34
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6531 |
Heparin sodium salt
肝素钠,Sodium heparinate,Heparin sodium |
Factor Xa; Thrombin; Autophagy | Autophagy; Metabolism; Proteases/Proteasome |
Heparin sodium salt (Sodium heparinate) 是一种抗凝剂,可与抗凝血酶 III 可逆地结合,使凝血酶因子 IIa 和 Xa 的失活速度加快,显着抑制外泌体-细胞相互作用。 | |||
TP1153L |
Fibronectin Adhesion-promoting Peptide acetate
Fibronectin Adhesion-promoting Peptide acetate(125720-21-0 free base),Heparin Binding Peptide acetate |
Others | Others |
Fibronectin Adhesion-promoting Peptide acetate (Heparin Binding Peptide acetate)(125720-21-0 free base) 是在纤连蛋白的羧基末端肝素结合结构域中发现的肝素结合氨基酸序列之一。 | |||
T4076 |
Fondaparinux sodium
Natural heparin pentasaccharide Sodium,Fondaparin sodium,磺达肝素(癸)钠,磺达肝癸钠,SR-90107A,Arixtra |
Factor Xa | Metabolism |
Fondaparinux sodium (SR-90107A) 是抗凝血酶依赖性的 factor Xa 抑制剂。 | |||
TP2255 |
heparin cofactor II precursor fragment [Homo sapiens]
|
Others | Others |
Heparin cofactor II precursor fragment [Homo sapiens] is a peptide with the sequence H2N-Tyr-Glu-Ile-Thr-Thr-Ile-His-Asn-Leu-Phe-Arg-OH, MW=1406.58. | |||
TP2256 |
heparin cofactor II precursor (SERPIND1) fragment [Homo sapiens]
|
Others | Others |
Heparin cofactor II precursor (SERPIND1) fragment [Homo sapiens] is a peptide with the sequence H2N-Phe-Thr-Val-Asp-Arg- Pro-Phe-Leu-Phe-Leu-Ile-Tyr-Glu-His-Arg-OH, MW=1953.25. | |||
T64262 | Heparin Lithium salt | ||
Heparin Lithium salt 是一种抗凝剂,能够可逆的结合抗凝血酶III (ATIII)。Heparin Lithium salt 明显阻碍外泌体-细胞相互作用。 | |||
TP1153 |
Fibronectin Adhesion-promoting Peptide
Heparin Binding Peptide |
||
Fibronectin Adhesion-promoting Peptide (Heparin Binding Peptide) is one of the heparin-binding amino acid sequences found in the carboxy-terminal heparin-binding domain of fibronectin. | |||
TP1152 |
Fibronectin Adhesion-promoting Peptide TFA
Heparin Binding Peptide TFA |
||
Fibronectin Adhesion-promoting Peptide (Heparin Binding Peptide) is one of the heparin-binding amino acid sequences found in the carboxy-terminal heparin-binding domain of fibronectin. It promotes assembly of mesenchymal stem cell (MSC) spheroids into lar | |||
T40711 |
H-D-Phe-Pip-Arg-pNA dihydrochloride
S-2238 dihydrochloride,H-D-Phe-Pip-Arg-pNA dihydrochloride |
Others | Others |
H-D-Phe-Pip-Arg-pNA dihydrochloride (S-2238 dihydrochloride), a chromogenic substrate, mimics the N-terminal fragment of the A alpha chain of fibrinogen, the native substrate of thrombin. Specifically designed for thrombin detection, H-D-Phe-Pip-Arg-pNA dihydrochloride is employed for the quantification of antithrombin-heparin cofactor (AT-III). The AT-III assay utilizing this substrate is characterized by its sensitivity, accuracy, and ease of implementation. | |||
T26240 |
Surfen dihydrochloride
Aminokinuride dihydrochloride,Aminoquinuride dihydrochloride,NSC-12155,Aminokinuride 2HCl,Aminoquinuride 2HCl |
FGFR; Antiviral; Antibiotic | Angiogenesis; Immunology/Inflammation; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Surfen dihydrochloride (Aminoquinuride dihydrochloride) 是一种有效的硫酸肝素小分子拮抗剂,具有抗菌和抗病毒活性,抑制炭疽致死因子、凝血因子 X 和致死因子。Surfen dihydrochloride 可抑制普通肝素和低分子量肝素的抗凝活性,抑制肝素的硫酸化和肝素裂解酶的降解。Surfen dihydrochloridn 抑制阻断硫酸乙酰肝素介导的 FGF2 结合和信号转导。Surfen 抑制 SEVI 和精液介导的 HIV 1 型感染增强。 | |||
T10820L1 |
Ciraparantag acetate
Ciraparantag acetate(1438492-26-2 Free base) |
Others | Others |
Ciraparantag acetate 是一种抗凝逆转剂,是一种小分子,专门设计用于通过电荷-电荷相互作用与普通肝素和低分子量肝素非共价结合。它显示出与直接口服抗凝剂 (DOAC) 相似的结合特性。 | |||
T0155 |
Argatroban
MCI-9038,阿加曲班,MD-805,Argipidine |
Thrombin | Proteases/Proteasome |
Argatroban (MCI-9038) 是一种选择性的凝血酶抑制剂。 | |||
T22246 |
Argatroban Monohydrate
阿加曲班一水合物,阿加曲班 |
Thrombin | Proteases/Proteasome |
Argatroban Monohydrate 是一种 thrombin 选择性抑制剂。 | |||
T13720 |
Hexadimethrine bromide
1,5-Dimethyl-1,5-diazaundecamethylene polymethobromide,海美溴铵,聚凝胺,Polybrene |
Others | Others |
Hexadimethrine bromide (1,5-Dimethyl-1,5-diazaundecamethylene polymethobromide) 是阳离子聚合物,常用于提高逆转录病毒载体介导的基因转移效率。 | |||
T22323 |
Enoxaparin sodium
|
Thrombin | Proteases/Proteasome |
Enoxaparin sodium 是一种低分子量肝素 (LMWH),已获得美国 FDA 批准,可用于医疗管理的 ST 段心肌梗死 (STEMI) 或 STEMI 及随后的经皮冠状动脉介入治疗 (PCI) 患者。它与抗凝血酶结合并增强其作用,并抑制凝血因子 XIa、IXa、Xa 和 IIa(凝血酶),从而防止血栓形成。 | |||
T68002 |
Naroparcil
|
Thrombin | Proteases/Proteasome |
Naroparcil 是一种可口服的硫代苷类化合物,是一种 4-甲基伞形 β-D-木糖苷类似物,在静脉血栓形成(颈静脉)的Wessler淤滞模型中显示出抗血栓形成作用。Naroparcil 增强了凝血酶/肝素辅因子II复合物的形成,诱导了处理兔血浆中硫酸皮肤素样物质的出现,但减少了与(125I)-人α-凝血酶孵育的血浆中的凝血酶/抗凝血酶III复合物的形成。 | |||
T24531 |
NIC
|
||
NIC is an inhibitor of host invasion. It is also an inhibitor of VEGF binding to immobilized heparin. | |||
TP1959 |
PM 102
|
||
Peptide that reverses the anticoagulant effect of heparin. Potently binds heparin (Kd = 36 nM in vitro). | |||
T10820 |
Ciraparantag
PER977 |
Others | Others |
Ciraparantag is an inhibitor of thrombin and factor Xa. Ciraparantag is a broad-spectrum reversal agent for anticoagulants, including unfractionated heparin, low-molecular-weight heparin, and certain direct oral anticoagulants. | |||
T11341 |
FXIa-IN-1
|
Others | Others |
FXIa-IN-1 is a potent β-lactam covalent heparin-derived factor XIa (fXIa) inhibitor. | |||
T71532 | Fondaparinux free base | ||
Fondaparinux Free Base is a synthetic pentasaccharide that mediates the interaction of HEPARIN with ANTITHROMBINS and inhibits FACTOR Xa; it is used for prevention of VENOUS THROMBOEMBOLISM after surgery. Fondaparinux is a clinically approved anticoagulant pentasaccharide for the treatment of thrombotic diseases, displays better efficacy and biosafety than other heparin-based anticoagulant drugs. | |||
T31522 |
Dipropyl sulfone
|
||
Dipropyl sulfone may function as an enhancer of heparin absorption in the intestine. | |||
T37568 |
4-Methylumbelliferyl 2-sulfamino-2-deoxy-α-D-Glucopyranoside (sodium salt)
|
||
4-Methylumbelliferyl 2-sulfamino-2-deoxy-α-D-Glucopyranoside (4-MU-α-GlcNS) is a fluorogenic substrate of heparin sulphamidase. Heparin sulphamidase cleaves 4-MU-α-GlcNS to yield 4-MU-α-GlcNH2, which is then cleaved by α-glucosaminidase to release the fluorescent product 4-MU, which displays an emission maxima of 445-454 nm. The excitation maxima for 4-MU is pH-dependent: 330, 370, and 385 nm at pH 4.6, 7.4, and 10.4, respectively. 4-MU-α-GlcNS has been used to quantify heparin sulphamidase defi... | |||
T10820L |
Ciraparantag TFA
PER977 TFA |
Others | Others |
Ciraparantag TFA is an inhibitor of thrombin and factor Xa. Ciraparantag is a broad-spectrum reversal agent for anticoagulants, including unfractionated heparin, low-molecular-weight heparin, and certain direct oral anticoagulants. | |||
T36292 |
NSC 12
|
||
NSC 12 is an extracellular trap for fibroblast growth factor 2 (FGF2) that binds FGF2 (Kd = 51 μM) and interferes with its interaction with FGFR1, without affecting the ability of FGF2 to bind heparin or heparin sulfate proteoglycans (HSPGs). NSC 12 also binds several other, but not all, FGF isoforms with Kd values ranging between 16 and 120 μM, preventing them from forming HSPG/FGF/FGFR ternary complexes. NSC 12 inhibits FGF-dependent angiogenesis and tumor cell proliferation in vitro and reduc... | |||
T16377 |
Odiparcil
SB-424323 |
Thrombin | Proteases/Proteasome |
Odiparcil is an orally active beta-d-thioxyloside analog. Odiparcil is an indirect thrombin inhibitor that exerts its anticoagulant effect through activation of antithrombin II (heparin cofactor II). It also has an antithrombotic activity associated with a reduced risk of adverse bleeding events. | |||
T82890 |
bFGF (119-126)
|
||
bFGF (119-126) 为具备生物活性的肽段,对应人类、牛(119-126)、小鼠、大鼠(118-125)以及肝素结合生长因子2(118-125)的相应残基。该肽能够抑制bFGF受体的二聚化及其激活作用。 | |||
T36111 |
L-Iduronic acid sodium salt
|
||
L-Iduronic acid sodium salt 是一种单糖,是肝素、硫酸乙酰肝素和硫酸皮肤素等糖胺聚糖 (GAG) 的重要成分。 | |||
T73751 |
Lepirudin
|
||
Lepirudin为高效的不可逆凝血酶抑制剂,同时是重组水蛭素,主要在肝素诱导的血小板减少症(HIT)中发挥抗凝作用。 | |||
T83672 |
TTAPE-Me
1,1,2,2-tetrakis[4-(2-Trimethylammonioethoxy)-phenylethene |
||
TTAPE-Me是一种聚集诱导发光(AIE)荧光团。它被用于检测阴离子磷脂,包括心磷脂、磷脂酰甘油(PG)和磷脂酰丝氨酸(PS)、核酸,以及阴离子多糖肝素。 | |||
T8926 |
Salcaprozate sodium
8-(2-羟基苯甲酰胺基)辛酸钠,SNAC |
Others | Others |
Salcaprozate sodium (SNAC) 是口服吸收促进剂,有作为口服形式的肝素和胰岛素递送剂的潜力。它可提高非共价大分子络合引起的亲脂性,从而增加小肠上皮细胞的被动跨细胞渗透。 | |||
T39066 |
H-D-Phe-Pip-Arg-pNA hydrochloride
S-2238 hydrochloride,H-D-Phe-Pip-Arg-pNA hydrochloride |
||
H-D-Phe-Pip-Arg-pNA hydrochloride, a chromogenic substrate, mimics the N-terminal segment of the A alpha chain of fibrinogen, the native substrate of thrombin. It displays specificity towards thrombin and is employed for quantifying antithrombin-heparin cofactor (AT-III). The utilization of H-D-Phe-Pip-Arg-pNA hydrochloride in the AT-III assay enables a sensitive, accurate, and straightforward measurement process. | |||
T36370 |
4-Methylumbelliferyl-α-L-Iduronide (free acid)
|
||
4-Methylumbelliferyl-α-L-iduronide (free acid) is a fluorogenic substrate for α-L-iduronidase, an enzyme found in cell lysosomes that is involved in the degradation of glycosaminoglycans such as dermatan sulfate and heparin sulfate. 4-Methylumbelliferyl-α-L-iduronide is cleaved by α-L-iduronidase to release the fluorescent moiety 4-methylumbelliferyl (4-MU). 4-MU fluorescence is pH-dependent with excitation maxima of 320 and 360 nm at low (1.97-6.72) and high (7.12-10.3) pH, respectively, and an... | |||
T36714 |
Sucrose octasulfate (potassium salt)
|
||
Sucrose octasulfate (SOS), a component of the gastrointestinal protectant sucralfate, is an alkaline aluminum-sucrose complex that inhibits peptic hydrolysis and raises gastric pH, protecting esophageal epithelium against acid injury. It can bind to exosite II of thrombin (KD = ~1.4 μM) and inhibit its catalytic activity (IC50 = 4.5 μM) and, as such, has been used as a surrogate for heparin. Furthermore, SOS has been shown to inhibit tumor growth in mouse melanoma and lung carcinoma models by pr... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20654 |
Heparin
Certoparin,Bemiparin,Dalteparin,Adomiparin |
Thrombin; Endogenous Metabolite; Antibacterial; Autophagy | Autophagy; Metabolism; Microbiology/Virology; Proteases/Proteasome |
Heparin (Adomiparin) 是硫酸粘多糖,常在临床医学上当抗凝剂使用。Heparin 在体内实验中显示出部分抗炎活性。 | |||
T41031 |
Protamine sulfate
|
Thrombin | Proteases/Proteasome |
Protamine sulfate是一种多阳离子肽类,作为一种抗肝素剂。该化合物能中和肝素的抗凝作用并增强脂质介导的基因转移。 | |||
Fr16605 |
Lupinine
鲁冰花,羽扇豆碱 |
AChR; AChE | Neuroscience |
Lupinine 是一种能够抵消乙醇麻醉的生物碱。 Lupinine 是一种 AChE 和 BChE 抑制剂和潜在的 CD69 激活剂,存在于 Loranthus、Calia 和 Lupinus 物种中。它还可以抑制肝素。 | |||
T2O2721 |
L-Cysteine
Thioserine,L-半胱氨酸,cysteine,半胱氨酸,L-(+)-Cysteine |
Endogenous Metabolite | Metabolism |
L-Cysteine (L-(+)-Cysteine) 是人体非必需的含硫氨基酸。L-Cysteine 对蛋白质合成、解毒和多种代谢功能很重要。L-Cysteine 存在于指甲、皮肤和头发的主要蛋白质-角蛋白中,对胶原蛋白的生成、皮肤弹性和质地都很重要。L-Cysteine 是抗氧化剂谷胱甘肽的一种成分,在辅酶A、肝素和生物素等基本生化物质的代谢中起着重要作用,也是氨基酸牛磺酸的制造所必需的。 | |||
T4S0797 |
Berberine
小檗碱,Berberin,Umbellatine,黄连素 |
Reactive Oxygen Species; Topoisomerase; Endogenous Metabolite; Antibacterial; Antibiotic; Autophagy | Autophagy; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Berberine (Umbellatine) 是从中草药黄连中分离出来的一种生物碱抗生素。它诱导活性氧生成并抑制 DNA 拓扑异构酶,具有抗肿瘤特性。 |