NP-MRD: Showing NP-Card for (4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate (NP0292716)

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Record Information

Version

2.0

Created at

2022-09-10 00:23:00 UTC

Updated at

2022-09-10 00:23:00 UTC

NP-MRD ID

NP0292716

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate

Description

Floridanine belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. (4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate is found in Doronicum macrophyllum, Packera aurea, Senecio inaequidens and Jacobaea othonnae. Based on a literature review very few articles have been published on Floridanine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102202232D          

 31 32  0  0  1  0            999 V2000
    5.0056   -0.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6295    0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4089   -0.0594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4741    1.0213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6947    1.2918    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5636    0.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698    1.2794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4466    1.9876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4680    0.5588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6431    0.5464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200    1.2546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4626    0.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6957    1.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3686    1.9891    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4563    1.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6729    2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4302    3.0831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1985    2.6834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6002    3.4040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4252    3.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8269    4.1370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8483    2.7082    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9794    3.5227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4723    3.2479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2517    2.9774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3169    4.0581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6732    2.7206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0964    2.0124    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9213    2.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217    1.9752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818    2.4701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 24 26  1  1  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  1  0  0  0
 18 30  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  2  0  0  0  0
M  END

     RDKit          3D

 62 63  0  0  0  0  0  0  0  0999 V2000
   -2.1904    2.5162    2.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5466    1.7390    0.9975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7134    1.3433    0.8946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6642    1.4510    0.0036 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8866    0.7376   -1.1770 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8099    1.4757   -2.1319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5780    0.6844   -1.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4058   -0.3468   -2.6387 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3865    1.6182   -1.9129 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6841    2.6167   -0.9760 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6378    2.0202   -0.0003 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    2.8146   -0.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2174    2.7456   -0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4797    1.4362    0.5877 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8855    1.2899    0.8599 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9322    0.3436   -0.1780 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2280   -0.6925    0.6596 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7118   -0.6013    0.4230 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0082   -1.4718    1.2396 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2055   -2.5398    0.9544 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5969   -3.7277    1.2191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1446   -2.5005    0.3405 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0592   -2.8994   -1.0115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9655   -3.5946    1.0277 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2834   -3.8498    0.3483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1493   -3.3423    2.3722 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8486   -1.1990    0.3997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3390   -0.6888   -0.9601 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8363   -0.8333   -1.0453 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023    0.8515    0.7926 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8813    0.8568    1.9647 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4237    1.9139    3.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8105    3.4338    2.3004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1034    2.7347    2.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2126    2.2141   -2.7108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1540    0.7369   -2.8806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6887    1.9187   -1.6551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1700    3.1520   -0.5725 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2032    3.4175   -1.6010 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4475    3.8488   -0.3681 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6040    3.5040    0.6629 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7200    2.7737   -0.9915 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5379    1.7727    0.1212 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1327    1.7201    1.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1555    0.2208    0.8914 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8391   -0.1904   -0.6007 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3513    0.6325   -1.0576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5634   -1.7186    0.4686 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3722   -0.4082    1.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5736   -0.7702   -0.6605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1772   -3.2683   -1.2308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3902   -4.5686    0.9912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2473   -3.6526   -0.7408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1087   -3.3270    0.8754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4758   -4.9619    0.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3685   -3.6221    2.9337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2841   -0.3796    0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7599   -1.3156    1.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8980   -1.3119   -1.7778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1175   -1.6595   -1.7375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2884   -1.1476   -0.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3660    0.0552   -1.4237 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 26  1  0
 24 22  1  0
 22 23  1  6
 22 27  1  0
 27 28  1  0
 28 29  1  0
 28  5  1  0
  5  6  1  0
  5  4  1  1
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 18 30  1  0
 30 31  2  0
 20 22  1  0
 30 11  1  0
 25 53  1  0
 25 54  1  0
 25 55  1  0
 24 52  1  1
 26 56  1  0
 23 51  1  0
 27 57  1  0
 27 58  1  0
 28 59  1  6
 29 60  1  0
 29 61  1  0
 29 62  1  0
  6 35  1  0
  6 36  1  0
  6 37  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
 10 38  1  0
 10 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 15 43  1  0
 15 44  1  0
 15 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 17 49  1  0
 18 50  1  6
M  END


  Mrv1652309102202232D          

 31 32  0  0  1  0            999 V2000
    5.0056   -0.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6295    0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4089   -0.0594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4741    1.0213    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6947    1.2918    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5636    0.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8698    1.2794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4466    1.9876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4680    0.5588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6431    0.5464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200    1.2546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4626    0.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6957    1.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3686    1.9891    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4563    1.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6729    2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4302    3.0831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1985    2.6834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6002    3.4040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4252    3.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8269    4.1370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8483    2.7082    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9794    3.5227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4723    3.2479    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2517    2.9774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3169    4.0581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6732    2.7206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0964    2.0124    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9213    2.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6217    1.9752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818    2.4701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
 24 25  1  0  0  0  0
 24 26  1  1  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 28  1  0  0  0  0
 28 29  1  1  0  0  0
 18 30  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0292716

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](O)[C@@]1(O)C[C@@H](C)[C@@](C)(OC(C)=O)C(=O)OC\C2=C\CN(C)CCC(OC1=O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H31NO9/c1-12-10-21(28,13(2)23)19(27)30-16-7-9-22(5)8-6-15(17(16)25)11-29-18(26)20(12,4)31-14(3)24/h6,12-13,16,23,28H,7-11H2,1-5H3/b15-6-/t12-,13+,16?,20-,21+/m1/s1

> <INCHI_KEY>
MPJBVZKNLCGQHF-OXDPSKHNSA-N

> <FORMULA>
C21H31NO9

> <MOLECULAR_WEIGHT>
441.477

> <EXACT_MASS>
441.199881582

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
43.68978271504851

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,6R,7R,11Z)-4-hydroxy-4-[(1S)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate

> <JCHEM_LOGP>
0.19386539499999927

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.69990315135303

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.46776863713402

> <JCHEM_PKA_STRONGEST_BASIC>
6.930381814959512

> <JCHEM_POLAR_SURFACE_AREA>
139.67000000000002

> <JCHEM_REFRACTIVITY>
108.2444

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4S,6R,7R,11Z)-4-hydroxy-4-[(1S)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       9.344  -0.614   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.508   0.394   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      11.963  -0.111   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      10.218   1.906   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.763   2.411   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.519   0.891   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.224   2.388   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.434   3.710   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       6.474   1.043   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.934   1.020   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.144   2.342   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.730   1.731   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.299   2.299   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       0.688   3.713   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -0.852   3.690   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.256   5.145   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.670   5.755   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.104   5.009   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.854   6.354   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.394   6.377   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.144   7.722   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.184   5.055   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.428   6.576   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.348   6.063   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.803   5.558   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.058   7.575   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.723   5.078   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.513   3.756   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.053   3.780   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.894   3.687   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.126   4.611   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7   28                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   30                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   30                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24   27                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   22   28                                                       
CONECT   28   27    5   29                                                  
CONECT   29   28                                                            
CONECT   30   18   11   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₁NO₉

Average Mass

441.4770 Da

Monoisotopic Mass

441.19988 Da

IUPAC Name

(4S,6R,7R,11Z)-4-hydroxy-4-[(1S)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate

Traditional Name

(4S,6R,7R,11Z)-4-hydroxy-4-[(1S)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@H](O)[C@@]1(O)C[C@@H](C)[C@@](C)(OC(C)=O)C(=O)OC\C2=C\CN(C)CCC(OC1=O)C2=O

InChI Identifier

InChI=1S/C21H31NO9/c1-12-10-21(28,13(2)23)19(27)30-16-7-9-22(5)8-6-15(17(16)25)11-29-18(26)20(12,4)31-14(3)24/h6,12-13,16,23,28H,7-11H2,1-5H3/b15-6-/t12-,13+,16?,20-,21+/m1/s1

InChI Key

MPJBVZKNLCGQHF-OXDPSKHNSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Doronicum macrophyllum	LOTUS Database	35616633
Senecio aureus	LOTUS Database	35616633
Senecio inaequidens	LOTUS Database	35616633
Senecio othonnae	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Alpha-acyloxy ketone
Tertiary alcohol
Tertiary aliphatic amine
Tertiary amine
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Amino acid or derivatives
1,2-diol
Oxacycle
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	0.19	ChemAxon
pKa (Strongest Acidic)	11.47	ChemAxon
pKa (Strongest Basic)	6.93	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	139.67 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	108.24 m³·mol⁻¹	ChemAxon
Polarizability	43.69 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

81423667

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139291965

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate (NP0292716)

MOL for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

3D MOL for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

3D SDF for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

3D-SDF for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

PDB for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

3D PDB for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

SMILES for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

INCHI for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

Structure for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)

3D Structure for NP0292716 ((4s,6r,7r,11z)-4-hydroxy-4-[(1s)-1-hydroxyethyl]-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-7-yl acetate)