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HLCL-61 HCL - 10mM in DMSO, high purity , CAS No.1158279-20-9

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
H420735
Grouped product items
SKU Size
Availability
Price Qty
H420735-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$197.90

PRMT Inhibitors

Basic Description

Synonyms HLCL619H-​Carbazole-​3-​methanamine,9-​ethyl-​N-​[(2-​methoxyphenyl)​methyl]​-​,hydrochloride (1:1)
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms HLCL-61 hydrochloride is a potent and selective PRMT5 inhibitor for the treatment of acute myeloid leukemia.
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Information

HLCL-61 HCL HLCL-61 hydrochloride is a potent and selective PRMT5 inhibitor for the treatment of acute myeloid leukemia.

Targets

PRMT5 (In THP-1 cells) 16.74 μM

In vitro

HLCL-61 shows no inhibitory activity against the type I (PRMT1 and PRMT4) and type II (PRMT7) PRMT family members. HLCL-61 shows effective inhibition of symmetric arginine dimethylation (me2) of histones H3 and H4 in AML samples.Treatment of AML cell lines (MV4-11 and THP-1) and primary blasts with HLCL-61 also results in a decrease of cell viability. HLCL-61 is also effective in promoting apoptosis in MV4-11 and THP-1 cells after 48 h.

Cell Research(from reference)

Cell lines:AML cell lines 

Concentrations:25,50uM 

Incubation Time:48h 

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Indoles and derivatives
Subclass Carbazoles
Intermediate Tree Nodes Not available
Direct Parent Carbazoles
Alternative Parents N-alkylindoles  Indoles  Phenylmethylamines  Phenoxy compounds  Methoxybenzenes  Benzylamines  Anisoles  Aralkylamines  Alkyl aryl ethers  Substituted pyrroles  Heteroaromatic compounds  Dialkylamines  Azacyclic compounds  Hydrochlorides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Carbazole - N-alkylindole - Indole - Phenoxy compound - Anisole - Benzylamine - Methoxybenzene - Phenylmethylamine - Phenol ether - Alkyl aryl ether - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Azacycle - Secondary aliphatic amine - Ether - Secondary amine - Amine - Hydrochloride - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.
External Descriptors Not available

Product Properties

ALogP 5.364
HBD Count 1
Rotatable Bond 6

Names and Identifiers

IUPAC Name 1-(9-ethylcarbazol-3-yl)-N-[(2-methoxyphenyl)methyl]methanamine;hydrochloride
INCHI InChI=1S/C23H24N2O.ClH/c1-3-25-21-10-6-5-9-19(21)20-14-17(12-13-22(20)25)15-24-16-18-8-4-7-11-23(18)26-2;/h4-14,24H,3,15-16H2,1-2H3;1H
InChIKey XYAVCNMZZKTEGR-UHFFFAOYSA-N
Smiles CCN1C2=C(C=C(C=C2)CNCC3=CC=CC=C3OC)C4=CC=CC=C41.Cl
Isomeric SMILES CCN1C2=C(C=C(C=C2)CNCC3=CC=CC=C3OC)C4=CC=CC=C41.Cl
PubChem CID 17208222
Molecular Weight 380.91

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

DMSO(mg / mL) Max Solubility 76
DMSO(mM) Max Solubility 199.5221968
Water(mg / mL) Max Solubility <1
Molecular Weight 380.900 g/mol
XLogP3
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 6
Exact Mass 380.166 Da
Monoisotopic Mass 380.166 Da
Topological Polar Surface Area 26.200 Ų
Heavy Atom Count 27
Formal Charge 0
Complexity 442.000
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

Reviews

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