NP-MRD: Showing NP-Card for 2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one (NP0084835)

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Record Information

Version

2.0

Created at

2022-04-29 05:28:08 UTC

Updated at

2022-04-29 05:28:08 UTC

NP-MRD ID

NP0084835

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one

Description

2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one is found in Mammea americana .

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292207282D          

 27 29  0  0  0  0            999 V2000
    5.0626    1.6514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3613    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267    1.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7959    0.5156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   -1.7170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6283   -2.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -3.1452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6729   -3.8465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529   -2.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3691   -1.7427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4944    1.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0598    2.5677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4498    3.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    0.3610    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  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  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
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 13 18  2  0  0  0  0
 12 19  2  0  0  0  0
  8 19  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 10 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
 21 27  2  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
   -2.1305    4.9088   -0.1834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7375    3.8742    0.7018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1927    2.4825    0.5107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7582    2.3515    0.7704 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0277    3.3859    1.2309 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3635    3.1473    1.4412 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0747    4.0957    1.8613 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8968    1.9475    1.2087 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1567    0.9528    0.7694 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7836   -0.2775    0.5481 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2150   -0.4366    0.8052 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8392    0.5542    1.2663 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9390   -1.6829    0.5504 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8950   -2.0839   -0.9083 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.1109   -0.4658    0.2406 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8777    0.0108    0.0759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1929    1.1024    0.5307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2456   -0.0739   -0.2340 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3995   -1.2093   -1.1009 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7451   -1.8644   -0.8741 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8495   -3.0705   -1.7802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8897   -2.3556    0.5465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7375   -0.9270   -1.1486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3177   -2.1478   -0.6290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2697    4.5579   -0.7839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9002    5.2185   -0.9516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9160    5.8547    0.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6700    4.1301    1.7840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8478    3.7901    0.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8095    1.8162    1.1693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3751    2.2240   -0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3761    4.3587    1.4291 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5145   -2.5201    1.1459 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5263   -3.1009   -1.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2238   -1.3687   -1.4206 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9073   -1.9715   -1.3590 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3668   -1.3353    2.0760 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9204   -2.5151    0.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.0525   -0.8571   -0.1937 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3073    0.3589    0.9323 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4835   -2.3385   -0.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.9112   -2.7863   -2.8492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9371   -3.6903   -1.6185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7044   -3.7121   -1.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2079   -1.8136    1.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7994   -3.4518    0.6204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9238   -2.1130    0.9308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7709   -0.2920   -0.3789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6685   -2.7113    0.2565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9433   -2.8063   -1.4349 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 20  2  0
 20 19  1  0
 19 18  2  0
 18 27  1  0
 27 22  1  0
 22 21  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 23 26  1  6
 18 17  1  0
 17 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 20  4  1  0
 21 19  1  0
 10  9  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  2 32  1  0
  3 33  1  0
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  5 35  1  0
 27 54  1  0
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 13 36  1  1
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 14 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 16 44  1  0
M  END


  Mrv1652304292207282D          

 27 29  0  0  0  0            999 V2000
    5.0626    1.6514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3613    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267    1.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7959    0.5156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6601    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8963    1.0941    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5995   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7983   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5391    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5837   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   -1.7170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6283   -2.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -3.1452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6729   -3.8465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529   -2.3925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3691   -1.7427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4083   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1101    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2799    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1045    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4944    1.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0598    2.5677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4498    3.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9347    0.3610    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  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  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
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 13 18  2  0  0  0  0
 12 19  2  0  0  0  0
  8 19  1  0  0  0  0
 11 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 10 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
 21 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0084835

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1=CC(=O)OC2=C1C1=C(CC(O1)C(C)(C)O)C=C2C(=O)C(C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O5/c1-6-8-13-11-17(23)27-21-15(19(24)12(3)7-2)9-14-10-16(22(4,5)25)26-20(14)18(13)21/h9,11-12,16,25H,6-8,10H2,1-5H3

> <INCHI_KEY>
KIVXXMQDTGBKDM-UHFFFAOYSA-N

> <FORMULA>
C22H28O5

> <MOLECULAR_WEIGHT>
372.461

> <EXACT_MASS>
372.193674002

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.98760579006842

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2-hydroxypropan-2-yl)-5-(2-methylbutanoyl)-9-propyl-2H,3H,7H-furo[2,3-f]chromen-7-one

> <ALOGPS_LOGP>
4.07

> <JCHEM_LOGP>
4.166663850999999

> <ALOGPS_LOGS>
-4.52

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.364302647036876

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.29638789274064

> <JCHEM_PKA_STRONGEST_BASIC>
-3.106395327051149

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
104.03009999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.12e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2-hydroxypropan-2-yl)-5-(2-methylbutanoyl)-9-propyl-2H,3H-furo[2,3-f]chromen-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       9.450   3.083   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.141   2.271   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.330   3.580   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.952   0.962   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.832   1.460   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.406   2.042   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.719  -0.076   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.223  -0.443   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.412   0.866   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.873   0.818   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.145  -0.539   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.956  -1.848   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.228  -3.205   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.040  -4.514   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.312  -5.871   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.123  -7.180   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.579  -4.466   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.689  -3.253   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.495  -1.800   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.606  -0.587   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.206   0.722   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.522   2.079   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.062   2.127   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.790   3.484   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.978   4.793   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.706   6.150   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.745   0.674   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6    7                                                  
CONECT    6    5    9                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8    6   10                                                  
CONECT   10    9   11   23                                                  
CONECT   11   10   12   20                                                  
CONECT   12   11   13   19                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14                                                            
CONECT   18   13                                                            
CONECT   19   12    8                                                       
CONECT   20   11   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   10   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   21                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈O₅

Average Mass

372.4610 Da

Monoisotopic Mass

372.19367 Da

IUPAC Name

2-(2-hydroxypropan-2-yl)-5-(2-methylbutanoyl)-9-propyl-2H,3H,7H-furo[2,3-f]chromen-7-one

Traditional Name

2-(2-hydroxypropan-2-yl)-5-(2-methylbutanoyl)-9-propyl-2H,3H-furo[2,3-f]chromen-7-one

CAS Registry Number

Not Available

SMILES

CCCC1=CC(=O)OC2=C1C1=C(CC(O1)C(C)(C)O)C=C2C(=O)C(C)CC

InChI Identifier

InChI=1S/C22H28O5/c1-6-8-13-11-17(23)27-21-15(19(24)12(3)7-2)9-14-10-16(22(4,5)25)26-20(14)18(13)21/h9,11-12,16,25H,6-8,10H2,1-5H3

InChI Key

KIVXXMQDTGBKDM-UHFFFAOYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Mammea americana	Plant	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	4.07	ALOGPS
logP	4.17	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	14.3	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	104.03 m³·mol⁻¹	ChemAxon
Polarizability	41.99 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

Not Available

Showing NP-Card for 2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one (NP0084835)

MOL for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

3D MOL for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

3D SDF for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

3D-SDF for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

PDB for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

3D PDB for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

SMILES for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

INCHI for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

Structure for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)

3D Structure for NP0084835 (2,3-Dihydro-4-hydroxy-2-(1-hydroxy-1-methylethyl)-5-(2-methyl-1-oxobutyl)-9-propyl-7H-furo[2,3-f][1]benzopyran-7-one)