19
17
11
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T68146 |
Sufotidine
AH 25352X,AH25352X,AH-25352X |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Sufotidine (AH 25352X) 是一种具有高度选择性的竞争性 H2 受体拮抗剂。 | |||
T15390 |
Glufosfamide
D 19575,Glucosylifosfamide mustard |
Others | Others |
Glufosfamide 是一种新型噁唑磷胺化合物,具有抗癌活性,可用于研究晚期非小细胞肺癌。 | |||
T20029 |
Buformin hydrochloride
NSC528218,NSC-528218,盐酸丁双胍,NSC 528218 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Buformin hydrochloride (NSC-528218) 是一种有效的 AMPK 激活剂,是一种双胍类的口服抗糖尿病药物。Buformin 延缓胃肠道对葡萄糖的吸收,增加胰岛素敏感性和葡萄糖对细胞的吸收,并抑制肝脏对葡萄糖的合成。Buformin 也具有抗癌活性,可用于各种癌症研究。 | |||
T15391 |
Glufosinate ammonium
|
Others | Others |
Glufosinate ammonium 是谷氨酸的一种膦酸类似物,是一种除草剂,在植物细胞中转化为 PT (L-phosphinothricin) 。Glufosinate ammonium 显示出神经毒性作用。 | |||
T31224 |
Piflufolastat
DCFPYL |
Epigenetic Reader Domain | Chromatin/Epigenetic |
Piflufolastat (DCFPYL) 是一种针对前列腺癌 PSMA 的 PET 显像剂。是一种含氟前列腺特异性膜抗原(PSMA)制剂。Piflufolastat 可用于制备 piflufolastat F 18 (DCFPyL F-18)。 | |||
T61011 | Izuforant | ||
Izuforant (JW1601) (Compound 24) 具有有效的抗炎和止痒活性。 Izuforant 对人血清素3受体 (h5-HT3R) 具有结合亲和力,IC50值为 9.1 μM。它也是组胺 H4 受体 (H4R) 的口服活性拮抗剂,对人 H4R 的IC50值为 36 nM。 | |||
T32590 |
Lauformine
|
||
Lauformine is a isoquinoline alkaloid. | |||
T131542 |
Arenobufagin (Arenobufogenin)
|
||
Arenobufagin (Arenobufogenin) 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 T131542。 | |||
T30610 |
Bufotoxin
Vulgarobufotoxin |
||
Bufotoxin, a toxic steroid lactone, exists in the parotoid glands, skin, and poison of many toads and other amphibians, and in some plants and mushrooms. | |||
T15391L |
Glufosinate
|
Others | Others |
Glufosinate, a phosphinic acid analog of glutamic acid, is a herbicide that is converted by plant cells into PT (L-phosphinothricin). It has neurotoxic activity. | |||
T10116 | 3-O-Acetylbufotalin | Others | Others |
3-O-Acetylbufotalin is a derivate of bufadienolide with anti-cancer activity. | |||
T125720 |
Ajuforrestin A
|
||
Ajuforrestin A 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 T125720。 | |||
T27146 |
Denufosol tetrasodium
INS37217,INS 37217,INS-37217 |
||
Denufosol is a P2Y2 agonist potentially for the treatment of cystic fibrosis. | |||
T20772 |
Crufomate
Ruelene,M 1261,M1261,Crufomatum,M-1261 |
||
Crufomate, an insecticide, is used extensively for the control of hornflies, cattle grubs and cattle lice. | |||
T23837 |
Buformin
丁双胍,W37,W 37,H 224,W-37 |
||
Buformin (1-butylbiguanide) is an oral antidiabetic drug of the biguanide class. It also inhibits the synthesis of glucose by the liver. Buformin delays absorption of glucose from the gastrointestinal tract increases insulin sensitivity and glucose uptake | |||
T75992 |
Buforin II
|
||
Buforin II,来源于 buforin I,从亚洲蟾蜍 Bufo bufo gargarizans 胃中分离得到的蛋白,是一种高效的抗菌 (antimicrobial) 肽。Buforin II 对广谱的革兰氏阳性和革兰氏阴性细菌具有抗菌活性。 | |||
T124283 |
5beta-Hydroxybufotalin
|
||
5beta-Hydroxybufotalin 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 T124283。 | |||
T131543 |
Gamabufotalin (Gamabufagin; Gamabufogenin)
|
||
Gamabufotalin (Gamabufagin; Gamabufogenin) 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 T131543。 | |||
T76864 |
Enapotamab
|
TAM Receptor | Tyrosine Kinase/Adaptors |
Enapotamab 是一种 AXL/UFO 相关抗体,可用于合成抗体-药物偶联物 (Enapotamab Vedotin)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4A2399 |
Cinobufotalin
华蟾毒它灵,华蟾素 |
IL Receptor; Akt; MRP; P-gp | Cytoskeletal Signaling; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; PI3K/Akt/mTOR signaling |
Cinobufotalin 是一种从蟾蜍的皮肤分泌物中提取的强心类固醇或丁二烯内酯。它已被用作强心药,利尿药和止血药,也是潜在的抗肺癌药物。 | |||
T4A2456 |
Gamabufotalin
Gamabufagin,日本蟾蜍毒苷元 |
COX | Immunology/Inflammation; Neuroscience |
Gamabufotalin (Gamabufagin) 是一种蟾蜍甾烯,存在于蟾酥中。它稳定性高,毒性低,被广泛用于癌症的研究。 | |||
T4A2458 |
Resibufogenin
酯蟾毒配基,Bufogenin,Recibufogenin,酯蟾毒配基,蟾力苏 |
Others | Others |
Resibufogenin (Bufogenin) 是华蟾素的成分之一,表现出抑制氧化应激及肿瘤再生的活性。 | |||
TN7062L |
Bufotenidine hydrochloride(487-91-2 Free base)
|
||
Bufotenidine hydrochloride(487-91-2 Free base) 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN7062L,CAS号为 40581-89-3。 | |||
T5A2461 |
Bufotalin
蟾蜍他灵,Bufotaline,蟾毒它灵,蟾蜍他灵 |
Apoptosis; Others; Reactive Oxygen Species | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; Others |
Bufotalin (Bufotaline) 是一种从蟾酥中分离的类固醇内酯,可诱导癌细胞凋亡,也诱导内质网应激的激活,具有强大的抗肿瘤活性。 | |||
TN2877 |
3,4-Dihydroxy-2-O-methylanigorufone
|
Others | Others |
3,4-Dihydroxy-2-O-methylanigorufone 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN2877,CAS号为 1392307-42-4。 | |||
TN4238 |
Hydroxyanigorufone
|
Others | Others |
Hydroxyanigorufone is a natural product from Musa itinerans Cheesm. | |||
TN1912 |
Marinobufogenin
南美蟾毒精,Marinobufagenin |
ATPase; EGFR | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Marinobufagenin, a cardiotonic steroid, its increased concentrations are important in the cardiac disease and oxidant stress state seen with renal failure. | |||
TN2787 |
2-O-Methylanigorufone
|
Others | Others |
2-O-Methylanigorufone is a natural product from Monochoria vaginalis. | |||
TN3035 |
4'-Hydroxy-2-O-methylanigorufone
|
Others | Others |
9-(4'-Hydroxyphenyl)-2-methoxyphenalen-1-one(4'-Hydroxy-2-O-methylanigorufone) is a phytoalexin. It shows a strong α-glucosidase inhibitory effect. | |||
T5527 |
Anigorufone
|
Antifection | Microbiology/Virology |
Anigorufone is a phytoalexin, it shows striking antinematode activity. Anigorufone has shown inhibitory activity on the growth of the germinative tube of Fusarium oxysporum f. sp. cubense race 4. | |||
T83282 |
5β-Hydroxybufotalin
|
||
5β-Hydroxybufotalin (化合物 6) 是一种来源于中药蟾酥的天然产物,具有有效的抗癌作用,能够抑制癌细胞的生长活性。 | |||
T82808 |
Bufoserotonin C
|
||
Bufoserotonin C为蟾酥中新发现的吲哚生物碱,展现出对抗肿瘤的活性。其在A549细胞系中的IC50为34.3 μM。 | |||
TN1200 |
19-Oxocinobufotalin
|
Others | Others |
19-Oxocinobufotalin 3-adipoylarginine ester shows significant inhibition effect against human hepatocellular carcinoma cell line SMMC-7721 in vitro. | |||
T82807 |
Bufospirostenin A
|
||
Bufospirostenin A是首次从动物体内分离得到的螺甾醇类化合物。 | |||
TN1572 |
Desacetylcinobufotalin
|
Others | Others |
Desacetylcinobufotalin has significant antitumor activity through induction apoptosis via mitochondria pathway, it also shows potent cytotoxic activities against HL-60 cell lines. | |||
T31876 |
Frangufoline
|
||
Frangufoline is a sedative 14-membered frangulanine-type cyclopeptide alkaloid. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-01601 |
AXL Protein, Human, Recombinant (His)
UFO,ARK,JTK11,AXL receptor tyrosine kinase,Tyro7 |
Human | HEK293 Cells |
AXL Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 46.5 kDa and the accession number is AAB20305.1. | |||
TMPJ-00449 |
AXL Protein, Human, Recombinant (hFc)
UFO,Tyrosine-protein kinase receptor UFO,A... |
Human | HEK293 Cells |
AXL Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-Fc tag. The predicted molecular weight is 90-115 KDa and the accession number is AAA61243. | |||
TMPJ-00399 |
AXL Protein, Mouse, Recombinant (hFc)
Tyrosine-protein kinase receptor UFO,UFO,A... |
Mouse | HEK293 Cells |
AXL Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-Fc tag. The predicted molecular weight is 85-120 KDa and the accession number is Q00993. | |||
TMPY-01021 |
AXL Protein, Mouse, Recombinant (His & hFc)
AI323647,AXL receptor tyrosine kinase,Tyro7,Ufo,Ark |
Mouse | HEK293 Cells |
AXL Protein, Mouse, Recombinant (His & hFc) is expressed in HEK293 mammalian cells with His and hFc tag. The predicted molecular weight is 74.5 kDa and the accession number is Q00993. | |||
TMPY-06478 |
AXL Protein, Human, Recombinant (mFc)
UFO,JTK11,ARK,Tyro7,AXL receptor tyrosine kinase |
Human | HEK293 Cells |
AXL Protein, Human, Recombinant (mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 72.11 kDa and the accession number is AAH32229.1. | |||
TMPY-01364 |
AXL Protein, Mouse, Recombinant (His)
Ark,AXL receptor tyrosine kinase,Ufo,Tyro7,AI323647 |
Mouse | HEK293 Cells |
AXL Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 47.8 kDa and the accession number is Q00993. | |||
TMPK-00410 |
AXL Protein (Primary Amine Labeling), Human, Recombinant (hFc), Biotinylated
ARK,EC 2.7.10.1,EC 2.7.10,Axl,JTK11,AXL oncogene,UFO |
Human | HEK293 Cells |
Axl, a member of the TAM (Tyro3, Axl, Mer) family, and its inhibitors can specifically break the kinase signaling nodes, allowing advanced patients to regain drug sensitivity with improved therapeutic efficacy. Overexpression and activation of Axl receptor tyrosine kinase have been widely accepted to promote cell proliferation, chemotherapy resistance, invasion, and metastasis in several human cancers, such as lung, breast, and pancreatic cancers. AXL Protein (Primary Amine Labeling), Human, Rec... | |||
TMPK-00408 |
AXL Protein, Human, Recombinant (His & Avi), Biotinylated
AXL oncogene,EC 2.7.10.1,AI323647,Axl,JTK11,ARK,EC 2.7.10, |
Human | HEK293 Cells |
Axl, a member of the TAM (Tyro3, Axl, Mer) family, and its inhibitors can specifically break the kinase signaling nodes, allowing advanced patients to regain drug sensitivity with improved therapeutic efficacy. Overexpression and activation of Axl receptor tyrosine kinase have been widely accepted to promote cell proliferation, chemotherapy resistance, invasion, and metastasis in several human cancers, such as lung, breast, and pancreatic cancers. AXL Protein, Human, Recombinant (His & Avi), Bio... | |||
TMPK-00407 |
AXL Protein, Human, Recombinant (His & Avi)
AXL oncogene,Axl,EC 2.7.10.1,Tyro7,UFO,ARK,EC 2.7.1... |
Human | HEK293 Cells |
Axl, a member of the TAM (Tyro3, Axl, Mer) family, and its inhibitors can specifically break the kinase signaling nodes, allowing advanced patients to regain drug sensitivity with improved therapeutic efficacy. Overexpression and activation of Axl receptor tyrosine kinase have been widely accepted to promote cell proliferation, chemotherapy resistance, invasion, and metastasis in several human cancers, such as lung, breast, and pancreatic cancers. AXL Protein, Human, Recombinant (His & Avi) is e... | |||
TMPK-00472 |
AXL Protein, Cynomolgus, Recombinant (His)
Tyro7,JTK11,AI323647,AXL oncogene,EC 2.7.10.1,EC 2.7.10,... |
Cynomolgus | HEK293 Cells |
Axl, a member of the TAM (Tyro3, Axl, Mer) family, and its inhibitors can specifically break the kinase signaling nodes, allowing advanced patients to regain drug sensitivity with improved therapeutic efficacy. Overexpression and activation of Axl receptor tyrosine kinase have been widely accepted to promote cell proliferation, chemotherapy resistance, invasion, and metastasis in several human cancers, such as lung, breast, and pancreatic cancers. AXL Protein, Cynomolgus, Recombinant (His) is ex... | |||
TMPJ-01081 |
Dtk Protein, Human, Recombinant (His)
RSE,SKY,DTK,Tyrosine-protein kinase DTK,Tyrosine-protein kin... |
Human | HEK293 Cells |
Axl (Ufo, Ark), Dtk (Sky, Tyro3, Rse, Brt) and Mer (human and mouse homologues of chicken cEyk)constitute a new receptor tyrosine kinase subfamily. The extracellular domain of these proteins contain two Ig-like motifs and two fibronectin type III motifs. This characteristic topology is also found in neural cell adhesion molecules and in receptor tyrosine phosphatases. All three receptors bind the vitamin K-dependent protein growth-arrest specific gene 6 (Gas6) which is structurally related to th... |