Alobresib - ≥98% , CAS No.1637771-14-2

CAS: 1637771-14-2 Cat. No.: A414297 Molecular Weight: 437.49
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
[2-cyclopropyl-6-(3,5-dimethyl-1,2-oxazol-4-yl)-1H-benzimidazol-4-yl]-dipyridin-2-ylmethanol | Gs 5829 | GS-5829;GS 5829;GS5829 | EX-A3724 | DB14970 | F81315 | UNII-3QBL0BLP3D | HY-109050 | (2-Cyclopropyl-6-(3,5-dimethyl-1,2-oxazol-4-yl)-1hbenzimidazol-4-
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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5mg
A414297-5mg
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A414297-25mg
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50mg
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100mg
A414297-100mg
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A414297-500mg
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

Alobresib (GS-5829) Alobresib (GS-5829) is a novel BET inhibitor that represents a highly effective therapeutics agent against recurrent/chemotherapy-resistant USC-overexpressing c-Myc. Alobresib (GS-5829) inhibits CLL cell proliferation and induces leukemia cell apoptosis through deregulation of key signaling pathways, such as BLK , AKT , ERK1/2 , and MYC . Alobresib (GS-5829) also inhibits NF-κB signaling.


Targets

BET ; BLK ; Akt ; ERK1/2 ; MYC 33297,


In vitro

In-vitro experiments demonstrates high sensitivity of USC cell-lines to the exposure to GS-5829 causing a dose-dependent decrease in the phosphorylated levels of c-Myc and a dose-dependent increase in caspase activation (apoptosis). GS-5829 inhibits CLL cell proliferation and induces leukemia cell apoptosis through deregulation of key signaling pathways, such as BLK, AKT, ERK1/2, and MYC. IκBα modulation indicates that GS-5829 also inhibits NF-κB signaling. GS-5829-induced apoptosis results from an imbalance between positive (BIM) and negative regulators (BCL-XL) of the intrinsic apoptosis pathway.


In vivo

GS-5829 has impressive activity against USC primary tumors as well as USC xenografts. Assessment of c-Myc expression in tumors exposed to the GS-5829 demonstrates down-regulation of both total and phospho c-Myc proteins. GS-5829 demonstrates excellent bioavailability after oral administration and is significantly more effective than JQ1 at the doses used in comparative experiments in vivo against USC xenografts. Clinical studies with GS-5829 in USC patients harboring disease resistant to standard salvage chemotherapy are warranted.


Cell Research(from reference)

Cell lines:PBMC, MEC-1 

Concentrations:100 nM, 200 nM, 400 nM, 800 nM 

Incubation Time:72 h, 24 h 

Specifications

Synonyms
[2-cyclopropyl-6-(3, 5-dimethyl-1, 2-oxazol-4-yl)-1H-benzimidazol-4-yl]-dipyridin-2-ylmethanol | Gs 5829 | GS-5829;GS 5829;GS5829 | EX-A3724 | DB14970 | F81315 | UNII-3QBL0BLP3D | HY-109050 | (2-Cyclopropyl-6-(3, 5-dimethyl-1, 2-oxazol-4-yl)-1hbenzimidazol-4-
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Alobresib (GS-5829) is a novel BET inhibitor that represents a highly effective therapeutics agent against recurrent/chemotherapy-resistant USC-overexpressing c-Myc. Alobresib (GS-5829) inhibits CLL cell proliferation and induces leukemia cell apoptosis t
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Product Properties
ALogP3.767
hba_count5
HBD Count1
Rotatable Bond5
Names and Identifiers
Pubchem Sid504772486
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504772486
Canonical SmilesCC1=C(C(=NO1)C)C2=CC(=C3C(=C2)NC(=N3)C4CC4)C(C5=CC=CC=N5)(C6=CC=CC=N6)O
IUPAC Name[2-cyclopropyl-6-(3,5-dimethyl-1,2-oxazol-4-yl)-1H-benzimidazol-4-yl]-dipyridin-2-ylmethanol
InChIKeyCMSUJGUHYXQSOK-UHFFFAOYSA-N
INCHI1S/C26H23N5O2/c1-15-23(16(2)33-31-15)18-13-19(24-20(14-18)29-25(30-24)17-9-10-17)26(32,21-7-3-5-11-27-21)22-8-4-6-12-28-22/h3-8,11-14,17,32H,9-10H2,1-2H3,(H,29,30)
Isomeric SMILES CC1=C(C(=NO1)C)C2=CC(=C3C(=C2)NC(=N3)C4CC4)C(C5=CC=CC=N5)(C6=CC=CC=N6)O
Molecular Weight 437.49
Reaxy-Rn 27474280
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=27474280&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassBenzimidazoles
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzimidazoles
Alternative Parents Pyridines and derivatives  Benzenoids  Tertiary alcohols  Isoxazoles  Imidazoles  Heteroaromatic compounds  Oxacyclic compounds  Azacyclic compounds  Organonitrogen compounds  Hydrocarbon derivatives  Aromatic alcohols  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzimidazole - Pyridine - Benzenoid - Azole - Imidazole - Isoxazole - Tertiary alcohol - Heteroaromatic compound - Azacycle - Oxacycle - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic alcohol - Hydrocarbon derivative - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzimidazoles. These are organic compounds containing a benzene ring fused to an imidazole ring (five member ring containing a nitrogen atom, 4 carbon atoms, and two double bonds).
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
BRD4 Tchem Bromodomain-containing protein 4 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate TypeDateItem
E2615043Certificate of AnalysisMay 28, 2026 A414297
K2219094Certificate of AnalysisSep 04, 2025 A414297
K2219095Certificate of AnalysisSep 04, 2025 A414297
K2219137Certificate of AnalysisSep 04, 2025 A414297
K2219138Certificate of AnalysisSep 04, 2025 A414297
K2219139Certificate of AnalysisSep 04, 2025 A414297
K2219140Certificate of AnalysisSep 04, 2025 A414297
K2219142Certificate of AnalysisSep 04, 2025 A414297
C2504075Certificate of AnalysisSep 13, 2022 A414297
Chemical and Physical Properties
SolubilitySolubility (25°C) In vitro DMSO: 87 mg/mL (198.86 mM); Ethanol: 11 mg/mL (25.14 mM); Water: ˂1 mg/mL
DMSO(mg / mL) Max Solubility87
DMSO(mM) Max Solubility198.86168826716
Water(mg / mL) Max Solubility˂1
Molecular Weight437.500 g/mol
XLogP33.200
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count5
Exact Mass437.185 Da
Monoisotopic Mass437.185 Da
Topological Polar Surface Area101.000 Ų
Heavy Atom Count33
Formal Charge0
Complexity672.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
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