108
10
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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)。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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)。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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 |
||
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. | |||
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. | |||
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. | |||
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 | |||
T12435 |
Adriforant hydrochloride
PF-3893787 hydrochloride |
Others | Others |
Adriforant hydrochloride is an antagonist of histamine H4 receptor. | |||
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. | |||
T69151 |
Adrenaline sulfate
|
||
Adrenaline sulfate 是一种由肾上腺髓质分泌的口服活性激素。Adrenaline sulfate 是一种 α-adrenergic 和 β-adrenergic 受体激动剂。Adrenaline sulfate 可用于治疗过敏反应。Adrenaline sulfate 具有心脏骤停研究潜力[4]。 | |||
T11196 |
Enazadrem
|
Lipoxygenase | Metabolism |
Enazadrem is a 5-lipoxygenase inhibitor with antiinflammatory activities. | |||
T9097 |
Guanadrel
|
Others | Others |
Guanadrel 是一种抗高血压药。 | |||
TP1764 |
Adrenomedullin (1-50), rat
|
||
Adrenomedullin (1-50), rat is a 50 amino acid peptide, which induces a selective arterial vasodilation via activation of CGRP1 receptor. Adrenomedullin (1-50) is a peptide hormone with RNA expressed in rat adrenal glands, lung, kidney, heart, and spleen, |
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。 | |||
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。 | |||
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。 | |||
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。 |