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抑制剂 & 化合物

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Cat. No. Product Name Target Signaling Pathways
T72319 Lewis y tetrasaccharide

Lewis y

Lewis Y tetrasaccharide (Lewis Y, LeY) 是Lewis X trisaccharide 的四糖衍生物。Lewis Y tetrasaccharide 是一种与恶性卵巢癌转移和预后不良相关的抗原。
T35884 Sialyl-Lewis X

Sialyl-Lewis X (sLeX), a sialylated fucosylated tetrasaccharide and endogenous antigen, serves as a high-affinity ligand for selectins (E-, P-, and L-selectin)[1]. It interacts with ELAM-1 and CD62, consequently inhibiting CD62-mediated neutrophil recruitment to inflammation sites[2].
T77243 Sialyl lewis x-lactose

Sialyl Lewis X-Lactose 是一种生化试剂,可作为生物材料或有机化合物,用于生命科学相关研究。
T9616 PD-1/PD-L1-IN-10

PD-1/PD-L1 Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation
PD-1/PD-L1-IN-10 是一种口服有效的PD-1/PD-L1抑制剂 (IC50of 2.7 nM),显示出抗肿瘤活性。
T73592 N′-(2-Chloroethyl)-N-(4-methylcyclohexyl)-N-nitrosourea

N′-(2-Chloroethyl)-N-(4-methylcyclohexyl)-N-nitrosourea 具有抗肿瘤活性,可用于治疗 Lewis 肺癌和结肠肿瘤。
TP1358L Peptide M acetate

Peptide M acetate(110652-62-5 free base),Peptide M 醋酸盐

Others Others
Peptide M acetate 是一种合成多肽 (长度为 18 个氨基酸,对应于牛 S 抗原的氨基酸位置303-322: DTNLASSTIIKEGIDKTV),能够在猴子和 Hartley 豚鼠以及 Lewis 大鼠中诱导实验性自身免疫性葡萄膜炎。
T40925 Peripheral Myelin Protein P2 (53-78), bovine

Peripheral Myelin Protein P2 (53-78), bovine

Bovine Peripheral Myelin Protein P2 (53-78) is a derivative composed of amino acid residues 53 to 78 from the peripheral myelin P2 protein of bovine origin. It acts as a T cell epitope and is used to induce experimental autoimmune neuritis (EAN) in Lewis rats.
T83334 4-(Phenylazo)diphenylamine

4-(Phenylazo)diphenylamine 是一种用于准确测定强碱、路易斯酸和氢化物还原剂浓度的优异比色指示剂。
T37542 Anguinomycin A

Anguinomycin A is an antibiotic first isolated from a Streptomyces sp. and analog of leptomycin B that is highly cytotoxic to mouse P388 leukemia cells in vitro (IC50 = 0.1-0.2 ng/ml). It also demonstrates antitumor activity at 62.5 μg/kg/day against Lewis lung carcinoma in mice.
T36040 16,16-dimethyl Prostaglandin A1

16,16-dimethyl Prostaglandin A1

16,16-dimethyl Prostaglandin A1 是一种前列腺素类似物,可以抑制 Lewis 肺癌和 B 16无黑色素瘤细胞中的 DNA 合成 (DNA synthesis),以及抑制 HSV 和 HIV-1的病毒复制。
TP1974 Obtustatin

Highly potent integrin α1β1 inhibitor (IC50 = 0.8 nM for α1β1 binding to type IV collagen). Selective for α1β1 over α2β1, αIIbβ3, αvβ3, α4β1, α5β6, α9β1 and α4β7. Inhibits FGF2-stimulated angiogenesis in the chicken chorioallantoic model. Displays antitum
T68631 Carbetimer

Carbetimer is a partially imidized copolymer of ethylene & maleic anhydride with average MW approx 1,200 daltons; capable of specific stimulation of immune response. Carbetimer is a low molecular weight polymer derived from ethylene and maleic anhydride with potent antineoplastic activity. Preclinical studies have shown antitumor effects against many tumor cell lines including B 16 melanoma. Its antitumor actions are felt to include both reduction of uridine and cytidine nucleoside triphosphate ...
T36460 CAY10736

CAY10736

CAY10736 is an anticancer compound.1 It inhibits proliferation in a panel of melanoma and breast, pancreatic, and lung cancer cell lines (IC50s = 0.827-9.89 μM). CAY10736 inhibits migration and epithelial-to-mesenchymal transition (EMT) of A375 and B16/F10 melanoma cells in vitro in a concentration-dependent manner. It reduces the viability of spheroid A375 and B16/F10 cells (IC50s = 2.4 and 1.59 μM, respectively) and increases the production of reactive oxygen species (ROS) in these cells in a ...
T36497 CAY10735

CAY10735

CAY10735 is an anticancer compound.1 It inhibits proliferation in a panel of melanoma and breast, pancreatic, and lung cancer cell lines (IC50s = 0.674-11.56 μM). CAY10735 inhibits migration of and the epithelial-to-mesenchymal transition (EMT) in A375 and B16/F10 melanoma cells in vitro in a concentration-dependent manner. It reduces the viability of spheroid A375 and B16/F10 cells (IC50s = 3.04 and 1.24 μM, respectively) and increases production of reactive oxygen species (ROS) in these cells ...
T37631 tetranor-12(S)-HETE

12(S)-HETE is a product of arachidonic acid metabolism through the 12-lipoxygenase pathway. It is primarily found in platelets, leukocytes, and to a lesser extent in smooth muscle cells. It enhances tumor cell adhesion to endothelial cells, fibronectin, and the subendothelial matrix. tetranor-12(S)-HETE is the major β-oxidation product resulting from peroxisomal metabolism of 12(S)-HETE in numerous tissues, and Lewis lung carcinoma cells. No biological function has yet been determined for tetran...
T69966 Roxadustat-d5

Roxadustat-d5 is intended for use as an internal standard for the quantification of roxadustat by GC- or LC-MS. Roxadustat is an inhibitor of hypoxia-inducible factor prolyl hydroxylase (HIF-PH; IC50s = 1.4, 1.26, and 1.32 µM for HIF-PH1, HIF-PH2, and HIF-PH3, respectively). It is selective for HIF-PH over other 2-oxoglutarate-dependent dioxygenases, including lysine-specific demethylase 5A (KDM5A), KDM5B, -5C, -5D, and -6B (IC50s = >100 µM for all). Roxadustat (10-200 µM) stabilizes HIF-1α and ...
T36695 TAS-103

TAS-103 is a dual inhibitor of DNA topoisomerase I/II, used for cancer research. TAS-103 is a dual inhibitor of DNA topoisomerase I/II. TAS-103 (0.1-10 μM) is active on CCRF-CEM cells, with an IC50 value of 5 nM. TAS-103 (0.1 μM) significantly increases levels of topo IIα FITC immunofluorescence in individual CCRF-CEM cells[1]. TAS-103 (0.01-1 μM) is highly cytotoxic to Lewis lung carcinoma (LLC) cells, and Liposomal TAS-103 is almost as active as free TAS-103[2]. TAS-103 inhibits the viability ...
T36053 D-Lysine lactam

D-Lysine lactam is a chiral building block.1,2It has been used in the synthesis of a chiral antibiotic synthetic intermediate, as well as in the stereoselective synthesis of neurokinin (NK) receptor antagonists. 1.Kumar, A., Bhashkar, B., Bhavsar, J., et al.Catalytic reduction: Efficient synthesis of chiral key intermediate of besifloxacin hydrochlorideDer Pharma Chemica7(9)297-3000(2015) 2.Gerspacher, M., Lewis, C., Ball, H.A., et al.Stereoselective preparation of N-[(R,R)-(E)-1-(3,4-dichlorobe...
T36373 Urocortin II (mouse) (trifluoroacetate salt)

Urocortin II is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin III , frog sauvagine, and piscine urotensin I.1 Mouse urocortin II shares 34 and 42% sequence homology with rat CRF and urocortin . It is expressed in mouse paraventricular, supraoptic, and arcuate nuclei of the hypothalamus, the locus coeruleus, and in motor nuclei of the brainstem and spinal ventral horn. Urocortin II selectively binds to CRF...
T35814 Urocortin III (human) (trifluoroacetate salt)

Urocortin III is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin II , frog sauvagine, and piscine urotensin I.1 Human urocortin III shares 90, 40, 37, and 21% identity to mouse urocortin III , mouse urocortin II , human urocortin , and mouse urocortin, respectively. Urocortin III selectively binds to type 2 CRF receptors (Kis = 21.7, 13.5, and >100 nM for rat CRF2α, rat CRF2β, and human CRF1, respectively)....

化合物

Lewis y tetrasaccharide
Cat.No: T72319
Synonym: Lewis y
Target:
Sialyl-Lewis X
Cat.No: T35884
Synonym:
Target:
Sialyl lewis x-lactose
Cat.No: T77243
Synonym:
Target:
PD-1/PD-L1-IN-10
Cat.No: T9616
Synonym:
Target: PD-1/PD-L1
N′-(2-Chloroethyl)-N-(4-methylcyclohexyl)-N-nitrosourea
Cat.No: T73592
Synonym:
Target:
Peptide M acetate
Cat.No: TP1358L
Synonym: Peptide M acetate(110652-62-5 free base),Peptide M 醋酸盐
Target: Others
Peripheral Myelin Protein P2 (53-78), bovine
Cat.No: T40925
Synonym: Peripheral Myelin Protein P2 (53-78), bovine
Target:
4-(Phenylazo)diphenylamine
Cat.No: T83334
Synonym:
Target:
Anguinomycin A
Cat.No: T37542
Synonym:
Target:
16,16-dimethyl Prostaglandin A1
Cat.No: T36040
Synonym: 16,16-dimethyl Prostaglandin A1
Target:
Obtustatin
Cat.No: TP1974
Synonym:
Target:
Carbetimer
Cat.No: T68631
Synonym:
Target:
CAY10736
Cat.No: T36460
Synonym: CAY10736
Target:
CAY10735
Cat.No: T36497
Synonym: CAY10735
Target:
tetranor-12(S)-HETE
Cat.No: T37631
Synonym:
Target:
Roxadustat-d5
Cat.No: T69966
Synonym:
Target:
TAS-103
Cat.No: T36695
Synonym:
Target:
D-Lysine lactam
Cat.No: T36053
Synonym:
Target:
Urocortin II (mouse) (trifluoroacetate salt)
Cat.No: T36373
Synonym:
Target:
Urocortin III (human) (trifluoroacetate salt)
Cat.No: T35814
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T81937 Lewis a trisaccharide

Lewis a

Lewis a trisaccharide 是精子聚糖结构和 HL-60 细胞表面聚糖结构的主要组分。
T7203 Oglufanide

奥谷法奈,L-Glutamyl-L-tryptophan,H-Glu-Trp-OH

VEGFR; HCV Protease; Endogenous Metabolite Angiogenesis; Metabolism; Microbiology/Virology; Proteases/Proteasome; Tyrosine Kinase/Adaptors
Oglufanide (H-Glu-Trp-OH) 是一种从小牛胸腺中分离出来的二肽免疫调节剂,可抑制血管内皮生长因子,可刺激细胞内细菌感染和对丙型肝炎病毒的免疫反应。
T75670 Lacto-N-fucopentaose II

Lacto-N-fucopentaose II (LNFP II)作为人Lewis血型决定因子的半抗原,其单唾液神经节苷/糖脂以及唾液酰衍生物CA 19-9,都是胆胰恶性肿瘤中的分子肿瘤标记物(TM)。
T81961 Lacto-N-difucohexaose I

LDFH I

LNDFH I是一种连接子,它能够将含Lewis b糖链的寡糖有效结合形成水不溶性多糖。
TN4455 Lucialdehyde B

Integrase; HSV Microbiology/Virology
Lucialdehyde B exhibits potent inhibitory activity against herpes simplex virus. It shows cytotoxic effects on Lewis lung carcinoma (LLC), T-47D, Sarcoma 180, and Meth-A tumor cell lines.

天然产物

Lewis a trisaccharide
Cat.No: T81937
Synonym: Lewis a
Target:
Oglufanide
Cat.No: T7203
Synonym: 奥谷法奈,L-Glutamyl-L-tryptophan,H-Glu-Trp-OH
Target: VEGFR, HCV Protease, Endogenous Metabolite
Lacto-N-fucopentaose II
Cat.No: T75670
Synonym:
Target:
Lacto-N-difucohexaose I
Cat.No: T81961
Synonym: LDFH I
Target:
Lucialdehyde B
Cat.No: TN4455
Synonym:
Target: Integrase, HSV
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