Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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C338042-1mg | 1mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $53.90 | |
C338042-5mg | 5mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $132.90 | |
C338042-10mg | 10mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $227.90 | |
C338042-25mg | 25mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $453.90 | |
C338042-50mg | 50mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $663.90 | |
C338042-100mg | 100mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $943.90 |
an HDAC inhibitor
Synonyms | HDAC-IN-7 | HBI-8000;CS-055 | N-(2-amino-5-fluorophenyl)-4-[[[(E)-3-pyridin-3-ylprop-2-enoyl]amino]methyl]benzamide | (E)-N-(2-amino-5-fluorophenyl)-4-((3-(pyridin-3-yl)acrylamido)methyl)benzamide |
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Specifications & Purity | Moligand™, ≥98% |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of histone deacetylase 1 |
Product Description | Chidamide is an HDAC (histone deacetylase) inhibitor that increases histone H3 acetylation levels in LoVo and HT29 colon cancer cells at concentrations as low as 4 μM. |
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IUPAC Name | N-(2-amino-5-fluorophenyl)-4-[[[(E)-3-pyridin-3-ylprop-2-enoyl]amino]methyl]benzamide |
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INCHI | InChI=1S/C22H19FN4O2/c23-18-8-9-19(24)20(12-18)27-22(29)17-6-3-16(4-7-17)14-26-21(28)10-5-15-2-1-11-25-13-15/h1-13H,14,24H2,(H,26,28)(H,27,29)/b10-5+ |
InChi Key | WXHHICFWKXDFOW-BJMVGYQFSA-N |
Canonical SMILES | C1=CC(=CN=C1)C=CC(=O)NCC2=CC=C(C=C2)C(=O)NC3=C(C=CC(=C3)F)N |
Isomeric SMILES | C1=CC(=CN=C1)/C=C/C(=O)NCC2=CC=C(C=C2)C(=O)NC3=C(C=CC(=C3)F)N |
Alternate CAS | 1883690-47-8 |
PubChem CID | 9800555 |
Molecular Weight | 390.41 |
PubChem CID | 53394037 |
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CAS Registry No. | 743420-02-2 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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G2402192 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402193 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402204 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402211 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402238 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402239 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402254 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402255 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402256 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402257 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402258 | Certificate of Analysis | Mar 27, 2024 | C338042 |
G2402259 | Certificate of Analysis | Mar 27, 2024 | C338042 |
Solubility | Soluble in DMSO (~20 mg/ml), DMF (~20 mg/ml), and 1: 1 DMSO: PBS(pH 7.2) (~0.5 mg/ml). |
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Refractive Index | n20D1.69 (Predicted) |
Boil Point(°C) | ~600.16° C at 760 mmHg (Predicted) |
Melt Point(°C) | 284.63° C (Predicted) |
1. Liu L, Chen B, Qin S, Li S, He X, Qiu S, Zhao W, Zhao H. (2010) A novel histone deacetylase inhibitor Chidamide induces apoptosis of human colon cancer cells.. Biochem Biophys Res Commun, 392 (2): (190-5). [PMID:20060381] |
2. Dong M, Ning ZQ, Xing PY, Xu JL, Cao HX, Dou GF, Meng ZY, Shi YK, Lu XP, Feng FY. (2012) Phase I study of chidamide (CS055/HBI-8000), a new histone deacetylase inhibitor, in patients with advanced solid tumors and lymphomas.. Cancer Chemother Pharmacol, 69 (6): (1413-22). [PMID:22362161] |
3. Gong K, Xie J, Yi H, Li W. (2012) CS055 (Chidamide/HBI-8000), a novel histone deacetylase inhibitor, induces G1 arrest, ROS-dependent apoptosis and differentiation in human leukaemia cells.. Biochem J, 443 (3): (735-46). [PMID:22339555] |
4. Wang H, Guo Y, Fu M, Liang X, Zhang X, Wang R, Lin C, Qian H. (2012) Antitumor activity of Chidamide in hepatocellular carcinoma cell lines.. Mol Med Rep, 5 (6): (1503-8). [PMID:22484326] |
5. Qiao Z, Ren S, Li W, Wang X, He M, Guo Y, Sun L, He Y, Ge Y, Yu Q. (2013) Chidamide, a novel histone deacetylase inhibitor, synergistically enhances gemcitabine cytotoxicity in pancreatic cancer cells.. Biochem Biophys Res Commun, 434 (1): (95-101). [PMID:23541946] |
6. Yao Y, Zhou J, Wang L, Gao X, Ning Q, Jiang M, Wang J, Wang L, Yu L. (2013) Increased PRAME-specific CTL killing of acute myeloid leukemia cells by either a novel histone deacetylase inhibitor chidamide alone or combined treatment with decitabine.. PLoS ONE, 8 (8): (e70522). [PMID:23940586] |
7. Jiang Z, Li W, Hu X, Zhang Q, Sun T, Cui S, Wang S, Ouyang Q, Yin Y, Geng C et al.. (2019) Tucidinostat plus exemestane for postmenopausal patients with advanced, hormone receptor-positive breast cancer (ACE): a randomised, double-blind, placebo-controlled, phase 3 trial.. Lancet Oncol, 20 (6): (806-815). [PMID:31036468] |