NP-MRD: Showing NP-Card for SB236050 (NP0004171)

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Record Information

Version

2.0

Created at

2020-12-09 01:40:07 UTC

Updated at

2021-07-15 16:48:26 UTC

NP-MRD ID

NP0004171

Secondary Accession Numbers

None

Natural Product Identification

Common Name

SB236050

Provided By

NPAtlas

Description

7,8-Dihydroxy-1-methoxy-3-methyl-10-oxo-4,10-dihydro-1H,3H-pyrano[4,3-b]chromene-9-carboxylic acid, also known as SB236050, belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety. 7,8-Dihydroxy-1-methoxy-3-methyl-10-oxo-4,10-dihydro-1H,3H-pyrano[4,3-b]chromene-9-carboxylic acid is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. SB236050 is found in Chaetomium and Dichotomopilus funicola. SB236050 was first documented in 2002 (PMID: 12019104). Based on a literature review very few articles have been published on 7,8-dihydroxy-1-methoxy-3-methyl-10-oxo-4,10-dihydro-1H,3H-pyrano[4,3-b]chromene-9-carboxylic acid (PMID: 24013408).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118043D          

 37 39  0  0  0  0            999 V2000
    2.0616    3.3028    0.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7904    2.1658    0.9259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0945    0.9963    0.2573 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0824    0.2598    0.8472 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2222   -1.0377    0.4705 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6926   -1.3909    0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4974   -1.4361   -0.7968 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0806   -1.0520   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0377   -1.7579   -0.8392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060   -1.3174   -0.6022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2429   -2.1660   -0.9252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5243   -1.7774   -0.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5945   -2.6296   -1.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8735   -0.5288   -0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1756   -0.2342    0.0161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975    0.3164    0.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1012    1.5934    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3318    2.4827    1.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4602    1.9410    0.9198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4766   -0.0773   -0.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3925    0.7181    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4860    1.8383    0.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8709    0.1933   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1317    3.3481   -0.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4968    3.2065   -0.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6926    4.2134    0.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4849    1.2961   -0.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922   -1.7015    1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122   -0.7386    1.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1079   -1.2737   -0.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607   -2.4353    0.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6366   -2.5250   -0.9165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9398   -0.8505   -1.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288   -3.1420   -1.3514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5465   -2.3479   -0.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7283    0.4535    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8197    2.0943    1.8397 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  1  0  0  0  0
  4  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  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
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 16 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23  3  1  0  0  0  0
 23  8  2  0  0  0  0
 20 10  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  3 27  1  6  0  0  0
  5 28  1  1  0  0  0
  6 29  1  0  0  0  0
  6 30  1  0  0  0  0
  6 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
 11 34  1  0  0  0  0
 13 35  1  0  0  0  0
 15 36  1  0  0  0  0
 19 37  1  0  0  0  0
M  END

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
    2.0616    3.3028    0.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7904    2.1658    0.9259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0945    0.9963    0.2573 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0824    0.2598    0.8472 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2222   -1.0377    0.4705 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6926   -1.3909    0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4974   -1.4361   -0.7968 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0806   -1.0520   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0377   -1.7579   -0.8392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060   -1.3174   -0.6022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2429   -2.1660   -0.9252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5243   -1.7774   -0.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5945   -2.6296   -1.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8735   -0.5288   -0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1756   -0.2342    0.0161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975    0.3164    0.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1012    1.5934    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3318    2.4827    1.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4602    1.9410    0.9198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4766   -0.0773   -0.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3925    0.7181    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4860    1.8383    0.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8709    0.1933   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1317    3.3481   -0.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4968    3.2065   -0.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6926    4.2134    0.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4849    1.2961   -0.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922   -1.7015    1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122   -0.7386    1.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1079   -1.2737   -0.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607   -2.4353    0.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6366   -2.5250   -0.9165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9398   -0.8505   -1.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288   -3.1420   -1.3514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5465   -2.3479   -0.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7283    0.4535    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8197    2.0943    1.8397 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  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23  3  1  0
 23  8  2  0
 20 10  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  6
  5 28  1  1
  6 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
 11 34  1  0
 13 35  1  0
 15 36  1  0
 19 37  1  0
M  END


  Mrv1652306242118043D          

 37 39  0  0  0  0            999 V2000
    2.0616    3.3028    0.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7904    2.1658    0.9259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0945    0.9963    0.2573 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0824    0.2598    0.8472 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2222   -1.0377    0.4705 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6926   -1.3909    0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4974   -1.4361   -0.7968 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0806   -1.0520   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0377   -1.7579   -0.8392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060   -1.3174   -0.6022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2429   -2.1660   -0.9252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5243   -1.7774   -0.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5945   -2.6296   -1.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8735   -0.5288   -0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1756   -0.2342    0.0161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975    0.3164    0.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1012    1.5934    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3318    2.4827    1.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4602    1.9410    0.9198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4766   -0.0773   -0.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3925    0.7181    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4860    1.8383    0.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8709    0.1933   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1317    3.3481   -0.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4968    3.2065   -0.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6926    4.2134    0.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4849    1.2961   -0.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922   -1.7015    1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122   -0.7386    1.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1079   -1.2737   -0.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607   -2.4353    0.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6366   -2.5250   -0.9165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9398   -0.8505   -1.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288   -3.1420   -1.3514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5465   -2.3479   -0.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7283    0.4535    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8197    2.0943    1.8397 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  1  0  0  0  0
  4  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  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
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 16 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23  3  1  0  0  0  0
 23  8  2  0  0  0  0
 20 10  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  3 27  1  6  0  0  0
  5 28  1  1  0  0  0
  6 29  1  0  0  0  0
  6 30  1  0  0  0  0
  6 31  1  0  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
 11 34  1  0  0  0  0
 13 35  1  0  0  0  0
 15 36  1  0  0  0  0
 19 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0004171

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C1=C2C(=O)C3=C(OC2=C([H])C(O[H])=C1O[H])C([H])([H])[C@]([H])(O[C@]3([H])OC([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O8/c1-5-3-7-10(15(21-2)22-5)13(18)9-8(23-7)4-6(16)12(17)11(9)14(19)20/h4-5,15-17H,3H2,1-2H3,(H,19,20)/t5-,15+/m1/s1

> <INCHI_KEY>
RSFJMLCZHPZXCW-UHFFFAOYSA-N

> <FORMULA>
C15H14O8

> <MOLECULAR_WEIGHT>
322.269

> <EXACT_MASS>
322.068867411

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
30.805660838405593

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R)-7,8-dihydroxy-1-methoxy-3-methyl-10-oxo-1H,3H,4H,10H-pyrano[4,3-b]chromene-9-carboxylic acid

> <ALOGPS_LOGP>
1.36

> <JCHEM_LOGP>
1.5570157979999997

> <ALOGPS_LOGS>
-2.40

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.64257013247919

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.2536250358549217

> <JCHEM_PKA_STRONGEST_BASIC>
-4.02603425603714

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000001

> <JCHEM_REFRACTIVITY>
77.55590000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.27e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R)-7,8-dihydroxy-1-methoxy-3-methyl-10-oxo-1H,3H,4H-pyrano[4,3-b]chromene-9-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
    2.0616    3.3028    0.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7904    2.1658    0.9259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0945    0.9963    0.2573 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0824    0.2598    0.8472 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2222   -1.0377    0.4705 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6926   -1.3909    0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4974   -1.4361   -0.7968 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0806   -1.0520   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0377   -1.7579   -0.8392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060   -1.3174   -0.6022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2429   -2.1660   -0.9252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5243   -1.7774   -0.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5945   -2.6296   -1.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8735   -0.5288   -0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1756   -0.2342    0.0161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975    0.3164    0.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1012    1.5934    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3318    2.4827    1.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4602    1.9410    0.9198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4766   -0.0773   -0.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3925    0.7181    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4860    1.8383    0.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8709    0.1933   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1317    3.3481   -0.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4968    3.2065   -0.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6926    4.2134    0.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4849    1.2961   -0.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922   -1.7015    1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122   -0.7386    1.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1079   -1.2737   -0.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607   -2.4353    0.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6366   -2.5250   -0.9165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9398   -0.8505   -1.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288   -3.1420   -1.3514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5465   -2.3479   -0.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7283    0.4535    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8197    2.0943    1.8397 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  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23  3  1  0
 23  8  2  0
 20 10  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  6
  5 28  1  1
  6 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
 11 34  1  0
 13 35  1  0
 15 36  1  0
 19 37  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       2.062   3.303   0.137  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.790   2.166   0.926  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.095   0.996   0.257  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.082   0.260   0.847  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.222  -1.038   0.471  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.693  -1.391   0.410  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.497  -1.436  -0.797  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.081  -1.052  -0.578  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.038  -1.758  -0.839  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.206  -1.317  -0.602  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.243  -2.166  -0.925  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.524  -1.777  -0.709  0.00  0.00           C+0
HETATM   13  O   UNK     0      -4.595  -2.630  -1.032  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.874  -0.529  -0.161  0.00  0.00           C+0
HETATM   15  O   UNK     0      -5.176  -0.234   0.016  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.797   0.316   0.159  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.101   1.593   0.718  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.332   2.483   1.069  0.00  0.00           O+0
HETATM   19  O   UNK     0      -4.460   1.941   0.920  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.477  -0.077  -0.061  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.393   0.718   0.238  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.486   1.838   0.721  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.871   0.193  -0.036  0.00  0.00           C+0
HETATM   24  H   UNK     0       3.132   3.348  -0.142  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.497   3.207  -0.834  0.00  0.00           H+0
HETATM   26  H   UNK     0       1.693   4.213   0.612  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.485   1.296  -0.761  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.792  -1.702   1.278  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.212  -0.739   1.153  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.108  -1.274  -0.612  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.861  -2.435   0.755  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.637  -2.525  -0.917  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.940  -0.851  -1.627  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.029  -3.142  -1.351  0.00  0.00           H+0
HETATM   35  H   UNK     0      -5.547  -2.348  -0.875  0.00  0.00           H+0
HETATM   36  H   UNK     0      -5.728   0.454   0.332  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.820   2.094   1.840  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   23   27                                             
CONECT    4    3    5                                                       
CONECT    5    4    6    7   28                                             
CONECT    6    5   29   30   31                                             
CONECT    7    5    8   32   33                                             
CONECT    8    7    9   23                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   20                                                  
CONECT   11   10   12   34                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   35                                                       
CONECT   14   12   15   16                                                  
CONECT   15   14   36                                                       
CONECT   16   14   17   20                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   37                                                       
CONECT   20   16   21   10                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    3    8                                                  
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    3                                                            
CONECT   28    5                                                            
CONECT   29    6                                                            
CONECT   30    6                                                            
CONECT   31    6                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
CONECT   34   11                                                            
CONECT   35   13                                                            
CONECT   36   15                                                            
CONECT   37   19                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   78    0
END

RDKit          3D

37 39  0  0  0  0  0  0  0  0999 V2000
    2.0616    3.3028    0.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7904    2.1658    0.9259 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0945    0.9963    0.2573 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0824    0.2598    0.8472 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2222   -1.0377    0.4705 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6926   -1.3909    0.4099 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4974   -1.4361   -0.7968 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0806   -1.0520   -0.5775 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0377   -1.7579   -0.8392 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060   -1.3174   -0.6022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2429   -2.1660   -0.9252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5243   -1.7774   -0.7089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5945   -2.6296   -1.0322 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8735   -0.5288   -0.1607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1756   -0.2342    0.0161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7975    0.3164    0.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1012    1.5934    0.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3318    2.4827    1.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4602    1.9410    0.9198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4766   -0.0773   -0.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3925    0.7181    0.2377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4860    1.8383    0.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8709    0.1933   -0.0362 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1317    3.3481   -0.1423 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4968    3.2065   -0.8341 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6926    4.2134    0.6124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4849    1.2961   -0.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922   -1.7015    1.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2122   -0.7386    1.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1079   -1.2737   -0.6116 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8607   -2.4353    0.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6366   -2.5250   -0.9165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9398   -0.8505   -1.6274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288   -3.1420   -1.3514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5465   -2.3479   -0.8745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7283    0.4535    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8197    2.0943    1.8397 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  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 16 20  2  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23  3  1  0
 23  8  2  0
 20 10  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  6
  5 28  1  1
  6 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
 11 34  1  0
 13 35  1  0
 15 36  1  0
 19 37  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
SB236050	ChEBI
7,8-Dihydroxy-1-methoxy-3-methyl-10-oxo-4,10-dihydro-1H,3H-pyrano[4,3-b]chromene-9-carboxylate	Generator
7,8-Dihydroxy-1-methoxy-3-methyl-10-oxo-3,4-dihydro-1H-pyrano[4,3-b]chromene-9-carboxylate	Generator

Chemical Formula

C₁₅H₁₄O₈

Average Mass

322.2690 Da

Monoisotopic Mass

322.06887 Da

IUPAC Name

(1S,3R)-7,8-dihydroxy-1-methoxy-3-methyl-10-oxo-1H,3H,4H,10H-pyrano[4,3-b]chromene-9-carboxylic acid

Traditional Name

(1S,3R)-7,8-dihydroxy-1-methoxy-3-methyl-10-oxo-1H,3H,4H-pyrano[4,3-b]chromene-9-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC1OC(C)CC2=C1C(=O)C1=C(C(O)=O)C(O)=C(O)C=C1O2

InChI Identifier

InChI=1S/C15H14O8/c1-5-3-7-10(15(21-2)22-5)13(18)9-8(23-7)4-6(16)12(17)11(9)14(19)20/h4-5,15-17H,3H2,1-2H3,(H,19,20)

InChI Key

RSFJMLCZHPZXCW-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
Chaetomium	NPAtlas	12019104
Dichotomopilus funicola	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Chromones

Alternative Parents

Substituents

Chromone
Hydroxybenzoic acid
Salicylic acid or derivatives
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Acetal
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Oxacycle
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

cyclic ketone (CHEBI:68709 )
monocarboxylic acid (CHEBI:68709 )
organic heterotricyclic compound (CHEBI:68709 )
catechols (CHEBI:68709 )
cyclic ether (CHEBI:68709 )

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	1.36	ALOGPS
logP	1.56	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	2.25	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	122.52 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	77.56 m³·mol⁻¹	ChemAxon
Polarizability	30.81 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	No	ChemAxon

External Links

NPAtlas ID

NPA007405

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4510270

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

68709

Good Scents ID

Not Available

References

General References

Payne DJ, Hueso-Rodriguez JA, Boyd H, Concha NO, Janson CA, Gilpin M, Bateson JH, Cheever C, Niconovich NL, Pearson S, Rittenhouse S, Tew D, Diez E, Perez P, De La Fuente J, Rees M, Rivera-Sagredo A: Identification of a series of tricyclic natural products as potent broad-spectrum inhibitors of metallo-beta-lactamases. Antimicrob Agents Chemother. 2002 Jun;46(6):1880-6. doi: 10.1128/aac.46.6.1880-1886.2002. [PubMed:12019104 ]
Lu K, Zhang Y, Li L, Wang X, Ding G: Chaetochromones A and B, two new polyketides from the fungus Chaetomium indicum (CBS.860.68). Molecules. 2013 Sep 5;18(9):10944-52. doi: 10.3390/molecules180910944. [PubMed:24013408 ]

Showing NP-Card for SB236050 (NP0004171)

MOL for NP0004171 (SB236050)

3D MOL for NP0004171 (SB236050)

3D SDF for NP0004171 (SB236050)

3D-SDF for NP0004171 (SB236050)

PDB for NP0004171 (SB236050)

3D PDB for NP0004171 (SB236050)

SMILES for NP0004171 (SB236050)

INCHI for NP0004171 (SB236050)

Structure for NP0004171 (SB236050)

3D Structure for NP0004171 (SB236050)