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  • T2143Bergapten5-Methoxypsoralen;佛手柑内酯;香柑内酯

    Bergapten, a psoralen, inhibits cell replication.

    价 格:¥电议型 号:T2143产 地:中国大陆

  • T2056LUNC0064-12 hydrochloride (1430089-64-7(free base))

    UNC0064-12 hydrochloride is an inhibitor of VEGFR2 extracted from patent WO2013055780A1

    价 格:¥电议型 号:T2056L产 地:中国大陆

  • T18143m-PEG12-OHDodecaethylene Glycol Monomethyl Ether

    m-PEG12-OH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. m-PEG12-OH is also a non-cleavable 12 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

    价 格:¥电议型 号:T18143产 地:中国大陆

  • T17143Toyocamycin丰加霉素;Vengicide

    Toyocamycin is an adenosine analog produced by Actinomycete, acts as an XBP1 inhibitor, inhibits IRE1α-induced ATP-dependent XBP1 mRNA cleavage (IC50: 80 nM). Toyocamycin induces apoptosis.

    价 格:¥电议型 号:T17143产 地:中国大陆

  • T16143MRTX-1257

    MRTX-1257 is a selective, irreversible, and covalent inhibitor of KRAS G12C. It has an IC50 of 900 pM for KRAS dependent ERK phosphorylation in H358 cells. MRTX1257 demonstrated 31% bioavailability in the mouse, with free fraction exposures well above the

    价 格:¥电议型 号:T16143产 地:中国大陆

  • T15623JNJ-61432059

    JNJ-61432059 is an oral active and selective negative modulator of TARP γ?8 Selective AMPAR(pIC50: 9.7).

    价 格:¥电议型 号:T15623产 地:中国大陆

  • T1485Methotrexate甲氨蝶呤;Amethopterin;CL14377;WR19039;NCI-C04671

    Methotrexate is a folate analog metabolic inhibitor with immunosuppressant and antineoplastic properties.

    价 格:¥电议型 号:T1485产 地:中国大陆

  • T14391Azidamfenicol

    Azidamfenicol inhibits ribosomal peptidyltransferase (Ki=22 μM)[1]. Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.

    价 格:¥电议型 号:T14391产 地:中国大陆

  • T1439Lacidipine拉西地平;SN-305;GR-43659X;GX-1048

    Lacidipine is a lipophilic dihydropyridine calcium antagonist with an intrinsically slow onset of activity. Due to its long duration of action, lacidipine does not lead to reflex tachycardia. It displays specificity in the vascular smooth muscle, where it

    价 格:¥电议型 号:T1439产 地:中国大陆

  • T14388AZD 4017

    AZD 4017 is an inhibitor of 11β-Hydroxysteroid Dehydrogenase Type 1(11β-HSD1) (IC50: 7 nM).

    价 格:¥电议型 号:T14388产 地:中国大陆

  • T14385AZD9056 hydrochloride

    AZD9056 hydrochloride is a P2X7 inhibitor,Which plays a significant role in pain-causing diseases and inflammation.

    价 格:¥电议型 号:T14385产 地:中国大陆

  • T14381AZD7624AZD-7624

    AZD7624 is an p38 inhibitor. It has potent anti-inflammatory activity.

    价 格:¥电议型 号:T14381产 地:中国大陆

  • T14380AZD7507

    AZD7507 is a CSF-1R inhibitor with an IC50 of 32 nM. AZD7507 has antitumor activity.

    价 格:¥电议型 号:T14380产 地:中国大陆

  • T1438Butoconazole nitrate硝酸布康唑;RS 35887

    Butoconazole Nitrate is the nitrate salt form of butoconazole, a synthetic imidazole derivative with fungistatic properties. Butoconazole nitrate interferes with steroid biosynthesis by inhibiting the conversion of lanosterol to ergosterol, thereby changi

    价 格:¥电议型 号:T1438产 地:中国大陆

  • T14379AZD5904

    AZD5904 is a potent and irreversible inhibitor of human Myeloperoxidase (MPO, IC50: 140 nM) which has similar potency in mouse and rat.

    价 格:¥电议型 号:T14379产 地:中国大陆

  • T14378LAZD5582 acetate (1258392-53-8 free base)

    AZD5582 acetate is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis.

    价 格:¥电议型 号:T14378L产 地:中国大陆

  • T14377AZD5423

    AZD5423 is an inhaled, potent, selective, and non-steroidal modulator of glucocorticoid receptor (GR) and it effectively reduces allergen-induced responses in subjects with mild allergic asthma.

    价 格:¥电议型 号:T14377产 地:中国大陆

  • T14376AZD4320

    AZD4320 is an inhibitor of BH3-mimicking dual BCL2/BCLxL. For KPUM-MS3, KPUM-UH1, and STR-428 cells, the IC50s values are 26 nM, 17 nM, and 170 nM , respectively.

    价 格:¥电议型 号:T14376产 地:中国大陆

  • T1437D-PanthenolD-Pantothenyl alcohol;Ilopan;Dexpanthenol;Pantothenol;D-泛醇;D-泛醇(维生素原B5)

    Dexpanthenol is an alcoholic analogue of D-pantothenic acid and cholinergic agent. Dexpanthenol acts as a precursor of coenzyme A necessary for acetylation reactions and is involved in the synthesis of acetylcholine. Although the exact mechanism of the ac

    价 格:¥电议型 号:T1437产 地:中国大陆

  • T14369AZD-0284

    AZD-0284 is an inverse agonist of the nuclear receptor RORγ. In development for the treatment of plaque psoriasis vulgaris and respiratory tract disorders[1].

    价 格:¥电议型 号:T14369产 地:中国大陆

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