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HDAC

Inhibitory Selectivity
Catalog No.Inhibitor Name HDAC HDAC1 HDAC2 HDAC3 HDAC4HDAC5 HDAC6 HDAC7 HDAC8 HDAC9 HDAC10 HDAC11 HD1 HD2
A10979Vorinostat
****
A10611Entinostat
**
*
A10518Panobinostat
****
A10947Trichostatin A
****
A10586Mocetinostat
**
**
*
*
A10122Belinostat
***
A11920Romidepsin
***
***
A10560MC1568
*
A11042Tubastatin A HCl
*
***
A10488Givinostat
****
****
A10516Dacinostat
***
A10246CUDC-101
****
****
***
****
***
***
****
**
**
**
***
A10830Pracinostat
***
**
***
***
***
*
**
**
**
***
**
A11152PCI-34051
*
*
****
*
A10337Droxinostat
*
*
*
A10700Abexinostat
****
***
****
***
**
***
A13218RGFP966
**
A11037AR-42
***
A11940Ricolinostat
**
***
***
*
*
****
*
**
A11964Tacedinaline
*
*
*
**
A11153CUDC-907
****
****
****
**
*
***
**
**
****
****
A11355M344
**
A10954Tubacin
****
A13139RG2833
***
****
A12556Resminostat
***
***
**
A15489BRD73954
*
***
**
A11361BG45
*
*
**
A143544SC-202
*
*
*
A16431CAY10603
**
****
A14341LMK-235
***
****
A14032Nexturastat A
****
A14128TMP269
**
**
***
***
A14197HPOB
*
*
*
***
*
*
A12722Scriptaid
A12616Tasquinimod
A11042Tubastatin A
***

Notes:
1.Hover mouse over " * " to view the IC50 value.(A few compounds have proven potency but without published IC50 data.)
2.For more details about the compound, click on the product name of your interest.
3.The higher the number of " * " is, the more potent the inhibitor or activator is.
4."" refers to compounds which do inhibitory effects on the related isoform, but without specific value.



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Catalog No. Product Name Application Product Information
A14128 SALE

TMP 269

HDAC 抑制剂
TMP 269 is a potent, selective class IIa HDAC inhibitor with IC50 of 157 nM, 97 nM, 43 nM and 23 nM for HDAC4, HDAC5, HDAC7 and HDAC9, respectively.
A16127

ITSA-1

HDAC 抑制剂
ITSA-1 is membrane permeable and specifically suppresses TSA inhibition of HDAC (histone deacetylase), but not other HDAC inhibitors.
A11361

BG45

HDAC 抑制剂
BG45 is an HDAC class I inhibitor with selectivity for HDAC3 (IC50 = 289 nM). It inhibits HDAC1, HDAC2, and HDAC6 with greatly reduced potency (IC50s = 2, 2.2, and >20 μM, respectively).
A11355

M344

HDAC 抑制剂
M344 is a potent inhibitor of HDAC with IC50 of 100 nM and able to induce cell differentiation.
A15935 SALE

BML-210

HDAC 抑制剂?€?
BML-210 is HDAC inhibitor. BML-210 induces growth inhibition and apoptosis and regulates HDAC and DAPC complex expression levels in cervical cancer cells.
A15934 SALE

ACY-738

HDAC6 抑制剂
ACY-738 is a potent and selective HDAC6 inhibitor with improved brain bioavailability. ACY-738 inhibits HDAC6 with low nanomolar potency and a selectivity of 60- to 1500-fold over class I HDACs.
A15437

R306465

HDAC 抑制剂
R306465 is a novel hydroxamate-based histone deacetylase (HDAC) inhibitor with broad-spectrum antitumour activity against solid and haematological malignancies in preclinical models.
A15387

TCS HDAC6 20b

HDAC6 抑制剂
TCS HDAC6 20b, selective inhibitor of histone deacetylase 6 (HDAC6). Inhibits HCT116 growth in combination with taxol. Also inhibits growth of MCF-7 cells stimulated by estrogen.
A15357

TC-H 106

HDAC 抑制剂
TC-H 106 is a slow, tight-binding inhibitor of class I HDACs (histone deacetylases).
A13139

RG2833 (RGFP109)

HDAC 抑制剂
RG2833 ( is a brain-penetrant HDAC inhibitor with IC50 of 60 nM and 50 nM for HDAC1 and HDAC3.
A15220

Resminostat hydrochloride

HDAC 抑制剂
Resminostat hydrochloride is a potent inhibitor of HDAC1/3/6(IC50=43-72 nM); less potent to HDAC8 with IC50 of 877 nM.
A15354

KD 5170

HDAC 抑制剂
KD 5170, a novel mercaptoketone-based histone deacetylase inhibitor that exhibits broad spectrum antitumor activity in vitro and in vivo.
A15355

NCH 51

HDAC 抑制剂
NCH 51 is a cell-permeable prodrug that is intracellularly converted to a potent HDAC inhibitor, with an IC50 of 48 nM.
A15356

NSC 3852

HDAC 抑制剂
NSC 3852 is an HDAC (histone deacetylase) inhibitor.
A14221

Splitomicin

NAD(+)-dependent histone deacetylase Sir2p 抑制剂
Splitomicin is a selective NAD(+)-dependent histone deacetylase Sir2p inhibitor with IC50 of 60 uM, showing a higher activity in a cell-based assay.
A14197 SALE

HPOB

HDAC6 抑制剂
HPOB is a potent inhibitor of histone deacetylase 6 (HDAC6; IC50 = 56 nM).
A14032

Nexturastat A

HDAC6 抑制剂
Nexturastat A is an aryl urea derivative that acts as a potent and highly selective inhibitor of histone deacetylase 6 (HDAC6) (IC50= 5.02 +/- 0.60 nM).
A12722

Scriptaid

HDAC 抑制剂
Scriptaid is an HDAC inhibitor (histone deacetylase).
A12556 SALE

Resminostat

HDAC 抑制剂
Resminostat, also known as RAS2410, is a potent inhibitor of histone deacetylase (HDAC) classes I and II. It binds to and inhibits HDACs leading to an accumulation of highly acetylated histones.
A12911

BRD9757

HDAC6 抑制剂
BRD9757 is a highly potent and selective HDAC6 inhibitor with an IC50 of 30 nM toward HDAC6.
A13218 SALE

RGFP966

HDAC3 抑制剂
RGFP966 is an HDAC3 inhibitor with IC50 of 0.08 μM, exhibits > 200-fold selectivity over other HDAC.
A12745

Apicidin

HDAC 抑制剂
Apicidin is a a potent histone deacetylases (HDAC) inhibitor with potential anticancer activity.
A11920 SALE

Romidepsin (FK228 ,Depsipeptide)

HDAC 抑制剂
Romidepsin strongly inhibits HDAC1 and HDAC2 with IC5N/A of 1.6 nM and 3.9 nM, respectively, but is relatively weak in inhibiting HDAC4 and HDAC6 with IC5N/A 25 nM and 79N/A nM, respectively.
A12616 SALE

Tasquinimod

HDAC4 抑制剂
Tasquinimod is an orally active antiangiogenic agent by allosterically inhibiting HDAC4 signalling.
A14236

Santacruzamate A

HDAC 抑制剂
Santacruzamate A (CAY10683) is a potent and selective HDAC inhibitor with IC50 of 119 pM for HDAC2, >3600-fold selectivity over other HDACs.
A16431

CAY10603

HDAC6 抑制剂
CAY10603 is a potent and selective HDAC6 inhibitor with IC50 of 2 pM, >200-fold selectivity over other HDACs.
A13405

HDAC inhibitor

HDAC 抑制剂
N/A
A12758 SALE

ACY-241

HDAC6 抑制剂
ACY-241 is a new, selective and orally available inhibitor of HDAC6.
A15781

UF010

HADC 抑制剂
UF010 is a potent and selective HADC inhibitor with IC50 ~0.06 uM, 0.1 uM, 0.5 uM and 1.5 uM for HDACs 3, 2, 1 and 8, respectively. It has > 6-fold selectivity over other HDACs.
A15489 SALE

BRD73954

HDAC 抑制剂
BRD73954 is a small molecule inhibitor that potently inhibits both HDAC6 and HDAC8 (IC50s = 36 and 120 nM, respectively).
A14326

TMP 195

HDAC 抑制剂
TMP195 is the most potent and selective class IIa HDAC inhibitor.
A14354 SALE

4SC-202

HDAC 抑制剂
4SC-202 is an orally bioavailable benzamide and inhibitor of human class I histone deacetylases (HDACs) isoenzymes 1, 2 and 3, with potential antineoplastic activity.
A14418

ST7612AA1

HDAC 抑制剂
ST7612AA1 is a new and potent HDAC inhibitor with potential anticancer activity.
A14341 SALE

LMK-235

HDAC4/5 抑制剂
LMK-235 is a selective histone deacetylase (HDAC) 4 and HDAC5 inhibitor.
A11964 SALE

CI994 (Tacedinaline)

HDAC 抑制剂
CI-994 is a histone deacetylase (HDAC) inhibitor and induces histone hyperacetylation in living cells.
A11940 SALE

ACY-1215 (Rocilinostat)

HDAC6 抑制剂
ACY-1215 selectively targets and binds to HDAC6, thereby disrupting the Hsp90 protein chaperone system through hyperacetylation of Hsp90 and preventing the subsequent aggresomal protein degradation.
A10516 SALE

LAQ824 (NVP-LAQ824, Dacinostat)

HDAC 抑制剂
LAQ824 (NVP-LAQ824) is a potent novel histone deacetylase inhibitor with significant activity against multiple myeloma.
A10488

ITF2357 (Givinostat)

HDAC 抑制剂
ITF2357 (Givinostat) is a HDACs inhibitor with potential anti-inflammatory, anti-angiogenic, and antineoplastic activities.
A10979 SALE

Vorinostat (SAHA)

HDAC 抑制剂
Vorinostat is an inhibitor of HDACs, inhibiting deacetylation and leading to an accumulation of both hyperacetylated histones and transcription factors.
A10586

MGCD0103 (Mocetinostat)

HDAC 抑制剂
MGCD0103 (Mocetinostat) is a benzamide histone deacetylase inhibitor by inhibiting mainly histone deacetylase 1 (HDAC1), but also HDAC2, HDAC3, and HDAC11.
A10246 SALE

CUDC-101

HDAC 抑制剂
CUDC-101 is a novel compound which inhibits multiple targets, which is designed to inhibit HDAC, EGFR and Her2.
A10560 SALE

MC1568

HDAC 抑制剂
MC1568 is a member of HDAC inhibitors that inhibits the histone deacetylase class II by modifying the genetic expression of various important genes of cell cycle mostly at G1 phase, resulting in the death of breast cancer cells by apoptosis.
A10518 SALE

LBH589 (Panobinostat)

HDAC 抑制剂
LBH589 is a hydroxamic acid and acts as a non-selective HDAC inhibitor with IC5o of HDAC1 to be 0.23 nM.
A10122 SALE

Belinostat (PXD101)

HDAC 抑制剂
Belinostat (PXD101) is a HDAC inhibitor that inhibits HDAC activity in HeLa cell extracts with an IC50 of 27 nM.
A10947 SALE

Trichostatin-A (TSA)

HDAC 抑制剂
Trichostatin A (TSA) inhibits the HDACs 1, 3, 4, 6 and 10 with IC50 values around 20 nM.
A10337 SALE

Droxinostat

HDAC 抑制剂
Droxinostat is a selective inhibitor of HDAC3, HDAC6, and HDAC8 that shows comparable inhibition of HDAC6 and HDAC8 with IC50 = 2.47 and 1.46 μmol/L, respectively.
A11037

AR-42 (HDAC-42)

HDAC 抑制剂
AR-42 is a novel HDAC inhibitor, exhibits biologic activity against malignant mast cell lines via down-regulation of constitutively activated Kit.
A10700 SALE

PCI-24781 (Abexinostat)

HDAC 抑制剂
PCI-24781 is a broad-spectrum phenyl hydroxamic acid HDAC inhibitor.
A10954

Tubacin

HDAC6 抑制剂
Tubacin (tubulin acetylation inducer) is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM.
A10698 SALE

Parthenolide ((-)-Parthenolide)

-
Parthenolide ((-)-Parthenolide) is a sesquiterpene lactone which occurs naturally in the plant feverfew (Tanacetum parthenium).

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