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AB120633

DAPT, gamma-Secretase inhibitor

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(29 Publications)

DAPT (CAS: 208255-80-5)(ab120633) is a γ-secretase inhibitor. Inhibits Notch signalling in vitro. Inhibits total Aβ and Aβ42 production in human primary cultures (IC50values are 115 and 200 nM, respectively) with no effect on APPα and APPβ levels. MW 432.5.

- Blood-brain barrier (BBB) permeable
- 3D Growth matrix component and component of cerebral organoid differentiation media
- Available in different sizes to fit your experimental needs. Larger volume format available upon request.
3 Images
Chemical Structure - DAPT, gamma-Secretase inhibitor (AB120633)
  • Chemical Structure

Lab

Chemical Structure - DAPT, gamma-Secretase inhibitor (AB120633)

2D chemical structure image of ab120633, DAPT, gamma-Secretase inhibitor

Functional Studies - DAPT, gamma-Secretase inhibitor (AB120633)
  • FuncS

Unknown

Functional Studies - DAPT, gamma-Secretase inhibitor (AB120633)

ab81283 staining AKT1 (phospho S473) in MCF7 cells treated with DAPT (ab120633), by ICC/IF. Decrease in expression of AKT1 (phospho S473) correlates with increased concentration of DAPT, as described in literature.
The cells were incubated at 37°C for 24h in media containing different concentrations of ab120633 (DAPT) in DMSO, fixed with 4% formaldehyde for 10 minutes at room temperature and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab81283 (1/200 dilution) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight® 488 goat anti-rabbit polyclonal antibody (ab96899) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.

Functional Studies - DAPT, gamma-Secretase inhibitor (AB120633)
  • FuncS

Collaborator

Functional Studies - DAPT, gamma-Secretase inhibitor (AB120633)

Kc167 cells were treated with varying concentrations of DAPT (ab120633) in DMSO for 16hr at 25°C; DMSO only was used as the negative control. The cells were further incubated for 30 minutes with 4mM EGTA in PBS (in the presence of DAPT), and were then lysed for analysis. To measure Notch activity, Notch targets E(spl)mβ-HLH and E(spl)m3-HLH mRNA levels were assayed. Data shows the fold change of mRNA levels of E(spl)mβ-HLH and E(spl)m3-HLH under different conditions, normalised to DMSO treatment (negative control). Notch activation by EGTA is abrogated by treatment with DAPT.

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Key facts

CAS number

208255-80-5

Purity

>99%

Form

Solid

form

Molecular weight

432.5 Da

Molecular formula

C<sub>2</sub><sub>3</sub>H<sub>2</sub><sub>6</sub>F<sub>2</sub>N<sub>2</sub>O<sub>4</sub>

PubChem

5311272

Nature

Synthetic

Biochemical name

Dapt

Biological description

γ-Secretase inhibitor. Inhibits Notch signalling in vitro. Inhibits total Aβ and Aβ42 production in human primary cultures (IC50 values are 115 and 200 nM, respectively) with no effect on APPα and APPβ levels. Blood-brain barrier permeable. 3D Growth matrix component and component of cerebral organoid differentiation media.

Canonical smiles

CC(C(=O)NC(C1=CC=CC=C1)C(=O)OC(C)(C)C)NC(=O)CC2=CC(=CC(=C2)F)F

Isomeric smiles

C[C@@H](C(=O)N[C@@H](C1=CC=CC=C1)C(=O)OC(C)(C)C)NC(=O)CC2=CC(=CC(=C2)F)F

InChi

InChI=1S/C23H26F2N2O4/c1-14(26-19(28)12-15-10-17(24)13-18(25)11-15)21(29)27-20(16-8-6-5-7-9-16)22(30)31-23(2,3)4/h5-11,13-14,20H,12H2,1-4H3,(H,26,28)(H,27,29)/t14-,20-/m0/s1

InChiKey

DWJXYEABWRJFSP-XOBRGWDASA-N

IUPAC Name

tert-butyl (2S)-2-[[(2S)-2-[[2-(3,5-difluorophenyl)acetyl]amino]propanoyl]amino]-2-phenylacetate

Product details

Check out our range of gamma-Secretase inhibitors here

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
The product can be stored for up to 12 months

Product protocols

Publications (29)

Recent publications for all applications. Explore the full list and refine your search

Neuron 112:3602-3617.e9 PubMed39406239

2024

Synaptic neoteny of human cortical neurons requires species-specific balancing of SRGAP2-SYNGAP1 cross-inhibition.

Applications

Unspecified application

Species

Unspecified reactive species

Baptiste Libé-Philippot,Ryohei Iwata,Aleksandra J Recupero,Keimpe Wierda,Sergio Bernal Garcia,Luke Hammond,Anja van Benthem,Ridha Limame,Martyna Ditkowska,Sofie Beckers,Vaiva Gaspariunaite,Eugénie Peze-Heidsieck,Daan Remans,Cécile Charrier,Tom Theys,Franck Polleux,Pierre Vanderhaeghen

Bio-protocol 14:e5081 PubMed39399592

2024

Alternative Method for Obtaining Human-Induced Pluripotent Stem Cell Lines and Three-Dimensional Growth: A Simplified, Passage-Free Approach that Minimizes Labor.

Applications

Unspecified application

Species

Unspecified reactive species

Masaya Tsukamoto,Tomoyuki Kawasaki,Akihiro Umezawa,Hidenori Akutsu

Neuron 112:3058-3068.e8 PubMed39111306

2024

SYNGAP1 deficiency disrupts synaptic neoteny in xenotransplanted human cortical neurons in vivo.

Applications

Unspecified application

Species

Unspecified reactive species

Ben Vermaercke,Ryohei Iwata,Keimpe Wierda,Leïla Boubakar,Paula Rodriguez,Martyna Ditkowska,Vincent Bonin,Pierre Vanderhaeghen

Cell 186:4676-4693.e29 PubMed37729907

2023

Stepwise emergence of the neuronal gene expression program in early animal evolution.

Applications

Unspecified application

Species

Unspecified reactive species

Sebastián R Najle,Xavier Grau-Bové,Anamaria Elek,Cristina Navarrete,Damiano Cianferoni,Cristina Chiva,Didac Cañas-Armenteros,Arrate Mallabiabarrena,Kai Kamm,Eduard Sabidó,Harald Gruber-Vodicka,Bernd Schierwater,Luis Serrano,Arnau Sebé-Pedrós

iScience 26:107044 PubMed37426342

2023

Calcium dysregulation combined with mitochondrial failure and electrophysiological maturity converge in Parkinson's iPSC-dopamine neurons.

Applications

Unspecified application

Species

Unspecified reactive species

Dayne A Beccano-Kelly,Marta Cherubini,Yassine Mousba,Kaitlyn M L Cramb,Stefania Giussani,Maria Claudia Caiazza,Pavandeep Rai,Siv Vingill,Nora Bengoa-Vergniory,Bryan Ng,Gabriele Corda,Abhirup Banerjee,Jane Vowles,Sally Cowley,Richard Wade-Martins

Burns & trauma 11:tkad032 PubMed37397510

2023

Notch4 participates in mesenchymal stem cell-induced differentiation in 3D-printed matrix and is implicated in eccrine sweat gland morphogenesis.

Applications

Unspecified application

Species

Unspecified reactive species

Yuzhen Wang,Fanliang Zhang,Bin Yao,Linhao Hou,Zhao Li,Wei Song,Yi Kong,Yaxin Tan,Xiaobing Fu,Sha Huang

Stem cell research & therapy 14:19 PubMed36737811

2023

Generation of multilineage liver organoids with luminal vasculature and bile ducts from human pluripotent stem cells via modulation of Notch signaling.

Applications

Unspecified application

Species

Unspecified reactive species

Hyo Jin Kim,Gyeongmin Kim,Kyun Yoo Chi,Hyemin Kim,Yu Jin Jang,Seongyea Jo,Jihun Lee,Youngseok Lee,Dong-Hun Woo,Choongseong Han,Sang Kyum Kim,Han-Jin Park,Jong-Hoon Kim

iScience 26:105962 PubMed36718360

2023

Distinct but interchangeable subpopulations of colorectal cancer cells with different growth fates and drug sensitivity.

Applications

Unspecified application

Species

Unspecified reactive species

Roberto Coppo,Jumpei Kondo,Keita Iida,Mariko Okada,Kunishige Onuma,Yoshihisa Tanaka,Mayumi Kamada,Masayuki Ohue,Kenji Kawada,Kazutaka Obama,Masahiro Inoue

Current protocols 2:e341 PubMed35025140

2022

Stage-Specific Generation of Human Pluripotent Stem Cell Derived Lung Models to Measure CFTR Function.

Applications

Unspecified application

Species

Unspecified reactive species

Shuk Yee Ngan,Henry T Quach,Onofrio Laselva,Elena N Huang,Maria Mangos,Sunny Xia,Christine E Bear,Amy P Wong

Journal of experimental & clinical cancer research : CR 40:325 PubMed34656164

2021

M6A associated TSUC7 inhibition contributed to Erlotinib resistance in lung adenocarcinoma through a notch signaling activation dependent way.

Applications

Unspecified application

Species

Unspecified reactive species

Kai Li,Zi-Yang Peng,Shan Gao,Qing-Shi Wang,Rui Wang,Xiang Li,Guo-Dong Xiao,Jing Zhang,Hong Ren,Shou-Ching Tang,Xin Sun
View all publications

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