55
17
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T39710 |
ARV-471
Vepdegestrant |
Estrogen Receptor/ERR; PROTACs | Endocrinology/Hormones; PROTAC |
ARV-471 (Vepdegestrant) 是一种高效的,口服有效的基于 Cereblon 配体的雌激素受体降解剂 PROTAC 。ARV-471 常用于研究乳腺癌。 | |||
T6798 |
Tretazicar
5-Aziridino-2,4-dinitrobenzamide,CB1954,NSC 115829 |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
Tretazicar (NSC-115829) 是一种抗肿瘤前药,由 NAD(P)H 醌氧化还原酶 2 激活。它在酶促活化后生成细胞毒性双功能烷基剂,可以形成 DNA-DNA 链间交联。 | |||
T7750 |
N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(9R)-6'-Methoxycinchonan-9-yl]- Thiourea
N-[3,5-双(三氟甲基)苯基]-N′-[(9R)-6′-甲氧基-9-金鸡宁]硫脲 |
Others | Others |
N-[3,5-bis(trifluoroMethyl)phenyl]-N'-[(9R)-6'-Methoxycinchonan-9-yl]- Thiourea 是金鸡纳生物碱衍生的双功能催化剂。 | |||
T17159 |
Treosulfan
NSC 39069,曲奥舒凡,Treosulphan |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
Treosulfan (Treosulphan) 是一种双功能的烷化剂,对卵巢癌及其他的实体瘤都有抑制效果。 | |||
T15178 |
dTRIM24
|
Others; PROTACs | Others; PROTAC |
dTRIM24 是一种基于 PROTAC 技术的选择性双功能 TRIM24 降解剂,由von Hippel-Lindau 和TRIM24 两者配体构成。 | |||
T18728 |
Sulfo-SMCC sodium
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Sulfo-SMCC sodium 是一种异双功能、不可裂解的 ADC 交联剂,带有 N-羟基琥珀酰亚胺酯和马来酰亚胺基团,分别与伯胺和巯基反应。 | |||
T4382 |
Proguanil hydrochloride
Paludrine hydrochloride,盐酸氯胍,Chlorguanide hydrochloride,Chloroquanil |
Others; Dehydrogenase; DNA/RNA Synthesis; Antifolate; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; Others |
Proguanil hydrochloride (Chloroquanil) 是一种双胍类抗疟疾剂,在体内代谢形成环胍。它还是一种二氢叶酸还原酶抑制剂。 | |||
T26803 |
Bibw 22
Bibw22,Bibw-22 |
Others | Others |
Bibw 22 is a bifunctional modulator of P-glycoprotein and nucleoside transport. | |||
T19168 |
9-Azido-Neu5DAz
|
Others | Others |
9-Azido-Neu5DAz is a non-natural bifunctional carbohydrates as imaging agent. | |||
T14267 |
Aminooxy-PEG3-C2-NH-Boc
|
Others | Others |
Aminooxy-PEG3-C2-NH-Boc is a PEGylated PROTAC linker utilized in the synthesis of PROTACs, an emerging class of bifunctional molecules for targeted protein degradation[1]. | |||
T19207 |
BFCAs-1
|
Others | Others |
BFCAs-1 is a polyamine polycarboxylic bifunctional chelating agent (BFCAs) with a broad range of applications in biology, chemistry, medicine and diagnostic imaging. | |||
T16181 |
N-(Azido-PEG2)-N-Boc-PEG4-Boc
|
Others | Others |
N-(Azido-PEG2)-N-Boc-PEG4-Boc is a PEG-based bifunctional linker employed for the synthesis of PROTACs. | |||
T28846 |
SR16835
AT-202,AT202,SR 16835,SR-16835 |
Others | Others |
SR16835 is a NOP receptor agonist, with low-affinity bifunctional activity at the μ opioid receptor. | |||
T18744 |
t-Boc-Aminooxy-PEG7-bromide
|
Others | Others |
t-Boc-Aminooxy-PEG7-bromide is a polyethylene glycol (PEG)-based bifunctional linker utilized in the synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T70925 |
GS-5759
|
Others | Others |
GS-5759 is a bifunctional ß2-Adrenoceptor Agonist and Phosphodiesterase 4 Inhibitor for Chronic Obstructive Pulmonary Disease with a Unique Mode of Action. | |||
T68272 |
Batefenterol Succinate
|
Others | Others |
Batefenterol Succinate is a first-in-class inhaled bifunctional bronchodilator possessing muscarinic receptor antagonist and β2-adrenoceptor agonist properties. | |||
T25140 |
BCH 2763
BCH2763,BCH-2763 |
Others | Others |
BCH 2763 is an effective, selective bifunctional thrombin inhibitor that blocks both the anion binding exosite and the active catalytic site. | |||
T41024 |
FmocNH-PEG4-t-butyl acetate
FmocNH-PEG4-t-butyl acetate |
Others | Others |
FmocNH-PEG4-t-butyl acetate is a polyethylene glycol (PEG)-derived PROTAC linker employed for the synthesis of PROTACs, bifunctional molecules designed to degrade target proteins. | |||
T40648 |
NOTA
|
Others | Others |
NOTA, a bifunctional chelate, serves as a foundation for PET imaging tool construction, probe design, and signal amplification through the multivalent effect. | |||
T34173 |
p-SCN-Bn-HOPO
|
Others | Others |
p-SCN-Bn-HOPO is an excellent bifunctional chelating agent for (89)Zr ImmunoPET, with low background, good tumor-organ contrast, and importantly, very low bone uptake for BT474 breast cancer imaging. | |||
T81433 |
p-NH2-CHX-A"-DTPA
|
Others | Others |
p-NH2-CHX-A"-DTPA 是双功能螯合剂。 | |||
T14449 |
Azido-PEG4-hydrazide-Boc
|
Others | Others |
Azido-PEG4-hydrazide-Boc is a polyethylene glycol (PEG)-based bifunctional linker compound used in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1]. | |||
T16234 |
N-Mal-N-bis(PEG4-NHS ester)
|
Others | Others |
N-Mal-N-bis(PEG4-NHS ester) is a polyethylene glycol (PEG)-based bifunctional linker utilized for synthesizing Proteolysis Targeting Chimeras (PROTACs)[1]. | |||
T17469 |
Azide-PEG3-Sulfone-PEG3-azide
|
Others | Others |
Azide-PEG3-Sulfone-PEG3-azide is a polyethylene glycol (PEG)-based bifunctional molecule, specifically designed as a PROTAC linker for the synthesis of PROTACs[1]. | |||
T18080 |
m-PEG-acrylate (MW 30000)
|
Others | Others |
m-PEG-acrylate (MW 30000) is a polyethylene glycol (PEG)-based bifunctional linker commonly employed in the chemical synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T81384 |
PROTAC BRD9 Degrader-3
|
PROTACs | PROTAC |
PROTACBRD9 Degrader-3为BRD9靶向的双功能降解剂,用于癌症研究。 | |||
T14163 |
Ald-Ph-amido-C2-PEG3-NH-Boc
|
Others | Others |
Ald-Ph-amido-C2-PEG3-NH-Boc is a polyethylene glycol (PEG)-based bifunctional linker utilized for the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1]. | |||
T18413 |
N-Desthiobiotin-N-bis(PEG4-t-butyl ester)
|
Others | Others |
N-Desthiobiotin-N-bis(PEG4-t-butyl ester) is a PEG-based linker compound employed for the synthesis of PROTACs, which are bifunctional molecules designed for targeted protein degradation[1]. | |||
T18834 |
Thiol-PEG-CH2COOH (MW 5000)
|
Others | Others |
Thiol-PEG-CH2COOH (MW 5000) is a Polyethylene glycol (PEG) derived link molecule, commonly utilized in the construction of PROTACs, which are bifunctional compounds designed for targeted protein degradation [1]. | |||
T17962 |
Fmoc-N-PEG36-acid
|
Others | Others |
Fmoc-N-amido-PEG36-acid is a polyethylene glycol (PEG)-based linker utilized in PROTAC synthesis. It has been designed specifically for constructing PROTACs, which are bifunctional molecules capable of recruiting target proteins to an E3 ubiquitin ligase for degradation[1]. | |||
T81385 |
PROTAC BRD9 Degrader-2
|
PROTACs | PROTAC |
PROTACBRD9 Degrader-2是针对癌症研究的BRD9双功能性降解剂。 | |||
T31584 |
DST Crosslinker
DST Cross linker,DST Cross-linker |
Others | Others |
DST crosslinker(disuccinimide tartarate) is an isotype bifunctional, cleavable crosslinker (cleavable by an oxidizer) for applications that require crosslinking cleavability and that do not interfere with protein disulfide bonds with reducing agents. | |||
T77936 |
PROTAC BRD9 Degrader-4
|
PROTACs | PROTAC |
PROTACBRD9 Degrader-4 是一种针对BRD9的双功能降解剂,用于癌症研究。 | |||
T82537 |
D-MoDE-A (1)
|
LYTACs | PROTAC |
D-MoDE-A(1)是一种双功能小分子,它通过ASGPR(去唾液酸糖蛋白受体)介导外源蛋白的降解。 | |||
T77155 | Dalutrafusp alfa | ||
Dalutrafusp alfa (AGEN-1423; GS-1423) 为针对CD73与TGF-β的特异性双功能抗体,涉及免疫抑制路径。 | |||
T11938L |
Macropa-NH2
|
Others | Others |
Macropa-NH2 是 macropa 双功能类似物,是一种常与抗体偶联的载体分子,常作为螯合剂使用,参与癌症研究。 | |||
T26049 |
RB 6145
RB6145,RB-6145 |
Others | Others |
RB 6145是一种双功能硝基咪唑,低氧细胞放射增敏剂RSU 1069的前药,它的毒性较RSU 1069降低。它具有缺氧细胞优先细胞毒性和抗肿瘤治疗活性。 | |||
T81779 |
M-MoDE-A (2)
|
LYTACs | PROTAC |
M-MoDE-A (2)为双功能小分子,其作用机理包括促进通过ASGPR (去唾液酸糖蛋白受体) 介导的细胞外蛋白质降解。 | |||
T69149 |
L2-b
|
Others | Others |
L2-b is a bifunctional Aβ-interacting, metal-chelating molecule that modulates ROS production in, and improves survival of neuroblastoma cells incubated in the presence of Aβ along with Copper or Zinc. In cell-free aggregation studies, L2-b inhibits metal-induced Aβ aggregation, and also promotes the dissociation of Ab aggregates in homogenates of human AD brain samples. | |||
T31588 |
Dynasylan 1161
Y 9138 |
Others | Others |
Dynasylan 1161 是一种双官能有机硅烷,可以与合适的聚合物反应。在水存在时,Dynasylan 1161可与各种无机基材结合。 | |||
T32026 |
GYKI-13324
GYKI 13324,GYKI13324 |
Others | Others |
GYKI-13324 is bifunctional nitrosoureido derivative and alkylating agent. GYKI-13324 was studied on human colorectal tumor xenograft lines. Given orally in single or multiple daily doses, GYKI-13324 produced long-term or total regression of adenomatous, b | |||
T28464 |
p-SCN-Bn-TCMC HCl
p-SCN-Bn-TCMC |
Others | Others |
p-SCN-Bn-TCMC is a bifunctional chelator, it contains a powerful chelator TCMC and reactive tioisocyante linker. TCMC is a powerful chelator with capability to strongly bind radio-isotopic heavy metal ion, which are widely used for radio-diagnostic/imagin | |||
T82560 |
di-Ellipticine-RIBOTAC
|
PROTACs | PROTAC |
Di-Ellipticine-RIBOTAC是一款双功能小分子,在体外和体内肌萎缩侧索硬化(ALS)模型中能够减少c9ALS/FTD r(G4C2)的重复扩增。 | |||
T68942 |
Caricotamide
|
Others | Others |
Caricotamide is a synthetic co-substrate that activates the human endogenous enzyme NRH:quinone oxidoreductase 2 (NQO2) with potential chemoadjuvant activity. When caricotamide is administered simultaneously with the prodrug tretazicar, NQO2 converts tretazicar to the bifunctional alkylating agent dinitrobenzamide, which is capable of forming a high degree of DNA interstrand cross-links, resulting in the inhibition of DNA replication and the induction of apoptosis. NQO2 has been found to be over... | |||
T82866 |
Biotin-PEG-Biotin (MW 20000)
|
||
Biotin-PEG-azide (MW 2000) 为含有生物素标记的聚乙二醇 (PEG) 衍生物。该生物素(Biotin)作为酶辅因子,在蛋白质标记应用中具有重要作用,而PEG是低毒性且具亲水性的水溶性聚合物。 | |||
T81035 |
TAT-NSF222 Fusion Peptide
|
||
TAT-NSF222 Fusion Peptide为包含TAT和NSF两个结构域的融合多肽,TAT负责通过巨胞饮促进细胞摄取,而NSF结构域则抑制N-乙基马来酰亚胺敏感因子(NSF)活性。该融合多肽是exocytosis的抑制剂。 | |||
T80588 |
Bintrafusp alfa
M7824,MSB0011359C |
||
Bintrafusp alfa (M 7824) 是高端双功能融合蛋白,融合了转化生长因子β受体II (TGF-βRII) 的细胞外域与人源IgG1单克隆抗体 (mAb) 致程序性细胞死亡配体阻断功能。该化合物主要用于癌症研究领域。 | |||
T79618 |
M3/PDE4 modulator-1
|
Others | Others |
M3/PDE4 modulator-1 (10f) 为多功能化合物,具备M3mAChR拮抗和PDE4抑制作用。于OVA大鼠模型中,M3/PDE4 modulator-1 (10-1000 nM/kg;iv) 能降低半胱氨酸嗜酸性粒细胞内流。 | |||
T81675 |
NICE-01
AP1867-PEG2-JQ1,AP-PEG2-JQ1 |
||
NICE-01 (AP1867-PEG2-JQ1; AP-PEG2-JQ1)是一款具有双功能的化合物,它通过特异性结合到细胞内特定亚细胞区室中的蛋白质,并以BRD4蛋白的核定位含溴结构域作为诱导,实现将胞浆中的货物输送至细胞核。 | |||
T78352 |
N-acetylglucosamine-1-P uridyltransferase (AGX1)
GlcNAc1pUT |
Others | Others |
N-acetylglucosamine-1-P uridyltransferase (AGX1) (GlcNAc1pUT) 是具有双功能乙酰转移酶/尿苷转移酶活性的原核生物专有酶。该酶能结合GlcNAc-1-P与UTP,催化合成UDP-GlcNAc的尿苷酰转移反应。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00590 |
GlmU Protein, E. coli, Recombinant (His & Myc)
glmU,Bifunctional protein GlmU |
E. coli | E. coli |
Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP-GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5-monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain. | |||
TMPH-00176 |
PucL Protein, Bacillus subtilis, Recombinant (His & Myc)
Uric acid degradation bifunctional protein PucL,puc... |
Bacillus subtilis | E. coli |
Catalyzes two steps in the degradation of uric acid, i.e. the oxidation of uric acid to 5-hydroxyisourate (HIU) and the stereoselective decarboxylation of 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline (OHCU) to (S)-allantoin. PucL Protein, Bacillus subtilis, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 64.0 kDa and the accession number is O32141. | |||
TMPH-00589 |
SpoT Protein, E. coli, Recombinant (His & Myc)
Bifunctional (p)ppGpp synthase/hydrolase SpoT,spoT |
E. coli | E. coli |
In eubacteria ppGpp (guanosine 3'-diphosphate 5'-diphosphate) is a mediator of the stringent response which coordinates a variety of cellular activities in response to changes in nutritional abundance. This enzyme catalyzes both the synthesis and degradation of ppGpp. The second messengers ppGpp and c-di-GMP together control biofilm formation in response to translational stress; ppGpp represses biofilm formation while c-di-GMP induces it. ppGpp activates transcription of CsrA-antagonistic small ... | |||
TMPH-01008 |
PNKP Protein, Human, Recombinant (His & SUMO)
Polynucleotide kinase-3'-phosphatase,PNKP,DNA 5'-kinase/3'-p... |
Human | E. coli |
Plays a key role in the repair of DNA damage, functioning as part of both the non-homologous end-joining (NHEJ) and base excision repair (BER) pathways. Through its two catalytic activities, PNK ensures that DNA termini are compatible with extension and ligation by either removing 3'-phosphates from, or by phosphorylating 5'-hydroxyl groups on, the ribose sugar of the DNA backbone. PNKP Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The ... | |||
TMPH-00188 |
BioAB Protein, Bacteroides fragilis, Recombinant (His & Myc)
Adenosylmethionine-8-amino-7-oxononanoate aminotransferase B... |
Bacteroides fragilis | E. coli |
Catalyzes two activities which are involved in the biotine biosynthesis: the conversion of dethiobiotin (DTB) to biotin by the insertion of a sulfur atom into dethiobiotin via a radical-based mechanism, and the transfer of the alpha-amino group from S-adenosyl-L-methionine (SAM) to 7-keto-8-aminopelargonic acid (KAPA) to form 7,8-diaminopelargonic acid (DAPA). BioAB Protein, Bacteroides fragilis, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The p... | |||
TMPH-00160 |
Cytochrome P450 BM-3 Protein, Bacillus megaterium, Recombinant (His & Myc)
cyp102A1,Bifunctional cytochrome P450/NADPH--P450 r... |
Bacillus megaterium | E. coli |
Cytochrome P450 BM-3 Protein, Bacillus megaterium, Recombinant (His & Myc) is expressed in E. coli. | |||
TMPH-01007 |
NDST1 Protein, Human, Recombinant (His & SUMO)
Glucosaminyl N-deacetylase/N-sulfotransferase 1,[Heparan sul... |
Human | E. coli |
NDST1 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 73.5 kDa and the accession number is P52848. | |||
TMPH-03057 |
Chorismate synthase Protein, Neurospora crassa, Recombinant (His)
B7F21.10,NCU05420,aro-2,5-enolpyruvylshikimate-3-phosphate p... |
Neurospora crassa | E. coli |
Bifunctional enzyme that possesses chorismate synthase and intrinsic flavin reductase activity, it uses NADPH to reduce FMN. | |||
TMPH-00110 |
UGT72B1 Protein, Arabidopsis thaliana, Recombinant (His & Myc)
Probable hydroquinone glucosyltransferase,Arbutin synthase,U... |
Arabidopsis thaliana | E. coli |
Bifunctional O-glycosyltransferase and N-glycosyltransferase that can detoxify xenobiotics. Possesses high activity to metabolize the persistent pollutants 2,4,5-trichlorophenol (TCP) and 3,4-dichloroaniline (DCA). Also active on benzoates and benzoate derivatives in vitro. UGT72B1 Protein, Arabidopsis thaliana, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 60.4 kDa and the accession number is Q9M156. | |||
TMPH-03605 |
CHOD Protein, Streptomyces sp., Recombinant (GST)
choA,Cholesterol isomerase,CHOD,Cholesterol oxidase |
Streptomyces | E. coli |
Bifunctional enzyme that catalyzes the oxidation of the 3-beta-hydroxy group of cholesterol and the isomerization of the double bond of the resulting product. CHOD Protein, Streptomyces sp., Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 81.9 kDa and the accession number is P12676. | |||
TMPJ-00690 |
PGDS Protein, Human, Recombinant
Glutathione-Requiring Prostaglandin D Synthase,PGDS,Glutathi... |
Human | E. coli |
Hematopoietic Prostaglandin D Synthase (HPGDS) belongs to the GST superfamily and Sigma family. HPGDS contains one GST C-terminal domain and one GST N-terminal domain. HPGDS is highly expressed in adipose tissue, macrophages, and placenta, and it exists in the form of homodimer in living body. HPGDS is a cytosolic enzyme that isomerizes PGH(2). HPGDS is a bifunctional enzyme that catalyzes both the conversion of PGH2 to PGD2 and also shows low glutathione-peroxidase activity towards cumenehydrop... | |||
TMPY-02201 |
Peroxiredoxin 6 Protein, Human, Recombinant (His)
p29,PRX,1-Cys,HEL-S-128m,peroxiredoxin 6,NSGPx,AOP2,aiPLA2 |
Human | E. coli |
PRDX6, a member of antioxidant protein superfamily, plays an important role in oxidative stress, catabolism of lipids and phospholipid lipisomes. Peroxiredoxin 6 (PRDX6) is involved in redox regulation of the cell and is thought to be protective against oxidant injury. Peroxiredoxin 6 (PRDX6) is a bifunctional protein with both glutathione peroxidase (GPx) and iPLA2 activities,which are concomitantly increased with the expression of PRDX6. PRDX6 promoted lung tumor growth in an in vivo allograft... | |||
TMPY-03976 |
EEF1E1 Protein, Human, Recombinant (His)
eukaryotic translation elongation factor 1 ε 1,P18,eukaryoti... |
Human | E. coli |
EEF1E1, also known as AIMP3 and p18, is a multifunctional protein that localizes to both the cytoplasm and nucleus. In the cytoplasm, EEF1E1 is an auxiliary component of the macromolecular aminoacyl-tRNA synthase complex. It is comprised of a bifunctional glutamyl-prolyl-tRNA synthase, the monospecific isoleucyl, leucyl, glutaminyl, methionyl, lysyl, arginyl and aspartyl-tRNA synthases, and three auxiliary proteins, EEF1E1/p18, AIMP2/p38 and AIMP1/p43. EEF1E1 also plays a positive role in ATM/AT... | |||
TMPJ-00202 |
CD157 Protein, Human, Recombinant (hFc)
Cyclic ADP-ribose hydrolase 2,cADPr hydrolase 2,ADP-ribosyl ... |
Human | HEK293 Cells |
The cluster of differentiation (CD) system is a glycosyl phosphatidylinositol anchored membrane protein that belongs to the CD38 family.It is generally used in immunophynotyping. CD157 was discovered in a bone marrow stromal cell line where it facilitates pre-B-cell growth. CD157 is a bifunctional ectoenzyme that exhibits both ADP-ribosyl cyclase and cyclic ADP ribose hydrolase activities followed with CD38. It plays a role in rheumatoid arthritis (RA) due to its enhanced expression in RA-derive... | |||
TMPY-03338 |
GSTZ1 Protein, Human, Recombinant (His)
MAI,GSTZ1-1,glutathione S-transferase ζ 1,MAAI,GSTZ1,glutath... |
Human | E. coli |
GSTZ1 (Glutathione S-Transferase Zeta 1) is a Protein Coding gene. 3 alternatively spliced human isoforms have been reported. GSTZ1 gene is a member of the glutathione S-transferase (GSTs) super-family which encodes multifunctional enzymes important in the detoxification of electrophilic molecules, including carcinogens, mutagens, and several therapeutic drugs, by conjugation with glutathione. GSTZ1 is a bifunctional protein that has minimal glutathione-conjugating activity with ethacrynic acid ... | |||
TMPY-01680 |
Lumican Protein, Human, Recombinant (His)
lumican,LDC,SLRR2D |
Human | HEK293 Cells |
Lumican, a prototypic leucine-rich proteoglycan with keratan sulfate side chains, is a major component of the cornea, dermal, and muscle connective tissues. In these bifunctional molecules, the protein moiety binds collagen fibrils and the highly charged hydrophilic glycosaminoglycans regulate interfibrillar spacings. Lumican is the major keratan sulfate proteoglycan of the cornea but is also distributed in interstitial collagenous matrices throughout the body. Lumican regulates collagenous matr... | |||
TMPY-04474 |
PFKFB3 Protein, Human, Recombinant (His & GST)
IPFK2,6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3,... |
Human | Baculovirus Insect Cells |
Fructose-2,6-biphosphatase 3, also known as 6-phosphofructo-2-kinase or PFK2 or PFKFB3, is a potent activator of phosphofructokinase, which is a rate-limiting enzyme of glycolysis. Highly phosphorylated PFKFB3 protein was found in human tumor cells, vascular endothelial cells, and smooth muscle cells. Fructose 2,6-bisphosphate (Fru-2,6-BP) is an allosteric activator of 6-phosphofructo-1-kinase (PFK-1), a rate-limiting enzyme and essential control point in glycolysis. The concentration of PFK2 de... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIH-0457 |
Proguanil-d6 HCl
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Proguanil-d6 HCl 是 Proguanil HCl 的氘代化合物。Proguanil HCl 的 CAS 号为 637-32-1。Proguanil hydrochloride 是一种双胍类抗疟疾剂,在体内代谢形成环胍。它还是一种二氢叶酸还原酶抑制剂。 |