NP-MRD: Showing NP-Card for Hispidulactone A (NP0018563)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-01-06 03:09:50 UTC

Updated at

2021-07-15 17:28:33 UTC

NP-MRD ID

NP0018563

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Hispidulactone A

Provided By

NPAtlas

Description

(3R)-12-hydroxy-10-methoxy-3-methyl-3,4,5,6,7,8-hexahydro-1H-2-benzoxecin-1-one belongs to the class of organic compounds known as oxocins. Oxocins are compounds containing an oxocin ring, which is a eight-member unsaturated aromatic ring containing one oxygen atom and seven carbon atoms. Hispidulactone A is found in Chaetosphaeronema hispidulum. Based on a literature review very few articles have been published on (3R)-12-hydroxy-10-methoxy-3-methyl-3,4,5,6,7,8-hexahydro-1H-2-benzoxecin-1-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242104353D          

 39 40  0  0  0  0            999 V2000
    5.2846    1.1946    0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9716    0.0849   -0.3906 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6167   -0.2726   -0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3098   -1.3462   -1.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9516   -1.6830   -1.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7182   -2.7718   -2.2474 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.9591   -0.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839    0.1068    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    0.4324    0.1169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3520    0.9599    0.7610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7696    1.5656    0.0120 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8985    1.8573    0.9459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2518    1.4721    0.4130 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2545    0.1257   -0.2628 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4747   -0.9157    0.4979 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4982   -2.0433    0.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4409   -1.5211   -0.1105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4594   -1.4063   -0.9891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6719   -1.7083   -2.2308 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8918    2.1373    0.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8412    0.9987    1.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3962    1.2386    0.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0786   -1.9243   -1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9043   -3.2303   -2.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9372    1.2874    0.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0578    0.3317    1.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    1.7809    1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0655    1.0543   -0.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864    2.5668   -0.3625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6900    1.3812    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559    2.9502    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9476    1.4250    1.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5639    2.2454   -0.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748    0.2098   -1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3296   -0.1411   -0.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2442   -0.5386    1.5291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8779   -2.4039   -0.1894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9513   -2.8808    1.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3373   -1.6604    1.3665 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
  9  3  1  0  0  0  0
 18  7  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  4 23  1  0  0  0  0
  6 24  1  0  0  0  0
  9 25  1  0  0  0  0
 10 26  1  0  0  0  0
 10 27  1  0  0  0  0
 11 28  1  0  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 12 31  1  0  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
 14 34  1  0  0  0  0
 14 35  1  0  0  0  0
 15 36  1  1  0  0  0
 16 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
M  END

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    5.2846    1.1946    0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9716    0.0849   -0.3906 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6167   -0.2726   -0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3098   -1.3462   -1.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9516   -1.6830   -1.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7182   -2.7718   -2.2474 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.9591   -0.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839    0.1068    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    0.4324    0.1169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3520    0.9599    0.7610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7696    1.5656    0.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8985    1.8573    0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2518    1.4721    0.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2545    0.1257   -0.2628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4747   -0.9157    0.4979 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4982   -2.0433    0.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4409   -1.5211   -0.1105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4594   -1.4063   -0.9891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6719   -1.7083   -2.2308 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8918    2.1373    0.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8412    0.9987    1.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3962    1.2386    0.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0786   -1.9243   -1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9043   -3.2303   -2.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9372    1.2874    0.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0578    0.3317    1.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    1.7809    1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0655    1.0543   -0.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864    2.5668   -0.3625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6900    1.3812    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559    2.9502    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9476    1.4250    1.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5639    2.2454   -0.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748    0.2098   -1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3296   -0.1411   -0.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2442   -0.5386    1.5291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8779   -2.4039   -0.1894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9513   -2.8808    1.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3373   -1.6604    1.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
  9  3  1  0
 18  7  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  4 23  1  0
  6 24  1  0
  9 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  1
 16 37  1  0
 16 38  1  0
 16 39  1  0
M  END


  Mrv1652306242104353D          

 39 40  0  0  0  0            999 V2000
    5.2846    1.1946    0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9716    0.0849   -0.3906 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6167   -0.2726   -0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3098   -1.3462   -1.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9516   -1.6830   -1.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7182   -2.7718   -2.2474 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.9591   -0.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839    0.1068    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    0.4324    0.1169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3520    0.9599    0.7610 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7696    1.5656    0.0120 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8985    1.8573    0.9459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2518    1.4721    0.4130 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2545    0.1257   -0.2628 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4747   -0.9157    0.4979 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4982   -2.0433    0.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4409   -1.5211   -0.1105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4594   -1.4063   -0.9891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6719   -1.7083   -2.2308 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8918    2.1373    0.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8412    0.9987    1.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3962    1.2386    0.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0786   -1.9243   -1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9043   -3.2303   -2.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9372    1.2874    0.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0578    0.3317    1.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    1.7809    1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0655    1.0543   -0.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864    2.5668   -0.3625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6900    1.3812    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559    2.9502    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9476    1.4250    1.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5639    2.2454   -0.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748    0.2098   -1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3296   -0.1411   -0.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2442   -0.5386    1.5291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8779   -2.4039   -0.1894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9513   -2.8808    1.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3373   -1.6604    1.3665 H   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  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
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
  9  3  1  0  0  0  0
 18  7  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  4 23  1  0  0  0  0
  6 24  1  0  0  0  0
  9 25  1  0  0  0  0
 10 26  1  0  0  0  0
 10 27  1  0  0  0  0
 11 28  1  0  0  0  0
 11 29  1  0  0  0  0
 12 30  1  0  0  0  0
 12 31  1  0  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
 14 34  1  0  0  0  0
 14 35  1  0  0  0  0
 15 36  1  1  0  0  0
 16 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0018563

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=C([H])C(OC([H])([H])[H])=C1[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[C@]([H])(OC2=O)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-10-6-4-3-5-7-11-8-12(18-2)9-13(16)14(11)15(17)19-10/h8-10,16H,3-7H2,1-2H3/t10-/m1/s1

> <INCHI_KEY>
KIVUDNGCLPAVOB-SNVBAGLBSA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.321

> <EXACT_MASS>
264.136159124

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.982467513274873

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-12-hydroxy-10-methoxy-3-methyl-3,4,5,6,7,8-hexahydro-1H-2-benzoxecin-1-one

> <ALOGPS_LOGP>
3.64

> <JCHEM_LOGP>
4.200224383666667

> <ALOGPS_LOGS>
-3.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.74122078263351

> <JCHEM_PKA_STRONGEST_BASIC>
-4.055305403458326

> <JCHEM_POLAR_SURFACE_AREA>
55.76

> <JCHEM_REFRACTIVITY>
72.65979999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.26e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-12-hydroxy-10-methoxy-3-methyl-3,4,5,6,7,8-hexahydro-2-benzoxecin-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    5.2846    1.1946    0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9716    0.0849   -0.3906 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6167   -0.2726   -0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3098   -1.3462   -1.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9516   -1.6830   -1.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7182   -2.7718   -2.2474 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.9591   -0.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839    0.1068    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    0.4324    0.1169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3520    0.9599    0.7610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7696    1.5656    0.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8985    1.8573    0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2518    1.4721    0.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2545    0.1257   -0.2628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4747   -0.9157    0.4979 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4982   -2.0433    0.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4409   -1.5211   -0.1105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4594   -1.4063   -0.9891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6719   -1.7083   -2.2308 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8918    2.1373    0.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8412    0.9987    1.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3962    1.2386    0.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0786   -1.9243   -1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9043   -3.2303   -2.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9372    1.2874    0.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0578    0.3317    1.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    1.7809    1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0655    1.0543   -0.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864    2.5668   -0.3625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6900    1.3812    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559    2.9502    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9476    1.4250    1.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5639    2.2454   -0.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748    0.2098   -1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3296   -0.1411   -0.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2442   -0.5386    1.5291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8779   -2.4039   -0.1894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9513   -2.8808    1.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3373   -1.6604    1.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
  9  3  1  0
 18  7  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  4 23  1  0
  6 24  1  0
  9 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  1
 16 37  1  0
 16 38  1  0
 16 39  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       5.285   1.195   0.429  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.972   0.085  -0.391  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.617  -0.273  -0.526  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.310  -1.346  -1.319  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.952  -1.683  -1.439  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.718  -2.772  -2.247  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.948  -0.959  -0.781  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.284   0.107   0.004  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.623   0.432   0.117  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.352   0.960   0.761  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.770   1.566   0.012  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.899   1.857   0.946  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.252   1.472   0.413  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.255   0.126  -0.263  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.475  -0.916   0.498  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.498  -2.043   0.789  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.441  -1.521  -0.111  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.459  -1.406  -0.989  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.672  -1.708  -2.231  0.00  0.00           O+0
HETATM   20  H   UNK     0       4.892   2.137   0.008  0.00  0.00           H+0
HETATM   21  H   UNK     0       4.841   0.999   1.437  0.00  0.00           H+0
HETATM   22  H   UNK     0       6.396   1.239   0.531  0.00  0.00           H+0
HETATM   23  H   UNK     0       4.079  -1.924  -1.842  0.00  0.00           H+0
HETATM   24  H   UNK     0       0.904  -3.230  -2.497  0.00  0.00           H+0
HETATM   25  H   UNK     0       2.937   1.287   0.742  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.058   0.332   1.587  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.893   1.781   1.316  0.00  0.00           H+0
HETATM   28  H   UNK     0      -1.065   1.054  -0.924  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.386   2.567  -0.363  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.690   1.381   1.939  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.956   2.950   1.180  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.948   1.425   1.279  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.564   2.245  -0.306  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.875   0.210  -1.326  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.330  -0.141  -0.399  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.244  -0.539   1.529  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.878  -2.404  -0.189  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.951  -2.881   1.257  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.337  -1.660   1.367  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   23                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   24                                                       
CONECT    7    5    8   18                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    3   25                                                  
CONECT   10    8   11   26   27                                             
CONECT   11   10   12   28   29                                             
CONECT   12   11   13   30   31                                             
CONECT   13   12   14   32   33                                             
CONECT   14   13   15   34   35                                             
CONECT   15   14   16   17   36                                             
CONECT   16   15   37   38   39                                             
CONECT   17   15   18                                                       
CONECT   18   17   19    7                                                  
CONECT   19   18                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    4                                                            
CONECT   24    6                                                            
CONECT   25    9                                                            
CONECT   26   10                                                            
CONECT   27   10                                                            
CONECT   28   11                                                            
CONECT   29   11                                                            
CONECT   30   12                                                            
CONECT   31   12                                                            
CONECT   32   13                                                            
CONECT   33   13                                                            
CONECT   34   14                                                            
CONECT   35   14                                                            
CONECT   36   15                                                            
CONECT   37   16                                                            
CONECT   38   16                                                            
CONECT   39   16                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   80    0
END

RDKit          3D

39 40  0  0  0  0  0  0  0  0999 V2000
    5.2846    1.1946    0.4294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9716    0.0849   -0.3906 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6167   -0.2726   -0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3098   -1.3462   -1.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9516   -1.6830   -1.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7182   -2.7718   -2.2474 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.9591   -0.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2839    0.1068    0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6231    0.4324    0.1169 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3520    0.9599    0.7610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7696    1.5656    0.0120 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8985    1.8573    0.9459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2518    1.4721    0.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2545    0.1257   -0.2628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4747   -0.9157    0.4979 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4982   -2.0433    0.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4409   -1.5211   -0.1105 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4594   -1.4063   -0.9891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6719   -1.7083   -2.2308 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8918    2.1373    0.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8412    0.9987    1.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3962    1.2386    0.5314 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0786   -1.9243   -1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9043   -3.2303   -2.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9372    1.2874    0.7416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0578    0.3317    1.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    1.7809    1.3161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0655    1.0543   -0.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3864    2.5668   -0.3625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6900    1.3812    1.9392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9559    2.9502    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9476    1.4250    1.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5639    2.2454   -0.3060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748    0.2098   -1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3296   -0.1411   -0.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2442   -0.5386    1.5291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8779   -2.4039   -0.1894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9513   -2.8808    1.2574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3373   -1.6604    1.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  2  0
  9  3  1  0
 18  7  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  4 23  1  0
  6 24  1  0
  9 25  1  0
 10 26  1  0
 10 27  1  0
 11 28  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 13 32  1  0
 13 33  1  0
 14 34  1  0
 14 35  1  0
 15 36  1  1
 16 37  1  0
 16 38  1  0
 16 39  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₄

Average Mass

264.3210 Da

Monoisotopic Mass

264.13616 Da

IUPAC Name

(3R)-12-hydroxy-10-methoxy-3-methyl-3,4,5,6,7,8-hexahydro-1H-2-benzoxecin-1-one

Traditional Name

(3R)-12-hydroxy-10-methoxy-3-methyl-3,4,5,6,7,8-hexahydro-2-benzoxecin-1-one

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C(O)=C1)C(=O)O[C@H](C)CCCCC2

InChI Identifier

InChI=1S/C15H20O4/c1-10-6-4-3-5-7-11-8-12(18-2)9-13(16)14(11)15(17)19-10/h8-10,16H,3-7H2,1-2H3/t10-/m1/s1

InChI Key

KIVUDNGCLPAVOB-SNVBAGLBSA-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
Chaetosphaeronema hispidulum	NPAtlas	30095908

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxocins. Oxocins are compounds containing an oxocin ring, which is a eight-member unsaturated aromatic ring containing one oxygen atom and seven carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxocins

Sub Class

Not Available

Direct Parent

Oxocins

Alternative Parents

Substituents

Oxocin
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous acid
Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
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	3.64	ALOGPS
logP	4.2	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	9.74	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	72.66 m³·mol⁻¹	ChemAxon
Polarizability	28.98 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

NPAtlas ID

NPA027999

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

141731781

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Hispidulactone A (NP0018563)

MOL for NP0018563 (Hispidulactone A)

3D MOL for NP0018563 (Hispidulactone A)

3D SDF for NP0018563 (Hispidulactone A)

3D-SDF for NP0018563 (Hispidulactone A)

PDB for NP0018563 (Hispidulactone A)

3D PDB for NP0018563 (Hispidulactone A)

SMILES for NP0018563 (Hispidulactone A)

INCHI for NP0018563 (Hispidulactone A)

Structure for NP0018563 (Hispidulactone A)

3D Structure for NP0018563 (Hispidulactone A)