Showing NP-Card for Daturametelin A (NP0332989)
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Version | 1.0 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Created at | 2024-05-03 03:56:23 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
Updated at | 2024-05-03 03:59:44 UTC | |||||||||||||||||||||||||||||||||||||||||||||||||||
NP-MRD ID | NP0332989 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Secondary Accession Numbers | None | |||||||||||||||||||||||||||||||||||||||||||||||||||
Natural Product Identification | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Common Name | Daturametelin A | |||||||||||||||||||||||||||||||||||||||||||||||||||
Description | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Structure | MOL for NP0332989 (Daturametelin A)Mrv2104 01152306332D 43 48 0 0 1 0 999 V2000 -5.6543 0.3469 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1480 -0.3044 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3307 -0.1916 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4589 -1.0686 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.2761 -1.1815 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.5870 -1.9456 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.4043 -2.0585 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -7.7151 -2.8227 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -7.2088 -3.4740 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.9106 -1.4072 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.7279 -1.5200 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -9.2342 -0.8687 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.0515 -0.9815 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -9.0387 -2.2842 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -9.8560 -2.3970 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.5324 -2.9355 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -8.8433 -3.6997 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.9525 -1.7199 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1353 -1.6071 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.8244 -0.8429 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0071 -0.7301 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.6962 0.0341 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5008 -1.3814 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7301 -2.1739 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0473 -2.6369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3959 -2.1305 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5838 -2.2757 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3035 -3.0516 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5086 -3.1969 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0404 -2.5662 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7601 -1.7902 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.4798 -1.0143 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0520 -1.6450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3323 -0.8691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1444 -0.7239 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6762 -1.3546 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.0361 -0.6122 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8526 -2.7114 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3844 -2.0807 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1041 -1.3047 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2920 -1.1595 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0117 -0.3836 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.2634 -2.4841 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 3 1 0 0 0 0 2 4 2 0 0 0 0 4 5 1 0 0 0 0 5 6 1 0 0 0 0 7 6 1 1 0 0 0 8 7 1 0 0 0 0 8 9 1 6 0 0 0 7 10 1 0 0 0 0 11 10 1 0 0 0 0 11 12 1 1 0 0 0 12 13 1 0 0 0 0 14 11 1 0 0 0 0 14 15 1 6 0 0 0 16 14 1 0 0 0 0 8 16 1 0 0 0 0 16 17 1 1 0 0 0 4 18 1 0 0 0 0 18 19 1 0 0 0 0 19 20 1 0 0 0 0 3 20 1 0 0 0 0 21 20 1 0 0 0 0 21 22 1 1 0 0 0 21 23 1 0 0 0 0 23 24 1 0 0 0 0 24 25 1 0 0 0 0 25 26 1 0 0 0 0 26 27 1 0 0 0 0 27 28 1 0 0 0 0 28 29 1 0 0 0 0 29 30 2 0 0 0 0 31 30 1 0 0 0 0 31 32 1 6 0 0 0 31 33 1 0 0 0 0 27 33 1 0 0 0 0 33 34 1 0 0 0 0 34 35 1 0 0 0 0 36 35 1 0 0 0 0 36 26 1 0 0 0 0 36 23 1 0 0 0 0 36 37 1 6 0 0 0 30 38 1 0 0 0 0 38 39 1 0 0 0 0 39 40 2 0 0 0 0 40 41 1 0 0 0 0 31 41 1 0 0 0 0 41 42 2 0 0 0 0 18 43 2 0 0 0 0 M END 3D SDF for NP0332989 (Daturametelin A)Mrv2104 01152306332D 43 48 0 0 1 0 999 V2000 -5.6543 0.3469 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.1480 -0.3044 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.3307 -0.1916 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -5.4589 -1.0686 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.2761 -1.1815 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -6.5870 -1.9456 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.4043 -2.0585 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -7.7151 -2.8227 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -7.2088 -3.4740 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -7.9106 -1.4072 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.7279 -1.5200 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -9.2342 -0.8687 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -10.0515 -0.9815 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -9.0387 -2.2842 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -9.8560 -2.3970 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -8.5324 -2.9355 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -8.8433 -3.6997 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -4.9525 -1.7199 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -4.1353 -1.6071 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -3.8244 -0.8429 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -3.0071 -0.7301 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 -2.6962 0.0341 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.5008 -1.3814 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.7301 -2.1739 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -2.0473 -2.6369 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.3959 -2.1305 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.5838 -2.2757 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3035 -3.0516 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.5086 -3.1969 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0404 -2.5662 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7601 -1.7902 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 0.4798 -1.0143 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0520 -1.6450 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.3323 -0.8691 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.1444 -0.7239 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -1.6762 -1.3546 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 -2.0361 -0.6122 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.8526 -2.7114 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.3844 -2.0807 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1041 -1.3047 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.2920 -1.1595 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.0117 -0.3836 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 -5.2634 -2.4841 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 1 2 1 0 0 0 0 2 3 1 0 0 0 0 2 4 2 0 0 0 0 4 5 1 0 0 0 0 5 6 1 0 0 0 0 7 6 1 1 0 0 0 8 7 1 0 0 0 0 8 9 1 6 0 0 0 7 10 1 0 0 0 0 11 10 1 0 0 0 0 11 12 1 1 0 0 0 12 13 1 0 0 0 0 14 11 1 0 0 0 0 14 15 1 6 0 0 0 16 14 1 0 0 0 0 8 16 1 0 0 0 0 16 17 1 1 0 0 0 4 18 1 0 0 0 0 18 19 1 0 0 0 0 19 20 1 0 0 0 0 3 20 1 0 0 0 0 21 20 1 0 0 0 0 21 22 1 1 0 0 0 21 23 1 0 0 0 0 23 24 1 0 0 0 0 24 25 1 0 0 0 0 25 26 1 0 0 0 0 26 27 1 0 0 0 0 27 28 1 0 0 0 0 28 29 1 0 0 0 0 29 30 2 0 0 0 0 31 30 1 0 0 0 0 31 32 1 6 0 0 0 31 33 1 0 0 0 0 27 33 1 0 0 0 0 33 34 1 0 0 0 0 34 35 1 0 0 0 0 36 35 1 0 0 0 0 36 26 1 0 0 0 0 36 23 1 0 0 0 0 36 37 1 6 0 0 0 30 38 1 0 0 0 0 38 39 1 0 0 0 0 39 40 2 0 0 0 0 40 41 1 0 0 0 0 31 41 1 0 0 0 0 41 42 2 0 0 0 0 18 43 2 0 0 0 0 M END > <DATABASE_ID> NP0332989 > <DATABASE_NAME> NP-MRD > <SMILES> C[C@@H](C1CCC2C3CC=C4CC=CC(=O)[C@]4(C)C3CC[C@]12C)C1CC(C)=C(CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(=O)O1 > <INCHI_IDENTIFIER> InChI=1S/C34H48O9/c1-17-14-25(42-31(40)21(17)16-41-32-30(39)29(38)28(37)26(15-35)43-32)18(2)22-10-11-23-20-9-8-19-6-5-7-27(36)34(19,4)24(20)12-13-33(22,23)3/h5,7-8,18,20,22-26,28-30,32,35,37-39H,6,9-16H2,1-4H3/t18-,20?,22?,23?,24?,25?,26+,28+,29-,30+,32+,33+,34-/m0/s1 > <INCHI_KEY> BUUVUQOPURMCQD-YBINBGNBSA-N > <FORMULA> C34H48O9 > <MOLECULAR_WEIGHT> 600.749 > <EXACT_MASS> 600.329833126 > <JCHEM_ACCEPTOR_COUNT> 8 > <JCHEM_ATOM_COUNT> 91 > <JCHEM_AVERAGE_POLARIZABILITY> 67.43163451749338 > <JCHEM_BIOAVAILABILITY> 1 > <JCHEM_DONOR_COUNT> 4 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> 6-[(1S)-1-[(9aR,11aS)-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,6H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]ethyl]-4-methyl-3-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,6-dihydro-2H-pyran-2-one > <JCHEM_LOGP> 3.397054933999999 > <JCHEM_MDDR_LIKE_RULE> 1 > <JCHEM_NUMBER_OF_RINGS> 6 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA> 13.200060336175227 > <JCHEM_PKA_STRONGEST_ACIDIC> 12.210491423472027 > <JCHEM_PKA_STRONGEST_BASIC> -2.981083553717509 > <JCHEM_POLAR_SURFACE_AREA> 142.75 > <JCHEM_REFRACTIVITY> 159.871 > <JCHEM_ROTATABLE_BOND_COUNT> 6 > <JCHEM_RULE_OF_FIVE> 0 > <JCHEM_TRADITIONAL_IUPAC> 6-[(1S)-1-[(9aR,11aS)-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,6H,9bH,10H,11H-cyclopenta[a]phenanthren-1-yl]ethyl]-4-methyl-3-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,6-dihydropyran-2-one > <JCHEM_VEBER_RULE> 0 $$$$ PDB for NP0332989 (Daturametelin A)HEADER PROTEIN 15-JAN-23 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 15-JAN-23 0 HETATM 1 C UNK 0 -10.555 0.648 0.000 0.00 0.00 C+0 HETATM 2 C UNK 0 -9.610 -0.568 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 -8.084 -0.358 0.000 0.00 0.00 C+0 HETATM 4 C UNK 0 -10.190 -1.995 0.000 0.00 0.00 C+0 HETATM 5 C UNK 0 -11.715 -2.205 0.000 0.00 0.00 C+0 HETATM 6 O UNK 0 -12.296 -3.632 0.000 0.00 0.00 O+0 HETATM 7 C UNK 0 -13.821 -3.843 0.000 0.00 0.00 C+0 HETATM 8 C UNK 0 -14.402 -5.269 0.000 0.00 0.00 C+0 HETATM 9 O UNK 0 -13.456 -6.485 0.000 0.00 0.00 O+0 HETATM 10 O UNK 0 -14.766 -2.627 0.000 0.00 0.00 O+0 HETATM 11 C UNK 0 -16.292 -2.837 0.000 0.00 0.00 C+0 HETATM 12 C UNK 0 -17.237 -1.622 0.000 0.00 0.00 C+0 HETATM 13 O UNK 0 -18.763 -1.832 0.000 0.00 0.00 O+0 HETATM 14 C UNK 0 -16.872 -4.264 0.000 0.00 0.00 C+0 HETATM 15 O UNK 0 -18.398 -4.474 0.000 0.00 0.00 O+0 HETATM 16 C UNK 0 -15.927 -5.480 0.000 0.00 0.00 C+0 HETATM 17 O UNK 0 -16.507 -6.906 0.000 0.00 0.00 O+0 HETATM 18 C UNK 0 -9.245 -3.211 0.000 0.00 0.00 C+0 HETATM 19 O UNK 0 -7.719 -3.000 0.000 0.00 0.00 O+0 HETATM 20 C UNK 0 -7.139 -1.573 0.000 0.00 0.00 C+0 HETATM 21 C UNK 0 -5.613 -1.363 0.000 0.00 0.00 C+0 HETATM 22 C UNK 0 -5.033 0.064 0.000 0.00 0.00 C+0 HETATM 23 C UNK 0 -4.668 -2.579 0.000 0.00 0.00 C+0 HETATM 24 C UNK 0 -5.096 -4.058 0.000 0.00 0.00 C+0 HETATM 25 C UNK 0 -3.822 -4.922 0.000 0.00 0.00 C+0 HETATM 26 C UNK 0 -2.606 -3.977 0.000 0.00 0.00 C+0 HETATM 27 C UNK 0 -1.090 -4.248 0.000 0.00 0.00 C+0 HETATM 28 C UNK 0 -0.567 -5.696 0.000 0.00 0.00 C+0 HETATM 29 C UNK 0 0.949 -5.967 0.000 0.00 0.00 C+0 HETATM 30 C UNK 0 1.942 -4.790 0.000 0.00 0.00 C+0 HETATM 31 C UNK 0 1.419 -3.342 0.000 0.00 0.00 C+0 HETATM 32 C UNK 0 0.896 -1.893 0.000 0.00 0.00 C+0 HETATM 33 C UNK 0 -0.097 -3.071 0.000 0.00 0.00 C+0 HETATM 34 C UNK 0 -0.620 -1.622 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 -2.136 -1.351 0.000 0.00 0.00 C+0 HETATM 36 C UNK 0 -3.129 -2.529 0.000 0.00 0.00 C+0 HETATM 37 C UNK 0 -3.801 -1.143 0.000 0.00 0.00 C+0 HETATM 38 C UNK 0 3.458 -5.061 0.000 0.00 0.00 C+0 HETATM 39 C UNK 0 4.451 -3.884 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 3.928 -2.436 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 2.412 -2.164 0.000 0.00 0.00 C+0 HETATM 42 O UNK 0 1.888 -0.716 0.000 0.00 0.00 O+0 HETATM 43 O UNK 0 -9.825 -4.637 0.000 0.00 0.00 O+0 CONECT 1 2 CONECT 2 1 3 4 CONECT 3 2 20 CONECT 4 2 5 18 CONECT 5 4 6 CONECT 6 5 7 CONECT 7 6 8 10 CONECT 8 7 9 16 CONECT 9 8 CONECT 10 7 11 CONECT 11 10 12 14 CONECT 12 11 13 CONECT 13 12 CONECT 14 11 15 16 CONECT 15 14 CONECT 16 14 8 17 CONECT 17 16 CONECT 18 4 19 43 CONECT 19 18 20 CONECT 20 19 3 21 CONECT 21 20 22 23 CONECT 22 21 CONECT 23 21 24 36 CONECT 24 23 25 CONECT 25 24 26 CONECT 26 25 27 36 CONECT 27 26 28 33 CONECT 28 27 29 CONECT 29 28 30 CONECT 30 29 31 38 CONECT 31 30 32 33 41 CONECT 32 31 CONECT 33 31 27 34 CONECT 34 33 35 CONECT 35 34 36 CONECT 36 35 26 23 37 CONECT 37 36 CONECT 38 30 39 CONECT 39 38 40 CONECT 40 39 41 CONECT 41 40 31 42 CONECT 42 41 CONECT 43 18 MASTER 0 0 0 0 0 0 0 0 43 0 96 0 END SMILES for NP0332989 (Daturametelin A)C[C@@H](C1CCC2C3CC=C4CC=CC(=O)[C@]4(C)C3CC[C@]12C)C1CC(C)=C(CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(=O)O1 INCHI for NP0332989 (Daturametelin A)InChI=1S/C34H48O9/c1-17-14-25(42-31(40)21(17)16-41-32-30(39)29(38)28(37)26(15-35)43-32)18(2)22-10-11-23-20-9-8-19-6-5-7-27(36)34(19,4)24(20)12-13-33(22,23)3/h5,7-8,18,20,22-26,28-30,32,35,37-39H,6,9-16H2,1-4H3/t18-,20?,22?,23?,24?,25?,26+,28+,29-,30+,32+,33+,34-/m0/s1 3D Structure for NP0332989 (Daturametelin A) | |||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Formula | C34H48O9 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Average Mass | 600.7490 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
Monoisotopic Mass | 600.32983 Da | |||||||||||||||||||||||||||||||||||||||||||||||||||
IUPAC Name | 6-[(1S)-1-[(9aR,11aS)-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,6H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]ethyl]-4-methyl-3-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,6-dihydro-2H-pyran-2-one | |||||||||||||||||||||||||||||||||||||||||||||||||||
Traditional Name | 6-[(1S)-1-[(9aR,11aS)-9a,11a-dimethyl-9-oxo-1H,2H,3H,3aH,3bH,4H,6H,9bH,10H,11H-cyclopenta[a]phenanthren-1-yl]ethyl]-4-methyl-3-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-5,6-dihydropyran-2-one | |||||||||||||||||||||||||||||||||||||||||||||||||||
CAS Registry Number | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
SMILES | C[C@@H](C1CCC2C3CC=C4CC=CC(=O)[C@]4(C)C3CC[C@]12C)C1CC(C)=C(CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C(=O)O1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Identifier | InChI=1S/C34H48O9/c1-17-14-25(42-31(40)21(17)16-41-32-30(39)29(38)28(37)26(15-35)43-32)18(2)22-10-11-23-20-9-8-19-6-5-7-27(36)34(19,4)24(20)12-13-33(22,23)3/h5,7-8,18,20,22-26,28-30,32,35,37-39H,6,9-16H2,1-4H3/t18-,20?,22?,23?,24?,25?,26+,28+,29-,30+,32+,33+,34-/m0/s1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
InChI Key | BUUVUQOPURMCQD-YBINBGNBSA-N | |||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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Predicted Spectra | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Not Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical Shift Submissions | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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Species | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Species of Origin |
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Chemical Taxonomy | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Classification | Not classified | |||||||||||||||||||||||||||||||||||||||||||||||||||
Physical Properties | ||||||||||||||||||||||||||||||||||||||||||||||||||||
State | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
Experimental Properties |
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Predicted Properties |
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External Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||
External Links | Not Available | |||||||||||||||||||||||||||||||||||||||||||||||||||
References | ||||||||||||||||||||||||||||||||||||||||||||||||||||
General References |
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