HSP

HSP(热休克蛋白)

Heat shock proteins (HSPs) are a family of highly conserved proteins that are expressed, either constitutively or regulated inductively, in response to a wide range of physiological and environmental insults, such as heat shock. According to molecular weight, mammalian HSPs are classified into four subfamilies, including HSP90 (90 kDa), HSP70 (70 kDa), HSP60 (60 kDa) and small HSPs (15 to 30 kDa), among which HSP90 and HSP70 are two of the most studied stress-inducible HSPs. HSP90 is a highly abundant chaperone protein characterized by containing three relevant domains, including the N-terminal domain, the charged middle linker region and the C-terminal dimerization domain; while HSP70 is an ATP-dependent chaperone protein characterized by containing two distinct functional domains, including a peptide binding domain (PBD) and the amino-terminal ATPase domain (ABD). Collectively HSPs play a fundamental role in maintaining the stability of other cellular proteins.

HSP 相关产品(97)

  • GC17210 structure
    GC1721017-AAG Hydrochloride
    CAS: 911710-03-7

    Hsp90 inhibitor,geldanamycin analogue

  • GC17655 structure
    GC17655Ganetespib (STA-9090)
    CAS: 888216-25-9
    纯度: >99.50%

    Ganetespib (STA-9090) (STA-9090) 是一种热休克蛋白 90 (HSP90) 抑制剂,在多种血液和实体肿瘤细胞系中表现出强效细胞毒性。 Ganetespib (STA-9090) 通过抑制 HIF-1α 在结直肠癌中具有抗血管生成作用;和 STAT3。

  • GC17751 structure
    GC17751MKT 077
    CAS: 147366-41-4
    纯度: >98.00%

    An Hsp70 inhibitor

  • GC17901 structure
    GC17901Tamoxifen
    CAS: 10540-29-1
    纯度: >98.00% / >99.00%

    Tamoxifen(他莫西芬)是一种选择性雌激素受体调节剂 (SERM),可阻断乳腺细胞中的雌激素作用,并可激活不同组织细胞中的雌激素活性;Tamoxifen 还可以作为 Hsp90 激活剂,增强 Hsp90 分子伴侣 ATPase 的活性;Tamoxifen 还可以诱导 CreER(T2) 小鼠的基因敲除。

  • GC18170 structure
    GC18170ML-346
    CAS: 100872-83-1
    纯度: >98.00%

    An activator of the heat shock response

  • GC18832 structure
    GC18832Conglobatin
    CAS: 72263-05-9

    An Hsp90 inhibitor

  • GC19094 structure
    GC19094CCT251236
    CAS: 1693731-40-6
    纯度: >99.00%

    An inhibitor of Hsf1-mediated transcription

  • GC19121 structure
    GC19121Debio 0932
    CAS: 1061318-81-7
    纯度: >98.00%

    An Hsp90 inhibitor

  • GC19188 structure
    GC19188HA15
    CAS: 1609402-14-3
    纯度: >99.50%

    HA15是一种特异性靶向BiP/GRP78/HSPA5的分子,可结合并抑制其ATPase活性,导致BiP与PERK、IRE1α和ATF6分离,从而引发内质网应激。

  • GC19215 structure
    GC19215KRIBB11
    CAS: 342639-96-7
    纯度: >98.00%

    An Hsf1 inhibitor

  • GC31103 structure
    GC31103Arimoclomol maleate (BRX-220)
    CAS: 289893-26-1
    纯度: >99.50%

    A co-inducer of heat shock proteins

  • GC31118 structure
    GC31118KU-32
    CAS: 956498-70-7

    KU-32是一种新型的,基于新生霉素的Hsp90抑制剂,可以预防神经细胞死亡。

  • GC32008 structure
    GC32008Feretoside
    CAS: 27530-67-2

    Feretoside是一种从杜仲树皮中提取的酚类化合物。它是HSP诱导剂,可作为细胞保护剂。

  • GC32437 structure
    GC32437HSF1A
    CAS: 1196723-93-9
    纯度: >99.00%

    HSF1A是热休克转录因子1(HSF1)的激活剂。

  • GC32620 structure
    GC32620Bimoclomol
    CAS: 130493-03-7
    纯度: >99.00%

    Bimoclomol是一种heatshockprotein(HSP)辅诱导剂,可用于心血管疾病的研究。

  • GC32869 structure
    GC32869HSP70-IN-1
    CAS: 1268273-90-0
    纯度: >98.00%

    HSP70-IN-1是一种热休克蛋白(HSP)抑制剂;抑制Kasumi-1细胞的生长的IC50值为2.3μM。

  • GC32965 structure
    GC32965Ethoxyquin
    CAS: 91-53-2
    纯度: >98.00%

    An antioxidant used in animal feed

  • GC33047 structure
    GC33047SNX-5422 Mesylate (PF-04929113 (Mesylate))
    CAS: 1173111-67-5

    A prodrug for an Hsp90 inhibitor

  • GC33286 structure
    GC33286TAS-116
    CAS: 1260533-36-5
    纯度: >99.00%

    An Hsp90 inhibitor

  • GC33426 structure
    GC33426Rocaglamide (Rocaglamide A)
    CAS: 84573-16-0
    纯度: >98.50%

    Rocaglamide (Rocaglamide A) 是从 Aglaia 属(楝科)中分离出来的。

  • GC33663 structure
    GC33663Teprenone (Geranylgeranylacetone)
    CAS: 6809-52-5
    纯度: >99.50%

    An inducer of Hsp expression

  • GC34539 structure
    GC34539Col003
    CAS: 328565-16-8
    纯度: >95.00%

    Col003是一种有效的Hsp47抑制剂,竞争性地与Hsp47上的胶原结蛋白合位点结合(IC50,1.8μM),通过破坏胶原蛋白的三重螺旋结构抑制胶原蛋白的分泌。

  • GC34634 structure
    GC34634JG-98
    CAS: 1456551-16-8
    纯度: >98.00%

    JG-98 is an allosteric inhibitor of Hsp70 that binds tightly to a deep pocket that is conserved in members of the Hsp70 family. JG-98 induces classical apoptosis features, including morphological changes consistent with programmed cell death and positive annexin staining. JG-98 exhibits anticancer activity.

  • GC35757 structure
    GC35757Cucurbitacin D
    CAS: 3877-86-9
    纯度: >98.00%

    A triterpenoid with diverse biological activities