HMN-154
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MedKoo CAT#: 555217

CAS#: 173528-92-2

Description: HMN-154 is a benzenesulfonamide anticancer agent. HMN-154 inhibits DNA binding of NF-Y to the human major histocompatibility complex class II human leukocyte antigen DRA Y-box sequence in a dose-dependent manner.


Chemical Structure

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HMN-154
CAS# 173528-92-2

Theoretical Analysis

MedKoo Cat#: 555217
Name: HMN-154
CAS#: 173528-92-2
Chemical Formula: C20H18N2O3S
Exact Mass: 366.10
Molecular Weight: 366.435
Elemental Analysis: C, 65.56; H, 4.95; N, 7.65; O, 13.10; S, 8.75

Price and Availability

Size Price Availability Quantity
100mg USD 950
200mg USD 1450
500mg USD 1950
1g USD 2950
2g USD 4650
5g USD 7250
Bulk inquiry

Synonym: HMN-154; HMN 154; HMN154.

IUPAC/Chemical Name: (E)-4-(2-(2-(N-(4-Methoxybenzenesulfonyl)amino)phenyl)ethenyl)pyridine

InChi Key: CIJCDFMGZYKSSC-VOTSOKGWSA-N

InChi Code: InChI=1S/C20H18N2O3S/c1-25-18-8-10-19(11-9-18)26(23,24)22-20-5-3-2-4-17(20)7-6-16-12-14-21-15-13-16/h2-15,22H,1H3/b7-6+

SMILES Code: O=S(NC1=CC=CC=C1/C=C/C2=CC=NC=C2)(C3=CC=C(OC)C=C3)=O

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Product Data:
Biological target: HMN-154 is a novel benzenesulfonamide anticancer compound; inhibits KB and colon38 cells with IC50 values of 0.0026 and 0.003 μg/mL, respectively.
In vitro activity: Furthermore, HMN-154 inhibits DNA binding of NF-Y to the human major histocompatibility complex class II human leukocyte antigen DRA Y-box sequence in a dose-dependent manner. Reference: Mol Pharmacol. 1999 Feb;55(2):356-63. https://pubmed.ncbi.nlm.nih.gov/9927629/
In vivo activity: TBD

Solubility Data

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 15.0 40.93

Preparing Stock Solutions

The following data is based on the product molecular weight 366.44 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol: 1. Tanaka H, Ohshima N, Hidaka H. Isolation of cDNAs encoding cellular drug-binding proteins using a novel expression cloning procedure: drug-western. Mol Pharmacol. 1999 Feb;55(2):356-63. doi: 10.1124/mol.55.2.356. PMID: 9927629.
In vitro protocol: 1. Tanaka H, Ohshima N, Hidaka H. Isolation of cDNAs encoding cellular drug-binding proteins using a novel expression cloning procedure: drug-western. Mol Pharmacol. 1999 Feb;55(2):356-63. doi: 10.1124/mol.55.2.356. PMID: 9927629.
In vivo protocol: TBD

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1: Tanaka H, Ohshima N, Hidaka H. Isolation of cDNAs encoding cellular
drug-binding proteins using a novel expression cloning procedure: drug-western.
Mol Pharmacol. 1999 Feb;55(2):356-63. PubMed PMID: 9927629.