MePhe7]-Neurokinin B is a neurokinin NK-3 receptor (NK3R) agonist/activator with IC50 of 3 nM. |
|
V70815 | [MePhe8,Sar9] Substance P ([MePhe8-MeGly9] Substance P) | 77128-76-8 | [MePhe8,Sar9] Substance P ([MePhe8-MeGly9] Substance P) is an analog of Substance P (Substance P ). |
|
V70797 | [Pro9]-Substance P | 104486-69-3 | [Pro9]-Substance P is a potent, reversible, and selective NK-1 tachykinin receptor agonist (activator) with EC50 of 0.93 nM. |
|
V77491 | [Sar4] Substance P (4-11) | [Sar4] Substance P (4-11) is the analog of Substance P (4-11). | |
|
V70789 | [Sar9,Met(O2)11]-Substance P TFA | 2828433-10-7 | [Sar9,Met(O2)11]-Substance P TFA is a selective tachykinin NK1 receptor agonist (activator). |
|
V70816 | [Tyr8,Nle11] Substance P | 71890-48-7 | [Tyr8,Nle11] Substance P is the analog of Substance P. |
|
V4330 | APREPITANT | 170729-80-3 | Aprepitant (formerly known as MK-0869; MK-869; L-754030; trade name: Emend) is a novel, selective and high-affinity small molecule antagonist of neurokinin 1 receptor with a Kd of 86 pM. |
|
V70803 | Benzomalvin B | 157047-97-7 | Benzomalvin B is a less active analog of Benzomalvin A. |
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