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BS-181 HCl - 98%, high purity , CAS No.1397219-81-6

    Grade & Purity:
  • ≥98%
In stock
Item Number
B412709
Grouped product items
SKU Size
Availability
Price Qty
B412709-10mg
10mg
4
$157.90
B412709-50mg
50mg
3
$573.90
B412709-250mg
250mg
1
$2,583.90

CDK7 Selective Inhibitors

Basic Description

Synonyms BS-181 hydrochloride | N5-(6-aminohexyl)-N7-benzyl-3-isopropylpyrazolo[1,5-a]pyrimidine-5,7-diamine hydrochloride
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms BS-181 HCl is a highly selective CDK7 inhibitor with IC50 of 21 nM. It is more than 40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.
Storage Temp Store at -20°C
Shipped In
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Product Description

Information

BS-181 HCl is a highly selectiveCDK7inhibitor withIC50of 21 nM. It is more than 40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.


Targets

CDK7 (Cell-free assay) 21 nM


In vitro

BS-181 is a small molecule inhibitor of CDK7 in a cell-free environment, which displays more potential activity than roscovitine with IC 50 of 510 nM. Among the CDKs and other 69 kinases from many different classes, BS-181 shows high inhibitory selectivity for CDK7, inhibits CDK2 at concentrations lower than 1 μM which being inhibited 35-fold less potently (IC50 with 880 nM) than CDK7, shows slight inhibition for CDK1, CDK4, CDK5, CDK6 and CDK9 with IC50 values higher than 3.0 μM, and only shows inhibition for several kinases from other classes at high concentrations (>10 μM). BS-181 promotes cell cycle arrest and inhibits the cancer cell growth of a range of tumor types, including breast, lung, prostate and colorectal cancer with IC50 in the range of 11.5-37 μM. In MCF-7 cells, BS-181 inhibits the phosphorylation of the CDK7 substrate RNA polymerase II COOH-terminal domain (CTD), and promotes cell cycle arrest and apoptosis to inhibit the growth of cancer cell lines.


In vivo

BS-181 is stable in vivo with a plasma elimination half-life in mice of 405 minutes after i.p. administration of 10 mg/kg. BS-181 inhibits the growth of MCF-7 xenografts in the nude mice model in a dose-dependent manner, with 25% and 50% reduction in tumor growth after 2 weeks of treatment at 10 mg/kg/day and 20 mg/kg/day, respectively without apparent toxicity.


Cell Research(from reference)

Cell lines:MCF-7 cells 

Concentrations:Dissolved in DMSO, final concentration ~50 μM 

Incubation Time:24 hours 

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Pyrazolopyrimidines
Subclass Pyrazolo[1,5-a]pyrimidines
Intermediate Tree Nodes Not available
Direct Parent Pyrazolo[1,5-a]pyrimidines
Alternative Parents Benzylamines  Secondary alkylarylamines  Aminopyrimidines and derivatives  Imidolactams  Pyrazoles  Heteroaromatic compounds  Azacyclic compounds  Monoalkylamines  Hydrochlorides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Pyrazolo[1,5-a]pyrimidine - Benzylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Imidolactam - Heteroaromatic compound - Pyrazole - Azole - Secondary amine - Azacycle - Organic nitrogen compound - Primary amine - Organonitrogen compound - Primary aliphatic amine - Hydrocarbon derivative - Amine - Hydrochloride - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as pyrazolo[1,5-a]pyrimidines. These are aromatic heterocyclic compounds containing a pyrazolo[3,4-d]pyrimidine ring system, which consists of a pyrazole ring fused to and sharing exactly one nitrogen atom with a pyrimidine ring.
External Descriptors Not available

Product Properties

ALogP 4.684
hba_count 2
HBD Count 3
Rotatable Bond 11

Names and Identifiers

Pubchem Sid 488201443
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488201443
IUPAC Name 5-N-(6-aminohexyl)-7-N-benzyl-3-propan-2-ylpyrazolo[1,5-a]pyrimidine-5,7-diamine;hydrochloride
INCHI InChI=1S/C22H32N6.ClH/c1-17(2)19-16-26-28-21(25-15-18-10-6-5-7-11-18)14-20(27-22(19)28)24-13-9-4-3-8-12-23;/h5-7,10-11,14,16-17,25H,3-4,8-9,12-13,15,23H2,1-2H3,(H,24,27);1H
InChIKey NVIJWMOQODWNFN-UHFFFAOYSA-N
Smiles CC(C)C1=C2N=C(C=C(N2N=C1)NCC3=CC=CC=C3)NCCCCCCN.Cl
Isomeric SMILES CC(C)C1=C2N=C(C=C(N2N=C1)NCC3=CC=CC=C3)NCCCCCCN.Cl
Alternate CAS 1092443-52-1(free base)
Molecular Weight 416.99
Reaxy-Rn 26177980
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=26177980&ln=

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.

6 results found

Lot Number Certificate Type Date Item
D23141149 Certificate of Analysis Mar 06, 2023 B412709
D23141148 Certificate of Analysis Mar 06, 2023 B412709
D23141143 Certificate of Analysis Mar 06, 2023 B412709
D23141160 Certificate of Analysis Mar 06, 2023 B412709
D23141203 Certificate of Analysis Mar 06, 2023 B412709
D23141144 Certificate of Analysis Mar 06, 2023 B412709

Chemical and Physical Properties

Solubility Solubility (25°C) In vitro DMSO: 83 mg/mL (199.04 mM); Water: 83 mg/mL (199.04 mM); Ethanol: 22 mg/mL warmed with 50ºC Water: bath (52.75 mM);
DMSO(mg / mL) Max Solubility 83
DMSO(mM) Max Solubility 199.0455407
Water(mg / mL) Max Solubility 3
Water(mM) Max Solubility 7.194417132
Molecular Weight 417.000 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 11
Exact Mass 416.246 Da
Monoisotopic Mass 416.246 Da
Topological Polar Surface Area 80.300 Ų
Heavy Atom Count 29
Formal Charge 0
Complexity 425.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Solution Calculators

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