NP-MRD: Showing NP-Card for (1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one (NP0147359)

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Record Information

Version

2.0

Created at

2022-09-02 02:57:08 UTC

Updated at

2022-09-02 02:57:09 UTC

NP-MRD ID

NP0147359

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one

Description

Nemanolone I belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position. Based on a literature review very few articles have been published on Nemanolone I.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022204572D          

 29 33  0  0  1  0            999 V2000
   -1.0886    0.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2809    0.3813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9787   -0.1551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3329    1.0548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1515    0.9521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4719    0.1919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9737   -0.4657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1772   -1.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9291   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6633   -1.2283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1611   -1.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7113   -0.4356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6855   -0.4237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2966    0.2124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7994    0.8463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1551   -0.3630    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5968   -0.0077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0396    0.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9172   -0.7679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7358   -0.8706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2340   -0.2130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9136    0.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4118    1.2048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2304    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5508    0.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4291    0.5478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0526   -0.3157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6337   -1.0737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0950    0.6499    0.0000 C   0  0  2  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  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16  7  1  6  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 22  1  1  0  0  0
  5 29  1  0  0  0  0
 17 29  1  0  0  0  0
M  END

     RDKit          3D

 49 53  0  0  0  0  0  0  0  0999 V2000
   -1.0334    1.4690   -2.8123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3776    0.5633   -1.6879 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7251    0.1401   -1.7990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6307   -0.5783   -1.5855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3932   -1.0383   -0.2988 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6281   -0.8062    0.5319 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9811    0.5247    0.5661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9261    1.1276    1.3479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8170    0.4971    2.2372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0694   -0.8667    2.3610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2953   -1.2221    2.9303 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2359   -1.9164    1.9805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5169   -3.1459    2.5788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1672   -1.9308    1.0975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6432   -3.0281    0.7806 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2266    1.3715   -0.3773 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2820    1.3121   -0.1308 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6784    2.3751    0.8952 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8642    1.6741   -1.3209 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1615    1.4141   -1.5083 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7268    0.2594   -0.7964 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0002   -0.4673    0.0956 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5355   -1.5589    0.7683 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8487   -1.8851    0.4965 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5792   -1.1527   -0.4016 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9140   -1.5250   -0.6446 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0482   -0.0689   -1.0698 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8160    0.6499   -1.9721 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5987   -0.0652    0.3420 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8733    1.4553   -3.5663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1228    1.1914   -3.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9389    2.5408   -2.5217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2534    0.6147   -1.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0547   -2.0661   -0.2528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9831    2.2042    1.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3605    1.1259    2.8888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4822   -2.2097    3.0218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9526   -3.9495    2.3487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5961    2.3821   -0.4865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1898    3.2371    0.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2281    2.7991    1.3865 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3263    1.9014    1.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7883    2.3070   -1.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3470    1.2336   -2.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9433   -2.1123    1.4636 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2973   -2.7420    1.0130 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3281   -2.2987   -0.1819 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7702    0.3574   -2.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4687   -0.0937    1.4567 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  6
  2  4  1  0
  4  5  1  0
  5 29  1  0
 29 22  1  0
 22 21  2  0
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  1
 17 16  1  0
 16  7  1  0
  7  6  2  0
  6 14  1  0
 14 15  2  0
 14 12  1  0
 12 13  1  0
 12 10  2  0
 10 11  1  0
 10  9  1  0
  9  8  2  0
 21 27  1  0
 27 28  1  0
 27 25  2  0
 25 26  1  0
 25 24  1  0
 24 23  2  0
 16  2  1  0
  8  7  1  0
  6  5  1  0
 17 29  1  0
 23 22  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  5 34  1  6
 29 49  1  1
 20 43  1  0
 20 44  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
 16 39  1  6
 13 38  1  0
 11 37  1  0
  9 36  1  0
  8 35  1  0
 28 48  1  0
 26 47  1  0
 24 46  1  0
 23 45  1  0
M  END


  Mrv1652309022204572D          

 29 33  0  0  1  0            999 V2000
   -1.0886    0.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2809    0.3813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9787   -0.1551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3329    1.0548    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1515    0.9521    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4719    0.1919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9737   -0.4657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1772   -1.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9291   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6633   -1.2283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1611   -1.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7113   -0.4356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6855   -0.4237    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2966    0.2124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7994    0.8463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1551   -0.3630    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5968   -0.0077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0396    0.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9172   -0.7679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7358   -0.8706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2340   -0.2130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9136    0.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4118    1.2048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2304    1.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5508    0.3419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4291    0.5478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0526   -0.3157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6337   -1.0737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0950    0.6499    0.0000 C   0  0  2  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  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  6 14  1  0  0  0  0
 14 15  2  0  0  0  0
 16  7  1  6  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 22  1  1  0  0  0
  5 29  1  0  0  0  0
 17 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0147359

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(O)O[C@H]2[C@H]3C4=C(CO[C@@]3(C)[C@@H]1C1=C2C(=O)C(O)=C(O)C=C1)C(O)=C(O)C=C4

> <INCHI_IDENTIFIER>
InChI=1S/C21H20O8/c1-20-14(8-3-5-11(22)15(24)10(8)7-28-20)18-13-9(19(20)21(2,27)29-18)4-6-12(23)16(25)17(13)26/h3-6,14,18-19,22,24,27H,7H2,1-2H3,(H2,23,25,26)/t14-,18-,19+,20-,21?/m1/s1

> <INCHI_KEY>
GYHQGFLONZNARQ-QYYVQIJYSA-N

> <FORMULA>
C21H20O8

> <MOLECULAR_WEIGHT>
400.383

> <EXACT_MASS>
400.115817604

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
39.44052887473249

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,11R,12S)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0^{2,11}.0^{3,8}.0^{13,19}]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one

> <ALOGPS_LOGP>
1.13

> <JCHEM_LOGP>
0.8639756063333328

> <ALOGPS_LOGS>
-2.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.762819725626734

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.978470847113428

> <JCHEM_PKA_STRONGEST_BASIC>
1.8569368386231142

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
104.24510000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.78e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,11R,12S)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0^{2,11}.0^{3,8}.0^{13,19}]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.032   1.485   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.524   0.712   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.827  -0.290   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       0.621   1.969   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.149   1.777   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.747   0.358   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.817  -0.869   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.197  -2.362   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.601  -2.995   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.971  -2.293   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.901  -3.699   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.061  -0.813   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.880  -0.791   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.287   0.396   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.226   1.580   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.289  -0.678   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.114  -0.014   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.074   1.327   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.712  -1.433   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.240  -1.625   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.170  -0.398   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.572   1.022   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.502   2.249   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.030   2.057   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.628   0.638   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       8.268   1.023   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.698  -0.589   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.783  -2.004   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.044   1.213   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   16                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7   14                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    6   15                                                  
CONECT   15   14                                                            
CONECT   16    7    2   17                                                  
CONECT   17   16   18   19   29                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23   29                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   21   28                                                  
CONECT   28   27                                                            
CONECT   29   22    5   17                                                  
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀O₈

Average Mass

400.3830 Da

Monoisotopic Mass

400.11582 Da

IUPAC Name

(1S,2R,11R,12S)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0^{2,11}.0^{3,8}.0^{13,19}]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one

Traditional Name

(1S,2R,11R,12S)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0^{2,11}.0^{3,8}.0^{13,19}]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one

CAS Registry Number

Not Available

SMILES

CC1(O)O[C@H]2[C@H]3C4=C(CO[C@@]3(C)[C@@H]1C1=C2C(=O)C(O)=C(O)C=C1)C(O)=C(O)C=C4

InChI Identifier

InChI=1S/C21H20O8/c1-20-14(8-3-5-11(22)15(24)10(8)7-28-20)18-13-9(19(20)21(2,27)29-18)4-6-12(23)16(25)17(13)26/h3-6,14,18-19,22,24,27H,7H2,1-2H3,(H2,23,25,26)/t14-,18-,19+,20-,21?/m1/s1

InChI Key

GYHQGFLONZNARQ-QYYVQIJYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

2-benzopyrans

Direct Parent

2-benzopyrans

Alternative Parents

Substituents

2-benzopyran
Tropolone
Tropone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Oxane
Vinylogous acid
Hemiacetal
Oxacycle
Polyol
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	1.13	ALOGPS
logP	0.86	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	4.98	ChemAxon
pKa (Strongest Basic)	1.86	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	104.25 m³·mol⁻¹	ChemAxon
Polarizability	39.44 Å³	ChemAxon
Number of Rings	5	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139590194

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one (NP0147359)

MOL for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

3D MOL for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

3D SDF for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

3D-SDF for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

PDB for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

3D PDB for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

SMILES for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

INCHI for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

Structure for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)

3D Structure for NP0147359 ((1s,2r,11r,12s)-6,7,16,17,21-pentahydroxy-11,21-dimethyl-10,20-dioxapentacyclo[10.7.2.0²,¹¹.0³,⁸.0¹³,¹⁹]henicosa-3(8),4,6,13(19),14,16-hexaen-18-one)