518
35
3
1
45
13
Cat. No. | Product Name | ||
---|---|---|---|
DF4000 | Smart共价片段化合物库 | 511 compounds | |
ChemDiv’s Smart Library of Covalent Fragments contains 799 compounds | |||
L9410 | 共价抑制剂库 | 1920 compounds | |
1920 种小分子的独特集合,包含已发现的共价抑制剂以及包含某些共价反应基团常见弹头的分子,如氯乙酰基,2-氯丙酰基,丙烯酰基,1-丙-2-炔基,1-丁-2-炔基,酮羰基,二硫键等,可以用于共价抑制剂药物研发; | |||
L8110 | 细胞重编程化合物库 | 1813 compounds | |
1813 种重编程信号通路相关的生物活性小分子化合物的特有集合,可用于高通量、高内涵筛选 |
Cat. No. | Product Name | Form | Specificity Of Inhibition |
---|---|---|---|
C0048 |
Deacetylase Inhibitor Cocktail (100× in 70% DMSO)
去乙酰化酶抑制剂 Cocktail(100× in 70% DMSO) |
Solution (100× in 70% DMSO) | Class I/II/III HDAC |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T60061 |
RU-TRAAK-2
|
Potassium Channel | Membrane transporter/Ion channel |
RU-TRAAK-2 是 TWIK 相关的花生四烯酸刺激的 K+ 通道的可逆抑制剂,对包括 Kv1.2、GIRK2 和 Slo1 在内的非 K2P 通道没有活性。 | |||
T18918 |
Azure B
Azure B chloride,天青 B |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Azure B (Azure B chloride) 是一种 Methylene blue 的主要代谢物,是一种阳离子染料,用于 Azure 曙红染色剂以进行血液涂片染色。它是高选择性和可逆的抑制单胺氧化酶(MAO)-A 的抑制剂,对重组人的 MAO-A 和 MAO-B 的IC50分别为 11 和 968 nM。它具有显著的抗抑郁作用。 | |||
T7788 |
2-Phenyl-2-(1-piperidinyl)propane
|
Others | Others |
2-Phenyl-2-(1-piperidinyl)propane 是一种具有可逆性、选择性的人 CYP2B6抑制剂,其 IC50为 5.1 μM,Ki 为 5.6。它对 CYP2D6 、CYP3A 均有抑制作用,且 IC50值分别为74 μM、200 μM。 | |||
T12103 |
MR-L2
|
PDE | Metabolism |
MR-L2 是可逆的、非竞争性的长型异构体磷酸二酯酶 -4激活剂,可以激活代表性的 PDE4 长型异构体 (PDE4A4、PDE4B1、PDE4C3、PDE4D5)。它可抑制 PGE2- 诱导的 MDCK 细胞囊肿形成,其EC50=1.2 µM。 | |||
T12909 |
SID 26681509
|
Cysteine Protease; Parasite | Microbiology/Virology; Proteases/Proteasome |
SID 26681509 是可逆的,竞争性的人组织蛋白酶 L 选择性抑制剂,IC50为 56 nM。它抑制Plasmodium falciparum 的体外繁殖,IC50为15.4 μM,抑制Leishmania major,IC5012.5 μM。 | |||
T9121 |
AG-636
|
Dehydrogenase; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
AG-636 是一种选择性可逆和具有口服活性的二氢乳清酸脱氢酶(DHODH)抑制剂,IC50 为 17 nM,具有很强的抗癌作用。 | |||
T9192 |
BIIB068
|
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
BIIB068 是可逆的、选择性的、具有口服活性的 BTK 抑制剂 (IC50:1 nM;Kd:0.3 nM)。它对 BTK 的选择性比其他激酶高 400 倍。它可用于自身免疫性疾病的研究。 | |||
T11831 |
LDN-27219
|
Others | Others |
LDN-27219 是一种人组织型转谷氨酰胺酶抑制剂(IC50:600 nM)。 | |||
T28804 |
Slingshot inhibitor D3
JHN76359 |
Others | Others |
Slingshot inhibitor D3 (JHN76359) 是具有选择性、竞争性、可逆性的Slingshot 抑制剂。它对Slingshot 1和Slingshot 2具有相似的抑制活性。它对Slingshot 1 的IC50为 3 μM;对Slingshot 2 的Ki 为 3.9 μM。 | |||
T14897 |
CCG-63802
|
GTPase | GPCR/G Protein |
CCG-63802 是选择性的、可逆变构的G 蛋白信号调节子RGS4抑制剂。CCG-63802与RGS4特异性结合从而阻断 RGS4-Gαo 相互作用,IC50为 1.9 μM。 | |||
T4527 |
Seclidemstat
SP-2577 |
Histone Demethylase | Chromatin/Epigenetic |
Seclidemstat (SP-2577) 是非竞争性可逆KDM1A (LSD1)抑制剂,可用于尤文肉瘤的研究。它促进 SWI/SNF 复合物突变卵巢癌的抗肿瘤免疫,并抑制病毒产生、病毒 DNA 复制和晚期基因表达。 | |||
T3185 |
R112
|
Syk | Angiogenesis; Tyrosine Kinase/Adaptors |
R112 是 ATP 竞争性的 Syk 激酶抑制剂,它能够抑制 Syk 激酶活性,Ki=6 nM,IC50=226 nM。 | |||
T4337 |
PCI 29732
PCI29732,PCI-29732 |
Others; BCRP; BTK | Angiogenesis; Membrane transporter/Ion channel; Others; Tyrosine Kinase/Adaptors |
PCI 29732 是一种有效的可逆BTK 抑制剂,对 BTK、Lck 和 Lyn 的Kiapp 值分别为 8.2、4.6 和 2.5 nM。它通过竞争性结合ABCG2 的 ATP 结合位点来抑制ABCG2的功能。 | |||
T0220 |
Foscarnet sodium
Phosphonoformate,膦甲酸钠 |
Virus Protease; Reverse Transcriptase; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Foscarnet sodium (Phosphonoformate) 是一种病毒 DNA 聚合酶活性抑制剂,可逆地抑制病毒复制。它是一种用于治疗巨细胞病毒性视网膜炎的抗病毒剂。 | |||
T11882 |
Pulrodemstat benzenesulfonate
LSD1-IN-7 benzenesulfonate,CC-90011 benzenesulfonate |
Histone Demethylase | Chromatin/Epigenetic |
Pulrodemstat benzenesulfonate (CC-90011 benzenesulfonate) 是一种有效的口服活性赖氨酸特异性去甲基化酶 1 (LSD1) 抑制剂,IC50为 0.25 nM,具有抗癌活性。它诱导急性髓细胞性白血病和小细胞肺癌细胞分化,对 LSD2、MOA-A 和 MAO-B 的酶抑制作用较小。 | |||
T3109 |
SP600125
1PMV,JNK Inhibitor II,Nsc75890,Pyrazolanthrone |
Apoptosis; Ferroptosis; Trk receptor; JNK; Aurora Kinase; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; MAPK; Tyrosine Kinase/Adaptors |
SP600125 (JNK Inhibitor II) 是一种 JNK 抑制剂,抑制 JNK1、JNK2 和 JNK3 (IC50=40/40/90 nM),具有口服有效性、可逆性和 ATP 竞争性。SP600125 是一种有效的铁死亡抑制剂,可以抑制自噬,诱导凋亡。 | |||
T3041 |
ALK inhibitor 2
|
FAK; ALK | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
ALK inhibitor 2 是嘧啶类 ALK 的有效抑制剂。它是一种睾丸特异性丝氨酸/苏氨酸激酶 2 (TSSK2;IC50=37 nM) 和粘着斑激酶 (FAK;IC50=5 nM) 抑制剂。 | |||
T41143 |
pCPA methyl ester hydrochloride
4-氯-DL-苯基丙氨酸甲酯盐酸盐,4-Chloro-DL-phenylalanine methyl ester hydrochloride |
5-HT Receptor; Hydroxylase | GPCR/G Protein; Metabolism; Neuroscience |
pCPA methyl ester hydrochloride (4-Chloro-DL-phenylalanine methyl ester hydrochloride) 是色氨酸羟化酶抑制剂和5-HT 合成的抑制剂。 pCPA methyl ester hydrochloride 可穿过血脑屏障并降低 5-HT 中枢可用性。 | |||
T10285 |
ALK inhibitor 1
|
FAK; IGF-1R; ALK | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
ALK inhibitor 1 是嘧啶类 ALK 的有效抑制剂。它是一种睾丸特异性丝氨酸/苏氨酸激酶 2 (TSSK2;IC50=31 nM) 和粘着斑激酶 (FAK;IC50=2 nM) 抑制剂。 | |||
T25017 |
AKT-I-1
|
Akt | Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
AKT-I-1 是一种特异性和可逆的 Akt1 抑制剂。 | |||
T16682 |
Pumaprazole
BY-841,普马拉唑 |
Proton pump | Membrane transporter/Ion channel |
Pumaprazole (BY-841) 是一种有效的、可逆的质子泵拮抗剂。 | |||
T24030 |
Entacapone acid
AG1290,AG 1290,AG-1290,恩他卡朋酸 |
Transferase | Metabolism |
Entacapone acid (AG 1290) 是一种选择性和可逆的儿茶酚-O-甲基转移酶 (COMT) 抑制剂。 | |||
T26930 |
BW-1370U87
1370U-87,BW1370U87,1370U87,1370U 87,BW 1370U87 |
MAO | Metabolism; Neuroscience |
BW-1370U87 是一种可逆的竞争性单胺氧化酶-A抑制剂,可用于研究抑郁症和其他中枢神经系统疾病。 | |||
T5374 |
NAcM-OPT
|
E1/E2/E3 Enzyme; NEDD8 | Metabolism; Ubiquitination |
NAcM-OPT 是口服活性、有效的 cullin neddylation 1 抑制剂,可以抑制 DCN1-UBE2M 相互作用。 | |||
T8589 |
(±)-Amiflamine
4-(dimethylamino)-alpha,4-(2-氨基丙基)-N,N,3-三甲基苯胺,Amiflamine,2-dimethylphenethylamine |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
(±)-Amiflamine (2-dimethylphenethylamine) 是一种单胺氧化酶(MAO-A),pIC50=5.57。 | |||
T27320 |
Finrozole
MPV 2213ad,MPV-2213ad,MPV 2213,MPV-2213,MPV2213ad |
Aromatase | Endocrinology/Hormones |
Finrozole (MPV 2213ad) 是一种新型选择性芳香化酶抑制剂,对于乳房发育是部分可逆的。 | |||
T2468 |
A-769662
A 769662 |
AMPK; Fatty Acid Synthase | Chromatin/Epigenetic; Metabolism; PI3K/Akt/mTOR signaling |
A-769662 是一种可逆 AMPK 激活剂,EC50值为 0.8 μM。 | |||
T28339 |
PD 174265
PD174265,N-{4-[(3-Bromophenyl)amino]quinazolin-6-Yl}propanamide,PD-174265 |
EGFR | Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
PD 174265 是一种有效、选择性和可逆的表皮生长因子受体 (EGFR) 抑制剂,IC50 为 0.45 nM。 | |||
T13268 |
USP7-IN-1
|
DUB | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination |
USP7-IN-1 是泛素蛋白特异性蛋白酶的选择性、可逆性抑制剂,IC50为 77 μM,可用于癌症研究。 | |||
T22832 |
H-8 hydrochloride
|
PKA | Tyrosine Kinase/Adaptors |
H-8 hydrochloride 是一种具有可逆性和 ATP 竞争性的 PKA 抑制剂。可用研究代谢疾病。 | |||
T14681 |
BMS-935177
|
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
BMS-935177 是一种可逆的 BTK 抑制剂,IC50 值为 3 nM。 | |||
T3596 |
TB5
|
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
TB5 是一种选择性可逆 hMAO-B 有效抑制剂,Ki=0.11±0.01 μM。 | |||
T9096 |
Nω-Hydroxy-nor-L-Arginine Dihydrochloride
|
Arginase | Immunology/Inflammation |
Nω-Hydroxy-nor-L-Arginine Dihydrochloride 是一种竞争性和可逆的精氨酸酶抑制剂。 | |||
T6901 |
N6022
|
GSNOR | Metabolism |
N6022 是选择性可逆的S-Nitrosoglutathione reductase 抑制剂,IC50=8 nM。 | |||
T5323 |
Toloxatone
托洛沙酮,MD 69276 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Toloxatone (MD 69276) 是可逆的单胺氧化酶 A (MAOA) 抑制剂,是一种抗抑郁剂。 | |||
T11177 |
Elinogrel
PRT060128 |
P2Y Receptor | GPCR/G Protein; Neuroscience |
Elinogrel (PRT060128) 是一种竞争性和可逆的血小板 P2Y12 拮抗剂,IC50 为 20 nM,并表现出有效的抗血小板作用。 | |||
T27288 |
Esuprone
LU-43839,LU 43839,LU43839 |
MAO | Metabolism; Neuroscience |
Esuprone (LU-43839) 是一种新型可逆且具有高选择性的MAO-A 抑制剂,具有抗惊厥活性,可用于治疗抑郁症。 | |||
T22692 |
CPCCOEt
|
GluR | Neuroscience |
CPCCOEt 是mGluR1b 的一种低亲和力、选择性、非竞争性和可逆性拮抗剂 | |||
T4467 |
UAMC00039 dihydrochloride
UAMC 00039 dihydrochloride |
Proteasome | Proteases/Proteasome; Ubiquitination |
UAMC00039 dihydrochloride 是可逆、竞争性的 dipeptidyl peptidase II 高效抑制剂,IC50=为0.48 nM。 | |||
T2377 |
Pilaralisib analogue
XL147 analogue,SAR245408 |
Apoptosis; DNA-PK; PI3K | Apoptosis; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
Pilaralisib analogue (XL147 analogue) 是一种选择性和可逆的 I 类 PI3K 抑制剂,用于 PI3Kα/δ/γ。 | |||
T10988L |
Degarelix acetate(214766-78-6 free base)
|
GNRH Receptor | GPCR/G Protein |
Degarelix acetate(214766-78-6 free base) 是促性腺激素释放激素受体 (GnRHR) 的竞争性可逆拮抗剂。 | |||
T5053 |
Eprobemide
LIS 630,依普贝胺 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Eprobemide (LIS 630) 是一种非竞争性的、可逆的单胺氧化酶 A 抑制剂。 | |||
T2465 |
PF-562271
PF562271,PF 562271 |
FAK; PYK2; CDK | Angiogenesis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
PF-562271 是一种可逆的,有效的,ATP 竞争性的 FAK (IC50:1.5 nM)和 Pyk2 (IC50:13 nM)激酶抑制剂。 | |||
T1969 |
DBEQ
JRF 12 |
Apoptosis; p97; Autophagy | Apoptosis; Autophagy; Ubiquitination |
DBEQ (JRF 12) 是一种选择性的,ATP 竞争性p97抑制剂,对 p97(wt) 和 p97(C522A) 的IC50值分别为 1.5 μM 和 1.6 μM,也可抑制Vps4,IC50值为 11.5 μM。 | |||
T4736 |
Cruzain-IN-1
ML092 |
Antibiotic | Microbiology/Virology |
Cruzain-IN-1 (ML092) 是一种克鲁斯氏锥体虫半胱氨酸蛋白酶(Cruzain)的共价可逆抑制剂(IC50:10 nM)。 | |||
T6107 |
IU1
|
DUB; Autophagy | Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Ubiquitination |
IU1 是一种可逆的特异性人类 USP14 蛋白酶体抑制剂,可以穿透细胞,IC50为 4.7 μM。 | |||
T1950 |
PND-1186
PND1186,PND 1186,VS-4718,SR-2516 |
Apoptosis; FAK | Angiogenesis; Apoptosis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
PND-1186 (VS-4718) 是一种高特异性的FAK 可逆抑制剂,IC50为 1.5 nM。它选择性促进肿瘤细胞凋亡。 | |||
T14927 |
Centrinone
LCR-263 |
PLK; Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
Centrinone (LCR-263) 是 polo 样激酶 4 的可逆抑制剂,对PLK4的Ki 值为0.16 nM。 | |||
T12613L |
BAY-85-8501
|
Serine Protease | Proteases/Proteasome |
BAY-85-8501 是选择性的人类中性脂酶抑制剂,IC50=65 pM。 | |||
T5138 |
BMS-986142
|
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
BMS986142 是一种有效的、具有高选择性的 Bruton's 酪氨酸激酶 (BTK)可逆性抑制剂 (IC50:0.5 nM)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S2391 |
L-Chicoric Acid
(-)-Chicoric acid,trans-Caffeoyltartaric acid,Chicoric acid,L-菊苣酸,dicaffeoyltartaric acid,菊苣酸 |
Others; HIV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
L-Chicoric Acid (trans-Caffeoyltartaric acid) 是一种二咖啡酰酒石酸,是一种选择性可逆的 HIV-1 整合酶抑制剂,IC50约为 100 nM。它还可抑制 HIV-1 复制。 | |||
T4899 |
L-Histidinol dihydrochloride
|
Endogenous Metabolite | Metabolism |
L-Histidinol dihydrochloride 是内源性代谢产物的一种。 | |||
T5648 |
Purpurin
吡啉,1,2,4-Trihydroxyanthraquinone,Hydroxylizaric acid,Verantin |
MAO; Antibacterial; Antibiotic; Antifungal | Metabolism; Microbiology/Virology; Neuroscience |
Purpurin (Verantin) 是来自Rubia tinctorumL. 的天然蒽醌,具有抗抑郁样作用。 | |||
T3740 |
Isovanillin
3-羟基-4-甲氧基苯甲醛,3-Hydroxy-p-anisaldehyde,3-Hydroxy-4-methoxybenzaldehyde,5-Formylguaiacol |
Others | Others |
Isovanillin (5-Formylguaiacol) 是一种醛氧化酶抑制剂,具有解痉挛和止泻活性。 | |||
T13469 |
(±)-Huperzine A
|
AChE | Neuroscience |
(±)-Huperzine A 是一种从中药中提取的活性石松属生物碱。 (±)-Huperzine A 是一种特异性和可逆的乙酰胆碱酯酶抑制剂,可用于治疗阿尔茨海默病的研究。 | |||
T8044 |
Ajmalicine
阿吗里新,Lamuran,Delta-Yohimbine,Raubasine,Ajmalicin |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Ajmalicine (Raubasine) 是一种有效的抗肾上腺素 (adrenolytic) 剂,优先阻断 α1-肾上腺素受体 (α1-adrenoceptor)。Ajmalicine 是一种可逆性但非竞争性尼古丁受体 (nicotine receptor) 完全抑制剂,IC50 为 72.3 μM。Ajmalicine 还可用于降压、蛇毒,具有镇静活性。 | |||
T0130 |
Physostigmine Salicylate
水杨酸依色林,水杨酸毒扁豆碱 |
AChR; AChE | Neuroscience |
Physostigmine salicylate 是一种可逆的乙酰胆碱酯酶抑制剂,也一种是抗胆碱能中毒的解毒剂。它可透过血脑屏障并刺激中枢胆碱能神经传递。它能逆转阿尔茨海默病转基因小鼠的记忆缺陷。 | |||
T4590 |
(+)-Kavain
醉椒素,Kavain,L-KAWAIN,(R)-KAWAIN |
Calcium Channel; GABA Receptor; Sodium Channel; Monoamine Transporter | Membrane transporter/Ion channel; Metabolism; Neuroscience |
(+)-Kavain ((R)-KAWAIN) 是从卡瓦胡椒中提取的一种主要的卡瓦内酯,可通过电压依赖性的 Na+和 Ca2+通道相互作用,减弱血管平滑肌的收缩,具有抗惊厥作用。它可与α4β2δ GABAA 受体结合,加强 GABA 的功效,用于炎症疾病研究。 | |||
T20488 |
4-Isopropylbenzoic acid
NSC1907,NSC-1907,NSC 1907,Cumic acid |
Antifungal | Microbiology/Virology |
4-Isopropylbenzoic acid (Cumic acid) 是一种芳香单萜,从 Bridelia retusa 的茎皮中分离得到。4-Isopropylbenzoic acid 显示出抗真菌活性。4-Isopropylbenzoic acid 也是一种可逆的、非竞争性的蘑菇酪氨酸酶 (mushroom tyrosinase) 抑制剂。 | |||
T6740 |
Bafilomycin A1
巴佛洛霉素A1,巴佛洛霉素 A1 |
Apoptosis; Proton pump; Antibacterial; Antibiotic; Autophagy | Apoptosis; Autophagy; Membrane transporter/Ion channel; Microbiology/Virology |
Bafilomycin A1 属于大环内酯类抗生素,是一种 V-ATPase 抑制剂 (IC50=0.44 nM),具有特异性和可逆性。Bafilomycin A1 是自噬晚期阶段抑制剂,阻断自噬体与溶酶体的融合。Bafilomycin A1 也诱导凋亡。 | |||
T20754 |
Deltamethrin
Butoss,RU-22974,Esbecythrin,溴氰菊酯,K-Othrin,Decamethrin,RU 22974 |
Others | Others |
Deltamethrin (RU 22974) 是一种具有神经毒性的拟除虫菊酯杀虫剂,在大鼠中能够产生一系列可逆的运动症状(如包括后肢僵硬、舞蹈性关节炎)。 | |||
T40179 |
Sodium Camptothecin
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Sodium Camptothecin 是一种植物生物碱,具有抗肿瘤活性。它是可逆 RNA 合成抑制剂,可以抑制腺病毒的复制。它能抑制 DNA 合成,并引起细胞内预形成的病毒 DNA 断裂。 | |||
TN1120 |
Osthenol
|
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Osthenol 是一种前酰化香豆素,从独活干根中分离得到。它对重组 hMAO-A 具有潜在的选择性抑制作用,IC50=0.74 µM,对 hMAO-A 和 hMAO-B 表现出较高的选择性指数。它是一种可逆的,选择性的竞争性人单胺氧化酶-A(hMAO-A)抑制剂 (Ki=0.26 µM)。 | |||
T6270 |
Trichostatin A
曲古柳菌素A,曲古抑菌素A,TSA |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Trichostatin A (TSA) 属于二烯异羟肟酸类的天然衍生物。Trichostatin A 是一种组蛋白去乙酰化酶抑制剂 (IC50=1.8 nM),具有可逆性和特异性。Trichostatin A 导致核心组蛋白过度乙酰化,从而调节染色质结构。 | |||
T1658 |
Selenomethionine
DL-Selenomethionine,DL-硒代蛋氨酸,Seleno-DL-methionine,硒代蛋氨酸 |
Amino Acids and Derivatives; Endogenous Metabolite; Autophagy | Autophagy; Metabolism |
Selenomethionine (Seleno-DL-methionine) 是一种硒代氨基酸,是蛋氨酸的硒类似物。 它具有作为植物代谢物的作用。 它是硒代蛋氨酸和硒代氨基酸的成员。 | |||
T6564 |
Leupeptin Hemisulfate
亮肽素 |
Serine Protease; Cysteine Protease | Proteases/Proteasome |
Leupeptin hemisulfate 是一种蛋白酶抑制剂,具有细胞膜渗透性、可逆性、竞争性和口服活性。Leupeptin hemisulfate 可以抑制 Cathepsin B、Cathepsin H、Cathepsin L 的活性,阻断两性溶酶体的融合。Leupeptin hemisulfate 还具有抗炎活性。 | |||
TCS1709 |
BENZYLACETONE
苄基丙酮,4-Phenylbutan-2-one,Methyl 2-phenylethyl ketone,4-Phenyl-2-butanone |
Tyrosinase | Proteases/Proteasome |
Benzylacetone (4-Phenyl-2-butanone) 是一种从沉香木中提取的芳香族化合物。它具有增强食欲和减少运动的作用。它具有较强且可逆的抗蘑菇酪氨酸酶作用,对单酚酶和双酚酶作用的IC50值分别为 2.8 mM 和 0.6 mM。 | |||
T3026 |
(-)-Huperzine A
HupA,石杉碱,Huperzine A,石杉碱甲 |
Apoptosis; AChR; AChE; iGluR | Apoptosis; Membrane transporter/Ion channel; Neuroscience |
(-)-Huperzine A (HupA) 是从中国梅花苔中分离得到的一种生物碱,具有神经保护活性。它是高特异性可逆的,具有血脑屏障渗透性的一种乙酰胆碱酯酶抑制剂, 其IC50值为 82 nM。 它也是 N-甲基-D-天冬氨酸受体的非竞争性拮抗剂,可研究神经退行性疾病,如阿尔茨海默病。 | |||
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。 | |||
TN5166 |
Trans-Methylisoeugenol
|
Parasite; GST | Microbiology/Virology; oxidation-reduction |
Trans-Methylisoeugenol 是从 Acorus calamus L 中分离得到的具有杀虫活性的化合物。它 是一种天然食用香料,具有抗焦虑和抗抑郁等特性,可对谷胱甘肽 S-转移酶(GSTs)产生中度可逆性抑制作用(对人类 GSTs 的抑制浓度为 0.2 至 5.4 毫摩尔,对大鼠 GSTs 的抑制浓度为 0.4 至 4.9 毫摩尔)。 | |||
T3921 |
Punicalagin
安石榴甙,安石榴苷 |
SARS-CoV; HBV | Microbiology/Virology |
Punicalagin 是一种在石榴中发现的主要鞣花单宁,是可逆且非竞争性的 3CLpro 抑制剂。Punicalagin 具有抗氧化、抗炎和抗肿瘤活性。 | |||
TN3540 |
Broussonin C
|
Tyrosinase; Antifection | Microbiology/Virology; Proteases/Proteasome |
Broussonin C and broussin are antifungal compounds. Broussonin C exerts simple reversible slow-binding inhibition against diphenolase. | |||
T21438 |
Physostigmine
Physostol,Antilirium,Eserine,毒扁豆碱,Esromiotin,Ezerin |
Others | Others |
Physostigmine is a potent and reversible inhibitor of cholinesterase. It is also reported to form a slowly degrading carbamylated enzyme complex with acetylcholinesterase (AChE). | |||
T10664 |
Calcium 2-oxoglutarate
|
Others; Tyrosinase | Others; Proteases/Proteasome |
Calcium 2-oxoglutarate is an intermediate in the production of GTP or ATP in the Krebs cycle. It is a reversible inhibitor of tyrosinase (IC50: 15 mM). | |||
T74005 |
Urolithin D
|
Others | Others |
Urolithin D 是EphA 受体的竞争性可逆拮抗剂。Urolithin D 表现出类内选择性。 | |||
TN1320 |
6-O-Caffeoylarbutin
|
Others | Others |
6'-O-caffeoylarbutin may serve as a skin-whitening ingredient with the merits of potent melanin inhibition,less toxicity and reversible melanin synthesis after stopping use. | |||
T16381 |
Okadaic acid
|
Others | Others |
Okadaic acid is a non-comepetitive, selective and reversible serine/threonine-specific protein phosphatases 1 (PP1), PP2A, and PP3 inhibitor (IC50s: 10-15 nM, 0.5 nM, and 4 nM, respectively). Okadaic acid is extracted from black sponges of the genus Halic | |||
TN2517 |
1,7-Dihydroxy-2,3-dimethoxyxanthone
|
Others | Others |
1,7-Dihydroxy-2,3-dimethoxyxanthone may have medicinal use in the management of inflammation, asthma and allergy, it antagonises in a non competitive but, reversible manner the contractions induced by chemical inflammatory mediators in the guinea pig trac | |||
TN7557 |
Heronamide C
|
Others | Others |
Heronamide C, a polyketide macrolactam antifungal agent synthesized by marine Actinomycetes, exhibits selective toxicity by inhibiting growth and promoting abnormal cell wall material accumulation in wild-type fission yeast cells (MIC = 0.13-0.28 μM), without affecting Gram-positive bacteria or human cancer cell lines, HeLa and MDA-MB-231. At 20 μM, it triggers reversible morphological alterations, notably the development of large intracellular structures, in HeLa cells. | |||
TN7291 |
2-Deoxyribose 5-phosphate disodium
|
Others | Others |
2-Deoxyribose 5-phosphate disodium 是一种2-deoxyribose-5-phosphate aldolase (DERA) 的底物,该酶为I类醛缩酶,负责催化可逆醛缩反应,且在过程中不需要任何辅助因子。 | |||
TN2344 |
Swainsonine
Tridolgosir |
Apoptosis; Others; Antibiotic | Apoptosis; Microbiology/Virology; Others |
Swainsonine (Tridolgosir) 是一种从黄芪中分离出来的一种生物碱,是一种强效和可逆的α-甘露糖苷酶抑制剂。Swainsonine 具有抗肿瘤活性,可诱导细胞凋亡和细胞周期停滞在 G2/M 期。 | |||
T81030 |
Tauro-β-muricholic acid
TβMCA |
FXR | Metabolism |
Tauro-β-muricholic acid (TβMCA) 为一种具有三羟基结构的胆汁酸,是FXR的竞争性、可逆拮抗剂,IC50值为40 μM。此外,Tauro-β-muricholic acid 能够通过维持线粒体膜电位来阻抑胆汁酸引起的肝细胞凋亡,发挥抗凋亡功能。 | |||
T69254 |
Ajmalicine hydrochloride
Raubasine hydrochloride |
Others | Others |
Ajmalicine (Raubasine) hydrochloride 是一种有效的抗肾上腺素 (adrenolytic) 剂,优先阻断 α1-肾上腺素受体 (α1-adrenoceptor)。Ajmalicine hydrochloride 是一种可逆性但非竞争性尼古丁受体 (nicotine receptor) 完全抑制剂,其 IC50为 72.3 μM。Ajmalicine hydrochloride 还可用于降压、蛇毒,具有镇静活性。 | |||
T14121 |
Actinonin
(-)-Actinonin |
Aminopeptidase | Metabolism |
Actinonin ((-)-Actinonin) is a naturally occurring antibacterial agent produced by Actinomyces and a potent reversible peptide deformylase (PDF) inhibitor with a Ki of 0.28 nM, it also is an apoptosis inducer. Actinonin inhibits aminopeptidase M, aminopeptidase N and leucine aminopeptidase, it also inhibits MMP-1, MMP-3, MMP-8, MMP-9, and hmeprin α with Ki values of 300 nM, 1,700 nM, 190 nM, 330 nM, and 20 nM, respectively. Actinonin has antiproliferative and antitumor activities[1][2][3][4][5]. | |||
T16896 |
SL 0101-1
SL0101 |
S6 Kinase | MAPK; PI3K/Akt/mTOR signaling |
SL 0101-1 (SL0101) 是一种可透过细胞膜且具有选择性、高效性、可逆性、ATP竞争性的 p90核糖体S6激酶(RSK) 的抑制剂,对 RSK 的 IC50 值为 89 nM。SL 0101-1 (SL0101) 也是一种有效的 RSK1/2 抑制剂,其 Ki 值为 1 μM。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-02279 |
Nucleoside phosphorylase/PNP Protein, Human, Recombinant (His)
PUNP,PRO1837,purine nucleoside phosphorylase,NP |
Human | E. coli |
Purine nucleoside phosphorylase (PNP) is a purine-metabolizing enzyme that catalyzes the reversible phosphorolysis of 6-oxypurine (deoxy)nucleosides to their respective bases and (deoxy)ribose-1-phosphate. It is a key enzyme in the purine salvage pathway of mammalian cells. Purine nucleoside phosphorylase is a transferase that catalyzes the addition of phosphate and removal of a purine base from guanosine and similar nucleosides.PNP defects result in metabolic abnormalities and fatal T cell immu... | |||
TMPH-01038 |
CA5A Protein, Human, Recombinant
Carbonic anhydrase VA,Carbonic anhydrase 5A, mitochondrial,C... |
Human | HEK293 Cells |
Reversible hydration of carbon dioxide. Low activity. CA5A Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 30.6 kDa and the accession number is P35218. | |||
TMPH-00515 |
PPDK Protein, Entamoeba histolytica, Recombinant (His & SUMO)
PPDK,Pyruvate, orthophosphate dikinase,Pyruvate, phosphate d... |
Entamoeba histolytica | E. coli |
Catalyzes the reversible phosphorylation of pyruvate and phosphate. In E.histolytica and C.symbiosus, PPDK functions in the direction of ATP synthesis. | |||
TMPJ-00826 |
TXN Protein, Human, Recombinant (His)
ADF,TXN,TRX1,Thioredoxin,TRX,ATL-Derived Factor,TRDX,Surface... |
Human | E. coli |
Thioredoxin (TXN) is a member of the Thioredoxin family. Thioredoxin exists as a disulfide-linked homodimer and contains one Thioredoxin domain. Thioredoxin is up-regulated by ionizing radiation. Thioredoxin participates in various redox reactions through the reversible oxidation of its active center dithiol to a disulfide and catalyzes dithiol-disulfide exchange reactions. Thioredoxin also plays a role in the reversible S-nitrosylation of cysteine residues in target proteins, and thereby contri... | |||
TMPH-03258 |
Carbonic Anhydrase 1 Protein, Rat, Recombinant (His & SUMO)
Cyanamide hydratase CA1,CA-I,Carbonate dehydratase I,Car1,Ca... |
Rat | E. coli |
Reversible hydration of carbon dioxide. Carbonic Anhydrase 1 Protein, Rat, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 44.2 kDa and the accession number is B0BNN3. | |||
TMPH-01085 |
CHAT Protein, Human, Recombinant (His)
CHAT,Choline O-acetyltransferase,ChAT,CHOACTase,Choline acet... |
Human | E. coli |
Catalyzes the reversible synthesis of acetylcholine (ACh) from acetyl CoA and choline at cholinergic synapses. CHAT Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 72.7 kDa and the accession number is P28329. | |||
TMPH-00312 |
Malate dehydrogenase Protein, Brucella abortus, Recombinant (His & Myc & SUMO)
mdh,Malate dehydrogenase |
Brucella abortus | E. coli |
Catalyzes the reversible oxidation of malate to oxaloacetate. Malate dehydrogenase Protein, Brucella abortus, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 53.7 kDa and the accession number is B2S881. | |||
TMPH-00398 |
PPK2 Protein, Chlorobium tepidum, Recombinant (His & Myc)
ppk2,ATP-polyphosphate phosphotransferase 2,Polyphosphoric a... |
Chlorobaculum tepidum | E. coli |
Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP). PPK2 Protein, Chlorobium tepidum, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 34.4 kDa and the accession number is O68984. | |||
TMPH-03021 |
PstP Protein, Mycobacterium tuberculosis, Recombinant (His)
Mycobacterial Ser/Thr phosphatase,PP2C-family Ser/Thr phosph... |
Mycobacterium tuberculosis | E. coli |
Plays an important role in regulating cell division and growth by reversible phosphorylation signaling. May play important roles in regulating cellular metabolism and signaling pathways, which could mediate the growth and development of the cell. Plays a role in establishing and maintaining infection. | |||
TMPJ-01207 |
UPP1 Protein, Human, Recombinant (His)
UPP1,Uridine Phosphorylase 1,UPP1 Protein |
Human | E. coli |
Uridinephosphorylase 1 (UPP1) is a member of the family of pentosyltransferase. UPP1 catalyses the reversible phosphorolysis of uridine to uracil. The expression levels and the enzymatic activity of UPP1 are higher in human solid tumors than in adjacent normal tissues. The high level of UPP1 expression in some tumors makes it a potential prognosticfactor for some cancers, such as oral squamous cell carcinoma. UPP1 is important for the homeostatic regulation of intracellular and plasma uridine c... | |||
TMPH-00422 |
Ppdk Protein, Clostridium symbiosum, Recombinant (His & Myc)
ppdK,Pyruvate, orthophosphate dikinase,Pyruvate, phosphate d... |
Clostridium symbiosum | E. coli |
Catalyzes the reversible phosphorylation of pyruvate and phosphate. In E.histolytica and C.symbiosus, PPDK functions in the direction of ATP synthesis. Ppdk Protein, Clostridium symbiosum, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 20.5 kDa and the accession number is P22983. | |||
TMPH-02195 |
TXNDC17 Protein, Human, Recombinant (GST)
Thioredoxin-like protein 5,Protein 42-9-9,Thioredoxin domain... |
Human | E. coli |
Disulfide reductase. May participate in various redox reactions through the reversible oxidation of its active center dithiol to a disulfide and catalyze dithiol-disulfide exchange reactions. Modulates TNF-alpha signaling and NF-kappa-B activation. Has peroxidase activity and may contribute to the elimination of cellular hydrogen peroxide. | |||
TMPH-00739 |
Thioredoxin-1 Protein, E. coli, Recombinant (His)
Thioredoxin 1,trxA |
E. coli | E. coli |
Participates in various redox reactions through the reversible oxidation of its active center dithiol to a disulfide and catalyzes dithiol-disulfide exchange reactions. Thioredoxin-1 Protein, E. coli, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 15.7 kDa and the accession number is P0AA25. | |||
TMPH-00911 |
GPT Protein, Human, Recombinant (His)
Glutamic--alanine transaminase 1,Glutamate pyruvate transami... |
Human | E. coli |
Catalyzes the reversible transamination between alanine and 2-oxoglutarate to form pyruvate and glutamate. Participates in cellular nitrogen metabolism and also in liver gluconeogenesis starting with precursors transported from skeletal muscles. GPT Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 58.5 kDa and the accession number is P24298. | |||
TMPH-03259 |
Carbonic Anhydrase 2 Protein, Rat, Recombinant (His)
CA-II,Carbonate dehydratase II,Carbonic anhydrase II,Cyanami... |
Rat | E. coli |
Essential for bone resorption and osteoclast differentiation. Reversible hydration of carbon dioxide. Contributes to intracellular pH regulation in the duodenal upper villous epithelium during proton-coupled peptide absorption. Stimulates the chloride-bicarbonate exchange activity of SLC26A6. Carbonic Anhydrase 2 Protein, Rat, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 31.7 kDa and the accession number is P27139. | |||
TMPJ-01278 |
SENP8 Protein, Human, Recombinant (His)
DEN1,Protease Cysteine 2,NEDP1,Sentrin-Specific Protease 8,D... |
Human | E. coli |
Sentrin-Specific Protease 8 (SENP8) mediates the reversible covalent modification of proteins by NEDD8. SENP8 catalyzes the full-length NEDD8 to generate its mature form and deconjugation of NEDD8 from targeted proteins such as CUL2 , CUL4A in vivo, or p53. but it does not show activity against ubiquitin or SUMO proteins. | |||
TMPH-03503 |
Adenylate kinase Protein, Shigella flexneri, Recombinant (His & Myc & SUMO)
ATP-AMP transphosphorylase,AK,Adenylate monophosphate kinase... |
Shigella flexneri | E. coli |
Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism. Adenylate kinase Protein, Shigella flexneri, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 43.6 kDa and the accession number is Q83M40. | |||
TMPH-01678 |
MMUT Protein, Human, Recombinant (His)
MMUT,Methylmalonyl-CoA mutase, mitochondrial,Methylmalonyl-C... |
Human | E. coli |
Catalyzes the reversible isomerization of methylmalonyl-CoA (MMCoA) (generated from branched-chain amino acid metabolism and degradation of dietary odd chain fatty acids and cholesterol) to succinyl-CoA (3-carboxypropionyl-CoA), a key intermediate of the tricarboxylic acid cycle. MMUT Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 84.8 kDa and the accession number is P22033. | |||
TMPH-03584 |
Shikimate dehydrogenase Protein, S. epidermidis, Recombinant (His & Myc)
Shikimate dehydrogenase (NADP(+)),aroE |
Staphylococcus epidermidis | E. coli |
Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA). It can also use NAD to oxidize shikimate. Shikimate dehydrogenase Protein, S. epidermidis, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 37.4 kDa and the accession number is Q5HNV1. | |||
TMPH-03022 |
PstP Protein, Mycobacterium tuberculosis, Recombinant
PP2C-family Ser/Thr phosphatase,pstP,Serine/threonine protei... |
Mycobacterium tuberculosis | E. coli |
Plays an important role in regulating cell division and growth by reversible phosphorylation signaling. May play important roles in regulating cellular metabolism and signaling pathways, which could mediate the growth and development of the cell. Plays a role in establishing and maintaining infection. PstP Protein, Mycobacterium tuberculosis, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 25.3 kDa and the accession number is P9WHW4. | |||
TMPJ-00818 |
ALDOC Protein, Human, Recombinant (His)
Aldolase C,ALDC,zebrin II,Aldo3,Scrg2,Fructose-bisphosphate ... |
Human | HEK293 Cells |
Fructose-bisphosphate aldolase C (ALDOC) belongs to the class I fructose-bisphosphate aldolase family. It is an enzyme that, in humans, is encoded by the ALDOC gene. ALDOC is expressed exclusively in the hippocampus and Purkinje cells of the brain. ALDOC is a glycolytic enzyme which catalyzes the reversible aldol cleavage of fructose-1,6-biphosphate and fructose 1-phosphate to dihydroxyacetone phosphate and either glyceraldehyde-3-phosphate or glyceraldehydes respectively | |||
TMPY-03386 |
ART3 Protein, Human, Recombinant (His)
ADP-ribosyltransferase 3,ARTC3 |
Human | HEK293 Cells |
ART3 is an arginine-specific ADP-ribosyltransferase which belongs to the Arg-specific ADP-ribosyltransferase family. ART3 catalyzes a reversible reaction which modifies proteins by the addition or removal of ADP-ribose to an arginine residue to regulate the function of the modified protein. It is expressed specifically in testis. ART3 pseudogene is located on chromosome 11. ART3 was identified as a susceptibility gene for non-obstructive azoospermia (NOA). It is a novel therapeutic target in the... | |||
TMPJ-00956 |
MDH2 Protein, Human, Recombinant (His)
MDH2,Malate dehydrogenase,mitochondrial |
Human | HEK293 Cells |
Malate dehydrogenase, mitochondrial is a 338 amino acids protein that belongs to the LDH/MDH superfamily. MDH type 1 family. MDH2 catalyzes the reversible oxidation of malate to oxaloacetate, utilizing the NAD/NADH cofactor system in the citric acid cycle. MDH2 is localized to the mitochondria and takes part in the malate-aspartate shuttle that functions in the metabolic coordination between cytosol and mitochondria. MDH2 is highly expressed in the adrenal system, small intestine, heart and panc... | |||
TMPJ-00313 |
Fumarase Protein, Human, Recombinant
FH,Fumarase,Fumarate Hydratase Mitochondrial |
Human | E. coli |
Fumarase is an enzyme that catalyze the reversible hydration/dehydration of fumarate to S-malate and is involved in the tricarboxylic acid or Krebs cycle. Fumarase exists in both form, cytosolic formand N-terminal extend mitochondrial form. The N-terminal extended form is targeted to the mitochondrion, where the removal of the extension is the same form as in the cytoplasm. Fumarase is thought to act as a tumor suppressor, which deficiency can lead to progressive encephalopathy, cerebral atrophy... | |||
TMPJ-00484 |
SHMT1 Protein, Human, Recombinant (His)
Serine Methylase,Glycine Hydroxymethyltransferase,Serine Hyd... |
Human | HEK293 Cells |
Serine Hydroxymethyltransferase Cytosolic (SHMT1) is a member of the SHMT family. SHMT1 is a cytoplasmic protein and exists as a homotetramer. SHMT1 catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. This reaction provides one carbon unit for the synthesis of methionine, thymidylate, and purines in the cytoplasm. A reduction in SHMT1 levels would result in less glycine that could affect the nervous system by acting as an agonist to ... | |||
TMPJ-00701 |
Carbonic Anhydrase 11 Protein, Human, Recombinant (His)
Carbonic Anhydrase-Related Protein 2,CARP XI,CA11,CARP-2,Car... |
Human | HEK293 Cells |
Carbonic Anhydrase-Related Protein 11 (CA11) is a secreted protein member of the α-carbonic anhydrase family. Carbonic Anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. CA11 is expressed abundantly in the brain with moder... | |||
TMPJ-00601 |
Apolipoprotein C-II/APOC2 Protein, Human, Recombinant (His)
Apolipoprotein C2,Apolipoprotein C-II,APC2 and APOC2 |
Human | E. coli |
APOC2 activates the lipoprotein lipase in capillaries, which hydrolyzes triglycerides and thus provides free fatty acids for cells. APOC2 is component of the very low density lipoprotein (VLDL) fraction in plasma. It is also an activator of several triacylglycerol lipases. The association of APOC2 with plasma chylomicrons, VLDL, and HDL is reversible, a function of the secretion and catabolism of triglyceride-rich lipoproteins, and changes rapidly. Defects in APOC2 are the cause of hyperlipoprot... | |||
TMPJ-00283 |
Carbonic Anhydrase 9 Protein, Human, Recombinant (Avi & His), Biotinylated
G250,P54/58N,Carbonic Anhydrase IX,CA9,Carbonate dehydratase... |
Human | HEK293 Cells |
Carbonic anhydrases IX (CA IX), also known as membrane antigen MN or CA9, is a member of the carbonic anhydrase (CA) family and may be involved in cell proliferation and cellular transformation. CAs are zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide (H2O + CO2 = H+ + HCO3–) and thus participate in a variety of biological and physical processes. CA9 is a transmembrane enzyme expressed primarily in carcinoma cells. It is one of the best markers for hypoxia and for RCC... | |||
TMPJ-00731 |
Carbonic Anhydrase 1 Protein, Human, Recombinant (His)
Carbonic Anhydrase B,Carbonate Dehydratase I,CA-I,Carbonic A... |
Human | E. coli |
Carbonic Anhydrase 1 (CA1) is a cytosolic enzyme, belonging to the alpha-carbonic anhydrase family. It is highly expressed in erythrocytes and acts as an early marker for erythroid differentiation. Carbonic anhydrase 1 plays a improtant role in many biological processes such as calcification, cellular respiration, bone resorption, acid-base balance. It is activated by imidazole, histamine, L-adrenaline, L- and D-histidine, and L- and D-phenylalanine. At the same time, It is inhibited by sulfonam... | |||
TMPY-01877 |
CA5A Protein, Human, Recombinant (His)
CA5,GS1-21A4.1,CA5AD,carbonic anhydrase VA, mitochondrial,CA... |
Human | E. coli |
Carbonic anhydrase 5A, mitochondrial, also known as Carbonate dehydratase VA, Carbonic anhydrase VA, CA-VA and CA5A, is a member of thealpha-carbonic anhydrase family. Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes first discovered in 1933 that catalyze the reversible hydration of carbon dioxide. CAs participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospi... | |||
TMPY-02277 |
Carbonic Anhydrase 7 Protein, Human, Recombinant (His)
CAVII,carbonic anhydrase VII |
Human | E. coli |
Carbonic anhydrase 7, also known as carbonate dehydratase VII, carbonic anhydrase VII, CA-VII and CA7, is a cytoplasm protein which belongs to thealpha-carbonic anhydrase family. Carbonic anhydrases are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, ... | |||
TMPY-02453 |
CROT Protein, Human, Recombinant (474 Leu/Val, His)
carnitine O-octanoyltransferase,COT |
Human | Baculovirus Insect Cells |
Carnitine octanoyltransferase (CROT or COT), also known as octanoyl-CoA: L-carnitine O-octanoyltransferase, medium-chain/long-chain carnitine acyltransferase, and carnitine medium-chain acyltransferase, is a carnitine acyltransferase belonging to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups that catalyzes the reversible transfer of fatty acyl groups between CoA and carnitine. Carnitine octanoyltransferase (CROT or COT) facilitate... | |||
TMPJ-00497 |
CTSB Protein, Human, Recombinant (His)
APPS,CPSB,APP Secretase,Cathepsin B1,Cathepsin B,CTSB |
Human | HEK293 Cells |
Cathepsin B is an enzymatic protein belonging to the peptidase (or protease) families. The protein encoded by this gene is a lysosomal cysteine protease composed of a dimer of disulfide-linked heavy and light chains, both produced from a single protein precursor. It is a member of the peptidase C1 family. At least five transcript variants encoding the same protein have been found for this gene. Cystatin-B / CSTB is an intracellular thiol proteinase inhibitor. Tightly binding reversible inhibitor... | |||
TMPY-03755 |
Glycerol 3 Phosphate Dehydrogenase/GPD1 Protein, Human, Recombinant (His)
GPDH-C,HTGTI,GPD-C,glycerol-3-phosphate dehydrogenase 1 (sol... |
Human | E. coli |
GPD1 (Glycerol-3-Phosphate Dehydrogenase 1) is a Protein Coding gene. 2 alternatively spliced human isoforms have been reported. GPD1 is a member of the NAD-dependent glycerol-3-phosphate dehydrogenase family. The encoded protein plays a critical role in carbohydrate and lipid metabolism by catalyzing the reversible conversion of dihydroxyacetone phosphate (DHAP) and reduced nicotine adenine dinucleotide (NADH) to glycerol-3-phosphate (G3P) and NAD+. It also reduces nicotine adenine dinucleotide... | |||
TMPJ-01034 |
TIM Protein, Human, Recombinant (His)
TPI1,TPI,Triose-Phosphate Isomerase,Triosephosphate Isomeras... |
Human | E. coli |
Triose-phosphate isomerase, also named Triose-phosphate isomerase, TPI and TIM, is an enzyme that catalyzes the reversible interconversion of the triose phosphate isomers dihydroxyacetone phosphate and D-glyceraldehyde 3-phosphate. TPI has been found in nearly every organism searched for the enzyme, including animals such as mammals and insects as well as in fungi, plants, and bacteria. However, some bacteria that do not perform glycolysis, like ureaplasmas, lack TPI. TPI plays an important role... | |||
TMPY-04568 |
PDK1 Protein, Human, Recombinant (His)
pyruvate dehydrogenase kinase, isozyme 1,PDHK1 |
Human | Baculovirus Insect Cells |
Pyruvate dehydrogenase kinase, isozyme 1, also known as [Pyruvate dehydrogenase [lipoamide]] kinase isozyme 1, mitochondrial and PDK1, is a member of the PDK / BCKDK protein kinase family. PDK-1 is expressed predominantly in the heart. It contains one histidine kinase domain. Pyruvate dehydrogenase kinase (PDK) isoforms are molecular switches that downregulate the pyruvate dehydrogenase complex (PDC) by reversible phosphorylation in mitochondria. An inhibitory effect of lipoic acid on PDKs would... | |||
TMPY-01100 |
GPT2 Protein, Rat, Recombinant (His)
glutamic pyruvate transaminase (alanine aminotransferase) 2 |
Rat | Baculovirus Insect Cells |
Alanine aminotransferase (ALT), also known as glutamate pyruvate transaminase (Gpt), is a pyridoxal enzyme that catalyzes the reversible interconversion of L-alanine and 2-oxoglutalate to pyruvate and L-glutamate and plays a key role in the intermediary metabolism of glucose and amino acids. As a key enzyme for gluconeogenesis, Gpt is a widely-used serum marker for liver injury. Two ALT isoenzymes have been identified, ALT1 and ALT2 (GPT1 and GPT2), which are encoded by separate genes and share ... | |||
TMPJ-01106 |
NAD(P) transhydrogenase/NNT Protein, Human, Recombinant (His)
NAD(P) transhydrogenase,NNT |
Human | E. coli |
NAD(P)+transhydrogenase (NNT) is located in the inner mitochondrial membrane and catalyzes a reversible hydride transfer between NAD(H) and NADP(H) that is coupled to proton translocation between the intermembrane space and mitochondrial matrix. NNT activity has an essential role in maintaining the NADPH supply for antioxidant defense and biosynthetic pathways. Structurally, NNT is composed of three domains; domains I and III are hydrophilic and have binding sites for NAD and NADP, respectively,... | |||
TMPY-01099 |
GPT Protein, Rat, Recombinant (His)
Gpt1,ALAT,glutamic-pyruvate transaminase (alanine aminotrans... |
Rat | Baculovirus Insect Cells |
Alanine aminotransferase (ALT), also known as glutamate pyruvate transaminase (GPT), is a pyridoxal enzyme that belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family, Alanine aminotransferase subfamily. Gpt / Gpt1 / ALT catalyzes the reversible interconversion of L-alanine and 2-oxoglutalate to pyruvate and L-glutamate and plays a key role in the intermediary metabolism of glucose and amino acids. Gpt / Gpt1 / ALT is expressed in the liver, kidney, heart, and skeletal musc... | |||
TMPY-01734 |
CA13 Protein, Human, Recombinant (His)
carbonic anhydrase XIII,FLJ37995,CAXIII,MGC59868 |
Human | E. coli |
The carbonic anhydrases (or carbonate dehydratases) are classified as metalloenzyme for its zinc ion prosthetic group and form a family of enzymes that catalyze the rapid interconversion of carbon dioxide and water to bicarbonate and protons, a reversible reaction that takes part in maintaining acid-base balance in blood and other tissues. The carbonic anhydrasekl (CA) family consists of at least 11 enzymatically active members and a few inactive homologous proteins. The CAXIII is a member of th... | |||
TMPY-02090 |
Cystatin B Protein, Human, Recombinant (His)
PME,EPM1A,STFB,ULD,cystatin B (stefin B),EPM1,CST6 |
Human | E. coli |
Cystatin-B, also known as CPI-B, Liver thiol proteinase inhibitor, Stefin-B, CSTB and CST6, is a cytoplasm and nucleus protein which belongs to thecystatin family. Cystatin-B / CSTB is an intracellular thiol proteinase inhibitor. Tightly binding reversible inhibitor of cathepsins L, H and B. Cystatin-B / CSTB is able to form a dimer stabilized by noncovalent forces, inhibiting papain and cathepsins l, h and b. Cystatin-B / CSTB is also thought to play a role in protecting against the prot... | |||
TMPY-02133 |
Carbonic Anhydrase VB Protein, Human, Recombinant (His)
carbonic anhydrase VB, mitochondrial,CA-VB,MGC39962 |
Human | E. coli |
Carbonic anhydrase 5B, also known as carbonate dehydratase VB, carbonic anhydrase VB, CA-VB and CA5B, is amember of the alpha-carbonic anhydrase family. The strongest expression of CA5B / CA-VB is in heart, pancreas, kidney, placenta, lung, and skeletal muscle. It is not expressed in liver. Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes first discovered in 1933 that catalyze the reversible hydration of carbon dioxide. CAs participate in a variety of biological process... | |||
TMPY-00583 |
ADPRH Protein, Human, Recombinant (His)
ADP-ribosylarginine hydrolase,ARH1 |
Human | E. coli |
Cholera toxin (CT) produced by Vibrio cholerae causes the devastating diarrhea of cholera by catalyzing the ADP-ribosylation of the alpha subunit of the intestinal Gs protein (Gsalpha), leading to characteristic water and electrolyte losses. Mammalian cells contain ADP-ribosyltransferases similar to CT and an ADP-ribosyl(arginine)protein hydrolase (ADPRH), which cleaves the ADP-ribose-(arginine)protein bond, regenerating native protein and completing an ADP-ribosylation cycle. CT-catalyzed ADP-r... | |||
TMPY-02510 |
HIST2H2BE Protein, Human, Recombinant
MGC129734,H2BGL105,H2B.1,histone cluster 2, H2be,H2B,H2BFQ,G... |
Human | E. coli |
Histones are a complex family of highly conserved basic proteins responsible for packaging chromosomal DNA into nucleosomes. Histone proteins exhibit two levels of diversity: 1. evolutionary diversity between species and 2. subtype diversity in a class(H1, H2A, H2B, H3 or H4) within a species. It has become more and more evident that histone modifications are key players in the regulation of chromatin states and dynamics as well as in gene expression. Therefore, histone modifications and the enz... | |||
TMPY-01761 |
Carbonic Anhydrase 3 Protein, Human, Recombinant (His)
carbonic anhydrase III,CAIII,Car3 |
Human | E. coli |
Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes first discovered in 1933 that catalyze the reversible hydration of carbon dioxide. CAs participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. Carbonic anhydrases (CAs) form a family of enzymes that catalyze the rapid conversion of carbon dioxide and water to bicarbonate an... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T23983 |
Deutetrabenazine metabolite M4
SD-1018,Deuterated monohydroxy tetrabenazine,D6-tetrabenazine metabolite M4 |
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Deutetrabenazine metabolite M4 is believed to be related to its effect as a reversible depletion of monoamines from nerve terminals. The major circulating metabolites of Deutetrabenazine, are reversible inhibitors of VMAT2, resulting in decreased uptake | |||
T12587 |
Pyridostigmine-d6 bromide
Pyridostigmine D6 bromide,溴化吡啶斯的明 D6 |
Others | Others |
Pyridostigmine D6 bromide is the deuterium labeled Pyridostigmine, which is a parasympathomimetic and a reversible inhibitor of cholinesterase. | |||
T10950 |
Dabigatran D4 hydrochloride
BIBR-953 D4 hydrochloride |
Others | Others |
Dabigatran D4 hydrochloride is deuterium-labeled dabigatran, which is a reversible and selective direct thrombin inhibitor (DTI) with a Ki value of 4.5 nM. | |||
T10349 |
Apixaban 13C,d3
Apixaban 13CD3,BMS-562247-01 13CD3 |
Others | Others |
Apixaban 13CD3 (BMS-562247-01 13CD3) is a deuterium-labeled Apixaban. Apixaban is a reversible inhibitor of Factor Xa (Ki: 0.08 nM and 0.17 nM in human and rabbit). | |||
TMIJ-0516 |
Carbaryl-d3
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Carbaryl-d3 是 Carbaryl 的氘代化合物。Carbaryl 的 CAS 号为 63-25-2。Carbaryl 可作为一种杀虫剂。 | |||
TMID-0191 |
Moclobemide-d8
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Moclobemide-d8 是 Moclobemide 的氘代化合物。Moclobemide 的 CAS 号为 71320-77-9。Moclobemide 是可逆的、可透过血脑屏障的单胺氧化酶 (MAO-A) 抑制剂,能够抑制 hMAO-A (IC50=6.061 μM)。它上调慢性应激小鼠海马祖细胞的增殖。 | |||
TMIH-0352 |
Moclobemide-d4
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Moclobemide-d4 是 Moclobemide 的氘代化合物。Moclobemide 的 CAS 号为 71320-77-9。Moclobemide 是可逆的、可透过血脑屏障的单胺氧化酶 (MAO-A) 抑制剂,能够抑制 hMAO-A (IC50=6.061 μM)。它上调慢性应激小鼠海马祖细胞的增殖。 | |||
TMIJ-0120 |
Donepezil-d5
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Donepezil-d5 是 Donepezil 的氘代化合物。Donepezil 的 CAS 号为 120014-06-4。Donepezil 是一种AChE抑制剂,对牛 AChE 和人 AChE 的IC50分别为 8.12 nM 和 11.6 nM。 | |||
TMIJ-0100 |
(3R,11bR)-Tetrabenazine-d6
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(3R,11bR)-Tetrabenazine-d6 是 (3R,11bR)-Tetrabenazine 的氘代化合物。(3R,11bR)-Tetrabenazine 的 CAS 号为 1026016-83-0。(+)-Tetrabenazine是一种可逆的囊泡单胺转运蛋白2 (VMAT-2)抑制剂,对VMAT2转运的抑制作用是VMAT1的10倍。 | |||
TMIJ-0182 |
Avibactam sodium salt-13C5
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Avibactam sodium salt-13C5 是 Avibactam sodium salt 的 13C 的标记化合物。Avibactam sodium salt 的 CAS 号为 1192491-61-4。Avibactam sodium 是一种可逆的 β-内酰胺酶抑制剂,抑制 TEM-1,P99和KPC-2 β-内酰胺酶,IC50分别为8、80和38 nM。 | |||
TMIH-0281 |
Indobufen-d5
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Indobufen-d5 是 Indobufen 的氘代化合物。Indobufen 的 CAS 号为 63610-08-2。Indobufen 是一种血小板聚集抑制剂,是下调单核细胞中的组织因子,可逆抑制血小板环氧合酶 (Cox) 的活性和血栓素 A2 (TxA2) 的合成。 | |||
T70174 |
Pirlindole-d4 HCl
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Pirlindole-d4 is intended for use as an internal standard for the quantification of pirlindole by GC- or LC-MS. Pirlindole is a selective and reversible monoamine oxidase A (MAO-A) inhibitor. It is selective for MAO-A over MAO-B. In rats, it reverses the depressive-like effects induced by chronic mild stress (CMS), increases proliferation of hippocampal neural progenitor cells, and reverses dendritic atrophy in granule neurons. Pirlindole is also an inhibitor of enterovirus-D68 and coxsackieviru... | |||
TMIJ-0189 |
Ranitidine-d6 HCl
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Ranitidine-d6 HCl 是 Ranitidine HCl 的氘代化合物。Ranitidine HCl 的 CAS 号为 66357-59-3。Ranitidine hydrochloride 是一种具有口服活性的组胺 H2 受体选择性拮抗剂,IC50为 3.3 μM。它还是一种CYP2C19和CYP2C9的弱抑制剂,可抑制胃液分泌。 |