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Cat. No. | Product Name | ||
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L2700 | 肾上腺素能受体化合物库 | 193 compounds | |
193 种特异靶向肾上腺素受体的生物活性小分子化合物的集合,是相关疾病药物筛选的有效工具; |
Cat. No. | Product Name | Form | Specificity Of Inhibition |
---|---|---|---|
CL0051 |
Adrenergic Receptor antagonist/agonist kit
Adrenergic Receptor antagonist/agonist kit |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T29670 |
ADR-925
ICRF198,ICRF-198,ADR 925,ICRF 198,ADR925 |
Endogenous Metabolite | Metabolism |
ADR-925 (ICRF 198) 是右雷佐生的一种活性螯合铁代谢物,具有使新生大鼠心肌细胞免受阿霉素诱导的损伤的能力。 | |||
T23642 |
ADR-851 free base
ADR851 free base |
||
ADR-851 free base is an antagonist of the HT3 receptor. | |||
T23641 |
ADR 882
ADR882,ADR-882 |
||
ADR 882 is an antagonist of the 5-HT3 receptor. It has analgesic properties. | |||
T23642L |
ADR-851 HCl
Adr-851,Adr 851,Adr851 |
||
ADR-851 HCl is an HT3 receptor antagonist. It works against mechanical, acute thermal, and formalin-induced inflammatory pain. | |||
T6467 |
Cardioxane
ADR-529 Hydrochloride,ICRF-187 hydrochloride,ADR-529,右雷佐生盐酸盐,Dexrazoxane HCl,Cardioxane hydrochloride,ICRF-187 |
Topoisomerase | DNA Damage/DNA Repair |
Cardioxane (ADR-529) 是一种心脏保护剂。 | |||
T22305 |
Dexrazoxane
右雷佐生,ICRF-187 |
Others | Others |
Dexrazoxane (ICRF-187) 是一种心脏保护剂。 | |||
T9244 |
σ1 Receptor antagonist-1
|
Sigma receptor | GPCR/G Protein |
σ1 Receptor antagonist-1 是高选择性的 sigma 1受体拮抗剂,pKi 为10.28。它抑制细胞生长,在 G0/G1 期阻滞细胞周期并诱导 MCF-7/ADR 细胞凋亡。 | |||
T74734 |
Truncated ADR58
|
||
Truncated ADR58 通过将全长ADR58的71个碱基缩短至31个碱基而制得。该化合物维持了与全长ADR58相似的功能性,能够高效且选择性地担任人肿瘤抑制素M(OSM)的拮抗剂,阻碍OSM与gp130受体的结合,特异性地抗拒OSM介导的信号传递。Truncated ADR58在研究类风湿性关节炎等相关疾病中有应用。 | |||
T6018 |
Zosuquidar trihydrochloride
唑喹达三盐酸盐,Zosuquidar (LY335979) 3HCl,RS 33295-198 trihydrochloride,RS 33295-198 (D06387) 3HCl,Zosuquidar 3HCl,LY-335979 trihydrochloride |
P-gp | Membrane transporter/Ion channel; Neuroscience |
Zosuquidar trihydrochloride (LY-335979 trihydrochloride) 是一种P-糖蛋白抑制剂,Ki 值为 59 nM。 | |||
T3628 |
Madrasin
DDD00107587 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Madrasin (DDD00107587) 是剪接抑制剂,在体外能够阻止剪接中间体和产物的形成,并干扰剪接体组装途径中的一个或多个早期步骤。它能在体外抑制 pre-mRNA 的剪接,并修饰细胞中内源性 pre-mRNA 的剪接。 | |||
T7197 |
Fadrozole
|
Aromatase | Endocrinology/Hormones |
Fadrozole 是一种有效的、非甾体类的、选择性的芳香化酶抑制剂(IC50:6.4 nM)。 | |||
T68599 |
Orphenadrine
Orphenadrine (free base) |
Sodium Channel; NMDAR; AChR | Membrane transporter/Ion channel; Neuroscience |
Orphenadrine 是一种非竞争性的 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,以浓度依赖性方式抑制克隆的 HERG 通道,在 HEK 细胞中产生0.85μM 的 IC。Orphenadrine 是中枢和外周毒蕈碱受体的拮抗剂,通过孔残基 Y652或 F656突变阻断衰减。 Orphenadrine 具有抗痉挛、镇痛和抗胆碱能活性,对在体外和体内对谷氨酸神经毒性具有保护作用。Orphenadrine 对钠离子通道具有抑制作用,可用来治疗帕金森。 | |||
T70047 |
Bedoradrine
Bedoradrine free base |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bedoradrine free base 是一种新型高选择性 β2-肾上腺素受体激动剂,可用于治疗哮喘和慢性阻塞性肺疾病。 | |||
T0948 |
Adrenalone hydrochloride
Adrenalone HCl,肾上腺酮盐酸盐,盐酸肾上腺酮 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Adrenalone hydrochloride (Adrenalone HCl) 是一种多巴胺β氧化酶 (dopamine β oxidase) 抑制剂,结构与去甲肾上腺素转运蛋白 (NET) 配体相似,IC50=36.9 μM。它是一种肾上腺素能 (adrenergic) 激动剂,用作局部血管收缩剂和止血剂。 | |||
T20094 |
Adrenochrome
Adraxone |
Antioxidant | oxidation-reduction |
Adrenochrome (Adraxone) 是一种细胞毒性分子,可用于杀死细菌。Adrenochrome 是 Epinephrine 的氧化产物。Adrenochrome 是一种可作用于大鼠心脏的冠状动脉收缩化合物,与心脏毒性有关,可用于确定超氧化物歧化酶的活性。Adrenochrome 与可用于神经系统疾病研究,是拟精神病的潜在药物。 | |||
T7567L |
Adrenorphin 3TFA(88377-68-8(free base))
Metorphamide |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Adrenorphin 3TFA(88377-68-8(free base)) (Metorphamide) 是 μ-opioid 受体 (Ki :12 nM) 的激动剂。 | |||
T26760 |
Bedoradrine sulfate
KUR1246,MN 221 sulfate,KUR1246 sulfate,MN221 sulfate,KUR 1246 sulfate,MN-221 sulfate,KUR 1246,KUR-1246 sulfate,MN-221,MN 221,MN221,KUR-1246 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Bedoradrine sulfate(MN-221 sulfate) 是一种超选择性β2激动剂,可用于治疗哮喘加重和慢性阻塞性肺病。 | |||
TP1244L1 |
Adrenocorticotropic Hormone (ACTH) (1-10), human acetate
Adrenocorticotropic Hormone (ACTH) (1-10), human acetate(2791-05-1 Free base) |
Others | Others |
Adrenocorticotropic Hormone (ACTH) (1-10), human acetate 是促肾上腺皮质激素的一个片段。 Adrenocorticotropic Hormone (ACTH) (1-10), human acetate 仅在 100 和 1000 nM 时具有较弱的 α-MSH 效力。 | |||
T26939 |
Cadralazine
ISF 2469,卡屈嗪,ISF-2469,ISF2469 |
Others | Others |
Cadralazine (ISF 2469) 是一种外周小动脉血管扩张剂,可用于作为抗高血压药物的研究。 | |||
T1308 |
Orphenadrine hydrochloride
Mebedrol,Mephenamin,盐酸邻甲苯海拉明 |
Sodium Channel; NMDAR; Norepinephrine; iGluR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Orphenadrine hydrochloride (Mephenamin) 是一种非竞争性的NMDA 受体拮抗剂, Ki=6.0 ± 0.7 μM。 | |||
T2206 |
Quadrol
N,N,N′,N′-Tetrakis(2-hydroxypropyl)ethylenediamine,EDTP,依的托,Edetol |
Others | Others |
Quadrol (EDTP) 是一种免疫刺激剂,是潜在的能够加速伤口愈合的有用药物。 | |||
T10003 |
α1 adrenoceptor-MO-1
|
Others | Others |
α1 adrenoceptor-MO-1(S 对映体)对α1肾上腺素受体具有亲和力,具有抗α-肾上腺素能和镇痛作用。α1 adrenoceptor-MO-1比R 对映体更具活性。 | |||
T76664 |
Adropin (34-76) (human, mouse, rat)
|
||
Adropin (34-76) (human, mouse, rat) 是一种多肽,可减轻肝纤维化和胰岛素抵抗,而不依赖于肥胖或食物摄入。 | |||
TP1257L |
Adrenomedullin (AM) (22-52), human acetate
Adrenomedullin (AM) (22-52), human acetate(159899-65-7 Free base) |
CGRP Receptor | GPCR/G Protein; Neuroscience |
Adrenomedullin (AM) (22-52), human acetate 是猫后肢血管床中 CGRP 受体和肾上腺髓质素受体的拮抗剂。 | |||
T7556 |
Fadrozole hydrochloride
CGS 16949A,盐酸法倔唑 |
Aromatase | Endocrinology/Hormones |
Fadrozole hydrochloride (CGS 16949A) 是一种选择性的、有效,和非甾体类的芳香化酶抑制剂(IC50:6.4 nM)。 | |||
T8231 |
Adrenocorticotropic Hormone (ACTH) (1-39), human
ACTH (1-39), human,丝拉克肽 |
Others | Others |
Adrenocorticotropic Hormone (ACTH) (1-39), human (ACTH (1-39), human) 是黑皮质素受体激动剂。 | |||
TQ0053 |
Fadraciclib
CYC065 |
CDK | Cell Cycle/Checkpoint |
Fadraciclib (CYC065) 是一种口服有效的 ATP 竞争性的CDK2/CDK9激酶抑制剂,IC50分别为 5 和 26 nM。 | |||
T7627L |
Adrenocorticotropic Hormone (ACTH) (4-10) TFA
Adrenocorticotropic Hormone (ACTH) (4-10) TFA(4037-01-8(free base)),Acth (4-10) |
Melanocortin Receptor | GPCR/G Protein; Neuroscience |
Adrenocorticotropic Hormone (ACTH) (4-10) TFA (Acth (4-10)) 是一种有效的黑皮质素 (MC4R) 受体激动剂。 | |||
T0366 |
Cefadroxil
BL-S 578,头孢羟氨苄 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefadroxil (BL-S 578) 是头孢菌素类广谱抗生素, 有效抑制革兰氏阳性和阴性菌感染。 | |||
T0871 |
Noradrenaline bitartrate
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Noradrenaline bitartrate 直接作用于 α 和 β 肾上腺素能受体。它是去甲肾上腺素的酒石酸氢盐,去甲肾上腺素是一种合成苯乙胺,可模拟内源性去甲肾上腺素的拟交感神经作用。临床上,去甲肾上腺素用作外周血管收缩剂,通过其α-肾上腺素能作用导致动脉和静脉床收缩。它还被用作通过其 β-1 肾上腺素能作用介导的强效正性肌力和变时性心脏刺激剂。 | |||
T10250 |
ADRA1D receptor antagonist 1 HCl
ADRA1D receptor antagonist 1 HCl(1191908-24-3 free base) |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
ADRA1D receptor antagonist 1 HCl 是一种具有口服活性、高效性和选择性的 α1D 肾上腺素受体拮抗剂(Ki:1.6 nM),具有潜在的抗增殖活性。 | |||
T6618 |
Orphenadrine Citrate
Flexon,Flexoject,Banflex,枸酸芬那君,奥芬那君 |
AChR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Orphenadrine Citrate (Flexon) 是NMDA 受体拮抗剂,Ki 为6.0μM,还是HERG 钾离子通道阻断剂。它是一种骨骼肌松弛剂,它作用于中枢神经系统以产生肌肉松弛作用。 | |||
TP1240 |
Adrenocorticotropic Hormone (ACTH) (18-39), human TFA
CLIP (human) (TFA) |
Others | Others |
Adrenocorticotropic Hormone (ACTH) (18-39), human TFA (CLIP human TFA) 是一种似皮质促素中叶肽,由垂体中叶的促黑素细胞产生。 | |||
T2558 |
Cladribine
2-chlorodeoxyadenosine,克拉屈滨,2-Chloro-2′-deoxyadenosine,CldAdo,2CdA |
Apoptosis; Adenosine deaminase | Apoptosis; Metabolism |
Cladribine (2CdA) 是一种嘌呤核苷类似物,是具有口服活性的腺苷脱氨酶抑制剂。它能作为 DNA 合成的抑制剂,可阻断受损 DNA 的修复。它可抑制 DNA 甲基化,具有抗淋巴瘤活性,可研究血液恶性肿瘤和多发性硬化。 | |||
T125154 | Quadranoside III | Antioxidant; Antibacterial | Microbiology/Virology; oxidation-reduction |
Quadranoside III 是从 Melissa officinalis 的干燥茎和叶中分离出三萜化合物,具有潜在的抗菌和抗氧化活性。 | |||
T38424 |
(R)-Fadrozole
FAD286,(R)-CGS 16949A free base,(R)-Fadrozole |
||
(R)-Fadrozole ((R)-CGS 16949A; FAD286) is a potent nonsteroidal inhibitor. (R)-Fadrozole also inhibits human placental aromatase (pIC 50 = 6.17) and aldosterone biosynthesis. (R)-Fadrozole reverses cardiac fibrosis in spontaneously hypertensive heart failure rats.. | |||
T76473 |
Adrenotensin (human)
|
||
Adrenotensin (human) (Pro-ADM-153-185 (human)) 是一种肾上腺髓质素前体肽的特定片段,具体为153至185位点。Adrenotensin (ADM)作为一个含有52个氨基酸的多功能肽,隶属于血管活性肽激素CGRP超家族。 | |||
TP2214 |
Adrenomedullin (1-12), human
|
Others | Others |
Adrenomedullin (AM) (1-12), human, is a peptide with the sequence Tyr-Arg-Gln-Ser-Met-Asn-Asn-Phe-Gln-Gly-Leu-Arg. Adrenomedullin (AM) (1-12), human, was initially identified as a vasodilator, and as such, it has the ability to relax vascular tone. Other | |||
T76011 |
Adrenomedullin (16-31), human TFA
|
||
Adrenomedullin(16-31), human TFA 为人类肾上腺髓质素(hADM)之16至31氨基酸片段,对CGRP1受体显示高亲和力。该化合物在大鼠体内可提高全身血压,但对猫无效。 | |||
TP1857 |
Adrenomedullin (AM) (13-52), human
|
||
Adrenomedullin (13-52) is a 40 amino acid peptide with one intramolecular disulfide bridge, Adrenomedullin (13-52) is a high affinity ligand for the adrenomedullin receptor. | |||
T35851 |
Etzadroxil
Ethyl 2-Ethylbutyrate |
Antibacterial | Microbiology/Virology |
Etzadroxil (Ethyl 2-Ethylbutyrate) 是一种可口服且具有挥发性的酯化物。Etzadroxil 具有广谱的抗菌活性,可用于治疗由多重耐药细菌引起的尿路感染。 | |||
T32536 |
l-Adrenalin ascorbinate
Tonhormon |
||
l-Adrenalin ascorbinate is a bioactive chemical. | |||
T29674 |
Adrogolide HCl
ABT 431,DAS 431,A-93431.1,ABT 431;ABT-431;ABT431,ABT-431,Adrogolide Hydrochloride,ABT431 |
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Adrogolide Hydrochloride is a selective dopamine receptor D1 agonist. | |||
T36817 |
Quadrone
|
||
Quadrone is a sesquiterpene originally isolated from A. terreus. It is cytotoxic to human carcinoma KB cells in vitro (EC50 = 1.3 μg/ml). | |||
T32748 |
Lidadronic Acid
Lidadronate |
||
Lidadronic Acid is a bioactive chemical. | |||
T10251 |
Adrenocorticotropic Hormone (ACTH) (1-39), rat TFA
ACTH (1-39) (mouse, rat) TFA |
Others | Others |
Adrenocorticotropic Hormone (ACTH) (1-39), rat (TFA) is a potent melanocortin 2 receptor (MC2) agonist. | |||
TP1256 |
Adrenomedullin (AM) (22-52), human TFA
22-52-Adrenomedullin (human) (TFA) |
||
Adrenomedullin (AM) (22-52), human (22-52-Adrenomedullin human) TFAis a kind of NH2 TFA truncated at the end of the quality of adrenal medullary analogue, is a kind of quality of adrenal medullary receptor antagonist. | |||
T12435 |
Adriforant hydrochloride
PF-3893787 hydrochloride |
Others | Others |
Adriforant hydrochloride is an antagonist of histamine H4 receptor. | |||
T80503 |
Proadrenomedullin (N-20) (bovine, porcine)
ProADM N20(bovine, porcine),PAMP-20(bovine, porcine) |
||
Proadrenomedullin (N-20) (bovine, porcine) 是一种来源于嗜铬细胞的、具有降压及抑制 catecholamine release 的非竞争性肽类。该化合物能显著抑制 PC12 嗜铬细胞瘤细胞的 catecholamine 分泌,显示出 350 nM 的 IC50 值。此外,Proadrenomedullin (N-20) (bovine, porcine) 作为 EC50 约为 270 nM 的阻断剂,能够有效抵抗烟碱能激动剂引起的 catecholamine release 脱敏现象和烟碱相关的信号通道 (22Na+摄取)。 | |||
T71150 |
Incadronic acid
|
||
Incadronate, also known as Cimadronate and YM-175, is a bone resorption inhibitor. Incadronate disodium inhibits macrophage migration to site of inflammation in vivo and proliferation and causes apoptosis in cancer cells in vitro. Incadronate disodium is a bone density conservation, antitumor and anti-inflammatory agent. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19768 |
γ-Tocotrienol
gamma Tocotrienol,gammaTocotrienol,gamma-Tocotrienol,D-gamma-Tocotrienol,Plastochromanol,γ-生育三烯酚 |
Others | Others |
γ-Tocotrienol (Plastochromanol) 是一种维生素 E 的活性形式。 | |||
T19180 |
Adrenic Acid
二十二碳四烯酸,廿二碳四烯酸,cis-7,10,13,16-Docosatetraenoic acid |
Endogenous Metabolite | Metabolism |
Adrenic Acid (cis-7,10,13,16-Docosatetraenoic acid) 是一种天然的多不饱和脂肪酸,主要存在于肾上腺,肾脏,大脑和脉管系统中。Adrenic Acid 能够调节肾上腺皮质血管的血管紧张度。Adrenic Acid 也是非酒精性脂肪肝疾病的炎症增强剂。 | |||
T2207 |
Adrenosterone
肾上腺甾酮,11-ketoandrostenedione,11-oxoandrostenedione,Reichstein's substance G |
Androgen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Adrenosterone (11-ketoandrostenedione) 是一种人内源性代谢物,由肾上腺皮质产生。Adrenosterone 是一种竞争性羟基类固醇脱氢酶 1 抑制剂。它是一种的类固醇激素,具有较弱的雄激素特性。它是一种膳食补充剂,能够减少脂肪并提高肌肉质量。它能够抑制人类癌细胞的转移进展。 | |||
T1071L |
DL-Adrenaline Hydrochloride
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
DL-Adrenaline Hydrochloride 是天然存在的拟交感神经胺的盐酸盐,具有收缩血管、降低眼内压的活性。 | |||
T20173 |
Noradrenaline tartrate
NSC 169106,NSC-169106,l-Noradrenaline d-bitartrate,NSC169106,Norepinephrine bitartrate |
||
Norepinephrine bitartrate is a precursor of epinephrine. Norepinephrine is the principal transmitter of most postganglionic sympathetic fibers and of the diffuse projection system in the brain arising from the locus ceruleus. | |||
T5132 |
9-dihydro-13-acetylbaccatin III
13-乙酰基-9-羟基巴卡丁 III,13-Acetyl-9-dihydrobaccatin III,9-DHAB III |
Apoptosis | Apoptosis |
9-dihydro-13-acetylbaccatin III (9-DHAB III) 是一种制备紫杉醇类似物的中间体。 | |||
T4085 |
Paris saponin VII
重楼皂苷 VII,Chonglou Saponin VII,Polyphyllin-VII,Dioscinin,Paris saponin-VII |
Apoptosis; BCL; Others; PARP; p38 MAPK; Akt; Caspase; P-gp; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; MAPK; Membrane transporter/Ion channel; Neuroscience; Others; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Paris saponin VII (Dioscini) 是从延龄草的根和根茎中分离的一种甾体皂苷。它减弱线粒体膜电位,增加凋亡相关蛋白的表达,并降低Bcl-2、caspase-9、caspase-3、PARP-1和p-Akt 的蛋白表达水平。它在 K562/ADR 细胞中诱导强烈的自噬,可研究白血病。 | |||
T4A2399 |
Cinobufotalin
华蟾毒它灵,华蟾素 |
IL Receptor; Akt; MRP; P-gp | Cytoskeletal Signaling; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; PI3K/Akt/mTOR signaling |
Cinobufotalin 是一种从蟾蜍的皮肤分泌物中提取的强心类固醇或丁二烯内酯。它已被用作强心药,利尿药和止血药,也是潜在的抗肺癌药物。 | |||
T83368 |
3,5-Dimethoxy-2,7-phenanthrenediol
|
||
3,5-Dimethoxy-2,7-phenanthrenediol (compound 2),一種從Combretum laxum根部分離的菲類化合物,對786-0、MCF-7及NCI/ADR-RES人癌細胞系展現出顯著的細胞毒性,其IC50s值分別為73.26 μM、118.40 μM以及83.99 μM。該化合物還表現出自由基清除活性,其IC50為20.4 μM。 | |||
TN5153 |
Torilin
|
MMP; ERK; IκB/IKK; p38 MAPK; NF-κB; Tyrosinase; Reductase; DNA/RNA Synthesis; JNK | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Endocrinology/Hormones; MAPK; Metabolism; NF-κB; Proteases/Proteasome |
Torilin 是一种睾酮5α还原酶抑制剂,它(IC50=31.7+/-4.23μM)对5α还原酶的抑制作用强于α-亚麻酸(IC50=160.3+/-24.62μM),但弱于非那雄胺(IC50=0.38+/-0.06μM)。Torilin 具有免疫调节、肝脏保护和抗炎特性,它通过限制 TAK1介导的 MAP 激酶和 NF-βB 活化来抑制炎症,它可以减轻关节炎的严重程度,改变 dLN 或关节中的白细胞活化,并恢复血清和脾细胞细胞因子失衡。托利林抑制α-黑素细胞刺激激素激活的 B16黑色素瘤细胞中的黑色素生成,IC(50)值为25μM。Torilin 对枯草芽孢杆菌 ATCC 6633孢子和营养细胞表现出优异的抗菌活性。Torilin 在体内和体外都具有强大的抗血管生成活性,它可能通过抑制肿瘤侵袭来抑制肿瘤发生,逆转癌细胞的多药耐药性,它可以增强阿霉素、长春碱、紫杉醇和秋水仙碱对多药耐药 KB-V1和 MCF7/ADR 细胞的细胞毒性。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02438 |
AKR1B1 Protein, Human, Recombinant (His)
ALDR1,AR,ADR,aldo-keto reductase family 1, member B... |
Human | E. coli |
Aldose reductase (AKR1B1) belongs to the aldo/keto reductase superfamily. AKR1B1 is a NADPH-dependent aldo-keto reductase best known as the rate-limiting enzyme of the polyol pathway. Expression of AKR1B1 was the highest in lens and retina. It is the first enzyme in the polyol pathway through which glucose is converted to sorbitol which is important for the function of various organs in the body, and has been implicated in the etiology of diabetic complications. AKR1B1 is quite abundant in the c... | |||
TMPY-02121 |
CXADR/CAR Protein, Human, Recombinant (His)
coxsackie virus and adenovirus receptor,CAR,CXADR,C... |
Human | HEK293 Cells |
CXADR/CAR Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 25.6 kDa and the accession number is P78310-1. | |||
TMPY-00738 |
CXADR/CAR Protein, Mouse, Recombinant (His & hFc)
AW553441,coxsackie virus and adenovirus receptor,MCAR,261020... |
Mouse | HEK293 Cells |
CXADR/CAR Protein, Mouse, Recombinant (His & hFc) is expressed in HEK293 mammalian cells with His and hFc tag. The predicted molecular weight is 52 kDa and the accession number is P97792-1. | |||
TMPJ-00237 |
CXADR/CAR Protein, Mouse, Recombinant (hFc)
CVB3 BP,Cxadr,CAR,Coxsackievirus and adenovirus rec... |
Mouse | HEK293 Cells |
CXADR/CAR Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-Fc tag. The predicted molecular weight is 50-70 KDa and the accession number is P97792. | |||
TMPH-00288 |
Adrenodoxin reductase Protein, Bovine, Recombinant (His)
Ferredoxin reductase,Adrenodoxin reductase,Ferredox... |
Bovine | P. pastoris (Yeast) |
Serves as the first electron transfer protein in all the mitochondrial P450 systems including cholesterol side chain cleavage in all steroidogenic tissues, steroid 11-beta hydroxylation in the adrenal cortex, 25-OH-vitamin D3-24 hydroxylation in the kidney, and sterol C-27 hydroxylation in the liver. Adrenodoxin reductase Protein, Bovine, Recombinant (His) is expressed in yeast with N-10xHis tag. The predicted molecular weight is 52.8 kDa and the accession number is P08165. | |||
TMPY-02839 |
Adrenomedullin Protein, Human, Recombinant (hFc)
AM,PAMP,adrenomedullin |
Human | HEK293 Cells |
Adrenomedullin consists of 52 amino acids and is a member of the adrenomedullin family. It s a a hypotensive peptide and has 1 intramolecular disulfide bond. It seems that adrenomedullin has a slight homology with the calcitonin gene-related peptide. Adrenomedullin has a highly expression in pheochromocytoma and adrenal medulla. It also can be detected in lung, ventricle and kidney tissues. Adrenomedullin and PAMP are potent hypotensive and vasodilatator agents. Numerous actions have been report... | |||
TMPY-00739 |
CXADR/CAR Protein, Human, Recombinant (His & hFc)
CXADR,HCAR,CAR,coxsackie virus and adenovirus recep... |
Human | HEK293 Cells |
CXADR/CAR Protein, Human, Recombinant (His & hFc) is expressed in HEK293 mammalian cells with His and hFc tag. The predicted molecular weight is 52 kDa and the accession number is P78310-1. | |||
TMPY-01939 |
CXADR/CAR Protein, Mouse, Recombinant (His)
CAR,coxsackie virus and adenovirus receptor,MCAR,AU016810,MC... |
Mouse | HEK293 Cells |
CXADR/CAR Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 25.7 kDa and the accession number is P97792-1. | |||
TMPH-00220 |
Adrenodoxin, mitochondrial Protein, Bovine, Recombinant (His)
Hepato-ferredoxin,FDX1,Ferredoxin-1,Adrenodoxin, mi... |
Bovine | E. coli |
Essential for the synthesis of various steroid hormones. Participates in the reduction of mitochondrial cytochrome P450 for steroidogenesis. Transfers electrons from adrenodoxin reductase to CYP11A1, a cytochrome P450 that catalyzes cholesterol side-chain cleavage to produce pregnenolone, the precursor of most steroid hormones. Does not form a ternary complex with adrenodoxin reductase and CYP11A1 but shuttles between the two enzymes to transfer electrons. Adrenodoxin, mitochondrial Protein, Bov... | |||
TMPH-00287 |
Adrenodoxin reductase Protein, Bovine, Recombinant (E. coli, His)
Ferredoxin--NADP(+) reductase,ADXR,NADPH:adrenodoxi... |
Bovine | E. coli |
Serves as the first electron transfer protein in all the mitochondrial P450 systems including cholesterol side chain cleavage in all steroidogenic tissues, steroid 11-beta hydroxylation in the adrenal cortex, 25-OH-vitamin D3-24 hydroxylation in the kidney, and sterol C-27 hydroxylation in the liver. Adrenodoxin reductase Protein, Bovine, Recombinant (E. coli, His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 55.8 kDa and the accession number is ... | |||
TMPJ-00236 |
CXADR/CAR Protein, Mouse, Recombinant (Avi & His), Biotinylated
Cxadr,Coxsackievirus and adenovirus receptor homolo... |
Mouse | HEK293 Cells |
CXADR/CAR Protein, Mouse, Recombinant (Avi & His), Biotinylated is expressed in HEK293 mammalian cells with C-Avi-6xHis tag. The predicted molecular weight is 30-40 KDa and the accession number is P97792. |