Lonidamine chemical structure
Chemical structureResearch use only
CAT. NO. DCAPI1199Featured

Lonidamine

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TotalUS$250
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Product overview

Description & Application

Lonidamine is an orally administered small molecule hexokinase inactivator.Target: OthersLonidamine is a derivative of indazole-3-carboxylic acid, which for a long time, has been known to inhibit aerobic glycolysis in cancer cells. It seems to enhance aerobic glycolysis in normal cells, but suppress glycolysis in cancer cells. This is most likely through the inhibition of the mitochondrially bound hexokinase. Later studies in Ehrlich ascites tumor cells showed that lonidamine inhibits both respiration and glycolysis leading to a decrease in cellular ATP. Clinical trials of lonidamine in combination with other anticancer agents for a variety of cancers has begun. Lonidamine has been used in the treatment of brain tumours in combination with radiotherapy and temozolomide. Results showed that a combination of temozolomide and lonidamine at clinically achievable, low plasma concentrations, could inhibit tumour growth, and lonidamine could reduce the dose of temozolomide required for radiosensitization of brain tumours. From Wikipedia.

ParameterValue
Chemical NameLonidamine
CAS No.50264-69-2
Synonyms1-(2,4-Dichlorobenzyl)-1H-indazole-3-carboxylic acid;1-(2,4-Dichlorobenzyl)indazole-3-carboxylic acid;Lonidamine;1-[(2,4-Dichlorophenyl)methyl]-1H-indazole-3-carboxylic acid;1-[(2,4-dichlorophenyl)methyl]indazole-3-carboxylic acid;1-(2,4-Dichlorobenzyl)-1H-indazole-3-carboxylic acid Diclondazolic acid;AF1890;DICA;Diclondazolic acid;Doridamina;Lonidamin;Lonidamina;Lonidaminum;Lonidaminum [INN-Latin];AF 1890;Lonidamina [INN-Spanish];1-(2,4-Dichlorbenzyl)-indazole-3-carboxylic acid;MLS000028822;C15H10Cl2N2O;AF-1890;NCGC00025244-02;Lonidamine (INN);HMS2234H24;Lonidamine [INN:BAN];D07257;LONIDAMINE [WHO-DD];HMS3262O17;SR-01000075961;NCGC00261403-01;AB00597141_08;SR-01000075961-1;Lopac0_000718;LONIDAMINE [INN];Q3836670;GTPL12601;NS00032024;s2610;C15H10Cl2N2O2;SW219810-1;LONIDAMINE [MI];NCGC00015609-01;NCGC00015609-07;50264-69-2;HMS3874D03;HMS3676P05;NSC 758419;NCGC00015609-08;NCGC00015609-02;Tox21_110181;1H-Indazole-3-carboxylic acid, 1-[(2,4-dichlorophenyl)methyl]-;NSC741419;UNII-U78804BIDR;SCHEMBL7134;1H-Indazole-3-carboxylic acid, 1-(2,4-dichlorobenzyl)-;WDRYRZXSPDWGEB-UHFFFAOYSA-N;HMS3651F09;Q-201318;HY-B0486;SDCCGSBI-0050696.P003;NSC-758419;Lonidamine, mitochondrial hexokinase inhibitor;NSC-741419;BRD-K78513633-001-03-3;SR-01000075961-3;SMR000058467;EN300-345010;MFCD00866285;CCRIS 3516;LP00718;NSC 741419;SR-01000075961-6;Tox21_500718;KN-228;CHEMBL1257030;NCGC00015609-03;BRD-K78513633-001-06-6;HMS3369I01;EINECS 256-510-0;AF-1890;Diclondazolic Acid;DICA;HMS3412P05;cid_39562;L0283;DTXCID90782;CCG-204803;Z1137008901;BRN 0894483;HMS3268K09;DTXSID5020782;Doridamina (TN);BDBM59775;1-[(2,4-Dichlorophenyl)Methyl]-1H-indazole-3-carboxylicacid;BCP06555;HB0993;LONIDAMINE [MART.];AKOS012842739;FT-0650359;AM20060642;A929099;NSC758419;AS-11653;NCGC00025244-01;AB00597141_10;Tocris-1646;DB06266;CAS-50264-69-2;NCGC00015609-09;Tox21_110181_1;NCGC00015609-16;1H-Indazole-3-carboxylic acid, 1-((2,4-dichlorophenyl)methyl)-;NCGC00025244-03;1-[(2,4-dichlorophenyl)methyl]-3-indazolecarboxylic acid;EU-0100718;SBI-0050696.P002;NCGC00015609-05;NCGC00015609-04;NCGC00015609-06;Tox21_202306;TH-070;AC-5626;L 4900;CHEBI:50138;Dichlondazolic acid;U78804BIDR;NCGC00259855-01;Pharmakon1600-01503225;Lopac-L-4900;L01XX07;Lonidaminum (INN-Latin);BRD-K78513633-001-13-2;lonidamine;1H-Indazole-3-carboxylic acid, 1-((2,4-dichlorophenyl)methyl)-(9CI);BRD-K78513633-001-14-0;LONIDAMINE (MART.);1-[(2,4-dichlorophenyl)methyl]-1H-indazole-3-carboxylic acid;1-(2,4-dichlorobenzyl)indazole-3-carboxylic acid;Lonidamine?;1-((2,4-dichlorophenyl)methyl)indazole-3-carboxylic acid;Lonidamina (INN-Spanish);1-(2,4-dichlorophenyl)-1h-indazol-3-carboxylic acid;BRD-K78513633-001-15-7;Diclondazolic Acid
FormulaC15H10Cl2N2O2
M.Wt321.1581
SMILESClC1C([H])=C(C([H])=C([H])C=1C([H])([H])N1C2=C([H])C([H])=C([H])C([H])=C2C(C(=O)O[H])=N1)Cl
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological Activity

Lonidamine is an orally administered small molecule hexokinase inactivator.Target: OthersLonidamine is a derivative of indazole-3-carboxylic acid, which for a long time, has been known to inhibit aerobic glycolysis in cancer cells. It seems to enhance aerobic glycolysis in normal cells, but suppress glycolysis in cancer cells. This is most likely through the inhibition of the mitochondrially bound hexokinase. Later studies in Ehrlich ascites tumor cells showed that lonidamine inhibits both respiration and glycolysis leading to a decrease in cellular ATP. Clinical trials of lonidamine in combination with other anticancer agents for a variety of cancers has begun. Lonidamine has been used in the treatment of brain tumours in combination with radiotherapy and temozolomide. Results showed that a combination of temozolomide and lonidamine at clinically achievable, low plasma concentrations, could inhibit tumour growth, and lonidamine could reduce the dose of temozolomide required for radiosensitization of brain tumours. From Wikipedia.

In Vitro

No in vitro data are provided in the current product source. Contact us for further information.

In Vivo

No in vivo data are provided in the current product source. Contact us for further information.

References & source

DC Chemicals original product information

Published experimental findings depend on the model and assay conditions. They do not guarantee equivalent performance in every application. For laboratory research use only.

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Solution calculator

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