TOP
Nav Bar
  1. General Info
  2. Effects Info
  3. Reference
Drug Details
01. General Information
Name 3-methyladenine
PubChem CID 135398661
Molecular Weight 149.15g/mol
Synonyms

3-methyladenine, 5142-23-4, 3-Methyl-3H-purin-6-amine, 6-Amino-3-methylpurine, 3-MA, 3H-Purin-6-amine, 3-methyl-, 3-Methyl-3H-adenine, 3-methylpurin-6-amine, ADENINE, 3-METHYL-, NSC 66389, C6H7N5, 3-methyl adenine, MFCD00010531, CHEBI:38635, DR88TV7SNU, 3-METHYL-3H-PURIN-6-YLAMINE, 3-Methyladenine (3-MA), Autophagy Inhibitor, 3-MA, 3,9-dihydro-3-methyl-6H-Purin-6-imine, 60192-57-6, 3899G64TKW, 3-Methyladenine autophagy inhibitor, NSC-66389, Purine, 3,6-dihydro-6-imino-3-methyl-, 6H-Purin-6-imine, 3,7-dihydro-3-methyl-, 6H-Purin-6-imine, 3,9-dihydro-3-methyl-, n3-methyladenine, 3-MA nucleobase, N(3)-methyladenine, EINECS 225-908-6, BRN 0146087, 3-methyl-7H-purin-6-imine, 3-methyl-Adenine, 3-Methyladenine?, NSC66389, 1p7m, 4ai5, UNII-DR88TV7SNU, NCIOpen2_000270, purine, 6-amino-3-methyl-, SCHEMBL48369, 5-26-17-00151 (Beilstein Handbook Reference), MLS006010995, SCHEMBL254058, UNII-3899G64TKW, METHYLADENINE, N(3)-, CHEMBL292268, 3-METHYL-6-AMINOPURINE, CHEMBL4303725, SCHEMBL15764619, 3-Methyl-3H-purin-6-amine #, DTXSID80199406, EX-A130, FSASIHFSFGAIJM-UHFFFAOYSA-N, ZPBYVFQJHWLTFB-UHFFFAOYSA-N, Bio1_000422, Bio1_000911, Bio1_001400, DTXSID901346127, GLXC-04639, HMS3656P04, AMY11868, BCP02452, 3-Methyladenine, autophagy inhibitor, BDBM50488841, HB2267, s2767, AKOS003382321, AKOS006228458, CCG-206388, CS-5207, DB04104, NCGC00345447-02, AC-28818, AS-19224, HY-19312, PD019337, SMR002530641, SY026559, DB-051961, A7582, FT-0635560, FT-0671432, M2518, NS00005696, SW220216-1, 3-methyl-3H-purin-6-amine (ACD/Name 4.0), C00913, 3-methyl-3H-purin-6-ylamine (ACD/Name 4.0), 3-MA , NSC 66389, J-640198, J-800199, W-202935, BRD-K81647657-001-01-9, Q27094948, InChI=1/C6H7N5/c1-11-3-10-5(7)4-6(11)9-2-8-4/h2-3H,7H2,1H

Drug Type Small molecule
Formula C₆H₇N₅
SMILES CN1C=NC(=N)C2=C1N=CN2
InChI 1S/C6H7N5/c1-11-3-10-5(7)4-6(11)9-2-8-4/h2-3,7H,1H3,(H,8,9)
InChIKey ZPBYVFQJHWLTFB-UHFFFAOYSA-N
CAS Number 5142-23-4
ChEMBL ID CHEMBL292268
ChEBI ID CHEBI:38635
Drug Bank ID DB04104
KEGG ID C00913
Toxicity Organism Test Type Route(Dose)
rat LD50 intraperitoneal(165 mg/kg)
mouse LD50 intraperitoneal(254 mg/kg)
rat LD50 oral(322 mg/kg)
Structure 2D-img
Download
2D MOL 3D MOL
02. Combinatorial Therapeutic Effect(s)
Synergistic Effect
Hide/Show
Enhancing Drug Efficacy
Hide/Show
Combination Pair ID: 800
Pair Name Pterostilbene, 3-methyladenine
Partner Name Pterostilbene
Disease Info [ICD-11: 2C60] Breast cancer Investigative
Biological Phenomena Induction-->Autophagy
Gene Regulation Down-regulation Expression VIM hsa7431
In Vitro Model MDA-MB-231 Breast adenocarcinoma Homo sapiens (Human) CVCL_0062
BT-549 Invasive breast carcinoma Homo sapiens (Human) CVCL_1092
Result These data showed that Fas signaling and autophagy accelerated the aggressiveness of TNBC. Inhibition of autophagy or Fas signaling may provide novel targets for TNBC therapy.
03. Reference
No. Title Href
1 The anti-tumor efficiency of pterostilbene is promoted with a combined treatment of Fas signaling or autophagy inhibitors in triple negative breast cancer cells. Food Funct. 2014 Aug;5(8):1856-65. doi: 10.1039/c4fo00145a. Click
It has been 132451 visits since 2024.08
If you find any error in data or bug in web service, please kindly report it to Dr. Zhang
TOP