Showing NP-Card for Noonindole K (NP0331480)
Record Information | ||||||||||||||||
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Version | 1.0 | |||||||||||||||
Created at | 2023-02-01 04:00:33 UTC | |||||||||||||||
Updated at | 2024-05-13 01:13:54 UTC | |||||||||||||||
NP-MRD ID | NP0331480 | |||||||||||||||
Secondary Accession Numbers | None | |||||||||||||||
Natural Product Identification | ||||||||||||||||
Common Name | Noonindole K | |||||||||||||||
Description | Not Available | |||||||||||||||
Structure | MOL for NP0331480 (Noonindole K)Mrv1652302012305002D 47 53 0 0 1 0 999 V2000 3.4402 0.7048 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4433 -0.1202 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 3.3601 -0.9410 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 4.1126 -0.6026 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5538 -1.1156 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1957 0.2182 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 4.2789 1.0390 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0313 1.3773 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7005 0.8949 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 6.3698 0.4125 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 5.6174 0.0741 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 5.5342 -0.7467 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.2035 -1.2291 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.2866 -0.4083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.0390 -0.0699 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.1222 0.7509 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 7.8746 1.0893 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.2130 0.3368 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.6270 1.4276 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.2963 0.9452 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 10.0487 1.2836 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 10.1319 2.1044 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.7179 0.8012 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 11.4704 1.1396 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.6348 -0.0196 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 11.3040 -0.5020 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.8824 -0.3580 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 9.7992 -1.1788 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.0468 -1.5172 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.2131 0.1244 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.5362 1.8417 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.2054 1.5717 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4530 1.2333 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.7083 0.8838 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.8650 -0.2643 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 4.9481 0.5565 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 4.7818 -1.0851 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0294 -1.4234 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6884 0.2125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1386 -0.4026 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3837 -0.0699 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6313 -0.4083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0379 0.0741 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0452 0.8949 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7976 1.2333 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4669 0.7509 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2732 0.9254 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 2 1 1 1 0 0 0 2 3 1 0 0 0 0 3 4 1 6 0 0 0 3 5 1 0 0 0 0 2 6 1 0 0 0 0 6 7 1 0 0 0 0 7 8 1 0 0 0 0 8 9 1 0 0 0 0 9 10 1 1 0 0 0 9 11 1 0 0 0 0 11 12 1 6 0 0 0 12 13 1 0 0 0 0 11 14 1 0 0 0 0 14 15 1 0 0 0 0 15 16 1 0 0 0 0 16 17 1 6 0 0 0 17 18 1 0 0 0 0 17 19 1 0 0 0 0 20 19 1 1 0 0 0 20 21 1 0 0 0 0 21 22 1 1 0 0 0 21 23 1 0 0 0 0 23 24 1 1 0 0 0 23 25 1 0 0 0 0 25 26 1 6 0 0 0 25 27 1 0 0 0 0 27 28 1 1 0 0 0 28 29 1 0 0 0 0 27 30 1 0 0 0 0 20 30 1 0 0 0 0 17 31 1 0 0 0 0 16 32 1 1 0 0 0 16 33 1 0 0 0 0 9 33 1 0 0 0 0 6 34 1 6 0 0 0 6 35 1 0 0 0 0 11 35 1 0 0 0 0 35 36 1 1 0 0 0 35 37 1 0 0 0 0 37 38 1 0 0 0 0 3 38 1 0 0 0 0 2 39 1 0 0 0 0 39 40 2 0 0 0 0 5 40 1 0 0 0 0 40 41 1 0 0 0 0 41 42 2 0 0 0 0 42 43 1 0 0 0 0 43 44 2 0 0 0 0 44 45 1 0 0 0 0 45 46 2 0 0 0 0 41 46 1 0 0 0 0 46 47 1 0 0 0 0 39 47 1 0 0 0 0 M END 3D SDF for NP0331480 (Noonindole K)Mrv1652302012305002D 47 53 0 0 1 0 999 V2000 3.4402 0.7048 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 3.4433 -0.1202 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 3.3601 -0.9410 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 4.1126 -0.6026 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 2.5538 -1.1156 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.1957 0.2182 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 4.2789 1.0390 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.0313 1.3773 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 5.7005 0.8949 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 6.3698 0.4125 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 5.6174 0.0741 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 5.5342 -0.7467 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 6.2035 -1.2291 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6.2866 -0.4083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.0390 -0.0699 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.1222 0.7509 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 7.8746 1.0893 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.2130 0.3368 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.6270 1.4276 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.2963 0.9452 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 10.0487 1.2836 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 10.1319 2.1044 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.7179 0.8012 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 11.4704 1.1396 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 10.6348 -0.0196 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 11.3040 -0.5020 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.8824 -0.3580 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0 9.7992 -1.1788 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.0468 -1.5172 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 9.2131 0.1244 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 7.5362 1.8417 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 7.2054 1.5717 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 6.4530 1.2333 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 3.7083 0.8838 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.8650 -0.2643 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0 4.9481 0.5565 0.0000 H 0 0 0 0 0 0 0 0 0 0 0 0 4.7818 -1.0851 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 4.0294 -1.4234 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.6884 0.2125 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.1386 -0.4026 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.3837 -0.0699 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.6313 -0.4083 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 -0.0379 0.0741 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.0452 0.8949 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 0.7976 1.2333 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 1.4669 0.7509 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 2.2732 0.9254 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0 2 1 1 1 0 0 0 2 3 1 0 0 0 0 3 4 1 6 0 0 0 3 5 1 0 0 0 0 2 6 1 0 0 0 0 6 7 1 0 0 0 0 7 8 1 0 0 0 0 8 9 1 0 0 0 0 9 10 1 1 0 0 0 9 11 1 0 0 0 0 11 12 1 6 0 0 0 12 13 1 0 0 0 0 11 14 1 0 0 0 0 14 15 1 0 0 0 0 15 16 1 0 0 0 0 16 17 1 6 0 0 0 17 18 1 0 0 0 0 17 19 1 0 0 0 0 20 19 1 1 0 0 0 20 21 1 0 0 0 0 21 22 1 1 0 0 0 21 23 1 0 0 0 0 23 24 1 1 0 0 0 23 25 1 0 0 0 0 25 26 1 6 0 0 0 25 27 1 0 0 0 0 27 28 1 1 0 0 0 28 29 1 0 0 0 0 27 30 1 0 0 0 0 20 30 1 0 0 0 0 17 31 1 0 0 0 0 16 32 1 1 0 0 0 16 33 1 0 0 0 0 9 33 1 0 0 0 0 6 34 1 6 0 0 0 6 35 1 0 0 0 0 11 35 1 0 0 0 0 35 36 1 1 0 0 0 35 37 1 0 0 0 0 37 38 1 0 0 0 0 3 38 1 0 0 0 0 2 39 1 0 0 0 0 39 40 2 0 0 0 0 5 40 1 0 0 0 0 40 41 1 0 0 0 0 41 42 2 0 0 0 0 42 43 1 0 0 0 0 43 44 2 0 0 0 0 44 45 1 0 0 0 0 45 46 2 0 0 0 0 41 46 1 0 0 0 0 46 47 1 0 0 0 0 39 47 1 0 0 0 0 M END > <DATABASE_ID> NP0331480 > <DATABASE_NAME> NP-MRD > <SMILES> [H][C@]12CC3=C(NC4=CC=CC=C34)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(CC[C@@]3(CO)[C@]1([H])CC2)C(C)(C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O > <INCHI_IDENTIFIER> InChI=1S/C34H49NO8/c1-31(2,43-30-28(40)27(39)26(38)22(16-36)41-30)24-12-14-34(17-37)23-10-9-18-15-20-19-7-5-6-8-21(19)35-29(20)33(18,4)32(23,3)13-11-25(34)42-24/h5-8,18,22-28,30,35-40H,9-17H2,1-4H3/t18-,22+,23+,24-,25-,26+,27-,28-,30-,32-,33+,34+/m0/s1 > <INCHI_KEY> ZXLLAVVXCSIHAT-CGSQOTMISA-N > <FORMULA> C34H49NO8 > <MOLECULAR_WEIGHT> 599.765 > <EXACT_MASS> 599.345817542 > <JCHEM_ACCEPTOR_COUNT> 8 > <JCHEM_ATOM_COUNT> 92 > <JCHEM_AVERAGE_POLARIZABILITY> 68.07235951270582 > <JCHEM_BIOAVAILABILITY> 0 > <JCHEM_DONOR_COUNT> 6 > <JCHEM_FORMAL_CHARGE> 0 > <JCHEM_GHOSE_FILTER> 0 > <JCHEM_IUPAC> (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-({2-[(1S,2S,5S,7S,10S,11R,14S)-10-(hydroxymethyl)-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-yl}oxy)oxane-3,4,5-triol > <JCHEM_LOGP> 2.584315337333332 > <JCHEM_MDDR_LIKE_RULE> 0 > <JCHEM_NUMBER_OF_RINGS> 7 > <JCHEM_PHYSIOLOGICAL_CHARGE> 0 > <JCHEM_PKA> 13.193978879926679 > <JCHEM_PKA_STRONGEST_ACIDIC> 12.209381498958729 > <JCHEM_PKA_STRONGEST_BASIC> -2.789449285075439 > <JCHEM_POLAR_SURFACE_AREA> 144.63 > <JCHEM_REFRACTIVITY> 159.21469999999997 > <JCHEM_ROTATABLE_BOND_COUNT> 5 > <JCHEM_RULE_OF_FIVE> 0 > <JCHEM_TRADITIONAL_IUPAC> (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-({2-[(1S,2S,5S,7S,10S,11R,14S)-10-(hydroxymethyl)-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-yl}oxy)oxane-3,4,5-triol > <JCHEM_VEBER_RULE> 0 $$$$ PDB for NP0331480 (Noonindole K)HEADER PROTEIN 01-FEB-23 NONE TITLE NULL COMPND NULL SOURCE NULL KEYWDS NULL EXPDTA NULL AUTHOR Marvin REVDAT 1 01-FEB-23 0 HETATM 1 C UNK 0 6.422 1.316 0.000 0.00 0.00 C+0 HETATM 2 C UNK 0 6.428 -0.224 0.000 0.00 0.00 C+0 HETATM 3 C UNK 0 6.272 -1.757 0.000 0.00 0.00 C+0 HETATM 4 H UNK 0 7.677 -1.125 0.000 0.00 0.00 H+0 HETATM 5 C UNK 0 4.767 -2.082 0.000 0.00 0.00 C+0 HETATM 6 C UNK 0 7.832 0.407 0.000 0.00 0.00 C+0 HETATM 7 C UNK 0 7.987 1.939 0.000 0.00 0.00 C+0 HETATM 8 C UNK 0 9.392 2.571 0.000 0.00 0.00 C+0 HETATM 9 C UNK 0 10.641 1.671 0.000 0.00 0.00 C+0 HETATM 10 H UNK 0 11.890 0.770 0.000 0.00 0.00 H+0 HETATM 11 C UNK 0 10.486 0.138 0.000 0.00 0.00 C+0 HETATM 12 C UNK 0 10.331 -1.394 0.000 0.00 0.00 C+0 HETATM 13 O UNK 0 11.580 -2.294 0.000 0.00 0.00 O+0 HETATM 14 C UNK 0 11.735 -0.762 0.000 0.00 0.00 C+0 HETATM 15 C UNK 0 13.140 -0.131 0.000 0.00 0.00 C+0 HETATM 16 C UNK 0 13.295 1.402 0.000 0.00 0.00 C+0 HETATM 17 C UNK 0 14.699 2.033 0.000 0.00 0.00 C+0 HETATM 18 C UNK 0 15.331 0.629 0.000 0.00 0.00 C+0 HETATM 19 O UNK 0 16.104 2.665 0.000 0.00 0.00 O+0 HETATM 20 C UNK 0 17.353 1.764 0.000 0.00 0.00 C+0 HETATM 21 C UNK 0 18.758 2.396 0.000 0.00 0.00 C+0 HETATM 22 O UNK 0 18.913 3.928 0.000 0.00 0.00 O+0 HETATM 23 C UNK 0 20.007 1.496 0.000 0.00 0.00 C+0 HETATM 24 O UNK 0 21.411 2.127 0.000 0.00 0.00 O+0 HETATM 25 C UNK 0 19.852 -0.037 0.000 0.00 0.00 C+0 HETATM 26 O UNK 0 21.101 -0.937 0.000 0.00 0.00 O+0 HETATM 27 C UNK 0 18.447 -0.668 0.000 0.00 0.00 C+0 HETATM 28 C UNK 0 18.292 -2.200 0.000 0.00 0.00 C+0 HETATM 29 O UNK 0 16.887 -2.832 0.000 0.00 0.00 O+0 HETATM 30 O UNK 0 17.198 0.232 0.000 0.00 0.00 O+0 HETATM 31 C UNK 0 14.068 3.438 0.000 0.00 0.00 C+0 HETATM 32 H UNK 0 13.450 2.934 0.000 0.00 0.00 H+0 HETATM 33 O UNK 0 12.046 2.302 0.000 0.00 0.00 O+0 HETATM 34 C UNK 0 6.922 1.650 0.000 0.00 0.00 C+0 HETATM 35 C UNK 0 9.081 -0.493 0.000 0.00 0.00 C+0 HETATM 36 H UNK 0 9.237 1.039 0.000 0.00 0.00 H+0 HETATM 37 C UNK 0 8.926 -2.025 0.000 0.00 0.00 C+0 HETATM 38 C UNK 0 7.522 -2.657 0.000 0.00 0.00 C+0 HETATM 39 C UNK 0 5.018 0.397 0.000 0.00 0.00 C+0 HETATM 40 C UNK 0 3.992 -0.752 0.000 0.00 0.00 C+0 HETATM 41 C UNK 0 2.583 -0.131 0.000 0.00 0.00 C+0 HETATM 42 C UNK 0 1.178 -0.762 0.000 0.00 0.00 C+0 HETATM 43 C UNK 0 -0.071 0.138 0.000 0.00 0.00 C+0 HETATM 44 C UNK 0 0.084 1.671 0.000 0.00 0.00 C+0 HETATM 45 C UNK 0 1.489 2.302 0.000 0.00 0.00 C+0 HETATM 46 C UNK 0 2.738 1.402 0.000 0.00 0.00 C+0 HETATM 47 N UNK 0 4.243 1.727 0.000 0.00 0.00 N+0 CONECT 1 2 CONECT 2 1 3 6 39 CONECT 3 2 4 5 38 CONECT 4 3 CONECT 5 3 40 CONECT 6 2 7 34 35 CONECT 7 6 8 CONECT 8 7 9 CONECT 9 8 10 11 33 CONECT 10 9 CONECT 11 9 12 14 35 CONECT 12 11 13 CONECT 13 12 CONECT 14 11 15 CONECT 15 14 16 CONECT 16 15 17 32 33 CONECT 17 16 18 19 31 CONECT 18 17 CONECT 19 17 20 CONECT 20 19 21 30 CONECT 21 20 22 23 CONECT 22 21 CONECT 23 21 24 25 CONECT 24 23 CONECT 25 23 26 27 CONECT 26 25 CONECT 27 25 28 30 CONECT 28 27 29 CONECT 29 28 CONECT 30 27 20 CONECT 31 17 CONECT 32 16 CONECT 33 16 9 CONECT 34 6 CONECT 35 6 11 36 37 CONECT 36 35 CONECT 37 35 38 CONECT 38 37 3 CONECT 39 2 40 47 CONECT 40 39 5 41 CONECT 41 40 42 46 CONECT 42 41 43 CONECT 43 42 44 CONECT 44 43 45 CONECT 45 44 46 CONECT 46 45 41 47 CONECT 47 46 39 MASTER 0 0 0 0 0 0 0 0 47 0 106 0 END SMILES for NP0331480 (Noonindole K)[H][C@]12CC3=C(NC4=CC=CC=C34)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(CC[C@@]3(CO)[C@]1([H])CC2)C(C)(C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O INCHI for NP0331480 (Noonindole K)InChI=1S/C34H49NO8/c1-31(2,43-30-28(40)27(39)26(38)22(16-36)41-30)24-12-14-34(17-37)23-10-9-18-15-20-19-7-5-6-8-21(19)35-29(20)33(18,4)32(23,3)13-11-25(34)42-24/h5-8,18,22-28,30,35-40H,9-17H2,1-4H3/t18-,22+,23+,24-,25-,26+,27-,28-,30-,32-,33+,34+/m0/s1 3D Structure for NP0331480 (Noonindole K) | |||||||||||||||
Synonyms | Not Available | |||||||||||||||
Chemical Formula | C34H49NO8 | |||||||||||||||
Average Mass | 599.7650 Da | |||||||||||||||
Monoisotopic Mass | 599.34582 Da | |||||||||||||||
IUPAC Name | Not Available | |||||||||||||||
Traditional Name | Not Available | |||||||||||||||
CAS Registry Number | Not Available | |||||||||||||||
SMILES | [H][C@]12CC3=C(NC4=CC=CC=C34)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(CC[C@@]3(CO)[C@]1([H])CC2)C(C)(C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O | |||||||||||||||
InChI Identifier | InChI=1S/C34H49NO8/c1-31(2,43-30-28(40)27(39)26(38)22(16-36)41-30)24-12-14-34(17-37)23-10-9-18-15-20-19-7-5-6-8-21(19)35-29(20)33(18,4)32(23,3)13-11-25(34)42-24/h5-8,18,22-28,30,35-40H,9-17H2,1-4H3/t18-,22+,23+,24-,25-,26+,27-,28-,30-,32-,33+,34+/m0/s1 | |||||||||||||||
InChI Key | ZXLLAVVXCSIHAT-CGSQOTMISA-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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