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2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T79260 |
MCI
|
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
MCI具有针对性地清除活性氧(ROS)并降低环氧合酶-2(COX-2)表达的功能,COX-2的IC50值为1.23μM。在胶原诱导的关节炎(CIA)模型中展现出的抗炎效果明显,适用于类风湿性关节炎(RA)的研究。 | |||
T8443 |
MCI-225
|
Norepinephrine | Neuroscience |
MCI-225 是一种选择性的 NA 再摄取抑制剂,具有 5-HT3 受体拮抗作用。 | |||
T16026 |
MCI826
|
P-gp; LTR | Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
MCI826 是一种具有有效性和选择性的 P-glycoprotein (P-gp)和肽白三烯 (p-LTs) 拮抗剂,在豚鼠晚期哮喘模型中显示出抗哮喘活性。 | |||
T28270 |
Osemozotan HCl
Osemozotan hydrochloride,MN-305,MCI-242,MKC-242,MKC242,MCI242 |
||
Osemozotan is a 5-HT1A receptor agonist potentially for the treatment of generalized anxiety disorder. | |||
T4978 |
Sarpogrelate hydrochloride
盐酸沙格雷酯,MCI-9042 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Sarpogrelate hydrochloride (MCI-9042) 是一种选择性5-HT2R 拮抗剂,可用于研究与血栓形成有关的血管疾病,对 5-HT2A、5-HT2B 和 5-HT2C 受体的pKi 值分别为 8.52、6.57 和 7.43。 | |||
T0155 |
Argatroban
MCI-9038,阿加曲班,MD-805,Argipidine |
Thrombin | Proteases/Proteasome |
Argatroban (MCI-9038) 是一种选择性的凝血酶抑制剂。 | |||
T0407 |
Edaravone
依达拉奉右莰醇,依达拉奉,MCI-186 |
Apoptosis; MMP; Free radical scavengers | Apoptosis; oxidation-reduction; Proteases/Proteasome |
Edaravone (MCI-186) 是一种新型自由基清除剂,能够抑制大鼠与 MMP-9有关的脑出血。 | |||
T71574 | Mci 176 | ||
Mci 176 is a quinazolinone calcium antagonist. | |||
T8443L |
MCI-225 hydrochloride hydrate
AA-10021,AA10021,MCI225,DDP-225,AA-10025,AA-10026 |
||
MCI-225 is a norepinephrine reuptake/5-HT3/5-HT reuptake inhibitor. MCI-225 could be effective in the treatment of senile dementia of the Alzheimer type, which is accompanied with both deficit in the BF-cortex cholinergic neuron and cerebral glucose hypom | |||
T82695 |
Colestilan
MCI-196,Colestimide |
||
Colestilan (MCI-196),一种口服活性的非吸收、非钙基磷酸盐粘合剂,同时为非金属阴离子交换树脂,主要应用于高胆固醇血症的研究。 | |||
T28752 |
Senazodan hydrochloride
Senazodan HCl,MCI-154,MCI154,MCI 154 |
||
Senazodan HCl, a phosphodiesterase inhibitor, is used potentially for the treatment of heart failure. | |||
T11152 |
Edaravone-d5
MCI-186 D5 |
Others | Others |
Edaravone, a novel and potent free radical scavenger, effectively prevents MMP-9-related brain hemorrhage in rats treated with tissue plasminogen activator. Its deuterium-labeled variant, Edaravone D5, retains the original compound's attributes while offering isotopic labeling benefits. | |||
T22605 |
Bifemelane hydrochloride
|
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Bifemelane hydrochloride 是一种选择性的,有效的,和竞争性的单胺氧化酶A (MAO-A)抑制剂,Ki=4.20 μM,它也非竞争性地抑制MAO-B,Ki=46.0 μM。它具有显著的抗抑郁作用,可用于研究与脑血管疾病有关的认知和情绪障碍。 | |||
T22246 |
Argatroban Monohydrate
阿加曲班一水合物,阿加曲班 |
Thrombin | Proteases/Proteasome |
Argatroban Monohydrate 是一种 thrombin 选择性抑制剂。 | |||
T71572 |
HOE-K86-4321
|
||
HOE-K86-4321 is a Bradykinin antagonist. | |||
T15378L |
Gemcitabine elaidate hydrochloride
CO-101 hydrochloride,Gemcitabine elaidate hydrochloride(210829-30-4(free base)),Gemcitabine 5'-elaidate hydrochloride,CP-4126 hydrochloride |
Others | Others |
Gemcitabine elaidate (CP-4126) hydrochloride 是 Gemcitabine 的亲脂性前药。Gemcitabine elaidate hydrochloride 通过酯酶转化为 Gemcitabine 以被磷酸化。Gemcitabine elaidate hydrochloride 可以口服给药,具有抗肿瘤活性。 | |||
T6069 |
Gemcitabine hydrochloride
Gemcitabine HCl,吉西他滨盐酸盐,Gemzar,LY188011,盐酸吉西他滨,LY 188011 hydrochloride |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Gemcitabine hydrochloride (LY 188011 hydrochloride) 是一种人工合成的胞嘧啶核苷衍生物,一种 DNA 合成抑制剂。Gemcitabine 具有抗肿瘤活性和抗代谢活性。Gemcitabine 可以引起细胞自噬和凋亡。 | |||
T0820 |
Triamcinolone acetonide
曲安奈德,Aristogel,Azmacort,Aristoderm |
Glucocorticoid Receptor | Endocrinology/Hormones |
Triamcinolone acetonide (Azmacort) 是皮质类固醇。 它是皮质类固醇激素受体激动剂。 它是抗炎糖皮质激素,局部用于治疗各种皮肤疾病。它的有效性是 prednisone 的八倍。 | |||
T0251 |
Gemcitabine
吉西他滨,NSC 613327,LY188011 |
Apoptosis; Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Gemcitabine (LY188011) 是一种人工合成的胞嘧啶核苷衍生物,一种 DNA 合成抑制剂。Gemcitabine 具有抗肿瘤活性和抗代谢活性。Gemcitabine 可以引起细胞自噬和凋亡。 | |||
T76788 |
Demcizumab
OMP 21M18 |
Gamma-secretase | Neuroscience; Proteases/Proteasome; Stem Cells |
Demcizumab (OMP 21M18) 是一种抗 DLL4 单克隆抗体。Demcizumab 是一种有效的 Notch 通路抑制剂。Demcizumab 在多种癌症模型中无论使单独还联合化疗试剂使用都是有效的。 | |||
T1646 |
Famciclovir
泛昔洛韦,BRL 42810 |
DNA/RNA Synthesis; HSV | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Famciclovir (BRL 42810) 是一种单纯疱疹病毒核苷类似物 DNA 聚合酶抑制剂。 | |||
T0261 |
Amcinonide
安西奈德,CL-34699 |
Glucocorticoid Receptor; Annexin A | Endocrinology/Hormones; GPCR/G Protein |
Amcinonide (CL-34699) 是皮质类固醇。它能够抑制NO 从活化的小胶质细胞释放(IC50:3.38 nM),具有糖皮质激素受体亲和力。 它是皮质类固醇激素受体激动剂。 | |||
T15378 |
Gemcitabine elaidate
Gemcitabine 5'-elaidate,反油酸吉西他滨,吉西他滨反油酸酯,Gemcitabine (elaidate),CO-101,CP-4126 |
Apoptosis; Nucleoside Antimetabolite/Analog; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Gemcitabine elaidate (CP-4126) 是 Gemcitabine 的亲脂性前药。它通过酯酶转化为 Gemcitabine 以被磷酸化。它具有抗肿瘤活性。 | |||
T80122 |
Dermcidin-1L (human)
|
Antibiotic | Microbiology/Virology |
Dermcidin-1L (human) 是由汗腺分泌的抗菌肽,具备抗菌活性,适用于研究炎症性皮肤疾病。 | |||
T17162 |
Triamcinolone hexacetonide
|
Others | Others |
Triamcinolone hexacetonide is used long-acting steroids in the treatment of subacute and chronic inflammatory joint diseases. | |||
T17985 |
Gemcitabine-O-Si(di-iso)-O-Mc
|
Others | Others |
Gemcitabine-O-Si(di-iso)-O-Mc, a drug-linker conjugate for Antibody-Drug Conjugates (ADC), exhibits potent antitumor activity. It incorporates Gemcitabine, a pyrimidine nucleoside analog antimetabolite and antineoplastic agent, connected through the ADC linker[1]. | |||
T80579 |
Suvemcitug
|
VEGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
Suvemcitug是一种IgG1κ抗体,它靶向VEGF并且源自非洲野兔(Oryctolagus cuniculus)。 | |||
T35461 |
δ14-Triamcinolone acetonide
|
||
δ14-Triamcinolone acetonide is a potential impurity found in commercial preparations of triamcinolone acetonide. Triamcinolone acetonide is a synthetic corticosteroid. It decreases cytokine levels, the firing rate of sensory neurons, and mechanical hypersensitivity in a rat spinal nerve ligation model when used at a dose of 1.5 mg/kg prior to and following surgery for three days. Triamcinolone acetonide also decreases outflow facility in a mouse model of steroid-induced glaucoma when 20 μl of a ... | |||
T29855 |
Alemcinal
|
||
Alemcinal is a Gastrointestinal Agent. | |||
T4187 |
Gemcitabine monophosphate sodium salt hydrate
|
Others; DNA; DNA/RNA Synthesis; Autophagy | Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others |
Gemcitabine monophosphate sodium salt hydrate 是Gemcitabine 的单磷酸盐衍生物。 | |||
T70464 |
Mitemcinal
|
||
Mitemcinal is a motilin agonist. | |||
T10996 |
Deramciclane
EGIS-3886 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Deramciclane has high affinity for 5-HT2A and 5-HT2C receptors. It acts as an antagonist in both receptor subtypes and has inverse agonist properties for 5-HT2C receptors, but no direct stimulant agonists. | |||
T14207 |
Amcinafal
安西法尔,SQ 15102 |
Others | Others |
Amcinafal is an active diol,and used against virus replication and interferon production. | |||
T21329 |
Gemcitabine monophosphate disodium salt
Gemcitabine monophosphate disodium salt monohydrate,Gemcitabine monophosphate disodium,GemMP |
||
R306465 is a novel HDAC inhibitor with broad-spectrum antitumor activity against solid (IC50: 30 to 300 nM) and hematological malignancies. R306465 was found to be a potent inhibitor of HDAC1 and -8 (class I) in vitro. | |||
T27584 |
Idremcinal
EM574,EM 574,EM-574 |
||
Idremcinal is a motilin receptor agonist. | |||
T33402 |
Mitemcinal fumarate
GM 611,Kita-ku Tokyo,GM-611,Kita-ku Toyko,GM611 |
||
Mitemcinal fumarate is a erythromycin derivative that is used to treat gastroesophageal reflux disease. | |||
T13200 | Triamcinolone Benetonide | Others | Others |
Triamcinolone benetonide is a synthetic glucocorticoid corticosteroid exhibiting potent anti-inflammatory properties. | |||
T27149 | Deramciclane fumarate | ||
Deramciclane fumarate is a 5-HT(2A/C) antagonist with putative anxiolytic activity. | |||
T75252 | Gemcitabine triphosphate | ||
Gemcitabine triphosphate (dFdCTP) 是 Gemcitabine 在细胞内的两种核苷代谢产物的一种。另一种是活性二磷酸 (dFdDTP)。Gemcitabine triphosphate 能够作为放射性标记探针成像研究的标准物,用于识别对 Gemcitabine 的肿瘤,并评估 Gemcitabine 被细胞摄取和保留性质。 | |||
T79863 |
Tibremciclib
|
CDK | Cell Cycle/Checkpoint |
Tibremciclib为CDK4抑制剂,展示出抗肿瘤活性。 | |||
T1884 |
CX516
Ampakine CX516,BDP 12,Ampalex,安帕来斯 |
GluR; iGluR | Membrane transporter/Ion channel; Neuroscience |
CX516 (Ampalex) 是AMPA 受体正向调节剂,可用于研究阿尔茨海默病,精神分裂等。 | |||
T62374 |
Sarpogrelate
|
||
Sarpogrelate (MCI-9042) 是一种新的、口服具有活力的、特异性的 5-HT2 受体拮抗剂。Sarpogrelate 能够提高血小板聚集,具有止血效果,能够用于研究伯格氏病。 | |||
T37963 |
Methylchloroisothiazolinone/Methylisothiazolinone Mixture
|
||
Methylchloroisothiazolinone/methylisothiazolinone mixture (MCIT/MIT) is a mixture of isothiazolinone-derived biocides.1,2It is effective against Gram-positive and Gram-negative bacteria with MIC values of 0.0002, 0.0002, 0.00005, and 0.00005% (w/w) forS. aureus,P. aeruginosa,A. niger, andC. albicans, respectively.2MCIT/MIT can elicit contact sensitization.3Formulations containing MCIT/MIT have been used for controlling microbial growth in industrial and household products. 1.Frenzel, E., Schmidt... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0798 |
Triamcinolone
Fluoxyprednisolone,曲安西龙,Aristocort,Rodinolone |
Glucocorticoid Receptor; COX | Endocrinology/Hormones; Immunology/Inflammation; Neuroscience |
Triamcinolone (Aristocort) 是一种皮质类固醇激素受体激动剂,也是一种合成的长效糖皮质激素,具有抗炎活性。 | |||
T20852 | Triamcinolone diacetate | ||
Triamcinolone diacetate is an antagonist of Lysyl oxidase. |