258
12
10
17
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37428 |
TRPC6-PAM-C20
TRPC6-PAM-C20,3-(6,7-Dimethoxy-3,3-dimethyl-3,4-dihydro-isoquinolin-1-yl)-chromen-2-one |
TRP/TRPV Channel | Membrane transporter/Ion channel |
TRPC6-PAM-C20 是一种选择性 TRPC6 正变构调节剂。 TRPC6-PAM-C20 在表达 TRPC6 的 HEK 细胞中诱导胞内 Ca2+ 瞬时增加,EC50 为 2.37 μM。 TRPC6-PAM-C20 增强 OAG 诱导的血小板聚集。 | |||
T37075 |
CB2R PAM
Ec2la |
Cannabinoid Receptor | GPCR/G Protein |
CB2R PAM 是一种口服活性大麻素 2 型受体(CB2Rs)阳性突变调节剂,它能增强 CP 55940 和 2-Arachidonylglycerol 刺激的 [35S]GTPγS 与 CB2 受体的结合,但在没有激动剂的情况下没有作用。CB2R PAM 在神经病理性疼痛小鼠模型中显示出抗损伤活性。 | |||
T1111 |
Pralidoxime Chloride
2-PAM chloride,吡啶醛肟甲氯,2-Pyridinealdoxime methochloride,2-PAM (chloride) |
AChE | Neuroscience |
Pralidoxime Chloride (2-PAM chloride) 是一种肟类化合物,对中毒乙酰胆碱酯酶具有恢复作用,可用于有机磷中毒的研究。 | |||
T33872 |
Pam 1392
AI3 52841,AI352841,AI3-52841 |
Others | Others |
Pam 1392 is a chemotherapeutic agent. | |||
TP1067 |
Pam3CSK4 TFA (112208-00-1 free base)
Pam3CSK4 TFA,Pam3Cys-Ser-(Lys)4 TFA |
TLR | Immunology/Inflammation |
Pam3CSK4 TFA (Pam3Cys-Ser-(Lys)4 TFA) 是 Toll 样受体 1/2 激动剂,对人 TLR1/2 的EC50为 0.47 ng/mL。 | |||
T22404 |
Pralidoxime Iodide
2-PAM,碘解磷定 |
Others | Others |
Pralidoxime Iodide, also named 2-PAM, is an antidote approved for reactivation of inhibited acetylcholinesterase (AChE) in organophosphate poisoning. | |||
TP2399 |
Palmitoyl tetrapeptide
Pam-ser-ser-asn-ala |
||
Palmitoyl tetrapeptide is an analog of the N-terminal part of lipoprotein from the outer membrane of E. coli. | |||
T9177 |
BPAM344
|
iGluR | Membrane transporter/Ion channel; Neuroscience |
BPAM344 是一种红藻氨酸受体亚基GluK1b、GluK2a 和GluK3a 的正变构调节剂。 | |||
T9021 |
Ro0711401
Ro-0711401,Ro 0711401 |
GluR | Neuroscience |
Ro0711401 是一种可口服的 mGlu1受体选择性正变构调节剂,EC50为 56 nM。 | |||
T29123 |
VU0152099
VU 0152099,VU-0152099 |
AChR | Neuroscience |
VU0152099 是选择性和可透过血脑屏障的 mAChR M4正变构调节剂,可增强 M4 对乙酰胆碱的反应,对大鼠 M4 受体的 EC50为 0.4 µM。 | |||
T28069 |
ML380
ML 380,ML-380 |
AChR | Neuroscience |
ML380 是一种高效的中枢神经系统渗透剂 M5 正变构调节剂,对人和大鼠 M5 的 EC50值分别为 190 和 610 nM。它对 M1 和 M3 mAChR 亚型具有中等选择性,可增加 Ach 对 M5 mAChR 的亲和力。 | |||
T23514 |
VU-1545
VU 1545 |
GluR | Neuroscience |
VU-1545 是一种代谢型谷氨酸受体 5 正变构调节剂,Ki 为 156 nM,EC50为 9.6 nM。 | |||
T29137 |
VU0453595
VU 0453595,VU-0453595 |
AChR | Neuroscience |
VU0453595 是有效的、高选择性的、全身活性的M1正变构调节剂 (PAM, EC50=2140 nM),在精神分裂症方面有研究价值。 | |||
T8991 |
BMS986187
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
BMS986187 是一种有效的δ-阿片受体选择性正变构调节剂 (PAM),其 EC50= 0.03 μM,pKB= 6.02 (~1 μM)。BMS986187 对 μ 受体无明显 PAM 活性 (EC50=3 μM)。 | |||
TP1962 |
Pam2CSK4
|
||
Toll-like receptor 2/6 (TLR2/6) agonist. Induces TNF-α production in human mononuclear cells. Also induces proliferation and activation of mouse splenic B cells. | |||
T7699 |
AZD7325
AZD-7325 |
P450; GABA Receptor | Membrane transporter/Ion channel; Metabolism; Neuroscience |
AZD7325 (AZD-7325) 是具有口服活性的α2和α3受体正向别构调节剂,Ki 分别是 0.3 和 1.3 nM。它是中等 CYP1A2和强效 CYP3A4诱导剂,有用于焦虑和 dravet 综合征相关的研究潜力。 | |||
TP2282 |
Pam2CSK4 Biotin
|
Others | Others |
biotinylated Pam2CSK4, a toll-like receptor 2/6 agonist | |||
T70460 |
HM5023507
|
Others | Others |
HM5023507, an orally active dual inhibitor of δγ isoforms in immune signaling. HM5023507 inhibited PI3Kδ and PI3Kγ isoforms with greater than 100-fold selectivity against PI3Kα and PI3Kβ in recombinant enzymatic assays and in primary human immune cells with an exquisite selectivity against other targets. | |||
T81559 |
Pam3-Cys-Ala-Gly
|
||
Pam3-Cys-Ala-Gly为合成细菌脂肽,具备激活巨噬细胞与B细胞的高效能力。 | |||
TP2282L |
Pam2CSK4 TFA
PUL-042 TFA,ODN-M362 TFA,Pam2CSK4 trifluoroacetate-salt,Pam2CSK4 TFA(868247-72-7 Free base) |
TLR; Antifungal | Immunology/Inflammation; Microbiology/Virology |
Pam2CSK4 TFA (PUL-042 TFA) 是一种有效的 TLR2 和 TLR6 双重激动剂,是一种模拟细菌脂蛋白的多肽。Pam2CSK4 TFA 可促进血小板聚集,可用来研究脂蛋白对牙周的影响。 | |||
TP1068 |
Pam3CSK4
Pam3Cys-Ser-(Lys)4 |
||
Pam3CSK4 is a synthetic triacylated lipopeptide (LP) that mimics the acylated amino terminus of bacterial LPs. | |||
TP1066 |
Pam3CSK4-Biotin
Pam3Cys-Ser-(Lys)4-Biotin |
||
Pam3CSK4-Biotin is a biotinylated derivative of Pam3CSK4, functioning as a Toll-like receptor 1/2 (TLR1/2) agonist. | |||
T60047 |
V-0219
|
Glucagon Receptor | GPCR/G Protein |
V-0219 是 GLP-1 的正变构调节剂,可用于肥胖相关糖尿病的研究。 | |||
T34896 |
Tofisopam
Emandaxin,托非索洋,Grandaxin |
Others | Others |
Tofisopam (Grandaxin) 是2,3-苯二氮卓类化合物,具有抗焦虑活性,可口服。 | |||
T13957 |
Verilopam
|
Others | Others |
Verilopam 具有镇痛作用,可用于疼痛研究。 | |||
T15645 |
Pamicogrel
KBT3022,帕米格雷 |
COX | Immunology/Inflammation; Neuroscience |
Pamicogrel (KBT3022) 是一种环氧合酶 (COX) 抑制剂。 | |||
T0053 |
Hydroxyzine Pamoate
Hydroxyzine embonate,双羟萘酸羟嗪,Bobsule,Equipose |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Hydroxyzine Pamoate (Bobsule) 是一种组胺 H1 受体拮抗剂,可有效治疗慢性荨麻疹、皮炎和组胺介导的瘙痒。它可作为止吐剂和镇静剂,缓解焦虑和紧张。 | |||
T1230 |
Pamabrom
巴马溴,帕马溴 |
Others | Others |
Pamabrom 是一种利尿剂,有效成分为8-bromotheophylline,能够缓解月经相关症状。 | |||
T7333 |
Pyrvinium pamoate
Pyrvinium embonate,扑蛲灵 |
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
Pyrvinium pamoate (Pyrvinium embonate) 是一种古老的驱虫药,用于治疗蛲虫病,由于其在某些类型的癌症中抑制 Wnt/β-catenin 通路,它作为抗癌药物再次引起人们的关注。 | |||
T28159 |
Nerisopam
EGIS-6775,GYKI 52322,GYKI52322,EGIS6775,GYKI-52322 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Nerisopam 是一种γ-氨基丁酸(GABA)受体激动剂。 | |||
T60075 |
Dopamine D2 receptor agonist-2
Dopamine D2 Receptor |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Dopamine D2 receptor agonist-2 (Dopamine D2 Receptor) 是靶向多巴胺D2受体的配体。 | |||
T68081 |
Girisopam
|
Others | Others |
Girisopam 是一种用于2,3-苯二氮卓结合位点的新型选择性苯二氮卓类化合物,是一种非典型精神安定药,具有抗焦虑作用。 | |||
T12352 |
Oxidopamine hydrochloride
6-Hydroxydopamine hydrochloride,6-OHDA hydrochloride,6-羟基多巴胺盐酸盐 |
Mitophagy; Dopamine Receptor; Autophagy | Autophagy; GPCR/G Protein; Neuroscience |
Oxidopamine hydrochloride (6-Hydroxydopamine hydrochloride) 是一种神经递质多巴胺拮抗剂,可选择性地破坏多巴胺能神经元,是一种广泛使用的神经毒素。 | |||
T11077 |
Dopamine D2 receptor antagonist-1
|
Others | Others |
Dopamine D2 receptor antagonist-1,一种对多巴胺D2受体(D2R)表现出亚毫摩尔级别亲和力的负变构调节剂(NAM)。 | |||
T1576 |
Iopamidol
SQ-13396,Niopam,Iopamiron,Iopamiro,碘帕醇,B-15000,Isovue |
Others | Others |
Iopamidol (SQ-13396) 是一种 benzenedicarboxamide 化合物。它具有放射性不透明介质、环境污染物和异种生物的作用。 | |||
T15257 |
Etripamil
MSP-2017,(-)-MSP-2017 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Etripamil (MSP-2017) 是一种短效L 型钙通道拮抗剂,可用于治疗阵发性室上性心动过速的研究。它通过抑制房室结细胞中钙慢通道的钙离子流入,显示房室结传导并延长房室结不应期 | |||
TP1223L |
Apamin acetate
Apamine acetate,Apamin acetate(24345-16-2 Free base) |
Potassium Channel | Membrane transporter/Ion channel |
Apamin acetate (Apamine acetate) 是一种具有选择性的 Ca2+ 激活的 K+ (SK) 通道的阻断剂,是在蜂毒素中发现的一种 18 个氨基酸的肽类神经毒素。Apamin acetate 可增强皮质神经元撕裂损伤后的神经突生长和再生。Apamin acetate 具有抗炎和抗纤维化的作用。 | |||
T6835 |
Fenoldopam mesylate
Fenoldopam methanesulfonate,SKF-82526 mesylate,Corlopam mesylate,mesylate,SKF 82526,非诺多泮甲磺酸盐 |
Dopamine Receptor | GPCR/G Protein; Neuroscience |
Fenoldopam mesylate (Corlopam mesylate) 是一种多巴胺受体D1选择性激动剂。 | |||
T13257 |
Upamostat
|
PAI-1; Serine/threonin kinase; Serine Protease | Cell Cycle/Checkpoint; Metabolism; Proteases/Proteasome |
Upamostat 是一种丝氨酸蛋白酶抑制剂,也是一种具有口服活性的 WX-UK1 前药,是一种尿激酶型纤溶酶原激活剂 (uPA) 抑制剂。 | |||
T13512 |
5-Hydroxydopamine hydrochloride
|
Antifungal | Microbiology/Virology |
5-Hydroxydopamine hydrochloride 是人体尿液中的一种天然胺,对卢克斯普受体的 IC50 值为 22 µM 。5-Hydroxydopamine hydrochloride 具有潜在的抗菌活性和抗癌活性。 | |||
T16339 |
Norverapamil hydrochloride
(±)-Norverapamil hydrochloride,D591 hydrochloride,盐酸去甲维拉帕米 |
Calcium Channel; P-gp; Drug Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Norverapamil hydrochloride (D591 hydrochloride) 是 Verapamil 的 N-去甲基代谢物,是 L 型钙通道阻滞剂和 P-糖蛋白 (P-gp) 功能抑制剂。 | |||
T6549 |
Isepamicin sulfate
Isepamicine (Isepamycin,硫酸异帕米星,Isepamicin Sulphate,Isepacin,sch21420) Sulphate |
Antibacterial; Antibiotic | Microbiology/Virology |
Isepamicin sulfate (sch21420) Sulphate) 是一种广谱氨基糖苷类抗生素,对产生 I 型 6-乙酰转移酶的菌株具有良好的活性,通过靶向细菌 30S 核糖体亚基来抑制细菌蛋白质合成。 | |||
T1337 |
Pamidronate Disodium
帕米膦酸钠,CGP 23339A,CGP 23339AE,Pamidronate disodium salt |
Others; HBV | Microbiology/Virology; Others |
Pamidronate Disodium (CGP 23339A) 是一种具有强化骨骼作用的物质。 | |||
T24064 |
Fipamezole
JP-1730,BVF-025,JP 1730,JP1730 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Fipamezole 是一种有效的 α2肾上腺素能受体拮抗剂,可能用于研究帕金森病自主神经功能障碍。 | |||
T68055 |
Devapamil
Devapamilo,Devapamilum |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Devapamil (Devapamilo) 是一种苯烷基胺,以使用依赖性方式阻断来自膜细胞内侧的 L 型钙电流。 | |||
TP1880L1 |
PAMP-12 (human, porcine) acetate
PAMP-12 (human, porcine) acetate(196305-05-2 free base) |
Others | Others |
PAMP-12 (human, porcine) acetate (PAMP-12 (human, porcine) acetate (196305-05-2 free base)) 是 ir-PAMP 的主要成分,由 AM 前体加工而成,PAMP-20 也是如此,并且可能参与心血管控制。 | |||
T7809L |
Ipamorelin 2 Pivalic acid
NNC-26-0161 |
Others | Others |
Ipamorelin 2 Pivalic acid (NNC-26-0161) 是一种生长激素释放肽,可诱导大鼠纵向骨生长。 | |||
T1010 |
Verapamil hydrochloride
Manidon,盐酸维拉帕米,(±)-Verapamil hydrochlorid,Verapamil HCl,Calcan hydrochloride |
P450; Calcium Channel; P-gp | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Verapamil hydrochloride (Verapamil HCl) 是一种钙通道阻滞剂,是一种可口服的 P 糖蛋白 (P-gp) 抑制剂,可抑制CYP3A4,用于高血压、心律不齐和心绞痛的研究。 | |||
T76804 |
Pamrevlumab
FG-3019 |
Apoptosis | Apoptosis |
Pamrevlumab (FG-3019) 是一种对缔组织生长因子(CTGF)有亲和力的人源抗体,参与抗结缔组织生长因子疗法,可用于治疗特发性肺纤维化 (IPF) 。 | |||
T11353 |
Gallopamil
Methoxyverapamil,戈洛帕米 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Gallopamil (Methoxyverapamil) 是一种苯烷基胺钙拮抗剂,以浓度依赖性方式抑制酸分泌 (IC50 = 10.9 μM)。Gallopamil 显示出抗心律失常和血管扩张剂的功效。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1970 |
N-trans-p-coumaroyloctopamine
N-p-Coumaroyloctopamine,N-对香豆酰真蛸胺,p-coumaroylnoradrenaline |
Others | Others |
N-trans-p-coumaroyloctopamine (p-coumaroylnoradrenaline) 来源于马铃薯的块茎组织。 | |||
T0469 |
Octopamine hydrochloride
章鱼胺盐酸盐,(±)-p-Octopamine hydrochlorid,(+,-)-Octopamine HCl,章胺盐酸盐 |
Dopamine Receptor; Endogenous Metabolite; Adrenergic Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Octopamine hydrochloride ((±)-p-Octopamine hydrochlorid) 是一种与去甲肾上腺素结构相关的生物单胺类物质,在无脊椎动物中起着神经调节剂、神经激素和神经递质的作用。它对转染人 alpha2-肾上腺素受体(ARs)的中国仓鼠卵巢细胞 α2-ARs 有刺激作用。它提高糖原分解、糖酵解、糖异生、摄氧量和门脉灌注压。 | |||
T2825 |
Cyclopamine
环巴胺,11-Deoxojervine |
Hedgehog/Smoothened; Endogenous Metabolite; Smo | GPCR/G Protein; Metabolism; Stem Cells |
Cyclopamine (11-Deoxojervine) 是Hedgehog 通路的拮抗剂,细胞实验中IC50=46 nM。它还是选择性Smo 抑制剂。 | |||
TN1968 |
N-Feruloyloctopamine
N-Feruloyloctopamine,N-阿魏酰章鱼胺 |
p38 MAPK; Akt | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
N-Feruloyloctopamine 是从木本曼陀罗提取的一种天然产物,有抗氧化作用,可显著降低Akt 和p38 MAPK 磷酸化水平。 | |||
T13108 |
Pamufetinib
H2OL3Q4XRD,4-(2-Fluoro-4-(3-(2-phenylacetyl)thioureido)phenoxy)-7-methoxy-N-methylquinoline-6-carboxamide,TAS-115 |
VEGFR; c-Met/HGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Pamufetinib (TAS-115) 是VEGFR 和c-Met/HGFR 抑制剂,能够抑制 rVEGFR2 (IC50:30 nM)和 rMET (IC50:32 nM)的活性。 | |||
T1644 |
Dopamine hydrochloride
盐酸多巴胺,Dopamine HCl,ASL279 |
Ferroptosis; Dopamine Receptor; 5-HT Receptor; Endogenous Metabolite | Apoptosis; GPCR/G Protein; Metabolism; Neuroscience |
Dopamine hydrochloride (ASL279) 是在脑黑质、脑腹侧被盖区和下丘脑中产生的一种天然儿茶酚胺,由二羟基苯丙氨酸脱羧形成,是去甲肾上腺素和肾上腺素的前体。它通过 D2 多巴胺受体来诱导 VEGFR2 的内吞作用,有促进血管生成活性。 | |||
T1537 |
Rapamycin
Sirolimus,AY 22989,雷帕霉素,NSC-2260804 |
Others; Endogenous Metabolite; Antibiotic; mTOR; Autophagy; Antifungal | Autophagy; Metabolism; Microbiology/Virology; Others; PI3K/Akt/mTOR signaling |
Rapamycin (AY 22989) 属于大环内酯类天然产物,是一种 mTOR 抑制剂,具有特异性(HEK293 细胞:IC50=0.1 nM)。Rapamycin 具有免疫抑制活性,并能诱导自噬。 | |||
T73775 |
Dopamine 3-O-sulfate
|
Others | Others |
Dopamine 3-O-sulfate,一种主要存在于血浆中的化合物,可作为芳香族氨基酸脱羧酶(AADC)缺乏症的生物标志物。 | |||
T40158 |
N-acetyldopamine
NADA,N-乙酰多巴胺 |
Others | Others |
N-acetyldopamine (NADA) is a catecholamine utilized by insects as a precursor for sclerotization, a process that strengthens their cuticle. | |||
TN6456 |
N-trans-caffeoyloctopamine
|
||
N-trans-Caffeoyltyramine has both arginase inhibitory property and antioxidant capacity. | |||
T25305 |
Demethoxyrapamycin
AY 24668,AY24668,AY-24668 |
Others | Others |
Demethoxyrapamycin is a new antifungal antibiotic agent which is co-produced with rapamycin by Streptomyces hygroscopicus. | |||
T81710 |
N-Acetyldopamine dimer-3
|
Others | Others |
N-Acetyldopamine dimer-3 (compound 11)为Aspongopus chinensis中检出的天然化合物。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-00392 |
PAM Protein, Human, Recombinant (His)
PAL,peptidylglycine alpha-amidating monooxygenase,peptidylgl... |
Human | HEK293 Cells |
PAM Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 94.4 kDa and the accession number is P19021-2. | |||
TMPK-00188 |
JAM-A Protein, Mouse, Recombinant (His)
F11R,JCAM1,PAM-1,PAM-1KAT,JAM-1,JAM,JCAM,J... |
Mouse | HEK293 Cells |
junctional adhesion molecule A (JAM-A), a cell adhesion molecule, is highly elevated in human GBM cancer stem cells and predicts poor patient prognosis. While JAM-A is also highly expressed in other cells in the tumor microenvironment, specifically microglia and macrophages,JAM-A functions to suppress pathogenic microglial activation in the female tumor microenvironment, highlighting an emerging role for sex differences in the GBM microenvironment and suggesting that sex differences extend beyon... | |||
TMPY-00149 |
PAM Protein, Human, Recombinant (hFc)
peptidylglycine alpha-amidating monooxygenase,PHM,peptidylgl... |
Human | HEK293 Cells |
PAM Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 104 kDa and the accession number is P19021-2. | |||
TMPY-00865 |
JAM-A Protein, Human, Recombinant (hFc)
F11 receptor,JAM1,JAMA,KAT,CD321,JCAM,JAM,PAM-1 |
Human | HEK293 Cells |
JAM-A Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 50 kDa and the accession number is Q9BQB4-1. | |||
TMPY-01035 |
JAM-A Protein, Human, Recombinant (His)
PAM-1,F11 receptor,JAMA,JAM1,KAT,CD321,JCAM,JAM |
Human | HEK293 Cells |
JAM-A Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 25 kDa and the accession number is Q9Y624-1. | |||
TMPJ-00965 |
TIM16 Protein, S. cerevisiae, Recombinant
TIM16,Mitochondrial import inner membrane translocase subuni... |
S. cerevisiae | E. coli |
Mitochondrial import inner membrane translocase subunit TIM16 (TIM16) is an ssential component of the PAM complex. PAM complex is required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. In the complex, TIM16 is required to regulate activity of mtHSP70 (SSC1) via its interaction with PAM18/TIM14. TIM16 may act by positioning PAM18/TIM14 in juxtaposition to mtHSP70 at the translocon to maximize ATPase s... | |||
TMPJ-01087 |
TIM14 Protein, S. cerevisiae, Recombinant
Mitochondrial import inner membrane translocase subunit TIM1... |
S. cerevisiae | E. coli |
Mitochondrial import inner membrane translocase subunit TIM14 (TIM14) is an essential component of the PAM complex. PAM complex is required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. In the complex, TIM14 is required to stimulate activity of mtHSP70 (SSC1). TIM14 belongs to the DnaJ family, which has been involved in Hsp40/Hsp70 chaperone systems. As a mitochondrial chaperone, TIM14 functions as p... | |||
TMPY-03852 |
Dopamine beta-Hydroxylase Protein, Human, Recombinant (His)
dopamine β-hydroxylase (dopamine β-monooxy... |
Human | HEK293 Cells |
DBH is a 29 kDa copper-containing oxygenase. It can be detected in noradrenergic nerve terminals of the central and peripheral nervous systems, and is also expressed in chromaffin cells of the adrenal medulla. DBH contains our identical subunits, and its activity requires ascorbate as a cofactor. It functions in in the synthesis of small-molecule neurotransmitters that is membrane-bound, making norepinephrine the only transmitter synthesized inside vesicles. DBH has been shown to be associated ... | |||
TMPH-01509 |
SPAM1 Protein, Human, Recombinant (His)
Sperm adhesion molecule 1,Hyaluronidase PH-20,Sperm surface ... |
Human | E. coli |
Involved in sperm-egg adhesion. Upon fertilization sperm must first penetrate a layer of cumulus cells that surrounds the egg before reaching the zona pellucida. The cumulus cells are embedded in a matrix containing hyaluronic acid which is formed prior to ovulation. This protein aids in penetrating the layer of cumulus cells by digesting hyaluronic acid. | |||
TMPH-01690 |
TIM14 Protein, Human, Recombinant (GST)
Mitochondrial import inner membrane translocase subunit TIM1... |
Human | E. coli |
Mitochondrial co-chaperone which forms a complex with prohibitins to regulate cardiolipin remodeling. May be a component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. May act as a co-chaperone that stimulate the ATP-dependent activity. |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMIH-0401 |
Octopamine-d3
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Octopamine-d3 是 Octopamine 的氘代化合物。 | |||
TMIH-0484 |
Ractopamine-d6 Hydrochloride (Mixture of Diastereomers)
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Ractopamine-d6 Hydrochloride (Mixture of Diastereomers) 是 Ractopamine Hydrochloride (Mixture of Diastereomers) 的氘代化合物。 | |||
TMIH-0399 |
Norverapamil-d7 HCl
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Norverapamil-d7 HCl 是 Norverapamil HCl 的氘代化合物。Norverapamil HCl 的 CAS 号为 67812-42-4。Norverapamil hydrochloride是 Verapamil 的 N-去甲基代谢物,是L型钙通道阻滞剂和 P-糖蛋白 (P-gp) 功能抑制剂。 | |||
TMIJ-0285 |
Verapamil-d7 Hydrochloride
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Verapamil-d7 Hydrochloride 是 Verapamil Hydrochloride 的氘代化合物。Verapamil Hydrochloride 的 CAS 号为 152-11-4。Verapamil hydrochloride 是一种钙通道阻滞剂,是一种可口服的 P 糖蛋白 (P-gp) 抑制剂,可抑制CYP3A4,用于高血压、心律不齐和心绞痛的研究。 | |||
TMIH-0547 |
S-Verapamil-d7 HCL
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S-Verapamil-d7 HCL 是 S-Verapamil HCL 的氘代化合物。S-Verapamil HCL 的 CAS 号为 1188265-55-5。 | |||
T12243 |
Norverapamil-d7
D591 D7,(±)-Norverapamil D7 |
Others | Others |
Norverapamil D7 is a deuterium labeled Norverapamil . Norverapamil is a blocker of L-type calcium channel and an inhibitor of P-glycoprotein (P-gp) function . | |||
TMIH-0482 |
Ractopamine-d5 Hydrochloride
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Ractopamine-d5 Hydrochloride 是 Ractopamine Hydrochloride 的氘代化合物。 | |||
TMIH-0508 |
R-Verapamil-d7 HCL
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R-Verapamil-d7 HCL 是 R-Verapamil HCL 的氘代化合物。R-Verapamil HCL 的 CAS 号为 1188265-55-5。 | |||
TMIH-0481 |
Ractopamine-d5
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Ractopamine-d5 是 Ractopamine 的氘代化合物。Ractopamine 的 CAS 号为 97825-25-7。 | |||
TMID-0019 |
Ractopamine-d3 hydrochloride
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Ractopamine-d3 hydrochloride 是 Ractopamine hydrochloride 的氘代化合物。Ractopamine hydrochloride 的 CAS 号为 90274-24-1。 | |||
T19453 |
N-Desmethylnefopam D5 hydrochloride
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Others | Others |
N-Desmethylnefopam D5 hydrochloride is a deuterium labeled N-Desmethylnefopam hydrochloride. | |||
TMIH-0483 |
Ractopamine-d6 (Mixture of Diastereomers)
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Ractopamine-d6 (Mixture of Diastereomers) 是 Ractopamine (Mixture of Diastereomers) 的氘代化合物。 | |||
TMIH-0047 |
3-Methoxy Dopamine-d4 Hydrochloride
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3-Methoxy Dopamine-d4 Hydrochloride 是 3-Methoxy Dopamine Hydrochloride 的氘代化合物。 | |||
TMIH-0002 |
(+/-)-Verapamil hydrochloride-d7
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(+/-)-Verapamil hydrochloride-d7 是 (+/-)-Verapamil hydrochloride 的氘代化合物。(+/-)-Verapamil hydrochloride 的 CAS 号为 152-11-4。Verapamil hydrochloride 是一种钙通道阻滞剂,是一种可口服的 P 糖蛋白 (P-gp) 抑制剂,可抑制CYP3A4,用于高血压、心律不齐和心绞痛的研究。 | |||
TMIH-0185 |
Desmethyl Nefopam-d5 HCl
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Desmethyl Nefopam-d5 HCl 是 Desmethyl Nefopam HCl 的氘代化合物。Desmethyl Nefopam HCl 的 CAS 号为 147656-98-2。 | |||
TMID-0252 |
Diazepam-d5
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Diazepam-d5 是 Diazepam 的氘代化合物。Diazepam 的 CAS 号为 439-14-5。 | |||
T12691 |
Rapamycin-d3
AY-22989-d3,Sirolimus-d3 |
Others | Others |
Rapamycin-d3 is the deuterium labeled Rapamycin. Rapamycin is a potent and specific inhibitor of mTOR(IC50 of 0.1 nM in HEK293 cells). |