NP-MRD: Showing NP-Card for (-)-Humirianthol (NP0075422)

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Record Information

Version

2.0

Created at

2022-04-28 20:42:34 UTC

Updated at

2022-04-28 20:42:34 UTC

NP-MRD ID

NP0075422

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Humirianthol

Description

(1S,2S,5R,6S,9S,12S,15R,16S,21R)-6,16-dihydroxy-5,15-dimethyl-8,13,17-trioxahexacyclo[14.2.2.1¹,¹².0²,¹⁰.0⁵,⁹.0¹⁵,²¹]Henicos-10-en-14-one belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (-)-Humirianthol is found in Casimirella ampla and Humirianthera ampla. Based on a literature review very few articles have been published on (1S,2S,5R,6S,9S,12S,15R,16S,21R)-6,16-dihydroxy-5,15-dimethyl-8,13,17-trioxahexacyclo[14.2.2.1¹,¹².0²,¹⁰.0⁵,⁹.0¹⁵,²¹]Henicos-10-en-14-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222422D          

 26 31  0  0  1  0            999 V2000
    4.8482   -0.7808    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0639    0.0155    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4821    0.6005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6847    0.3892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4689   -0.4071    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0507   -0.9921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -1.7964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682   -2.0704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3953   -1.4248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6171   -0.5273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0078    0.1657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1552   -0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9351   -1.0636    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5338   -1.7802    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6802   -2.6251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0924   -3.2040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5081   -2.7814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7852   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1311   -1.2482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6955   -1.1619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8313   -0.4178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8879    0.0564    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1814   -0.7146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5388   -1.2320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3391    0.7471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3617    0.7849    0.0000 C   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
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  8 17  1  6  0  0  0
 14 18  1  6  0  0  0
 13 19  1  1  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 10 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 24  1  1  0  0  0
 22 25  1  6  0  0  0
  2 26  1  1  0  0  0
M  END

     RDKit          3D

 52 57  0  0  0  0  0  0  0  0999 V2000
   -3.2271    0.3244   -1.3940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1025    0.2091    0.0902 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5642    1.3994    0.7914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0405    1.4185    0.8868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4180    0.5210   -0.1493 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9403   -0.8730    0.0020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1927   -1.9503   -0.3186 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1424   -1.6454   -0.8131 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1284   -2.6057   -0.7569 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3323   -1.9111   -0.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4214   -2.2323   -1.2428 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1352   -0.7036    0.1146 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8552   -0.9173    1.4275 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6579   -0.6578    0.2547 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0452    0.6680   -0.1832 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6552    1.6901    0.7453 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1510    1.7020    0.4237 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5377    0.5898   -0.5438 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9022    0.6181   -0.6742 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8616    0.6885   -1.7388 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5520    1.0576   -1.5813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2999   -1.0110    0.5315 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0592   -2.0168    0.0030 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3929   -1.7253    0.2647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4581   -0.2405    0.6507 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5084   -0.1117    2.0236 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0507    1.3567   -1.7895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6179   -0.4316   -1.9109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2895    0.1091   -1.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9810    1.4137    1.8351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9649    2.3082    0.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7446    2.4618    0.6499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6906    1.2100    1.9139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8048    0.9068   -1.1397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6466   -2.9115   -0.1804 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1664   -1.1819   -1.8159 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3485   -0.4529    2.2817 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9283   -2.0146    1.6489 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8965   -0.5453    1.3742 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2731   -0.8822    1.2467 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2729    2.7158    0.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5541    1.3268    1.7763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4534    2.6664   -0.0195 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7575    1.5251    1.3414 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3486    1.0622    0.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5296    2.1875   -1.6073 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8655    0.7473   -2.3748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2688   -1.0030    1.6397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9580   -1.8210   -0.6876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8452   -2.3615    1.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2520    0.2859    0.1113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4537   -0.9628    2.4976 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  6
 18 20  1  0
 20 21  1  0
  6 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 22  2  1  0
 25  2  1  0
 15  5  1  0
 15 21  1  6
 14  8  1  0
 18 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  7 35  1  0
  8 36  1  6
 13 37  1  0
 13 38  1  0
 13 39  1  0
 14 40  1  1
 16 41  1  0
 16 42  1  0
 17 43  1  0
 17 44  1  0
 19 45  1  0
 21 46  1  0
 21 47  1  0
 22 48  1  1
 24 49  1  0
 24 50  1  0
 25 51  1  6
 26 52  1  0
M  END


  Mrv1652304282222422D          

 26 31  0  0  1  0            999 V2000
    4.8482   -0.7808    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0639    0.0155    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4821    0.6005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6847    0.3892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4689   -0.4071    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0507   -0.9921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7704   -1.7964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9682   -2.0704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3953   -1.4248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6171   -0.5273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0078    0.1657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1552   -0.1816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9351   -1.0636    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5338   -1.7802    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6802   -2.6251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0924   -3.2040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5081   -2.7814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7852   -2.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1311   -1.2482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6955   -1.1619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8313   -0.4178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8879    0.0564    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1814   -0.7146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5388   -1.2320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3391    0.7471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3617    0.7849    0.0000 C   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
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  1  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  8 17  1  6  0  0  0
 14 18  1  6  0  0  0
 13 19  1  1  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 10 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
  1 24  1  1  0  0  0
 22 25  1  6  0  0  0
  2 26  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0075422

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12CC[C@@H]3C(=C[C@@H]4OC(=O)[C@]5(C)[C@H]4[C@]33CC[C@]5(O)OC3)[C@@H]1OC[C@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O6/c1-17-4-3-11-10(15(17)24-8-13(17)21)7-12-14-18(2,16(22)26-12)20(23)6-5-19(11,14)9-25-20/h7,11-15,21,23H,3-6,8-9H2,1-2H3/t11-,12+,13-,14+,15+,17-,18+,19+,20+/m1/s1

> <INCHI_KEY>
AWXCFXSOVHMZKV-DSMHVVIASA-N

> <FORMULA>
C20H26O6

> <MOLECULAR_WEIGHT>
362.422

> <EXACT_MASS>
362.172938557

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.774627665563614

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,5R,6S,9S,12S,15R,16S,21R)-6,16-dihydroxy-5,15-dimethyl-8,13,17-trioxahexacyclo[14.2.2.1^{1,12}.0^{2,10}.0^{5,9}.0^{15,21}]henicos-10-en-14-one

> <ALOGPS_LOGP>
1.00

> <JCHEM_LOGP>
0.8456473956666659

> <ALOGPS_LOGS>
-2.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.85134483387241

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.415506529442943

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3019219756110028

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
90.5824

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.05e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5R,6S,9S,12S,15R,16S,21R)-6,16-dihydroxy-5,15-dimethyl-8,13,17-trioxahexacyclo[14.2.2.1^{1,12}.0^{2,10}.0^{5,9}.0^{15,21}]henicos-10-en-14-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       9.050  -1.457   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.453   0.029   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.367   1.121   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.878   0.726   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.475  -0.760   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.561  -1.852   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.038  -3.353   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.541  -3.865   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.471  -2.660   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.885  -0.984   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.748   0.309   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.156  -0.339   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.746  -1.985   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.863  -3.323   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.136  -4.900   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.039  -5.981   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.682  -5.192   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.466  -3.970   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.245  -2.330   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       3.165  -2.169   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.418  -0.780   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.991   0.105   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.539  -1.334   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      10.339  -2.300   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      11.833   1.395   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.008   1.465   0.000  0.00  0.00           C+0
CONECT    1    2    6   24                                                  
CONECT    2    1    3   22   26                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9    5   11   21                                             
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   19   20                                             
CONECT   14   13    9   15   18                                             
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    8                                                       
CONECT   18   14                                                            
CONECT   19   13                                                            
CONECT   20   13   21                                                       
CONECT   21   20   10                                                       
CONECT   22    2   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23    1                                                       
CONECT   25   22                                                            
CONECT   26    2                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆O₆

Average Mass

362.4220 Da

Monoisotopic Mass

362.17294 Da

IUPAC Name

(1S,2S,5R,6S,9S,12S,15R,16S,21R)-6,16-dihydroxy-5,15-dimethyl-8,13,17-trioxahexacyclo[14.2.2.1^{1,12}.0^{2,10}.0^{5,9}.0^{15,21}]henicos-10-en-14-one

Traditional Name

(1S,2S,5R,6S,9S,12S,15R,16S,21R)-6,16-dihydroxy-5,15-dimethyl-8,13,17-trioxahexacyclo[14.2.2.1^{1,12}.0^{2,10}.0^{5,9}.0^{15,21}]henicos-10-en-14-one

CAS Registry Number

Not Available

SMILES

C[C@]12CC[C@@H]3C(=C[C@@H]4OC(=O)[C@]5(C)[C@H]4[C@]33CC[C@]5(O)OC3)[C@@H]1OC[C@H]2O

InChI Identifier

InChI=1S/C20H26O6/c1-17-4-3-11-10(15(17)24-8-13(17)21)7-12-14-18(2,16(22)26-12)20(23)6-5-19(11,14)9-25-20/h7,11-15,21,23H,3-6,8-9H2,1-2H3/t11-,12+,13-,14+,15+,17-,18+,19+,20+/m1/s1

InChI Key

AWXCFXSOVHMZKV-DSMHVVIASA-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
Casimirella ampla	LOTUS Database	35616633
Humirianthera ampla	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthofuran
Naphthalene
Furopyran
Pyran
Oxane
Gamma butyrolactone
Tetrahydrofuran
Furan
Cyclic alcohol
Secondary alcohol
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	1	ALOGPS
logP	0.85	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	11.42	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	90.58 m³·mol⁻¹	ChemAxon
Polarizability	37.77 Å³	ChemAxon
Number of Rings	6	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

162889831

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Humirianthol (NP0075422)

MOL for NP0075422 ((-)-Humirianthol)

3D MOL for NP0075422 ((-)-Humirianthol)

3D SDF for NP0075422 ((-)-Humirianthol)

3D-SDF for NP0075422 ((-)-Humirianthol)

PDB for NP0075422 ((-)-Humirianthol)

3D PDB for NP0075422 ((-)-Humirianthol)

SMILES for NP0075422 ((-)-Humirianthol)

INCHI for NP0075422 ((-)-Humirianthol)

Structure for NP0075422 ((-)-Humirianthol)

3D Structure for NP0075422 ((-)-Humirianthol)