1.0 2016-10-03 18:34:06 UTC 2020-04-22 15:49:01 UTC BMDB0012204 BMDB12204 Cis-zeatin (e)-2-Methyl-4-(1H-purin-6-ylamino)-2-buten-1-ol (e)-2-Methyl-4-(1H-purin-6-ylamino)but-2-en-1-ol (e)-2-Methyl-4-(purin-6-ylamino)-2-buten-1-ol (e)-Zeatin N6-(4-Hydroxyisopentenyl)adenine trans-Zeatin Zeatin (2E)-2-Methyl-4-(9H-purin-6-ylamino)-2-buten-1-ol 6-(4-Hydroxy-3-methyl-trans-2-butenylamino)purine N6-(4-Hydroxy-3-methyl-trans-2-butenyl)adenine ZT ZTA Zeatine trans-6-(4-Hydroxy-3-methylbut-2-enyl)amino purine C10H13N5O 219.2431 219.112010063 (2E)-2-methyl-4-[(1H-purin-6-yl)amino]but-2-en-1-ol (2E)-2-methyl-4-(1H-purin-6-ylamino)but-2-en-1-ol 32771-64-5 C\C(CO)=C/CNC1=C2N=CN=C2N=CN1 InChI=1S/C10H13N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h2,5-6,16H,3-4H2,1H3,(H2,11,12,13,14,15)/b7-2+ UZKQTCBAMSWPJD-FARCUNLSSA-N belongs to the class of organic compounds known as 6-alkylaminopurines. 6-alkylaminopurines are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring. Organic compounds Organoheterocyclic compounds Imidazopyrimidines Purines and purine derivatives 6-alkylaminopurines Aminopyrimidines and derivatives Azacyclic compounds Heteroaromatic compounds Hydrocarbon derivatives Imidazoles Imidolactams Organopnictogen compounds Primary alcohols Secondary alkylarylamines 6-alkylaminopurine Alcohol Amine Aminopyrimidine Aromatic heteropolycyclic compound Azacycle Azole Heteroaromatic compound Hydrocarbon derivative Imidazole Imidolactam Organic nitrogen compound Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Primary alcohol Pyrimidine Secondary aliphatic/aromatic amine Secondary amine Aromatic heteropolycyclic compounds zeatin Solid logp -0.32 ALOGPS logs -2.73 ALOGPS logp -0.34 ChemAxon pka_strongest_acidic 6.11 ChemAxon pka_strongest_basic 0.3 ChemAxon iupac (2E)-2-methyl-4-[(1H-purin-6-yl)amino]but-2-en-1-ol ChemAxon average_mass 219.2431 ChemAxon mono_mass 219.112010063 ChemAxon smiles C\C(CO)=C/CNC1=C2N=CN=C2N=CN1 ChemAxon formula C10H13N5O ChemAxon inchi InChI=1S/C10H13N5O/c1-7(4-16)2-3-11-9-8-10(13-5-12-8)15-6-14-9/h2,5-6,16H,3-4H2,1H3,(H2,11,12,13,14,15)/b7-2+ ChemAxon inchikey UZKQTCBAMSWPJD-FARCUNLSSA-N ChemAxon polar_surface_area 86.72 ChemAxon refractivity 63.3 ChemAxon polarizability 23 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 5 ChemAxon donor_count 3 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon number_of_rings 2 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::NmrOneD 3849 Specdb::NmrOneD 4116 Specdb::NmrOneD 95758 Specdb::NmrOneD 95759 Specdb::NmrOneD 95760 Specdb::NmrOneD 95761 Specdb::NmrOneD 95762 Specdb::NmrOneD 95763 Specdb::NmrOneD 95764 Specdb::NmrOneD 95765 Specdb::NmrOneD 95766 Specdb::NmrOneD 95767 Specdb::NmrOneD 95768 Specdb::NmrOneD 95769 Specdb::NmrOneD 95770 Specdb::NmrOneD 95771 Specdb::NmrOneD 95772 Specdb::NmrOneD 95773 Specdb::NmrOneD 95774 Specdb::NmrOneD 95775 Specdb::NmrOneD 95776 Specdb::NmrOneD 95777 Specdb::MsMs 87972 Specdb::MsMs 87973 Specdb::MsMs 87974 Specdb::MsMs 150600 Specdb::MsMs 150601 Specdb::MsMs 150602 Specdb::MsMs 374589 Specdb::MsMs 438608 Specdb::MsMs 438609 Specdb::MsMs 438610 Specdb::MsMs 438611 Specdb::MsMs 438612 Specdb::MsMs 439197 Specdb::MsMs 439460 Specdb::MsMs 439462 Specdb::MsMs 439464 Specdb::MsMs 439683 Specdb::MsMs 439684 Specdb::MsMs 439685 Specdb::MsMs 439686 Specdb::MsMs 447184 Specdb::MsMs 447185 Specdb::MsMs 447186 Specdb::MsMs 447187 Specdb::MsMs 447188 Specdb::CMs 2079 Specdb::CMs 6009 Specdb::CMs 31562 Specdb::CMs 39862 Specdb::CMs 137898 Specdb::CMs 145632 FDB002239 395716 449093 C00371 16522 DB11337 ZEA C00000091 CPD-4210 Zeatin