NP-MRD: Showing NP-Card for 10-Norparvulenone (NP0003582)

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Record Information

Version

2.0

Created at

2020-12-09 00:47:35 UTC

Updated at

2021-07-15 16:46:48 UTC

NP-MRD ID

NP0003582

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-Norparvulenone

Provided By

NPAtlas

Description

10-Norparvulenone is found in Microsphaeropsis and Microsphaeropsis sp. FO-5050. 10-Norparvulenone was first documented in 2000 (PMID: 11132970). Based on a literature review very few articles have been published on 4,8-dihydroxy-7-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117483D          

 31 32  0  0  0  0            999 V2000
    3.4109    1.9621    0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708    0.6335    0.3449 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842    0.1841    0.2384 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423    1.0786   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6675    0.6002   -0.1466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9311   -0.7159   -0.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -1.6454    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1935   -2.9598    0.3578 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4474   -1.1901    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5638   -2.0544    0.7555 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8161   -2.9094   -0.2748 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2786   -1.1659    0.0824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6420   -2.3138    0.0268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177   -0.0663    0.3049 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0518    0.8840   -0.8516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7184    1.5365   -0.6547 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7836    2.7032    0.0393 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3500    2.0300    0.8354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7193    2.7241    0.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079    2.1271   -0.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8193    2.0888   -0.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9885   -3.3966   -0.1394 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -1.5692    1.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892   -2.7582    1.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0374   -2.9728   -0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3151   -0.4651    0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9900    0.4644    1.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8586    1.6049   -0.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1200    0.2816   -1.7942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3679    1.7777   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4788    3.5018   -0.4688 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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  9  3  1  0  0  0  0
 16  5  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  4 21  1  0  0  0  0
  8 22  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
 11 25  1  0  0  0  0
 14 26  1  0  0  0  0
 14 27  1  0  0  0  0
 15 28  1  0  0  0  0
 15 29  1  0  0  0  0
 16 30  1  6  0  0  0
 17 31  1  0  0  0  0
M  END

     RDKit          3D

 31 32  0  0  0  0  0  0  0  0999 V2000
    3.4109    1.9621    0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708    0.6335    0.3449 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842    0.1841    0.2384 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423    1.0786   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6675    0.6002   -0.1466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9311   -0.7159   -0.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -1.6454    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1935   -2.9598    0.3578 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4474   -1.1901    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5638   -2.0544    0.7555 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8161   -2.9094   -0.2748 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2786   -1.1659    0.0824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6420   -2.3138    0.0268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177   -0.0663    0.3049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0518    0.8840   -0.8516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7184    1.5365   -0.6547 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7836    2.7032    0.0393 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3500    2.0300    0.8354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7193    2.7241    0.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079    2.1271   -0.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8193    2.0888   -0.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9885   -3.3966   -0.1394 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -1.5692    1.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892   -2.7582    1.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0374   -2.9728   -0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3151   -0.4651    0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9900    0.4644    1.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8586    1.6049   -0.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1200    0.2816   -1.7942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3679    1.7777   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4788    3.5018   -0.4688 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  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
  6 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
  9  3  1  0
 16  5  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  8 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 14 26  1  0
 14 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  6
 17 31  1  0
M  END


  Mrv1652306242117483D          

 31 32  0  0  0  0            999 V2000
    3.4109    1.9621    0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708    0.6335    0.3449 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842    0.1841    0.2384 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423    1.0786   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6675    0.6002   -0.1466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9311   -0.7159   -0.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -1.6454    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1935   -2.9598    0.3578 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4474   -1.1901    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5638   -2.0544    0.7555 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8161   -2.9094   -0.2748 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2786   -1.1659    0.0824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6420   -2.3138    0.0268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177   -0.0663    0.3049 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0518    0.8840   -0.8516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7184    1.5365   -0.6547 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7836    2.7032    0.0393 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3500    2.0300    0.8354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7193    2.7241    0.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079    2.1271   -0.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8193    2.0888   -0.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9885   -3.3966   -0.1394 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -1.5692    1.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892   -2.7582    1.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0374   -2.9728   -0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3151   -0.4651    0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9900    0.4644    1.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8586    1.6049   -0.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1200    0.2816   -1.7942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3679    1.7777   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4788    3.5018   -0.4688 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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  9  3  1  0  0  0  0
 16  5  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  4 21  1  0  0  0  0
  8 22  1  0  0  0  0
 10 23  1  0  0  0  0
 10 24  1  0  0  0  0
 11 25  1  0  0  0  0
 14 26  1  0  0  0  0
 14 27  1  0  0  0  0
 15 28  1  0  0  0  0
 15 29  1  0  0  0  0
 16 30  1  6  0  0  0
 17 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0003582

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C(OC([H])([H])[H])=C([H])C2=C1C(=O)C([H])([H])C([H])([H])[C@@]2([H])O[H])C([H])([H])O[H]

> <INCHI_IDENTIFIER>
InChI=1S/C12H14O5/c1-17-10-4-6-8(14)2-3-9(15)11(6)12(16)7(10)5-13/h4,8,13-14,16H,2-3,5H2,1H3/t8-/m1/s1

> <INCHI_KEY>
NXSUIALRPVXVTA-UHFFFAOYSA-N

> <FORMULA>
C12H14O5

> <MOLECULAR_WEIGHT>
238.239

> <EXACT_MASS>
238.084123551

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
23.807568511134267

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R)-4,8-dihydroxy-7-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-one

> <ALOGPS_LOGP>
0.26

> <JCHEM_LOGP>
0.47172724666666654

> <ALOGPS_LOGS>
-1.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.101453512384072

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.921146913227723

> <JCHEM_PKA_STRONGEST_BASIC>
-3.145659937600491

> <JCHEM_POLAR_SURFACE_AREA>
86.99

> <JCHEM_REFRACTIVITY>
61.1022

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.67e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R)-4,8-dihydroxy-7-(hydroxymethyl)-6-methoxy-3,4-dihydro-2H-naphthalen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 31 32  0  0  0  0  0  0  0  0999 V2000
    3.4109    1.9621    0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708    0.6335    0.3449 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842    0.1841    0.2384 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423    1.0786   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6675    0.6002   -0.1466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9311   -0.7159   -0.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -1.6454    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1935   -2.9598    0.3578 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4474   -1.1901    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5638   -2.0544    0.7555 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8161   -2.9094   -0.2748 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2786   -1.1659    0.0824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6420   -2.3138    0.0268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177   -0.0663    0.3049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0518    0.8840   -0.8516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7184    1.5365   -0.6547 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7836    2.7032    0.0393 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3500    2.0300    0.8354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7193    2.7241    0.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079    2.1271   -0.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8193    2.0888   -0.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9885   -3.3966   -0.1394 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -1.5692    1.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892   -2.7582    1.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0374   -2.9728   -0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3151   -0.4651    0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9900    0.4644    1.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8586    1.6049   -0.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1200    0.2816   -1.7942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3679    1.7777   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4788    3.5018   -0.4688 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  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
  6 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
  9  3  1  0
 16  5  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  8 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 14 26  1  0
 14 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  6
 17 31  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       3.411   1.962   0.257  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.971   0.634   0.345  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.684   0.184   0.238  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.642   1.079  -0.021  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.668   0.600  -0.147  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.931  -0.716  -0.016  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.098  -1.645   0.239  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.194  -2.960   0.358  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.447  -1.190   0.372  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.564  -2.054   0.756  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.816  -2.909  -0.275  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.279  -1.166   0.082  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.642  -2.314   0.027  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.318  -0.066   0.305  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.052   0.884  -0.852  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.718   1.537  -0.655  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.784   2.703   0.039  0.00  0.00           O+0
HETATM   18  H   UNK     0       4.350   2.030   0.835  0.00  0.00           H+0
HETATM   19  H   UNK     0       2.719   2.724   0.638  0.00  0.00           H+0
HETATM   20  H   UNK     0       3.708   2.127  -0.815  0.00  0.00           H+0
HETATM   21  H   UNK     0       0.819   2.089  -0.234  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.989  -3.397  -0.139  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.347  -1.569   1.269  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.089  -2.758   1.610  0.00  0.00           H+0
HETATM   25  H   UNK     0       2.037  -2.973  -0.879  0.00  0.00           H+0
HETATM   26  H   UNK     0      -4.315  -0.465   0.283  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.990   0.464   1.246  0.00  0.00           H+0
HETATM   28  H   UNK     0      -3.859   1.605  -0.873  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.120   0.282  -1.794  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.368   1.778  -1.732  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.479   3.502  -0.469  0.00  0.00           H+0
CONECT    1    2   18   19   20                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   21                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    7   12                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7   22                                                       
CONECT    9    7   10    3                                                  
CONECT   10    9   11   23   24                                             
CONECT   11   10   25                                                       
CONECT   12    6   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   26   27                                             
CONECT   15   14   16   28   29                                             
CONECT   16   15   17    5   30                                             
CONECT   17   16   31                                                       
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    4                                                            
CONECT   22    8                                                            
CONECT   23   10                                                            
CONECT   24   10                                                            
CONECT   25   11                                                            
CONECT   26   14                                                            
CONECT   27   14                                                            
CONECT   28   15                                                            
CONECT   29   15                                                            
CONECT   30   16                                                            
CONECT   31   17                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   64    0
END

RDKit          3D

31 32  0  0  0  0  0  0  0  0999 V2000
    3.4109    1.9621    0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9708    0.6335    0.3449 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6842    0.1841    0.2384 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6423    1.0786   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6675    0.6002   -0.1466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9311   -0.7159   -0.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0977   -1.6454    0.2385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1935   -2.9598    0.3578 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4474   -1.1901    0.3720 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5638   -2.0544    0.7555 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8161   -2.9094   -0.2748 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2786   -1.1659    0.0824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6420   -2.3138    0.0268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3177   -0.0663    0.3049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0518    0.8840   -0.8516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7184    1.5365   -0.6547 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7836    2.7032    0.0393 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3500    2.0300    0.8354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7193    2.7241    0.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079    2.1271   -0.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8193    2.0888   -0.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9885   -3.3966   -0.1394 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3467   -1.5692    1.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892   -2.7582    1.6104 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0374   -2.9728   -0.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3151   -0.4651    0.2830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9900    0.4644    1.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8586    1.6049   -0.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1200    0.2816   -1.7942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3679    1.7777   -1.7316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4788    3.5018   -0.4688 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  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
  6 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
  9  3  1  0
 16  5  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  4 21  1  0
  8 22  1  0
 10 23  1  0
 10 24  1  0
 11 25  1  0
 14 26  1  0
 14 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  6
 17 31  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₂H₁₄O₅

Average Mass

238.2390 Da

Monoisotopic Mass

238.08412 Da

IUPAC Name

(4R)-4,8-dihydroxy-7-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-one

Traditional Name

(4R)-4,8-dihydroxy-7-(hydroxymethyl)-6-methoxy-3,4-dihydro-2H-naphthalen-1-one

CAS Registry Number

Not Available

SMILES

COC1=C(CO)C(O)=C2C(=O)CCC(O)C2=C1

InChI Identifier

InChI=1S/C12H14O5/c1-17-10-4-6-8(14)2-3-9(15)11(6)12(16)7(10)5-13/h4,8,13-14,16H,2-3,5H2,1H3

InChI Key

NXSUIALRPVXVTA-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
Microsphaeropsis	NPAtlas	11132970
Microsphaeropsis sp. FO-5050	-	KNApSAcK

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Tetralins

Sub Class

Not Available

Direct Parent

Tetralins

Alternative Parents

Substituents

Tetralin
Anisole
Phenol ether
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Vinylogous acid
Ketone
Secondary alcohol
Ether
Aromatic alcohol
Hydrocarbon derivative
Organooxygen compound
Alcohol
Organic oxide
Primary alcohol
Organic oxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	0.26	ALOGPS
logP	0.47	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	8.92	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	61.1 m³·mol⁻¹	ChemAxon
Polarizability	23.81 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

NPA005003

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8167356

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9991774

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Fukami A, Nakamura T, Kim YP, Shiomi K, Hayashi M, Nagai T, Yamada H, Komiyama K, Omura S: A new anti-influenza virus antibiotic, 10-norparvulenone from Microsphaeropsis sp. FO-5050. J Antibiot (Tokyo). 2000 Oct;53(10):1215-8. doi: 10.7164/antibiotics.53.1215. [PubMed:11132970 ]

Showing NP-Card for 10-Norparvulenone (NP0003582)

MOL for NP0003582 (10-Norparvulenone)

3D MOL for NP0003582 (10-Norparvulenone)

3D SDF for NP0003582 (10-Norparvulenone)

3D-SDF for NP0003582 (10-Norparvulenone)

PDB for NP0003582 (10-Norparvulenone)

3D PDB for NP0003582 (10-Norparvulenone)

SMILES for NP0003582 (10-Norparvulenone)

INCHI for NP0003582 (10-Norparvulenone)

Structure for NP0003582 (10-Norparvulenone)

3D Structure for NP0003582 (10-Norparvulenone)