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17215925 ChemSpider C10H18O (S)-alpha-Terpineol 154.13577 3702 TAXONOMY 470-82-6 CAS CPD-4261 BioCyc CL:0000000 CELL TYPE ONTOLOGY 937 ChemSpider 7785-53-7 CAS SMILES CC(C)=CCC[C@](C)(O)C=C 14073-97-3 CAS HMDB00250 HMDB C00553 KEGG Compound CHEBI:17221 ChEBI 2216-52-6 CAS SMILES O 1.0 HMDB35763 HMDB SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS GERANYL-PP BioCyc ReactionCatalysis39973 ACTIVATION ReactionCatalysis39971 ACTIVATION C00843 KEGG Compound Terpenoid Backbone Biosynthesis SubPathway 1.0 ReactionCatalysis39972 ACTIVATION 5675 ChemSpider 1.0 ReactionCatalysis39970 ACTIVATION 442501 PubChem-compound SubPathwayInteraction6597 SubPathway6597Reaction SubPathwayReaction Q9LRZ6 UniProt HMDB36102 HMDB S-(+)-linalool synthase 1.0 BiologicalState151 Arabidopsis thaliana, Cell, Cytosol 439263 PubChem-compound 559142 ChemSpider tricyclene synthase ReactionCatalysis39968 ACTIVATION ReactionCatalysis39969 ACTIVATION Eucalyptol Geranyl-PP SubPathwayOutput Cell P0DI76 UniProt SMILES CC1=CC[C@@H](CC1)C(C)(C)O 53-59-8 CAS 28993 ChemSpider D-Linalool Water 1038 PubChem-compound HMDB01285 HMDB 7732-18-5 CAS 1.0 (S)-alpha-Terpineol CHEBI:16474 ChEBI GO:0005829 GENE ONTOLOGY HMDB59597 HMDB GO:0009507 GENE ONTOLOGY PW015068 PathWhiz 1,8-cineole synthase 1 beta-myrcene/(E)-beta-ocimene synthase 2 (+)-neomenthol dehydrogenase Q9M2E2 UniProt 31253 PubChem-compound C10H20O (+)-Neomenthol 156.15141 C00341 KEGG Compound http://identifiers.org/smpdb/SMP14204 SMPDB CHEBI:17211 ChEBI 1010 ChemSpider 1.0 PPI BioCyc HMDB36086 HMDB 2758 PubChem-compound (+)-Neomenthol C21H30N7O17P3 NADPH 745.0911 C21H29N7O17P3 NADP 744.08325 123-35-3 CAS 962 PubChem-compound 2656 ChemSpider NADPH BioCyc C10H18O (-)-Menthone 154.13577 Pyrophosphate 1.0 CHEBI:15402 ChEBI HMDB00217 HMDB 4.2.3.25 false 4.2.3.25 Geranyl-PP + Water → D-Linalool + Pyrophosphate LEFT_TO_RIGHT Cytosol (-)-Menthone Reaction49845 false Geranyl-PP → 7-Methyl-3-methylene-1,6-octadiene + Pyrophosphate LEFT_TO_RIGHT BiologicalState225 Arabidopsis thaliana, Cell, chloroplast Reaction49844 false Geranyl-PP → 7-Methyl-3-methylene-1,6-octadiene + Pyrophosphate LEFT_TO_RIGHT 7-Methyl-3-methylene-1,6-octadiene Reaction49847 false (S)-alpha-Terpineol → Eucalyptol LEFT_TO_RIGHT C09844 KEGG Compound HMDB02111 HMDB 1.0 4.2.3.108 false 4.2.3.108 Geranyl-PP + Water → (S)-alpha-Terpineol + Pyrophosphate LEFT_TO_RIGHT 388397 ChemSpider 1.1.1.208 false 1.1.1.208 (-)-Menthone + Hydrogen Ion + NADPH → (+)-Neomenthol + NADP LEFT_TO_RIGHT C00080 KEGG Compound beta-myrcene/(E)-beta-ocimene synthase 2 67179 PubChem-compound HMDB35162 HMDB C10H20O7P2 Geranyl-PP 314.06842 CHEBI:15377 ChEBI CHEBI:15410 ChEBI HMDB00221 HMDB C10H16 7-Methyl-3-methylene-1,6-octadiene 136.1252 SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O 1.0 CHEBI:15378 ChEBI SMILES [H+] C00006 KEGG Compound Hydrogen Ion CHEBI:18009 ChEBI C00001 KEGG Compound 1,8-cineole synthase 1 5886 PubChem-compound S-(+)-linalool synthase CHEBI:18361 ChEBI CHEBI:584235 ChEBI C00005 KEGG Compound 390927 ChemSpider NADPH tricyclene synthase HMDB38169 HMDB SMILES NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O SMILES NC(=O)C1=CN(C=CC1)[C@H]1O[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2O[C@@H]([C@@H](OP(O)(O)=O)[C@H]2O)N2C=NC3=C(N)N=CN=C23)[C@H](O)[C@@H]1O C06074 KEGG Compound CHEBI:300 ChEBI 1.0 393471 ChemSpider C10H18O Eucalyptol 154.13577 SMILES CC(C)[C@@H]1CC[C@@H](C)CC1=O 53-57-6 CAS 644102 PubChem-compound 1.0 1.0 763-10-0 CAS CHEBI:98 ChEBI HMDB04472 HMDB C09902 KEGG Compound C10H18O D-Linalool 154.13577 C00013 KEGG Compound O7P2 Pyrophosphate 173.91193 24636 ChemSpider 22833512 PubChem-compound NAD(P) BioCyc SMILES CC(C)=CCC\C(C)=C\CO[P@@](=O)(O)OP(=O)(O)O H2O Water 18.010565 (+)-neomenthol dehydrogenase C11389 KEGG Compound 26447 PubChem-compound Q84UV0 UniProt H Hydrogen Ion 1.007825 126-90-9 CAS SMILES CC(C)=CCCC(=C)C=C 445995 PubChem-compound Q9ZUH4 UniProt Monoterpenoid Biosynthesis chloroplast 391430 ChemSpider SMILES CC12CCC(CC1)C(C)(C)O2 NADP S-(+)-linalool synthase tricyclene synthase beta- myrcene/(E)- beta-ocimene synthase 2 1,8-cineole synthase 1,8-cineole synthase (+)-neomenthol dehydrogenase Geranyl-PP H 2 O D-Linalool PP i PP i 7-Methyl-3- methylene- 1,6-octadiene PP i H 2 O (S)-alpha- Terpineol PP i Eucalyptol (-)-Menthone NADPH H + (+)-Neomenthol NADP Magnesium Magnesium Magnesium Magnesium Magnesium Terpenoid Backbone Biosynthesis Chloroplast Stroma Cytosol
17215925 ChemSpider C10H18O (S)-alpha-Terpineol 154.13577 3702 TAXONOMY 470-82-6 CAS CPD-4261 BioCyc CL:0000000 CELL TYPE ONTOLOGY 937 ChemSpider 7785-53-7 CAS SMILES CC(C)=CCC[C@](C)(O)C=C 14073-97-3 CAS HMDB00250 HMDB C00553 KEGG Compound CHEBI:17221 ChEBI 2216-52-6 CAS SMILES O 1.0 HMDB35763 HMDB SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS GERANYL-PP BioCyc ReactionCatalysis39973 ACTIVATION ReactionCatalysis39971 ACTIVATION C00843 KEGG Compound Terpenoid Backbone Biosynthesis SubPathway 1.0 ReactionCatalysis39972 ACTIVATION 5675 ChemSpider 1.0 ReactionCatalysis39970 ACTIVATION 442501 PubChem-compound SubPathwayInteraction6597 SubPathway6597Reaction SubPathwayReaction Q9LRZ6 UniProt HMDB36102 HMDB S-(+)-linalool synthase 1.0 BiologicalState151 Arabidopsis thaliana, Cell, Cytosol 439263 PubChem-compound 559142 ChemSpider tricyclene synthase ReactionCatalysis39968 ACTIVATION ReactionCatalysis39969 ACTIVATION Eucalyptol Geranyl-PP SubPathwayOutput Cell P0DI76 UniProt SMILES CC1=CC[C@@H](CC1)C(C)(C)O 53-59-8 CAS 28993 ChemSpider D-Linalool Water 1038 PubChem-compound HMDB01285 HMDB 7732-18-5 CAS 1.0 (S)-alpha-Terpineol CHEBI:16474 ChEBI GO:0005829 GENE ONTOLOGY HMDB59597 HMDB GO:0009507 GENE ONTOLOGY PW015068 PathWhiz 1,8-cineole synthase 1 beta-myrcene/(E)-beta-ocimene synthase 2 (+)-neomenthol dehydrogenase Q9M2E2 UniProt 31253 PubChem-compound C10H20O (+)-Neomenthol 156.15141 C00341 KEGG Compound http://identifiers.org/smpdb/SMP14204 SMPDB CHEBI:17211 ChEBI 1010 ChemSpider 1.0 PPI BioCyc HMDB36086 HMDB 2758 PubChem-compound (+)-Neomenthol C21H30N7O17P3 NADPH 745.0911 C21H29N7O17P3 NADP 744.08325 123-35-3 CAS 962 PubChem-compound 2656 ChemSpider NADPH BioCyc C10H18O (-)-Menthone 154.13577 Pyrophosphate 1.0 CHEBI:15402 ChEBI HMDB00217 HMDB 4.2.3.25 false 4.2.3.25 Geranyl-PP + Water → D-Linalool + Pyrophosphate LEFT_TO_RIGHT Cytosol (-)-Menthone Reaction49845 false Geranyl-PP → 7-Methyl-3-methylene-1,6-octadiene + Pyrophosphate LEFT_TO_RIGHT BiologicalState225 Arabidopsis thaliana, Cell, chloroplast Reaction49844 false Geranyl-PP → 7-Methyl-3-methylene-1,6-octadiene + Pyrophosphate LEFT_TO_RIGHT 7-Methyl-3-methylene-1,6-octadiene Reaction49847 false (S)-alpha-Terpineol → Eucalyptol LEFT_TO_RIGHT C09844 KEGG Compound HMDB02111 HMDB 1.0 4.2.3.108 false 4.2.3.108 Geranyl-PP + Water → (S)-alpha-Terpineol + Pyrophosphate LEFT_TO_RIGHT 388397 ChemSpider 1.1.1.208 false 1.1.1.208 (-)-Menthone + Hydrogen Ion + NADPH → (+)-Neomenthol + NADP LEFT_TO_RIGHT C00080 KEGG Compound beta-myrcene/(E)-beta-ocimene synthase 2 67179 PubChem-compound HMDB35162 HMDB C10H20O7P2 Geranyl-PP 314.06842 CHEBI:15377 ChEBI CHEBI:15410 ChEBI HMDB00221 HMDB C10H16 7-Methyl-3-methylene-1,6-octadiene 136.1252 SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O 1.0 CHEBI:15378 ChEBI SMILES [H+] C00006 KEGG Compound Hydrogen Ion CHEBI:18009 ChEBI C00001 KEGG Compound 1,8-cineole synthase 1 5886 PubChem-compound S-(+)-linalool synthase CHEBI:18361 ChEBI CHEBI:584235 ChEBI C00005 KEGG Compound 390927 ChemSpider NADPH tricyclene synthase HMDB38169 HMDB SMILES NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O SMILES NC(=O)C1=CN(C=CC1)[C@H]1O[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2O[C@@H]([C@@H](OP(O)(O)=O)[C@H]2O)N2C=NC3=C(N)N=CN=C23)[C@H](O)[C@@H]1O C06074 KEGG Compound CHEBI:300 ChEBI 1.0 393471 ChemSpider C10H18O Eucalyptol 154.13577 SMILES CC(C)[C@@H]1CC[C@@H](C)CC1=O 53-57-6 CAS 644102 PubChem-compound 1.0 1.0 763-10-0 CAS CHEBI:98 ChEBI HMDB04472 HMDB C09902 KEGG Compound C10H18O D-Linalool 154.13577 C00013 KEGG Compound O7P2 Pyrophosphate 173.91193 24636 ChemSpider 22833512 PubChem-compound NAD(P) BioCyc SMILES CC(C)=CCC\C(C)=C\CO[P@@](=O)(O)OP(=O)(O)O H2O Water 18.010565 (+)-neomenthol dehydrogenase C11389 KEGG Compound 26447 PubChem-compound Q84UV0 UniProt H Hydrogen Ion 1.007825 126-90-9 CAS SMILES CC(C)=CCCC(=C)C=C 445995 PubChem-compound Q9ZUH4 UniProt Monoterpenoid Biosynthesis chloroplast 391430 ChemSpider SMILES CC12CCC(CC1)C(C)(C)O2 NADP Chloroplast TPS14 TPS10 TPS24 TPS27 TPS27 SDR1 Geranyl-PP Water D-Linalool Pyrophosphate Pyrophosphate 7-Methyl-3- methylene- 1,6-octadiene Pyrophosphate Water (S)-alpha- Terpineol Pyrophosphate Eucalyptol (-)-Menthone NADPH Hydrogen Ion (+)-Neomenthol NADP Terpenoid Backbone Biosynthesis