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Targets Recommended: Ligand for E3 Ligase

158

抑制剂 & 化合物

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Cat. No. Product Name Target Signaling Pathways
T18669L (S,R,S)-AHPC-Me-C10-NH2 hydrochloride

(S,R,S)-AHPC-Me-C10-NH2盐酸盐

Ligand for E3 Ligase PROTAC
(S,R,S)-AHPC-Me-C10-NH2 hydrochloride 是一种合成的 E3 连接酶配体-接头偶联物,包含 VHL 配体和接头。
T17881 (S,R,S)-AHPC-C10-NH2

VH032-C10-NH2

Others; Ligand for E3 Ligase Others; PROTAC
(S,R,S)-AHPC-C10-NH2 (VH032-C10-NH2) 包含基于 (S,R,S)-AHPC 的VHL 配体和 1 个 linker,是一种合成的 E3 连接酶配体-linker 偶联物 (E3 ligase ligand-linker conjugate)。用于 BET 的靶向 PROTAC 的合成。
T37863 9(S),10(S),13(S)-TriHOME

9(S),10(S),13(S)-TriHOME is an oxylipin derived from linoleic acid. It has been detected in beer and in bronchoalveolar lavage fluid (BALF) from female smokers.
T35447 10(S)-PAHSA

10(S)-PAHSA is a stereoisomer of 10-PAHSA , an endogenous lipid that belongs to a collection of branched fatty acid esters of hydroxy fatty acids (FAHFAs).
T37488 10(S),17(S)-DiHDHA

Protectin D1 (also known as neuroprotectin D1 when produced in neuronal tissues) is a DHA-derived dihydroxy fatty acid that exhibits potent protective and anti-inflammatory activities. 10(S),17(S)-DiHDHA is a DHA metabolite, also referred to as protectin DX (PDX). It is produced by an apparent double lipoxygenase (LO)-mediated reaction in murine peritonitis exudates, in suspensions of human leukocytes, or by soybean 15-LO incubated with DHA. It differs from protectin D1 with respect to the stere...
T60123 Chimmitecan

(S)-9-Allyl-10-hydroxycamptothecin,吉米替康

Topoisomerase DNA Damage/DNA Repair
Chimmitecan ((S)-9-Allyl-10-hydroxycamptothecin) 是一种topoisomerase I 抑制剂,在体内、外表现有效的活性。
T18661 (S,R,S)-AHPC-C10-NH2 dihydrochloride

VH032-C10-NH2 dihydrochloride,VH032-linker 10,(S,R,S)-AHPC-C10-NH2二盐酸盐,VH032 amide-alkylC10-amine

Others; Ligand for E3 Ligase Others; PROTAC
(S,R,S)-AHPC-C10-NH2 dihydrochloride (VH032-linker 10) 包含基于 (S,R,S)-AHPC 的VHL 配体和 1 个 linker,是一种合成的 E3 连接酶配体-linker 偶联物,用于合成 BET 的靶向 PROTAC。
T36999 7(S),17(S)-dihydroxy-8(E),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic Acid

Novel oxylipins, referred to as docosanoids, have been derived from C22polyunsaturated fatty acids 7(S),17(S)-dihydroxy-8(E),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic acid (7(S),17(S)-hydroxy DPA) is a DPA-derived analog of the 17(S)-dihydroxy series of docosanoids known as protectins. Protectin D1, a DHA-derived dihydroxy fatty acid, exhibits potent anti-inflammatory activities.1,2,3Potentially, 7(S),17(S)-hydroxy DPA demonstrates similar properties; however, its biological activity has yet to b...
T32781 Lipofundin S

Phospholipid - stabilized soybean oil,Intralipid,Intralipid 20,Medialipid,Lipofundin S 10

Lipofundin S is an emulsion containing soybean oil, glycerol, and soy phosphatides.
T34106 Polyglyceryl-10 stearate

Polyaldo 10-1-S,Decaglyceryl monostearate,Nikkol decaglyn 1-SV EX,Nikkol decaglyn 1-SV,Nikkol decaglyn 1-S

Polyglyceryl-10 stearate is a biochemical.
T18669 (S,R,S)-AHPC-Me-C10-NH2

Others Others
(S,R,S)-AHPC-Me-C10-NH2 is a chemical compound consisting of a synthesized E3 ligase ligand-linker conjugate that incorporates both a VHL ligand and a linker. This compound, (S,R,S)-AHPC-Me-C10-NH2, finds application in PROTAC MS432[1].
T18668 (S,R,S)-AHPC-Me-C10-Br

Others Others
(S,R,S)-AHPC-Me-C10-Br is a chemically synthesized conjugate that functions as a ligand-linker for E3 ligases. This compound incorporates a VHL E3 ligase linker and MS432, derived from the MEK1/2 inhibitor PD0325901[1].
T17926 (S,R,S)-AHPC-PEG6-C4-Cl

VHL Ligand-Linker Conjugates 10,E3 ligase Ligand-Linker Conjugates 9,VH032-PEG6-C4-Cl

Others Others
(S,R,S)-AHPC-PEG6-C4-Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 6-unit PEG linker. (S,R,S)-AHPC-PEG6-C4-Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
T17910 (S,R,S)-AHPC-PEG2-C4-Cl

E3 ligase Ligand-Linker Conjugates 10,VHL Ligand-Linker Conjugates 7,VH032-PEG2-C4-Cl

Others Others
(S,R,S)-AHPC-PEG2-C4-Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker. (S,R,S)-AHPC-PEG2-C4-Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
T63298 B10-S

B10-S 是有效的抗过敏剂,对 P 物质诱导的 LAD2 脱颗粒具有抑制作用。
T71726 TNFalpha-IN-S10

TNFalpha-IN-S10 is an inhibitor of TNF-α.
T65662 (1S)-(+)-(10-Camphorsulfonyl)oxaziridine

(1S)-(+)-(10-Camphorsulfonyl)oxaziridine 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T65662,CAS号为 104322-63-6。
T66968 (1S)-(+)-Camphor-10-sulphonic acid

(1S)-(+)-Camphor-10-sulphonic acid 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66968,CAS号为 3144-16-9。
T64990 (2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-10,13-Dimethyl-2,16-di(piperidin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol

(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-10,13-Dimethyl-2,16-di(piperidin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T64990,CAS号为 13522-16-2。
T131624 (3S,5S,6R,10R,13S,17S) androstane-3,6,17-triol

androstane-3,6,17-triol 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T131624。
T62433 (5S,8R)-HBV-IN-10

(5S,8R)-HBV-IN-10 是一种 compound 6 (WO2021204258A1) 的异构体。其中 Compound 6 是一种乙型肝炎表面抗原 (HBsAg) 的有效抑制剂 (0.1 μM< EC50≤1 μM)。
T66301 (3S,8R,9S,10R,13S,14S)-17-Iodo-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

(3S,8R,9S,10R,13S,14S)-17-Iodo-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66301,CAS号为 32138-69-5。
T64669 (R)-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-Trihydroxy-7,10,13-trimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid

(R)-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-Trihydroxy-7,10,13-trimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64669。
T66298 (8S,9S,10R,14S)-13-Ethyl-11-methylene-2,3,7,8,9,10,11,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(6H)-one

(8S,9S,10R,14S)-13-Ethyl-11-methylene-2,3,7,8,9,10,11,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(6H)-one 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66298,CAS号为 54024-21-4。
T65404 (2'R,7R,8R,10S,13S,14S)-Methyl 10,13-dimethyl-3,5'-dioxo-1,2,3,4',5',6,7,8,10,12,13,14,15,16-tetradecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-7-carboxylate

(2'R,7R,8R,10S,13S,14S)-Methyl 10,13-dimethyl-3,5'-dioxo-1,2,3,4',5',6,7,8,10,12,13,14,15,16-tetradecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-7-carboxylate 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T65404,CAS号为 95716-70-4。
T65075 (3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl (Z)-octadec-9-en-1-yl carbonate

(3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl (Z)-octadec-9-en-1-yl carbonate 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T65075,CAS号为 17110-51-9。
T66136 (R)-Methyl 4-((3R,5S,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate

(R)-Methyl 4-((3R,5S,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66136,CAS号为 10538-65-5。
T66656 (R)-Methyl 4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate

(R)-Methyl 4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66656,CAS号为 10538-59-7。
T66748 (R)-Methyl 4-((3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6-dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate

(R)-Methyl 4-((3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6-dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66748,CAS号为 2868-48-6。
T66741 (R)-4-((3R,5R,8S,9S,10R,13R,14S,17R,E)-6-Ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid

(R)-4-((3R,5R,8S,9S,10R,13R,14S,17R,E)-6-Ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66741,CAS号为 1516887-33-4。
T66990 (R)-Benzyl 4-((3R,5R,8S,9S,10R,13R,14S,17R,E)-6-ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate

(R)-Benzyl 4-((3R,5R,8S,9S,10R,13R,14S,17R,E)-6-ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66990,CAS号为 1352328-66-5。
T64690 (S)-2-Amino-5-((2,2,10,10-tetramethyl-4,8-dioxo-3,9-dioxa-5,7-diazaundecan-6-ylidene)amino)pentanoic acid

(S)-2-Amino-5-((2,2,10,10-tetramethyl-4,8-dioxo-3,9-dioxa-5,7-diazaundecan-6-ylidene)amino)pentanoic acid 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64690。
T67236 3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(8α,9S)-10,11-dihydro-6'-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione

3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(8α,9S)-10,11-dihydro-6'-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T67236,CAS号为 1352957-59-5。
T64502 (S)-Decarboxyl ofloxacin

(S)-Decarboxyl ofloxacin 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T64502。
T65298 (4aR,4bS,6aS,7S,9aS,9bS,11aR)-Methyl 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylate

(4aR,4bS,6aS,7S,9aS,9bS,11aR)-Methyl 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylate 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T65298。
T66996 (4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid

(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T66996,CAS号为 104239-97-6。
T2303 (S)-Afatinib

BIBW2992,阿法替尼

EGFR; HER Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
(S)-Afatinib (BIBW2992) 是一种不可逆的 EGFR 家族抑制剂,对 EGFRwt、EGFR (L858R)、EGFR (L858R/T790M)、HER2 和 HER4 的 IC50 分别为 0.5/0.4/10/14/1 nM。
T2012 Oclacitinib

PF-03394197

JAK Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
Oclacitinib (PF-03394197) 是一种有效的选择性 JAKs 抑制剂,IC50 为 10-99 nM;不抑制一组 38 种非 JAK 激酶 (IC50 > 1000 nM)。
T20828 Citalopram

Cipram,Lu 10-171,Lu-10-171 Lu10-171

5-HT Receptor GPCR/G Protein; Neuroscience
Citalopram (Lu 10-171) 是一种具有口服活性的、选择性的血清素再摄取抑制剂 (SSRI),是一种选择性5-羟色胺再摄取抑制剂,是一种 S(+)-对映体 (Escitalopram) 和 R(-)-对映体的外消旋混合物。Citalopram 具有抗抑郁活性,可增强血清素能神经传递,可用于研究老年痴呆。
T19649 PF-06273340

PF 6273340,PF 06273340,PF6273340,PF-6273340

Trk receptor Tyrosine Kinase/Adaptors
PF-06273340 是一种口服具有活力的、具有选择性的外周限制性Trk 泛抑制剂。
T1850 Balicatib

AAE581,巴利卡替

Cysteine Protease Proteases/Proteasome
Balicatib (AAE581) 是组织蛋白酶K 抑制剂,其对组织蛋白酶K 的抑制作用是组织蛋白酶B、L 和S 的抑制性的10100倍。
T2368L Edoxaban

Lixiana,依杜沙班

Factor Xa; Thrombin Metabolism; Proteases/Proteasome
Edoxaban (Lixiana) (DU-176) 是一种选择性的,口服有效的 factor Xa (FXa)抑制剂。Edoxaban 对游离 FXa 和凝血酶原的 Ki 分别为 0.561 nM 和 2.98 nM。Edoxaban 是一种抗凝剂,可用于预防中风。Edoxaban 还是一种凝血酶和凝血因子 IXaβ (FIXa) 的弱抑制剂,Ki 值分别为 6.00 μM 和 41.7 μM,对 FXa 的选择性超过 10000 倍。由于具有抗血栓形成的特性,Edoxaban 可用于预防血栓栓塞性疾病的研究。
T0153 Oltipraz

吡噻硫酮,NSC 347901,RP 35972

HIF/HIF Prolyl-Hydroxylase; HIV Protease; Reverse Transcriptase; Nrf2; HIF Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; Microbiology/Virology; Proteases/Proteasome
Oltipraz (RP 35972) 是一种 Nrf2的强效激活剂。它时间依赖性地抑制 HIF-1α激活,IC50为 10 μM,浓度 ≥ 10 μM 时完全消除 HIF-1α诱导。
T62694 (S)-GFB-12811

(S)-GFB-12811 (compound 596) 是一种选择性的、选择性的 CDK5 抑制剂 (IC50<10 nM)。(S)-GFB-12811 能够用于细胞周期进程、神经元发育、肿瘤发生的研究。
T37721 Dihydronovobiocin

Dihydronovobiocin is a coumarin antibiotic and derivative of novobiocin .1It is active against the bacteriaS. aureus,S. haemolyticus,D. pneumoniae,S. typhosa,K. pneumoniae, andP. multocida(MICs = 0.6, 2, 0.6, 10, 10, and 3 μg/ml, respectively).2Dihydronovobiocin inhibits DNA gyrase subunit B with an IC50value of 64.5 nM.3 1.Berger, J., and Batcho, A.D.Coumarin - glycoside antibioticsJ. Chromatogr. Lib.15101-158(1978) 2.Hoeksema, H.Dihydronovobiocin and derivatives thereof3,175,9441-9(1965) 3.Gev...
T28391 PF-9404C

PF9404C

PF-9404C is the S-S diesteroisomer of a beta adrenergic receptors blocker with vasodilatory properties. PF9404C increased the formation of cyclic GMP from 3 pmol mg−1 protein in basal conditions, to 53 pmol mg−1 protein in 10 μM in rat aorta smooth muscle
T29007 Trichostatin A S-isomer

(-)-Trichostatin A

Trichostatin A S-isomer is the s-isomer of Trichostatin A. Trichostatin A is a histone deacetylase inhibitors (HDIs or HDACIs) that have a broad spectrum of epigenetic activities. Trichostatin A inhibits HDACs 1, 3, 4, 6 and 10 with IC50 values around 20
T83699 LL-37 (18-37) (human) TFA

KR-20,hCAP-18,CAP-18,Cathelicidin,FALL-39

LL-37 (18-37) 是 LL-37 的一种抗菌肽片段。对S. aureus和C. albicans具有活性,最小致死浓度分别为4 µM 和10 µM。在10到50 µM 的浓度范围内,它还能抑制E. histolytica营养体的生长。
T71449 Capreomycin free base

Capreomycin is a polypeptide antibiotic originally isolated from S. capreolus. It is active against M. tuberculosis (MIC = 10 µg/ml). Capreomycin binds to both the 30S and 50S ribosomal subunits, inhibiting protein synthesis.
T35607 10'-Desmethoxystreptonigrin

10'-Desmethoxystreptonigrin is an antibiotic originally isolated from Streptomyces and a derivative of the antibiotic streptonigrin. It is active against a variety of bacteria, including S. aureus, S. faecalis, E. coli, K. pneumoniae, and P. vulgaris (MICs = 0.4, 1.6, 3.1, 3.1 and 0.4 μg/ml, respectively). 10'-Desmethoxystreptonigrin is cytotoxic to HCT116 colon and A2780 ovarian cancer cells (IC50s = 0.004 and 0.001 μg/ml, respectively), as well as HCT116 cells resistant to etoposide and tenipo...

化合物

(S,R,S)-AHPC-Me-C10-NH2 hydrochloride
Cat.No: T18669L
Synonym: (S,R,S)-AHPC-Me-C10-NH2盐酸盐
Target: Ligand for E3 Ligase
(S,R,S)-AHPC-C10-NH2
Cat.No: T17881
Synonym: VH032-C10-NH2
Target: Others, Ligand for E3 Ligase
9(S),10(S),13(S)-TriHOME
Cat.No: T37863
Synonym:
Target:
10(S)-PAHSA
Cat.No: T35447
Synonym:
Target:
10(S),17(S)-DiHDHA
Cat.No: T37488
Synonym:
Target:
Chimmitecan
Cat.No: T60123
Synonym: (S)-9-Allyl-10-hydroxycamptothecin,吉米替康
Target: Topoisomerase
(S,R,S)-AHPC-C10-NH2 dihydrochloride
Cat.No: T18661
Synonym: VH032-C10-NH2 dihydrochloride,VH032-linker 10,(S,R,S)-AHPC-C10-NH2二盐酸盐,VH032 amide-alkylC10-amine
Target: Others, Ligand for E3 Ligase
7(S),17(S)-dihydroxy-8(E),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic Acid
Cat.No: T36999
Synonym:
Target:
Lipofundin S
Cat.No: T32781
Synonym: Phospholipid - stabilized soybean oil,Intralipid,Intralipid 20,Medialipid,Lipofundin S 10
Target:
Polyglyceryl-10 stearate
Cat.No: T34106
Synonym: Polyaldo 10-1-S,Decaglyceryl monostearate,Nikkol decaglyn 1-SV EX,Nikkol decaglyn 1-SV,Nikkol decaglyn 1-S
Target:
(S,R,S)-AHPC-Me-C10-NH2
Cat.No: T18669
Synonym:
Target: Others
(S,R,S)-AHPC-Me-C10-Br
Cat.No: T18668
Synonym:
Target: Others
(S,R,S)-AHPC-PEG6-C4-Cl
Cat.No: T17926
Synonym: VHL Ligand-Linker Conjugates 10,E3 ligase Ligand-Linker Conjugates 9,VH032-PEG6-C4-Cl
Target: Others
(S,R,S)-AHPC-PEG2-C4-Cl
Cat.No: T17910
Synonym: E3 ligase Ligand-Linker Conjugates 10,VHL Ligand-Linker Conjugates 7,VH032-PEG2-C4-Cl
Target: Others
B10-S
Cat.No: T63298
Synonym:
Target:
TNFalpha-IN-S10
Cat.No: T71726
Synonym:
Target:
(1S)-(+)-(10-Camphorsulfonyl)oxaziridine
Cat.No: T65662
Synonym:
Target:
(1S)-(+)-Camphor-10-sulphonic acid
Cat.No: T66968
Synonym:
Target:
(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-10,13-Dimethyl-2,16-di(piperidin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol
Cat.No: T64990
Synonym:
Target:
(3S,5S,6R,10R,13S,17S) androstane-3,6,17-triol
Cat.No: T131624
Synonym:
Target:
(5S,8R)-HBV-IN-10
Cat.No: T62433
Synonym:
Target:
(3S,8R,9S,10R,13S,14S)-17-Iodo-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
Cat.No: T66301
Synonym:
Target:
(R)-4-((3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-Trihydroxy-7,10,13-trimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid
Cat.No: T64669
Synonym:
Target:
(8S,9S,10R,14S)-13-Ethyl-11-methylene-2,3,7,8,9,10,11,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(6H)-one
Cat.No: T66298
Synonym:
Target:
(2'R,7R,8R,10S,13S,14S)-Methyl 10,13-dimethyl-3,5'-dioxo-1,2,3,4',5',6,7,8,10,12,13,14,15,16-tetradecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-7-carboxylate
Cat.No: T65404
Synonym:
Target:
(3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl (Z)-octadec-9-en-1-yl carbonate
Cat.No: T65075
Synonym:
Target:
(R)-Methyl 4-((3R,5S,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
Cat.No: T66136
Synonym:
Target:
(R)-Methyl 4-((3R,5S,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
Cat.No: T66656
Synonym:
Target:
(R)-Methyl 4-((3R,5R,6S,8S,9S,10R,13R,14S,17R)-3,6-dihydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
Cat.No: T66748
Synonym:
Target:
(R)-4-((3R,5R,8S,9S,10R,13R,14S,17R,E)-6-Ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid
Cat.No: T66741
Synonym:
Target:
(R)-Benzyl 4-((3R,5R,8S,9S,10R,13R,14S,17R,E)-6-ethylidene-3-hydroxy-10,13-dimethyl-7-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate
Cat.No: T66990
Synonym:
Target:
(S)-2-Amino-5-((2,2,10,10-tetramethyl-4,8-dioxo-3,9-dioxa-5,7-diazaundecan-6-ylidene)amino)pentanoic acid
Cat.No: T64690
Synonym:
Target:
3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(8α,9S)-10,11-dihydro-6'-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione
Cat.No: T67236
Synonym:
Target:
(S)-Decarboxyl ofloxacin
Cat.No: T64502
Synonym:
Target:
(4aR,4bS,6aS,7S,9aS,9bS,11aR)-Methyl 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylate
Cat.No: T65298
Synonym:
Target:
(4aR,4bS,6aS,7S,9aS,9bS,11aR)-4a,6a-Dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid
Cat.No: T66996
Synonym:
Target:
(S)-Afatinib
Cat.No: T2303
Synonym: BIBW2992,阿法替尼
Target: EGFR, HER
Oclacitinib
Cat.No: T2012
Synonym: PF-03394197
Target: JAK
Citalopram
Cat.No: T20828
Synonym: Cipram,Lu 10-171,Lu-10-171 Lu10-171
Target: 5-HT Receptor
PF-06273340
Cat.No: T19649
Synonym: PF 6273340,PF 06273340,PF6273340,PF-6273340
Target: Trk receptor
Balicatib
Cat.No: T1850
Synonym: AAE581,巴利卡替
Target: Cysteine Protease
Edoxaban
Cat.No: T2368L
Synonym: Lixiana,依杜沙班
Target: Factor Xa, Thrombin
Oltipraz
Cat.No: T0153
Synonym: 吡噻硫酮,NSC 347901,RP 35972
Target: HIF/HIF Prolyl-Hydroxylase, HIV Protease, Reverse Transcriptase, Nrf2, HIF
(S)-GFB-12811
Cat.No: T62694
Synonym:
Target:
Dihydronovobiocin
Cat.No: T37721
Synonym:
Target:
PF-9404C
Cat.No: T28391
Synonym: PF9404C
Target:
Trichostatin A S-isomer
Cat.No: T29007
Synonym: (-)-Trichostatin A
Target:
LL-37 (18-37) (human) TFA
Cat.No: T83699
Synonym: KR-20,hCAP-18,CAP-18,Cathelicidin,FALL-39
Target:
Capreomycin free base
Cat.No: T71449
Synonym:
Target:
10'-Desmethoxystreptonigrin
Cat.No: T35607
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T2764 (S)-10-Hydroxycamptothecin

10-羟喜树碱,10-羟基喜树碱,10-Hydroxycamptothecin,10-HCPT

Apoptosis; Topoisomerase Apoptosis; DNA Damage/DNA Repair
(S)-10-Hydroxycamptothecin (10-HCPT) 是一种从喜树中分离的 DNA 拓扑异构酶 I 抑制剂。它显著诱导细胞凋亡,可研究肝癌、胃癌、结肠癌和白血病。
T83553 (4S)-10-Nor-calamenen-10-one

(4S)-10-Nor-calamenen-10-one(Compound 15)促进小胶质细胞通过LPS刺激产生的NO增强。该化合物为桉树倍半萜烯类,可从Alpinia oxyphylla中提取。
T83558 (3S,4aS,10aS)-3-(Acetyloxy)-2,3,4,4a,10,10a-hexahydro-6-hydroxy-1,1,4a-trimethyl-7-(1-methylethyl)-9(1H)-phenanthrenone

(3S,4aS,10aS)-3-(Acetyloxy)-2,3,4,4a,10,10a-hexahydro-6-hydroxy-1,1,4a-trimethyl-7-(1-methylethyl)-9(1H)-phenanthrenone(化合物3)是从丹参(Salvia miltiorrhiza)根提取的棕榈酸盐。该化合物展现出抗癌活性,对于不同的人类癌症细胞系具有显著的抑制效果,其DC50值分别为:HeLa细胞系25.5 μg/mL、HepG2细胞系37.5 μg/mL以及OVCAR-3细胞系30.2 μg/mL。
TN2413 Diacetylpiptocarphol

Others Others
Diacetylpiptocarphol has antiplasmodial activity
T4839 Ac-Ala-OH

N-Acetylalanine,N-Acetyl-L-alanine,N-乙酰-L-丙氨酸

Others; Endogenous Metabolite Metabolism; Others
Ac-Ala-OH (N-Acetyl-L-alanine) 是鸟嘌呤核苷酸结合蛋白G(I)/G(S)/G(O) γ -2亚基、髓鞘碱性蛋白、GTP-结合核蛋白 Ran、原肌球蛋白 α - 4链、HIV-1 Rev 结合蛋白2、Xaa-Pro 二肽酶、胸腺酶 β -10、肌动蛋白样蛋白3、丙氨酸转氨酶、丝氨酸/苏氨酸蛋白磷酸酶PP1 - β催化亚基、10 kda 热休克蛋白(线粒体)、钙调蛋白和 β -1-syntrophin 的底物。
T0486L Irinotecan Hydrochloride

盐酸伊立替康,伊立替康盐酸盐,Camptothecin 11 hydrochloride,CPT-11 hydrochloride

Topoisomerase; Autophagy Autophagy; DNA Damage/DNA Repair
Irinotecan Hydrochloride (CPT-11 hydrochloride) 是喜树碱半合成衍生物的盐酸盐,是一种拓扑异构酶 I 抑制剂,可研究结肠癌和直肠癌。
T83518 (S)-O-Methylencecalinol

(S)-O-Methylencecalinol (compound 10),一种从Ageratina grandfolia地上部分分离得到的化合物,目标是钙调素。
TN5264 Xanthoxyletin

TNF; NOS; ROS; COX; Antifection Apoptosis; Immunology/Inflammation; Microbiology/Virology; Neuroscience
Xanthoxyletin shows potent antibacterial, fungicidal, and algicidal properties, it also has anticancer, and anti-inflammatory activities. It shows an inhibitory effect on iNOS protein expression at 10 microM, it also can inhibit the synthesis of nitric oxide and the protein expression of tumor necrosis factor-alpha and cyclooxygenase-2. Xanthoxyletin induces S phase arrest and apoptosis in human gastric adenocarcinoma SGC-7901 cells, the effects are associated with the DNA damage, apoptosis thro...
T38097 Antibiotic PF 1052

Antibiotic PF 1052 is a fungal metabolite originally isolated from Phoma.1,2 It is active against S. aureus, S. parvulus, and C. perfringens (MICs = 3.13, 0.78, and 0.39 μg/ml, respectively), among others.1 It inhibits neutrophil migration in a wound assay using zebrafish larvae expressing GFP-labeled neutrophils, reducing pseudopodia formation and inducing rounding of neutrophils.2 Antibiotic PF 1052 is selective for neutrophil migration over macrophage migration in zebrafish larvae. It also in...
T83693 Magainin 2 TFA

MG2

Magainin 2是一种从非洲爪蟾(X. laevis)皮肤中分离出的阳离子肽,具有宿主防御和抗菌活性。该化合物对细菌E. coli、K. pneumoniae、S. epidermidisS. aureus及真菌C. albicans表现出活性(MICs分别为5、1010、50和80 µg/ml)。Magainin 2(20 µM)能降低猕猴桃花粉的萌发率和平均管长。在被单纯疱疹病毒1型(HSV-1)或2型(HSV-2)感染的Vero细胞中,它可减少病毒复制(EC50s分别为22.16和19.8 µM),同时不影响细胞活性,其50%细胞毒性浓度值(CC50)大于100 µM。
T37609 (rel)-Asperparaline A

Aspergillimide is a fungal metabolite originally isolated from A. japonicus.1 It reduces nicotinic acetylcholine receptor (nAChR) peak and slowly-desensitizing amplitudes induced by acetylcholine in silkworm (B. mori) larval neurons (IC50s = 20.2 and 39.6 nM, respectively) but has no effect on chicken α3β4-, α4β2-, and α7-containing nAChRs.2 Dietary administration of aspergillimide A (10 μg/g of diet) induces paralysis in silkworm fourth instar larvae.1 Aspergillimide A (10 and 20 mg/kg) reduces...
T35609 19-O-Acetylchaetoglobosin A

19-O-Acetylchaetoglobosin A is a fungal metabolite originally isolated fromC. globosumthat has actin polymerization inhibitory and cytotoxic activities.1,2It inhibits actin polymerization in a cell-free assay when used at a concentration of 2 μM.219-O-Acetylchaetoglobosin A (3.2, 10, and 32 μg/ml) is cytotoxic to HeLa cervical cancer cells.1 1.Umeda, M., Ohtsubo, K., Saito, M., et al.Cytotoxicity of new cytochalasans from Chaetomium globosumExperientia31(4)435-438(1975) 2.Sekita, S., Yoshihira, ...
TN5228 Vestitol

Antifection Microbiology/Virology
Vestitol is a phytoalexin with insect feeding-deterrent activity, it has antioxidant, anti-inflammatory and antimicrobial activities, it can inhibit neutrophil migration at a dose of 10 mg/kg, and shows MICs ranging from 25-50 to 50-100 ug/mL and MBCs ranging from 25-50 to 50-100 ug/mL.Vestitol exerts a limited inhibitory effect on S. hermonthica germination, it can significantly inhibit seedling growth, it also contributes, at least in part, to the host's defence mechanism and acts as a chemica...
T38258 Phanerosporic Acid

Phanerosporic acid is a fungal secondary metabolite originally isolated from P. chrysosporum that has antibacterial activity against B. cereus, B. subtilis, and E. coli and antifungal activity against S. cerevisiae, A. niger, O. ulmi, U. maydis, C. cucmerinum, C. cladosporioides, and B. cinerea.1 It has been used in the synthesis of macrolide derivatives.References1. Arnone, A., Assante, G., Nasini, G., et al. Phanerosporic acid, a β-resorcylate obtained from Phanerochaete chrysosporium. Phytoch...
T36226 Beauveriolide I

Beauveriolide I is a cyclodepsipeptide that has been found inBeauveriaand an inhibitor of lipid droplet formation.1It inhibits lipid droplet formation when used at concentrations of 3 and 10 μM, as well as inhibits cholesterol synthesis (IC50= 0.78 μM), in primary mouse peritoneal macrophages.1,2Beauveriolide I also inhibits acyl-coenzyme A:cholesterol acyltransferase (ACAT) activity in mouse macrophage membranes (IC50= 6 μM).2 1.Namatame, I., Tomoda, H., Si, S., et al.Beauveriolides, specific i...
T35409 (+)-δ-Cadinene

Apoptosis; Antibacterial Apoptosis; Microbiology/Virology
(+)-δ-Cadinene 是一种从G. hirsutum 中发现的倍半萜,具有抗菌、杀虫、抗癌和抗增殖活性。 它对肺炎双球菌的MIC 值为31.25 μg/ml,对 A. stephensi、A. aegypti 和 C. quinquefasciatust 三龄幼虫的LC50s 值分别8.23、9. 2和3。(+)-δ-Cadinene(10、50 和 100 μM)可诱导 OVCAR-3 人类卵巢癌细胞凋亡并抑制其增殖。
T36227 Beauveriolide III

Beauveriolide III is a cyclodepsipeptide that has been found inBeauveriaand an inhibitor of lipid droplet formation.1It inhibits lipid droplet formation when used at concentrations of 3 and 10 μM, as well as inhibits cholesterol synthesis (IC50= 0.41 μM), in primary mouse peritoneal macrophages.1,2Beauveriolide III also inhibits acyl-coenzyme A:cholesterol acyltransferase (ACAT) activity in mouse macrophage membranes (IC50= 5.5 μM).2Beauveriolide III (25 and 50 mg/kg) reduces the size of aortic ...
T37272 9(S),12(S),13(S)-TriHOME

9(S),12(S),13(S)-TriHOME is a linoleic acid-derived oxylipin that has diverse biological activities.1,2,3,4It has been found in various plants and is produced in human eosinophils in a 15-lipoxygenase-dependent, soluble epoxide hydrolase-independent manner.1,59(S),12(S)13(S)-TriHOME inhibits antigen-induced β-hexosaminidase release from RBL-2H3 mast cells (IC50= 28.7 μg/ml).2It inhibits LPS-induced nitric oxide (NO) production in BV-2 microglia (IC50= 40.95 μM).3In vivo, 9(S),12(S),13(S)-TriHOME...
T36448 (E)-Ajoene

(E)-Ajoene is a disulfide that has been found inA. sativumand has diverse biological activities.1,2,3,4It is active against Gram-positive and Gram-negative bacteria (MICs = 10-250 and 150->500 μg/ml, respectively) and fungi (MICs = 15-50 μg/ml).1(E)-Ajoene inhibits proliferation of a variety of cancer cells, including MDA-MB-231 breast, HeLa cervical, and WHCO1 esophageal cancer cells (IC50s = 18.6, 61, and 39.2 μM, respectively).2It also inhibits human glutathione reductase andT. cruzitrypanoth...

天然产物

(S)-10-Hydroxycamptothecin
Cat.No: T2764
Synonym: 10-羟喜树碱,10-羟基喜树碱,10-Hydroxycamptothecin,10-HCPT
Target: Apoptosis, Topoisomerase
(4S)-10-Nor-calamenen-10-one
Cat.No: T83553
Synonym:
Target:
(3S,4aS,10aS)-3-(Acetyloxy)-2,3,4,4a,10,10a-hexahydro-6-hydroxy-1,1,4a-trimethyl-7-(1-methylethyl)-9(1H)-phenanthrenone
Cat.No: T83558
Synonym:
Target:
Diacetylpiptocarphol
Cat.No: TN2413
Synonym:
Target: Others
Ac-Ala-OH
Cat.No: T4839
Synonym: N-Acetylalanine,N-Acetyl-L-alanine,N-乙酰-L-丙氨酸
Target: Others, Endogenous Metabolite
Irinotecan Hydrochloride
Cat.No: T0486L
Synonym: 盐酸伊立替康,伊立替康盐酸盐,Camptothecin 11 hydrochloride,CPT-11 hydrochloride
Target: Topoisomerase, Autophagy
(S)-O-Methylencecalinol
Cat.No: T83518
Synonym:
Target:
Xanthoxyletin
Cat.No: TN5264
Synonym:
Target: TNF, NOS, ROS, COX, Antifection
Antibiotic PF 1052
Cat.No: T38097
Synonym:
Target:
Magainin 2 TFA
Cat.No: T83693
Synonym: MG2
Target:
(rel)-Asperparaline A
Cat.No: T37609
Synonym:
Target:
19-O-Acetylchaetoglobosin A
Cat.No: T35609
Synonym:
Target:
Vestitol
Cat.No: TN5228
Synonym:
Target: Antifection
Phanerosporic Acid
Cat.No: T38258
Synonym:
Target:
Beauveriolide I
Cat.No: T36226
Synonym:
Target:
(+)-δ-Cadinene
Cat.No: T35409
Synonym:
Target: Apoptosis, Antibacterial
Beauveriolide III
Cat.No: T36227
Synonym:
Target:
9(S),12(S),13(S)-TriHOME
Cat.No: T37272
Synonym:
Target:
(E)-Ajoene
Cat.No: T36448
Synonym:
Target:
Cat. No. Product Name Species Expression System
TMPY-02450 Cathepsin D Protein, Human, Recombinant (His)

HEL-S-130P,CLN10,cathepsin D,CP

Human HEK293 Cells
Cathepsin D Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 44 kDa and the accession number is P07339.
TMPY-01431 L1CAM Protein, Human, Recombinant (His)

N-CAM-L1,MASA,HSAS,L1 cell adhe

Human HEK293 Cells
L1CAM Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 125 kDa and the accession number is P32004-1.
TMPY-02519 BLVRB Protein, Human, Recombinant (His)

HEL-S-10,biliverdin reductase B,F...

Human E. coli
Biliverdin reductase (hBVR) is a serine/threonine kinase that catalyzes reduction of the heme oxygenase (HO) activity product, biliverdin, to bilirubin. BVR consists of an N-terminal dinucleotide-binding domain (Rossmann-fold) and a C-terminal domain that contains a six-stranded β-sheet that is flanked on one face by several α-helices. The C-terminal and N-terminal domains interact extensively, forming the active site cleft at their interface. Biliverdin reductase (BVR) catalyzes the last step i...
TMPK-00811 L1CAM Protein, Mouse, Recombinant (His)

CALL,MGC132578,FLJ44930,NCAM-L1,MIC5,CHL-1,SPG1,H

Mouse HEK293 Cells
L1 cell adhesion molecule (L1CAM) is one of the first neural adhesion molecules described with important functions in the development of the nervous system. Subsequent work discovered that L1CAM is expressed in many human cancers and is often associated with bad prognosis. This is most likely due to the motility and invasion promoting function of L1CAM. L1CAM is a valuable diagnostic/prognostic marker and an attractive target for the therapy of several human cancers.
TMPY-02208 Peroxiredoxin 5 Protein, Human, Recombinant (His)

B166,HEL-S-55,prx-V,ACR1,PMP20,AOEB166,SBB...

Human E. coli
Peroxiredoxin 5 Protein, Human, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 18.5 kDa and the accession number is P30044-2.
TMPY-01926 S100A10 Protein, Human, Recombinant (His)

ANX2L,S100 calcium binding protein A10...

Human E. coli
S100 protein is a family of low molecular weight protein found in vertebrates characterized by two EF-hand calcium-binding motifs. There are at least 21 different S100 proteins, and the name is derived from the fact that the protein is 100% soluble in ammonium sulfate at neutral pH. Most S100 proteins are disulfide-linked homodimer, and is normally present in cells derived from the neural crest, chondrocytes, macrophages, dendritic cells, etc. S1 proteins have been implicated in a variety of int...
TMPY-02217 HSC70 Protein, Human, Recombinant (His)

HSP73,HSC54,HSP71,NIP71,LAP-1,HEL...

Human E. coli
HSPA8, also known as HSC70, is a member of the heat shock protein family due to homology with other heat shock proteins. The heat shock protein 70 family is comprised of both heat-inducible and constitutively expressed members. The latter are called heat-shock cognate proteins. HSPA8 belongs to the heat-shock cognate subgroup. Members of the human heat-shock protein multigene family have several highly conserved proteins with structural and functional properties in common but vary in the extent ...
TMPH-00503 60S ribosomal protein L10 Protein, Drosophila melanogaster, Recombinant (His)

QM protein homolog,Large ribosomal subunit...

Fruit fly E. coli
60S ribosomal protein L10 Protein, Drosophila melanogaster, Recombinant (His) is expressed in E. coli.
TMPY-06759 L1CAM Protein, Human, Recombinant (His & Avi), Biotinylated

CAML1,SPG1,MIC5,HSAS,N-CAM-L1,L1 ...

Human HEK293 Cells
L1CAM Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with His and Avi tag. The predicted molecular weight is 126.46 kDa and the accession number is NP_000416.1.
TMPY-06857 L1CAM Protein, Human, Recombinant (hFc)

N-CAM-L1,NCAM-L1,N-CAML1,MASA,HSAS

Human HEK293 Cells
L1CAM Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 149.93 kDa and the accession number is NP_000416.1.
TMPY-00017 Influenza A H10N3 (A/duck/Hunan/S11205/2012) Hemagglutinin/HA1 Protein (His)

Harvey rat sarcoma viral oncogene homolog

H10N3 HEK293 Cells
Influenza A H10N3 (A/duck/Hunan/S11205/2012) Hemagglutinin/HA1 Protein (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 36.8 kDa and the accession number is S0AUA5.
TMPK-00016 Cpn10/HSPE1 Protein, Human/Mouse/Goat, Recombinant (His & Avi), Biotinylated

Hsp10,Chaperonin 10,HSPE...

Human,Mouse,Goat E. coli
Cpn10/HSPE, a 10-kDa heat shock protein, is a novel interacting partner of NPAT. A pool of Cpn10 is colocalized with NPAT foci during G1 and S phases in nuclei.Cpn10 is important for S phase progression and cell proliferation. Interaction of Heat Shock Protein Cpn10 with the Cyclin E/Cdk2 Substrate Nuclear Protein Ataxia-Telangiectasia (NPAT) Is Involved in Regulating Histone Transcription. Cpn10/HSPE1 Protein, Human/Mouse/Goat, Recombinant (His & Avi), Biotinylated is expressed in E. coli expre...
TMPK-00015 Cpn10/HSPE1 Protein, Human/Mouse/Goat, Recombinant (His & Avi)

GROES,Hsp10,Chaperonin 10

Human,Mouse,Goat E. coli
Cpn10/HSPE, a 10-kDa heat shock protein, is a novel interacting partner of NPAT. A pool of Cpn10 is colocalized with NPAT foci during G1 and S phases in nuclei.Cpn10 is important for S phase progression and cell proliferation. Interaction of Heat Shock Protein Cpn10 with the Cyclin E/Cdk2 Substrate Nuclear Protein Ataxia-Telangiectasia (NPAT) Is Involved in Regulating Histone Transcription. Cpn10/HSPE1 Protein, Human/Mouse/Goat, Recombinant (His & Avi) is expressed in E. coli expression system w...
TMPY-01306 DNMT2 Protein, Human, Recombinant (GST)

PUMET,RNMT1,tRNA aspartic acid methyltrans...

Human Baculovirus Insect Cells
DNMT2, also known as tRNA (cytosine-5-)-methyltransferase, DNA methyltransferase homolog HsaIIP, and TRDMT1, is a member of the DNA methyltransferase family of enzymes. DNMT2 enzymes have been widely conserved during evolution and contain all of the signature motifs of DNA (cytosine-5)-methyltransferases. It contains all 10 sequence motifs that are conserved among m(5)C MTases, including the consensus S:-adenosyl-L-methionine-binding motifs and the active site ProCys dipeptide, and its structure...
TMPY-02300 BIN1 Protein, Human, Recombinant (His)

AMPHL,bridging integrator 1,AMPH2,SH3P9

Human E. coli
Amphiphysin 2, also named bridging integrator-1 (BIN1) or SH3P9, Amphiphysin2/BIN1 is a crescent-shaped N-BAR protein playing a key role in forming deeply invaginated tubes in muscle T-tubules, has been recently implicated in rare and common diseases affecting different tissues and physiological functions. BIN1 downregulation is linked to cancer progression and also correlates with ventricular cardiomyopathy and arrhythmia preceding heart failure. Increased BIN1 expression is linked to increased...
TMPY-05760 DR3/TNFRSF25 Protein, Human, Recombinant (hFc), Biotinylated

TRAMP,tumor necrosis factor receptor s...

Human HEK293 Cells
DR3/TNFRSF25 Protein, Human, Recombinant (hFc), Biotinylated is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 45.9 kDa and the accession number is Q93038-10.
TMPY-01751 DR3/TNFRSF25 Protein, Human, Recombinant (hFc)

TRAMP,TR3,WSL-1,TNFRSF12,DR3,WSL-...

Human HEK293 Cells
DR3/TNFRSF25 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 45.9 kDa and the accession number is Q93038-10.
TMPY-00961 ADAM15 Protein, Human, Recombinant (His)

MDC15,ADAM metallopeptidase domain 15

Human HEK293 Cells
ADAM15 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 54 kDa and the accession number is Q13444-10.

重组蛋白

Cathepsin D Protein, Human, Recombinant (His)
Cat.No: TMPY-02450
Species: Human
Expression System: HEK293 Cells
L1CAM Protein, Human, Recombinant (His)
Cat.No: TMPY-01431
Species: Human
Expression System: HEK293 Cells
BLVRB Protein, Human, Recombinant (His)
Cat.No: TMPY-02519
Species: Human
Expression System: E. coli
L1CAM Protein, Mouse, Recombinant (His)
Cat.No: TMPK-00811
Species: Mouse
Expression System: HEK293 Cells
Peroxiredoxin 5 Protein, Human, Recombinant (His)
Cat.No: TMPY-02208
Species: Human
Expression System: E. coli
S100A10 Protein, Human, Recombinant (His)
Cat.No: TMPY-01926
Species: Human
Expression System: E. coli
HSC70 Protein, Human, Recombinant (His)
Cat.No: TMPY-02217
Species: Human
Expression System: E. coli
60S ribosomal protein L10 Protein, Drosophila melanogaster, Recombinant (His)
Cat.No: TMPH-00503
Species: Fruit fly
Expression System: E. coli
L1CAM Protein, Human, Recombinant (His & Avi), Biotinylated
Cat.No: TMPY-06759
Species: Human
Expression System: HEK293 Cells
L1CAM Protein, Human, Recombinant (hFc)
Cat.No: TMPY-06857
Species: Human
Expression System: HEK293 Cells
Influenza A H10N3 (A/duck/Hunan/S11205/2012) Hemagglutinin/HA1 Protein (His)
Cat.No: TMPY-00017
Species: H10N3
Expression System: HEK293 Cells
Cpn10/HSPE1 Protein, Human/Mouse/Goat, Recombinant (His & Avi), Biotinylated
Cat.No: TMPK-00016
Species: Human,Mouse,Goat
Expression System: E. coli
Cpn10/HSPE1 Protein, Human/Mouse/Goat, Recombinant (His & Avi)
Cat.No: TMPK-00015
Species: Human,Mouse,Goat
Expression System: E. coli
DNMT2 Protein, Human, Recombinant (GST)
Cat.No: TMPY-01306
Species: Human
Expression System: Baculovirus Insect Cells
BIN1 Protein, Human, Recombinant (His)
Cat.No: TMPY-02300
Species: Human
Expression System: E. coli
DR3/TNFRSF25 Protein, Human, Recombinant (hFc), Biotinylated
Cat.No: TMPY-05760
Species: Human
Expression System: HEK293 Cells
DR3/TNFRSF25 Protein, Human, Recombinant (hFc)
Cat.No: TMPY-01751
Species: Human
Expression System: HEK293 Cells
ADAM15 Protein, Human, Recombinant (His)
Cat.No: TMPY-00961
Species: Human
Expression System: HEK293 Cells
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