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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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S357869-5mg | 5mg | In stock | $98.90 | |
S357869-10mg | 10mg | In stock | $147.90 | |
S357869-25mg | 25mg | In stock | $333.90 | |
S357869-50mg | 50mg | In stock | $444.90 | |
S357869-100mg | 100mg | In stock | $751.90 |
Specifications & Purity | Moligand™, ≥98% |
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Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of CREB binding protein;Inhibitor of E1A binding protein p300 |
Product Description | Product introduction SGC-CBP30 is a potent and highly selective CBP/p300 bromodomain (Kds of 21 nM and 32 nM for CBP and p300, respectively) inhibitor, displaying 40-fold selectivity over the first bromodomain of BRD4 [BRD4(1)] bound. SGC-CBP30 strongly reduces secretion of IL-17A in Th17 cells and has anti-inflammatory effects. |
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IUPAC Name | 4-[(2S)-1-[2-[2-(3-chloro-4-methoxyphenyl)ethyl]-5-(3,5-dimethyl-1,2-oxazol-4-yl)benzimidazol-1-yl]propan-2-yl]morpholine |
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INCHI | InChI=1S/C28H33ClN4O3/c1-18(32-11-13-35-14-12-32)17-33-25-8-7-22(28-19(2)31-36-20(28)3)16-24(25)30-27(33)10-6-21-5-9-26(34-4)23(29)15-21/h5,7-9,15-16,18H,6,10-14,17H2,1-4H3/t18-/m0/s1 |
InChi Key | GEPYBHCJBORHCE-SFHVURJKSA-N |
Canonical SMILES | CC1=C(C(=NO1)C)C2=CC3=C(C=C2)N(C(=N3)CCC4=CC(=C(C=C4)OC)Cl)CC(C)N5CCOCC5 |
Isomeric SMILES | CC1=C(C(=NO1)C)C2=CC3=C(C=C2)N(C(=N3)CCC4=CC(=C(C=C4)OC)Cl)C[C@H](C)N5CCOCC5 |
PubChem CID | 72201027 |
Molecular Weight | 509.04 |
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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G2209334 | Certificate of Analysis | Jun 05, 2022 | S357869 |
G2209335 | Certificate of Analysis | Jun 05, 2022 | S357869 |
G2209337 | Certificate of Analysis | Jun 05, 2022 | S357869 |
G2209338 | Certificate of Analysis | Jun 05, 2022 | S357869 |
G2209344 | Certificate of Analysis | Jun 05, 2022 | S357869 |
Solubility | DMSO: 93 mg/mL (182.7 mM);Ethanol: 93 mg/mL (182.7 mM);Water: <1 mg/mL |
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1. Hammitzsch A, Tallant C, Fedorov O, O'Mahony A, Brennan PE, Hay DA, Martinez FO, Al-Mossawi MH, de Wit J, Vecellio M et al.. (2015) CBP30, a selective CBP/p300 bromodomain inhibitor, suppresses human Th17 responses.. Proc Natl Acad Sci USA, 112 (34): (10768-73). [PMID:26261308] |
2. Chua MJ, Robaa D, Skinner-Adams TS, Sippl W, Andrews KT. (2018) Activity of bromodomain protein inhibitors/binders against asexual-stage Plasmodium falciparum parasites.. Int J Parasitol Drugs Drug Resist, 8 (2): (189-193). [PMID:29631126] |