6-Dimethylaminopurine
PubChem CID: 3134
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| Compound Synonyms | 6-dimethylaminopurine, 938-55-6, N,N-dimethyl-7H-purin-6-amine, 6-(Dimethylamino)purine, N,N-Dimethyladenine, N6,N6-Dimethyladenine, N(6),N(6)-Dimethyladenine, 6-Dimethyladenine, Dimethyladenine, 1H-Purin-6-amine, N,N-dimethyl-, Adenine, N,N-dimethyl-, N,N-Dimethyl-9H-purin-6-amine, 6,6-Dimethyladenine, n,n-dimethyl-adenine, 6-DMAP, N,N-Dimethyl-6-aminopurine, 6-(dimethylamino)-Purine, CCRIS 5216, CHEBI:60281, 6-Dimethylamino-9H-purine, EINECS 213-344-3, Adenine, N6,N6-dimethyl-, UNII-649SA4S2CV, Purine, 6-(dimethylamino)-, NSC 401568, N(6)-dimethyladenine, 6-Dimethylamine purine, N6,N6-dimethyl-Adenine, MFCD00005573, NSC-401568, 649SA4S2CV, CHEMBL407391, N,N-dimethyl-1H-purin-6-amine, DTXSID20239658, 9H-PURIN-6-AMINE, N,N-DIMETHYL-, 104245-07-0, Protein Kinase Inhibitor, DMAP, 42C, Adenine,N-dimethyl-, Kinome_3442, Purine, 6-dimethylamino, N6,N6 -dimethyladenine, Maybridge3_000221, purine, 6-dimethylamino-, Epitope ID:140948, SCHEMBL152593, PU09, 1H-Purin-6-amine,N-dimethyl-, BDBM92422, DTXCID70162149, Dimethyl-(9H-purin-6-yl)-amine, HMS1431K01, 6-(Dimethylamino)purine, >=98%, N,N-Dimethyl-9H-purin-6-amine #, BBL036342, MFCD00079113, NSC401568, s6088, STK370033, AKOS005445384, AKOS015850812, AKOS028109175, CS-W010844, DS-6256, FD04709, HY-W010128, IDI1_011608, SY050761, 6-(Dimethylamino)purineN,N-Dimethyladenine, D3894, NS00039689, EN300-63840, T71480, Q15632695, N6,N6-Dimethyladenine, N,N-Dimethyl-9H-purin-6-amine, Z1258992637, N6,N6-Dimethyladenine, N,N-Dimethyl-9H-purin-6-amine |
|---|---|
| Ghose Rule | True |
| Classyfire Kingdom | Organic compounds |
| Topological Polar Surface Area | 57.7 |
| Hydrogen Bond Donor Count | 1.0 |
| Pfizer 3 75 Rule | False |
| Scaffold Graph Level | C1CCC2CCCC2C1 |
| Np Classifier Class | Purine alkaloids |
| Deep Smiles | CNcncncc6[nH]cn5)))))))))C |
| Heavy Atom Count | 12.0 |
| Classyfire Class | Imidazopyrimidines |
| Description | 6-Dimethylaminopurine is a serine threonine protein kinase inhibitor. It inhibits the germinal vesicle breakdown and the meiotic maturation of oocytes. (PMID 2540051) 6-Dimethylaminopurine can be used to rtificially lengthen the pre-maturation period of oocyte growth, in vitro, by inhibiting germinal vesicle breakdown in mouse and human oocytes. (PMID: 10655310) [HMDB] |
| Scaffold Graph Node Level | C1NCC2NCNC2N1 |
| Classyfire Subclass | Purines and purine derivatives |
| Isotope Atom Count | 0.0 |
| Molecular Complexity | 160.0 |
| Database Name | fooddb_chem_all;hmdb_chem_all;imppat_phytochem;pubchem |
| Defined Atom Stereocenter Count | 0.0 |
| Iupac Name | N,N-dimethyl-7H-purin-6-amine |
| Class | Imidazopyrimidines |
| Veber Rule | True |
| Classyfire Superclass | Organoheterocyclic compounds |
| Xlogp | 0.7 |
| Superclass | Organoheterocyclic compounds |
| Subclass | Purines and purine derivatives |
| Gsk 4 400 Rule | True |
| Molecular Formula | C7H9N5 |
| Scaffold Graph Node Bond Level | c1ncc2[nH]cnc2n1 |
| Inchi Key | BVIAOQMSVZHOJM-UHFFFAOYSA-N |
| Silicos It Class | Soluble |
| Rotatable Bond Count | 1.0 |
| State | Solid |
| Synonyms | 6-(dimethylamino)-Purine, 6-(Dimethylamino)purine, 6-Dimethyladenine, 6-Dimethylamine purine, 6-Dimethylaminopurine, 6,6-Dimethyladenine, Dimethyladenine, DMAP, N,N-Dimethyl-1H-purin-6-amine, N,N-Dimethyl-6-aminopurine, N,N-dimethyl-Adenine, N,N-Dimethyladenine, N(6)-Dimethyladenine, N(6),N(6)-Dimethyladenine, N6,N6-dimethyl-Adenine, N6,N6-Dimethyladenine, 6-(Dimethylamino)-purine, N,N-Dimethyl-adenine, N6,N6-Dimethyl-adenine, 6-DMAP, Dimethylaminopurine, n,n-dimethyl-(1h)-purin-6-amine |
| Substituent Name | 6-alkylaminopurine, Dialkylarylamine, Aminopyrimidine, Imidolactam, Pyrimidine, Heteroaromatic compound, Imidazole, Azole, Tertiary amine, Azacycle, Hydrocarbon derivative, Organonitrogen compound, Amine, Aromatic heteropolycyclic compound |
| Esol Class | Very soluble |
| Functional Groups | cN(C)C, c[nH]c, cnc |
| Compound Name | 6-Dimethylaminopurine |
| Kingdom | Organic compounds |
| Exact Mass | 163.086 |
| Formal Charge | 0.0 |
| Monoisotopic Mass | 163.086 |
| Hydrogen Bond Acceptor Count | 4.0 |
| Molecular Weight | 163.18 |
| Gi Absorption | True |
| Covalent Unit Count | 1.0 |
| Total Atom Stereocenter Count | 0.0 |
| Total Bond Stereocenter Count | 0.0 |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Lipinski Rule Of 5 | True |
| Inchi | InChI=1S/C7H9N5/c1-12(2)7-5-6(9-3-8-5)10-4-11-7/h3-4H,1-2H3,(H,8,9,10,11) |
| Smiles | CN(C)C1=NC=NC2=C1NC=N2 |
| Np Classifier Biosynthetic Pathway | Alkaloids |
| Defined Bond Stereocenter Count | 0.0 |
| Egan Rule | True |
| Taxonomy Direct Parent | 6-alkylaminopurines |
| Np Classifier Superclass | Pseudoalkaloids |
- 1. Outgoing r'ship
FOUND_INto/from Plectranthus Glabratus (Plant) Rel Props:Reference:https://doi.org/10.1080/10412905.1993.9698226