N6-Benzyladenine
PubChem CID: 62389
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| Compound Synonyms | 6-Benzylaminopurine, 1214-39-7, Benzyladenine, N6-Benzyladenine, 6-Benzyladenine, N-Benzyladenine, N-Benzyl-9H-purin-6-amine, 6-(Benzylamino)purine, Benzylaminopurine, Cytokinin B, Adenine, N-benzyl-, N-benzyl-7H-purin-6-amine, 6-BAP, N(6)-Benzylaminopurine, Benzyl(purin-6-yl)amine, 6-(N-Benzylamino)purine, 1H-PURIN-6-AMINE, N-(PHENYLMETHYL)-, Pro-Shear, BA (Growth stimulant), BAP (growth stimulant), N(sup 6)-Benzyladenine, Verdan senescence inhibitor, Aminopurine, 6-benzyl, Caswell No. 081EE, N-Benzyl-adenine, N(sup 6)-(Benzylamino)purine, N-(Phenylmethyl)-1H-purin-6-amine, 6-Benzyl adenine, N-6-Benzyladenine, N(6)-(benzylamino)purine, Adenine, N(sup 6)-benzyl-, Adenine, N6-benzyl-, CCRIS 4351, SD 4901, SQ 4609, ABG 3034, Benzyl Aminopurine, 6-[(phenylmethyl)amino]-9H-purine, EINECS 214-927-5, KXG6A989PS, 6-(Benzylamino)-9H-purine, MFCD00005572, NSC 40818, n(6)-benzyladenine, CYTOPURINE, CHEBI:29022, HSDB 7667, NSC-40818, BENZYLADENINE [MI], BENZYLADENINE, 6-, 9H-Purin-6-amine, N-(phenylmethyl)-, BENZYLADENINE [HSDB], N-benzyl-1H-purin-6-amine, MLS000532693, BAP 99, CHEMBL228862, DTXSID7032630, SMR000140130, CAS-1214-39-7, 6-BA, 6-((phenylmethyl)amino)-9H-purine, benzylpurin-6-ylamine, 6-(n-benzyl)aminopurine, UNII-KXG6A989PS, NBenzyladenine, 6benzyladenine, ProShear, benzyl-(7h-purin-6-yl)-amine, Adenine, Nbenzyl, 6-benzylaminopurin, BAP (cytokinin), Prestwick_414, n6-benzylaminopurine, 6(Benzylamino)purine, Benzyl(purin6yl)amine, 6(NBenzylamino)purine, benzylaminopurine, 6-, N(6)Benzylaminopurine, 6-BA cpd, N(sup 6)Benzyladenine, N-Benzyladenine, 8CI, N(Sup6)-Benzyladenine, BA (growth stimulator), Opera_ID_868, Prestwick0_000189, Prestwick1_000189, Prestwick2_000189, Prestwick3_000189, Adenine, N(sup 6)benzyl, N(Sup 6)-benzyl-Adenine, CBKinase1_000521, CBKinase1_012921, Cambridge id 5131951, TimTec1_001722, BENZYLADENINE [INCI], Oprea1_747691, Oprea1_785203, Oprea1_830563, SCHEMBL35562, BSPBio_000117, CBDivE_001815, N(Phenylmethyl)1Hpurin6amine, MLS001074298, N(sup 6)(Benzylamino)purine, SPBio_002038, 6-Benzylaminopurine, 99.0%, 6-Benzylaminopurine (Standard), BPBio1_000129, 1HPurin6amine, N(phenylmethyl), 9HPurin6amine, N(phenylmethyl), DTXCID5012630, N-benzyladenine, monosodium salt, HY-B0941R, NWBJYWHLCVSVIJ-UHFFFAOYSA-, 6-Benzylaminopurine 100 microg/mL in Acetonitrile/Acetone, HMS1538O06, HMS1568F19, HMS1667I06, HMS2095F19, HMS2234B24, HMS3374C09, HMS3712F19, N-benzyladenine, monopotassium salt, 6-benzyladenine 6-benzylaminopurine, HY-B0941, NSC40818, STR06184, N-(phenylmethyl)-7H-purin-6-amine, Tox21_301307, AC7620, BDBM50205363, CCG-55533, GEO-00296, MFCD00051031, N-(Phenylmethyl)-9H-Purin-6-amine, s4511, STK858495, AKOS002304241, AKOS005257767, 7H-purin-6-amine, N-(phenylmethyl)-, AC-5488, CCG-220189, FB02966, KS-5285, PS-3425, 6-Benzylaminopurine, analytical standard, USEPA/OPP Pesticide Code: 116901, N-benzyl-9H-purin-6-amine, AldrichCPR, NCGC00016571-01, NCGC00016571-02, NCGC00016571-03, NCGC00016571-04, NCGC00016571-05, NCGC00255357-01, SY014632, 6-Benzylaminopurine, >=99.0% (HPLC), B1088, NS00005241, BA, N6-Benzyladenine, N6-Benzyladenine, BA, EN300-40176, 6-Benzylaminopurine, plant cell culture tested, Q419946, SR-01000644553, 6-Benzylaminopurine, Vetec(TM) reagent grade, 98%, SR-01000644553-1, SR-01000644553-2, BA, N6-Benzyladenine, N6-Benzyladenine, BA, BRD-K62929068-001-05-8, BRD-K62929068-001-15-7, BRD-K62929068-001-16-5, Z57245233, 6-Benzylaminopurine, ReagentPlus(R), >=99.0% (HPLC), F0578-0089, 2B76FFBD-3C3A-4349-9047-E5B8945B54A7, ((2r,3s,4r,5r)-5-(4-amino-2-oxopyrimidin-1(2h)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyltriphosph, InChI=1/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-12(15-7-14-10)17-8-16-11/h1-5,7-8H,6H2,(H2,13,14,15,16,17) |
|---|---|
| Topological Polar Surface Area | 66.5 |
| Hydrogen Bond Donor Count | 2.0 |
| Heavy Atom Count | 17.0 |
| Description | 6-Benzylaminopurine, benzyl adenine or BAP is a first-generation synthetic cytokinin which elicits plant growth and development responses, setting blossoms and stimulating fruit richness by stimulating cell division. It is an inhibitor of respiratory kinase in plants, and increases post-harvest life of green vegetables. Cytokinin B is found in wild celery and garden tomato (variety). |
| Isotope Atom Count | 0.0 |
| Molecular Complexity | 241.0 |
| Database Name | fooddb_chem_all;hmdb_chem_all;pubchem |
| Defined Atom Stereocenter Count | 0.0 |
| Iupac Name | N-benzyl-7H-purin-6-amine |
| Nih Violation | False |
| Class | Imidazopyrimidines |
| Xlogp | 2.1 |
| Superclass | Organoheterocyclic compounds |
| Is Pains | False |
| Subclass | Purines and purine derivatives |
| Molecular Formula | C12H11N5 |
| Inchi Key | NWBJYWHLCVSVIJ-UHFFFAOYSA-N |
| Rotatable Bond Count | 3.0 |
| State | Solid |
| Synonyms | 1H-Purin-6-amine, N-(phenylmethyl)-, 6-(Benzylamino)purine, 6-(N-Benzylamino)purine, 6-[(phenylmethyl)amino]-9H-purine, 6-BAP, 6-Benzyl adenine, 6-Benzyladenine, 6-Benzylaminopurine, 9H-Purin-6-amine, N-(phenylmethyl)-, 9H-Purine, 6-[(phenylmethyl)amino]-, Adenine, n-benzyl-, Adenine, N(sup 6)-benzyl-, Aminopurine, 6-benzyl, BAP, Benzyl(purin-6-yl)amine, Benzyladenine, Benzylaminopurine, Cytokinin B, N-(Phenylmethyl)-1H-purin-6-amine, N-(Phenylmethyl)-9H-purin-6-amine, N-6-Benzyladenine, N-benzyl-1H-purin-6-amine, N-Benzyl-9H-purin-6-amine, N-Benzyl-adenine, N-Benzyladenine, N-Benzyladenine, 8CI, N(6)-(benzylamino)purine, N(6)-Benzylaminopurine, N(sup 6)-(Benzylamino)purine, N(sup 6)-Benzyladenine, N(Sup6)-Benzyladenine, N6-Benzyladenine, 6-[(Phenylmethyl)amino]-9H-purine, Cytokinin b, N-BENZYL-9H-purin-6-amine, N(6)-(Benzylamino)purine, N-Benzyl-1H-purin-6-amine, N(6)-Benzyladenine, 6-BA CPD, 6-Benzylaminopurin, 6-BA, 6-Benzylaminoadenine, BA, N6-(Benzylamino)purine, N6-Benzylaminopurine |
| Substituent Name | 6-alkylaminopurine, Phenylmethylamine, Benzylamine, Aralkylamine, Secondary aliphatic/aromatic amine, Aminopyrimidine, Imidolactam, Benzenoid, Pyrimidine, Monocyclic benzene moiety, Heteroaromatic compound, Imidazole, Azole, Azacycle, Secondary amine, Hydrocarbon derivative, Organonitrogen compound, Amine, Aromatic heteropolycyclic compound |
| Compound Name | N6-Benzyladenine |
| Kingdom | Organic compounds |
| Exact Mass | 225.101 |
| Formal Charge | 0.0 |
| Brenk Violation | False |
| Monoisotopic Mass | 225.101 |
| Hydrogen Bond Acceptor Count | 4.0 |
| Molecular Weight | 225.25 |
| Covalent Unit Count | 1.0 |
| Total Atom Stereocenter Count | 0.0 |
| Total Bond Stereocenter Count | 0.0 |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Inchi | InChI=1S/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-12(15-7-14-10)17-8-16-11/h1-5,7-8H,6H2,(H2,13,14,15,16,17) |
| Smiles | C1=CC=C(C=C1)CNC2=NC=NC3=C2NC=N3 |
| Defined Bond Stereocenter Count | 0.0 |
| Taxonomy Direct Parent | 6-alkylaminopurines |
- 1. Outgoing r'ship
FOUND_INto/from Apium Graveolens (Plant) Rel Props:Source_db:fooddb_chem_all - 2. Outgoing r'ship
FOUND_INto/from Lycopersicon Esculentum (Plant) Rel Props:Source_db:fooddb_chem_all