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  • T1016011β-HSD1-IN-111β-HSD-1-IN-1,11βHSD1IN1,11β HSD1 IN 1

    11β-HSD1-IN-1 is an inhibitor of 11β-hydroxydehydrogenase 1 (11β-HSD1, IC50: 52 nM), and used for the treatment of pain.

    价 格：￥电议型 号：T10160产 地：中国大陆

  • T6014911β-HSD1-IN-1111βHSD1IN11

    11β-HSD1-IN-11 is a competitive 11β-HSD1 inhibitor with IC50s of 0.34 μM and 0.13 μM against rat and human 11β-HSD1, respectively.

    价 格：￥电议型 号：T60149产 地：中国大陆

  • T83120And1-IN-1；化合物 And1-IN-1And1-IN-1

    And1-IN-1, also known as compound III, is a potent inhibitor of And1 [1].

    价 格：￥电议型 号：T83120产 地：中国大陆

  • T7285911β-HSD1-IN-10；化合物 11β-HSD1-IN-1011β-HSD1-IN-10

    11β-HSD1-IN-10, a potent inhibitor of 11β-HSD1 with an IC50 value of 1.8 ?M for humans, is suitable for research into obesity, hyperglycemia, and cognitive impairment.

    价 格：￥电议型 号：T72859产 地：中国大陆

  • T7281411β-HSD1-IN-12；11β-HSD1抑制剂1211β-HSD1-IN-12

    11β-HSD1-IN-12 is an 11β-HSD1 inhibitor.11β-HSD1-IN-12 is implicated in the conversion of glucocorticoids in vivo and can be used to study metabolic syndrome and obesity.

    价 格：￥电议型 号：T72814产 地：中国大陆

  • T64321Octyl-beta-D-glucopyranoside；辛基-beta-D-吡喃葡萄糖苷Octyl glucoside|||11β-HSD1-IN-11；Octyl glucoside|||11β-

    Octyl-beta-D-glucopyranoside (11β-HSD1-IN-11) is a non-ionic detergent, it can be widely used in the research of biotechnical, biochemical applications, solubilization and crystallization of membrane proteins.

    价 格：￥电议型 号：T64321产 地：中国大陆

  • T64089BRD4 D1-IN-1；化合物 BRD4 D1-IN-1BRD4 D1-IN-1

    BRD4 D1-IN-1 is a selective inhibitor of BRD4 D1 with an IC50 <0.092 μM. BRD4 D1-IN-1 has an affinity of 18 nM and over 500-fold selectivity for BRD4 D1 and BRD4 D2.

    价 格：￥电议型 号：T64089产 地：中国大陆

  • T63920LSD1-IN-19；化合物 LSD1-IN-19LSD1-IN-19

    LSD1-IN-19 (compound 29) is a selective, potent, non-covalent inhibitor of LSD1 (Ki: 0.108 μM, KD: 0.068 μM). The 72h IC50 values were 0.17 and 0.40 μM, respectively.

    价 格：￥电议型 号：T63920产 地：中国大陆

  • T63716LSD1-IN-18；化合物 LSD1-IN-18LSD1-IN-18

    LSD1-IN-18 is a potent, non-covalent, selective inhibitor of LSD1 (Ki:0.156 μM; KD: 0.075 μM).LSD1-IN-18 exhibited anti-proliferative effects in THP-1 leukemia cells and MDA-MB-231 breast cancer cells with IC50 (72 h) of 0.16 and 0.21 μM, respectively.

    价 格：￥电议型 号：T63716产 地：中国大陆

  • T62679LSD1-IN-13 hydrochloride；化合物 LSD1-IN-13 hydrochlorideLSD1-IN-13 hydrochloride

    LSD1-IN-13 hydrochloride (compound 7e) is an orally active inhibitor of LSD1 (IC50: 24.43 nM). hydrochloride induces differentiation of AML (acute myeloid leukemia) cell lines.

    价 格：￥电议型 号：T62679产 地：中国大陆

  • T62099LSD1-IN-13；化合物 LSD1-IN-13LSD1-IN-13

    LSD1-IN-13 (compound 7e) is an orally active LSD1 inhibitor (IC50: 24.43 nM) that also activates CD86 expression (EC50: 470 nM).LSD1-IN-13 induces differentiation of AML (acute myeloid leukaemia) cell lines.

    价 格：￥电议型 号：T62099产 地：中国大陆

  • T62030BRD4-BD1-IN-1；化合物 BRD4-BD1-IN-1BRD4-BD1-IN-1

    BRD4-BD1-IN-1 (Compound 9a) is a BRD4-BD1 inhibitor(IC50= 38.20 μM).

    价 格：￥电议型 号：T62030产 地：中国大陆

  • T61841SCD1-IN-1；化合物 SCD1-IN-1SCD1-IN-1

    SCD1-IN-1, a potent inhibitor of SCD1 (IC50: 5.8 nM), is valuable in dermatologic research [1].

    价 格：￥电议型 号：T61841产 地：中国大陆

  • T61716Steroid sulfatase/17β-HSD1-IN-1；化合物 Steroid sulfatase/17β-HSD1-IN-1Steroid sulfatase/17β-HSD1-IN-1

    Steroid sulfatase/17β-HSD1-IN-1 is a highly effective inhibitor of both steroid sulfatase and 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) activities, displaying an IC50 value of 28 nM against cellular human steroid sulfatase. This compound holds significant potential for investigating estrogen-dependent diseases [1].

    价 格：￥电议型 号：T61716产 地：中国大陆

  • T61405LSD1-IN-14；化合物 LSD1-IN-14LSD1-IN-14

    LSD1-IN-14, a powerful and specific inhibitor of LSD1 (with an IC50 value of 0.89 μM), effectively suppresses the growth of A549 and THP-1 cells and promotes the apoptosis of tumor cells [1].

    价 格：￥电议型 号：T61405产 地：中国大陆

  • T6103417β-HSD1-IN-1；化合物 17β-HSD1-IN-117β-HSD1-IN-1

    17β-HSD1-IN-1 (Compound 1) can be used in the non-small cell lung cancer (NSCLC) research. 17β-HSD1-IN-1 is a highly selective inhibitor of 17β-HSD1 with IC50 values of 5.6 and 3155 nM for 17β-HSD1 and 17β-HSD2, respectively [1].

    价 格：￥电议型 号：T61034产 地：中国大陆

  • T61022LSD1-IN-17；化合物 LSD1-IN-17LSD1-IN-17

    LSD1-IN-17 (compound 5b) is a potent inhibitor of LSD1 that inhibits LSD1-CoREST, MAO-A and MAO-B, with IC 50 values of 0.005, 0.028, and 0.820 μM, respectively. LSD1-IN-17 exhibits cell growth arrest in prostate cancer LNCaP cells with an IC50 value of 17.2 μM [1].

    价 格：￥电议型 号：T61022产 地：中国大陆

  • T61021LSD1-IN-16；化合物 LSD1-IN-16LSD1-IN-16

    LSD1-IN-16 (compound 4b) is a potent inhibitor of LSD1 that inhibits LSD1-CoREST, MAO-A and MAO-B with IC50 values of 0.015, 0.024, and 0.366 μM, respectively. LSD1-IN-16 exhibits cell growth arrest in prostate cancer LNCaP cells with an IC50 value of 15.2 μM [1].

    价 格：￥电议型 号：T61021产 地：中国大陆

  • T60941LSD1-IN-15；化合物 LSD1-IN-15LSD1-IN-15

    LSD1-IN-15 (compound 1b) is a potent LSD1 inhibitor that inhibit LSD1-CoREST, MAO-A and MAO-B with IC 50 values of 0.149, 0.028, and 0.327 μM, respectively. LSD1-IN-15 shows cell growth arrest in LNCaP cells of prostate cancer. The IC50 value is 9.9 μM [1].

    价 格：￥电议型 号：T60941产 地：中国大陆

  • T60381LSD1-IN-12；化合物 LSD1-IN-12LSD1-IN-12

    LSD1-IN-12 (compound 2) is an effective inhibitor of LSD1, demonstrating inhibitory Ki values of 1.1 μM (LSD1), 61 μM (LSD2), 2.3 μM (MAO-A), and 3.5 μM (MAO-B), respectively [1].

    价 格：￥电议型 号：T60381产 地：中国大陆

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