95
11
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9466 |
RTICBM-189
|
Others | Others |
RTICBM-189 是可透过血脑屏障的大麻素 1 型受体变构调节剂,在 Ca2+动员试验中pIC50为 7.54,对 hCB1和 mCB1的 pIC50分别为 5.29 和 6.25。 | |||
T9452 |
PW0787
|
GPR | Endocrinology/Hormones; GPCR/G Protein |
PW0787 是一种可透过血脑屏障的,口服具有活性的GPR52选择性激动剂 (EC50=135 nM)。它能够抑制精神刺激行为。 | |||
T22976 |
MFZ 10-7
|
Others; GluR | Neuroscience; Others |
MFZ 10-7 是 mGluR5 的负变构调节剂。 | |||
T4385 |
PF-4840154
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
PF4840154 是有效的大鼠和人TrpA1通道选择性激动剂,EC50分别为 97 和 23 nM。PF-4840154 可以诱导 TrpA1 介导的小鼠伤害行为。 | |||
T16481 |
PF-04995274
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
PF-04995274 是强效,高亲和力,口服活性血清素 4 受体的部分激动剂。它是可脑渗透的,可用于与阿尔茨海默症相关的认知障碍的研究。 | |||
T2556 |
Nandrolone decanoate
癸酸诺龙,19-Nortestosterone decanoate |
Others; HIV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Nandrolone decanoate (19-Nortestosterone decanoate) 是一种合成代谢雄激素,通过涉及谷氨酸诱导的 N-甲基-D-天冬氨酸受体过度兴奋的机制诱导攻击性行为表征。 | |||
T23008L |
MMPIP hydrochloride
MMPIP hydrochloride (479077-02-6 Free base) |
GluR | Neuroscience |
MMPIP hydrochloride 是变构 mGluR7 的选择性拮抗剂。 MMPIP hydrochloride 可用于研究 mGluR7 对中枢神经系统功能的作用。 | |||
T0293 |
Metyrapone
美替拉酮,甲吡酮,NSC-25265,Su-4885 |
Others; P450; Dehydrogenase; Autophagy | Autophagy; Metabolism; Others |
Metyrapone (NSC-25265) 是 STEROID 11-BETA-MONOOXYGENASE 酶抑制剂。 它被用作库欣综合征诊断中下丘脑-垂体反馈机制的测试。 | |||
T23444 |
TCS 1105
N-(4-fluorobenzyl)-2-(1H-indol-3-yl)-2-oxoacetamide |
Others | Others |
TCS 1105是一种GABAA 苯并二氮卓受体(BZR)配体。TCS 1105阻断Sema3A 诱导的轴突生长锥塌陷。TCS 1105能减少小鼠的焦虑样行为,增强攻击性行为和社会支配力。 | |||
T40548 |
NH-3
|
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
NH-3 is a potent orally active thyroid hormone receptor (THR) antagonist which exhibits reversible behavior, demonstrated by an IC 50 of 55 nM. Derived from the selective thyromi-metic GC-1, NH-3 effectively inhibits the binding of thyroid hormones to their respective receptors, resulting in hindered cofactor recruitment. | |||
T60221 |
Tabernanthalog
TBG |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Tabernanthalog (TBG) 是一种5-HT2A 激动剂。在啮齿类动物中,Tabernanthalog 已被发现可促进结构神经可塑性并产生抗抑郁作用。 | |||
T20177 |
C.I. Vat Yellow 2
Caledon Printing Yellow 5G,Vat Yellow 2,Calcoloid Yellow GCD |
||
C.I. Vat Yellow 2 (Calcoloid Yellow GCD)是一种黄色染料剂,也可用于检测天然沉积物上的吸附行为。 | |||
T10038 |
11-cis-Vaccenyl acetate
(Z)-Octadec-11-enyl acetate |
Endogenous Metabolite | Metabolism |
11-cis-Vaccenyl acetate ((Z)-Octadec-11-enyl acetate) 激活位于触角 T1 感受器的嗅觉神经元,并介导雄性和雌性果蝇的聚集行为。 | |||
T2571 |
Benactyzine hydrochloride
Neuroleptone,胃复康,盐酸贝那替嗪,Tranquilline,Amitakon |
AChR; AChE | Neuroscience |
Benactyzine hydrochloride (Neuroleptone) 是丁酰胆碱酯酶抑制剂,其Ki=0.010 mM。 | |||
T5828 |
MS21570
5-(苄基硫代)-N-甲基-1,3,4-噻二唑-2-胺 |
GPR | Endocrinology/Hormones; GPCR/G Protein |
MS21570 作为 GPR171 拮抗剂基于其阻断能力,IC50 为 220 nM,可减少小鼠的焦虑样行为和恐惧条件反射。 | |||
T11839L |
Lesopitron HCl
Lesopitron HCl(132449-89-9 Free base) |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Lesopitron HCl 是一种5-HT1A 受体激动剂,具有抗焦虑化作用,可逆转与小鼠可卡因戒断相关的黑暗回避行为。 | |||
T0766 |
Promazine hydrochloride
Romtiazin hydrochloride,Sinophenin hydrochloride,盐酸丙嗪 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Promazine hydrochloride (Romtiazin hydrochloride) 是一种抗精神病药,也是一种多巴胺受体 (D2) 拮抗剂,能够抑制多巴胺能神经传递。 | |||
T9325 |
2-(2-Aminothiazole-4-yl)-2-methoxyiminoa
|
Others | Others |
2-(2-Aminothiazole-4-yl)-2-methoxyiminoa 是一种蛋白质酪氨酸磷酸酶的抑制剂,蛋白质酪氨酸磷酸酶可以导致细胞信号通路的变化,从而影响细胞的行为。 | |||
T3275 |
Nefazodone hydrochloride
Dutonin,MJ-13754-1,Serzone,BMY-13754-1,BMY-13754,萘法唑酮盐酸盐 |
5-HT Receptor; Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Nefazodone hydrochloride (Serzone) 是一种强效和选择性的5HT2A 拮抗剂,Ki 为5.8 nM,对 5-HT 和去甲肾上腺素摄取具有中度抑制作用,IC50分别为 290 和 300 nM。它是一种苯哌嗪类抗抑郁药,具有微弱的 α-肾上腺素阻断活性,用于治疗抑郁症、攻击性行为和恐慌症。 | |||
T33816 |
Ordopidine
ACR-325,ACR 325,ACR325 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Ordopidine (ACR325) 是一种多巴胺能稳定剂,可抑制精神刺激剂引起的多动症,并在不活动时刺激行为。Ordopidine 在体外作为多巴胺 D2 受体拮抗剂起作用,尽管亲和力低,但其依赖于特定状态的行为效应特征是 D2 受体拮抗剂所不具备的。 | |||
T15781 |
LP-935509
|
Serine/threonin kinase; AAK1 (AP2 associated kinase 1) | Cell Cycle/Checkpoint; Metabolism; Neuroscience |
LP-935509 是一种选择性的、具有脑渗透的、小分子的衔接蛋白-2 相关激酶1 (AAK1) ATP 竞争性抑制剂,其 IC50=3.3 nM,Ki=0.9 nM。它是一种 BIKE 的有效抑制剂 (IC50=14 nM) 和中度的 GAK 抑制剂 (IC50=320 nM)。它能够逆转 SNL 手术后的疼痛。 | |||
T38947 |
Udonitrectag
REC 0559 |
||
Udonitrectag (REC 0559) is a low molecular weight compound developed to emulate the behavior of NGF, with the objective of tackling the challenge of maintaining NGF stability. | |||
T10848 | CMLD012073 | Others | Others |
CMLD012073 is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor. It inhibits NIH/3T3 cells (IC50: 10 nM). CMLD012073 inhibits eukaryotic translation initiation by modifying the behavior of the RNA helicase (eIF4A). | |||
T31886 |
Fulicin
Phe-asn-glu-phe-val-NH2 |
||
Fulicin is a D-amino acid-containing neuropeptide and can control male copulatory behavior in the land snail, Achatina fulica. | |||
T33090 |
Lysyl-histidyl-phenylalanyl-arginyl-tryptophyl-glycinamide
|
||
Lysyl-histidyl-phenylalanyl-arginyl-tryptophyl-glycinamide is an ACTH fragment; cyclic analog evoked excessive grooming behavior in rabbits when administered intracerebroventricularly. | |||
TP1982 |
Neuropeptide S(Rat)
Neuropeptide S (Rat) |
||
Potent endogenous neuropeptide S receptor (NSPR) agonist (EC50 = 3.2 nM). Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice. | |||
T68189 |
Anpirtoline free base
|
||
Anpirtoline free base is a highly potent 5-HT1B receptor agonist. Anpirtoline has been shown to decreases central serotonin synthesis and attenuate aggressive behavior in vivo. Anpirtoline also acts as an antagonist at 5-HT3 receptors and can bypass the blood-brain barrier. | |||
T34418 |
RS-0406
RS0406,Phenol |
||
RS-0406 is a new type of β-flakes blocker, which can reverse amyloid β-induced cytotoxicity and long-term enhanced damage in vitro, and inhibit amyloid-oligomer-induced behavior deterioration in vivo. | |||
T75950 |
Neuropeptide S(Mouse) TFA
|
||
Neuropeptide S(Mouse) TFA, an endogenous agonist for the neuropeptide S receptor (NPSR) with an EC50 value of 3 nM, plays a significant role in physiological processes by inducing the mobilization of intracellular Ca2+. This compound elevates locomotor activity and wakefulness, and simultaneously decreases anxiety-like behavior in mice. | |||
T75951 |
Neuropeptide S(Rat) TFA
|
||
Neuropeptide S(Rat) TFA, a robust endogenous agonist for the neuropeptide S receptor (NSPR) with an EC50 of 3.2 nM, enhances locomotor activity and promotes wakefulness while concurrently diminishing anxiety-like behavior in mice. | |||
T81087 |
Stick Insect Hypertrehalosaemic Factor II
|
||
Stick Insect Hypertrehalosaemic Factor II为合成肽,展现出与天然样品一致的FAB光谱、反相高效液相色谱特性以及生物活性,适用于高海藻糖效应的研究。 | |||
T27550 |
HMR-1426
HMR 1426,HMR1426 |
||
HMR-1426 is gastric emptying inhibitor. HMR1426 shows an anorectic potential in rats and decreased body weight and fat mass. This was achieved solely by reducing food intake without influencing overall energy expenditure or behavior. | |||
TP1720 |
Pressinoic Acid
|
||
Pressinoic Acid is a peptide with potent corticotrophin-releasing activity. It is also an oxytocin inhibitor; it induces maternal behavior. | |||
T80498 |
Jingzhaotoxin-XII
JzTx-XII |
Potassium Channel | Membrane transporter/Ion channel |
Jingzhaotoxin-XII (JzTx-XII) 作为特异性 Kv4.1 通道抑制剂,表现出 0.363 μM 的 IC50 值,通过改变通道的门控行为来与其相互作用。 | |||
T39792 | AMPC | ||
AMPC, a powerful and efficient inhibitor of TFF3, demonstrates inhibitory effects on cell proliferation, survival, oncogenicity, and CSC-like behavior in TFF3-positive CMS4 CRC cells. It acts as a promising standalone anti-cancer agent and also enhances the effects of 5-FU when used in combination, making it a valuable tool for cancer research. | |||
TP1981 |
Neuropeptide S(Mouse)
Neuropeptide S (Mouse) |
||
Potent endogenous neuropeptide S receptor (NPSR) agonist (EC50 = 3 nM). Induces mobilization of intracellular Ca2+. Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice. | |||
TP1983 |
Neuropeptide S (human)
|
||
Potent endogenous neuropeptide S receptor agonist (EC50 = 9.4 nM). Increases locomotor activity and wakefulness in mice. Also reduces anxiety-like behavior in mice. | |||
TP1529 |
Galanin (1-19), human
|
||
Galanin (1-19), human, represents the fragment encompassing amino acids 1 to 19 of the human galanin neuropeptide. Galanin (GAL) is known for its extensive distribution and multifaceted biological roles, such as regulating hormone secretion, providing antinociceptive effects, and altering feeding behavior. | |||
T80913 |
Tyr-ACTH (4-9)
|
||
Tyr-ACTH(4-9)为行为活性肽,常应用于研究大鼠学习行为的消除。 | |||
T82425 |
Excitin 1
|
||
Excitin 1为具口服活性多肽,能改变大鼠行为并影响脑内单胺与氨基酸浓度。 | |||
T61820 | Ar-V7-IN-1 | ||
Ar-V7-IN-1 is a highly potent inhibitor specifically targeting Ar-V7, a splice variant of the androgen receptor that exhibits hormone-independent behavior. Its development shows promise for researching various indications, notably cancers such as prostate cancer[1]. | |||
T37647 |
5α-dihydro Levonorgestrel
|
||
5α-dihydro Levonorgestrel is a metabolite of the synthetic progestin levonorgestrel . It lacks in vitro and in vivo estrogenic activity, but induces copulatory behavior in male rats when administered at a dose of 1 mg per animal per day. | |||
TP2407 |
Small cardioactive peptide A
SCPA |
||
Small cardioactive peptide A, as a neuropeptide that modulates neuromuscular synapsis in Aplysia, can also function as a neural cotransmitter in molluscs and exert a role in both the central and peripheral modulation of the control of feeding behavior. | |||
T78514 |
Timiperone
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Timiperone对大脑多巴胺D2受体显示出高亲和力,具备抗精神病效果,能有效抑制刻板行为。该化合物在精神分裂症研究中可被广泛应用。 | |||
T69546 |
MP-135
|
||
MP135 is a Novel μ−δ Opioid Receptor Heteromer-Selective Agonist. MP135 maintains untoward side effects such as respiratory depression and reward behavior; together, these results suggest that optimization of MP135 is necessary for the development of therapeutics that suppress the classical side effects associated with conventional clinical opioids. | |||
TP2067 |
Cortagine
|
||
Potent and selective corticotrophin releasing factor receptor 1 (CRF1) agonist (EC50 = 0.18 nM for rat CRF1). Displays anxiolytic and antidepressant activity in vivo. Microinfusion into mouse prefrontal cortex reduces defensive behavior in vivo. | |||
T40528 |
Oxytocin free acid
9-Deamidooxytocin |
||
Oxytocin free acid, also known as 9-Deamidooxytocin, is an analog of oxytocin where the glycinamide residue at position 9 has been substituted with a glycine residue. Oxytocin, a pleiotropic peptide hormone, has wide-ranging implications for general health, adaptation, development, reproduction, and social behavior. | |||
T71262 |
AZD-8418
|
||
AZD-8418 is an mGlu2 receptor positive allosteric modulators that attenuates nicotine-taking and nicotine-seeking behavior. Acute treatment with AZD8418 (0.37, 1.12, 3.73, 7.46, and 14.92 mg/kg) and AZD8529 (1.75, 5.83, 17.5, and 58.3 mg/kg) deceased nicotine self-administration and had no effect on food-maintained responding. Chronic treatment with AZD8418 attenuated nicotine self-administration, but tolerance to this effect developed quickly. The inhibition of nicotine self-administration by c... | |||
T19386 |
ITIC
|
CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
ITIC, a non-fullerene acceptor, demonstrates exceptional thermal stability and exhibits a glass-crystal transition at a significantly lower temperature than its high glass transition temperature (Tg) of 180 °C. Furthermore, ITIC, which is an indacenodithienothiophene-based postfullerene electron acceptor, displays a distinct crystallization behavior, differing substantially from that of fullerenes. | |||
TP1131 |
β-CGRP, human TFA (101462-82-2 free base)
CGRP-II (Human) (TFA),Human β-CGRP (TFA),β-CGRP, human TFA |
||
β-CGRP,human tissue is one of the calcitonin peptide, through complex behavior of calcitonin receptor like receptor (CRLR) - and receptor activity - modifying proteins (increased), and 1 and 300 - nM CRLR IC50s/RAMP1 and CRLR/RAMP2 cells. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5145 |
Oxytocin acetate
Oxytocic hormone acetate,α-Hypophamine acetate,Oxytocin acetate (50-56-6 free base),醋酸催产素 |
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
Oxytocin acetate (α-Hypophamine acetate) 是哺乳动物的神经垂体激素,是多效的下丘脑肽,是催产素受体的配体,有助于分娩、哺乳和亲社会行为。它可作为一种压力应对分子,具有抗炎、抗氧化剂和保护作用。 | |||
TWS0704 |
N-Methylnuciferine
|
Others | Others |
N-Methylnuciferine 是一种从Lotus Plumule 提取的生物碱,可改善脂多糖诱导的抑郁样行为。 | |||
T4429 |
Rauwolscine hydrochloride
Corynanthidine hydrochloride,盐酸育亨宾碱,萝芙素盐酸盐,α-Yohimbine hydrochloride,Isoyohimbine hydrochloride |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Rauwolscine hydrochloride (Isoyohimbine hydrochloride) 是一种高选择性的 α2 adrenergic 受体拮抗剂,Ki=12 nM。 | |||
T5S2357 |
Acetylcorynoline
(+)-Corynoline Acetate,O-Acetylcorynoline,乙酰紫堇灵 |
Antifungal | Microbiology/Virology |
Acetylcorynoline (O-Acetylcorynoline) 是提取自 Corydalis bungeana 中的一种主要生物碱成分,具有抗炎活性。 | |||
T64353 |
4-tert-Octylphenol
|
Endogenous Metabolite | Metabolism |
4-tert-Octylphenol 是一种干扰内分泌的化学物质及雌激素药物,能诱导子代小鼠脑神经元祖细胞的凋亡,并通过减少溴脱氧尿苷(BrdU)、有丝分裂标志物Ki67以及磷酸组蛋白H3(p-Histone-H3)的表达,导致神经元祖细胞的增殖减少。这种物质不仅会干扰小鼠的大脑发育,还会影响其行为。 | |||
TN4994 |
Sequirin C
|
Others | Others |
Sequirin C can inhibit feeding behavior. | |||
T40667 | L-Azatyrosine | ||
L-Azatyrosine, an antitumor antibiotic derived from Streptomyces chibaensis, exhibits the ability to restore the normal phenotypic behavior of transformed cells that carry oncogenic Ras genes. | |||
TN1623 |
Escin IIB
|
Others; NOS | Immunology/Inflammation; Others |
Escin IIB has positive effects on acute inflammation in animals, it can inhibit the induced by serotonin in rats, the hind paw edema induced by carrageenin, and the scratching behavior induced by compound 48/80 in mice. | |||
TN2750 | 2-C-Methyl-D-erythrono-1,4-lactone | Others | Others |
(-)-2-C-Methyl-D-erythrono-1,4-lactone is inactive alone, but elicits oviposition behavior when mixes with other fractions. | |||
T36828 |
9(Z)-Tricosene
|
||
(9Z)-Tricosene is a pheromone released by insects, including D. melanogaster, M. domestica (house fly), and A. mellifera L. (honey bee). In Drosophila, it induces aggregation behavior and is an oviposition guidance cue for females. Due to its aggregation-inducing activity, it is used as a bait pesticide to attract insects to traps. The mechanism of action in Drosophila is the activation of antennal basiconic Or7a receptors. It is also highly produced by honey bees during the waggle dance, which ... | |||
TN4062 | Flavidin | COX; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Flavidin shows very good antioxidant capacity. Flavidin can enhance fluorescent imaging, allowing more sensitive and specific cell labeling in tissues, it should have wide application in molecular detection, providing a general insight into how to optimiz |