NP-MRD: Showing NP-Card for caryatin-3' sulfate (NP0040907)

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Record Information

Version

2.0

Created at

2021-06-20 22:56:54 UTC

Updated at

2021-06-30 00:15:07 UTC

NP-MRD ID

NP0040907

Secondary Accession Numbers

None

Natural Product Identification

Common Name

caryatin-3' sulfate

Provided By

JEOL Database JEOL Logo

Description

caryatin-3' sulfate is found in Carya illinoinensis (Wangenh) K. Koch (Juglandaceae). caryatin-3' sulfate was first documented in 2011 (Abdallah, H. M. et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100563D          

 42 44  0  0  0  0            999 V2000
    1.2027    1.2707   -1.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4234    1.4009    0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6636    0.5385    0.1101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9421   -0.1633    1.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1131   -0.0859    2.4470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1822    1.1424    3.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9462    1.1975    4.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216    0.0190    4.7974 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1428    0.0665    5.9618 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1475   -1.2102    4.1958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5538   -2.4118    4.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1360   -2.6990    4.9954 S   0  0  2  0  0  6  0  0  0  0  0  0
    3.9514   -1.8516    4.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296   -4.1334    5.0103 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3334   -2.1777    6.5101 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3648   -1.2635    3.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9988   -1.0448    1.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7909   -1.2947    0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7698   -2.2771    0.4378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5998   -2.6087   -0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5286   -3.5849   -0.4243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4726   -1.9677   -1.8505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5088   -0.9639   -2.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3858   -0.4097   -3.2510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2609    0.7113   -3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6505   -0.6289   -0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6014    0.4084   -1.0494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5135    1.1472   -2.0231 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2140    1.6216   -0.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8043    1.9083   -1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2752    0.2296   -1.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1863    2.0714    2.6242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1498    2.1676    4.6711 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    1.0068    6.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -1.2634    6.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1387   -2.2303    2.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8763   -2.7908    1.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0100   -3.7431   -1.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1010   -2.2359   -2.6942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0017    1.2256   -4.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1537    1.4237   -2.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3013    0.3770   -3.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 10  1  0  0  0  0
 23 26  2  0  0  0  0
 10  8  2  0  0  0  0
 20 22  2  0  0  0  0
  8  7  1  0  0  0  0
 18 19  2  0  0  0  0
  7  6  2  0  0  0  0
  6  5  1  0  0  0  0
 19 20  1  0  0  0  0
 23 24  1  0  0  0  0
 18 17  1  0  0  0  0
  8  9  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
  3  2  1  0  0  0  0
 27  3  1  0  0  0  0
 20 21  1  0  0  0  0
  3  4  2  0  0  0  0
  2  1  1  0  0  0  0
  4 17  1  0  0  0  0
 10 11  1  0  0  0  0
 18 26  1  0  0  0  0
 11 12  1  0  0  0  0
  4  5  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
  5 16  2  0  0  0  0
 12 15  1  0  0  0  0
 22 23  1  0  0  0  0
 24 25  1  0  0  0  0
 22 39  1  0  0  0  0
 19 37  1  0  0  0  0
 16 36  1  0  0  0  0
  7 33  1  0  0  0  0
  6 32  1  0  0  0  0
  9 34  1  0  0  0  0
 21 38  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
 15 35  1  0  0  0  0
 25 40  1  0  0  0  0
 25 41  1  0  0  0  0
 25 42  1  0  0  0  0
M  END

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    1.2027    1.2707   -1.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4234    1.4009    0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6636    0.5385    0.1101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9421   -0.1633    1.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1131   -0.0859    2.4470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1822    1.1424    3.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9462    1.1975    4.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216    0.0190    4.7974 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1428    0.0665    5.9618 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1475   -1.2102    4.1958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5538   -2.4118    4.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1360   -2.6990    4.9954 S   0  0  0  0  0  6  0  0  0  0  0  0
    3.9514   -1.8516    4.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296   -4.1334    5.0103 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3334   -2.1777    6.5101 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3648   -1.2635    3.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9988   -1.0448    1.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7909   -1.2947    0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7698   -2.2771    0.4378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5998   -2.6087   -0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5286   -3.5849   -0.4243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4726   -1.9677   -1.8505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5088   -0.9639   -2.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3858   -0.4097   -3.2510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2609    0.7113   -3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6505   -0.6289   -0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6014    0.4084   -1.0494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5135    1.1472   -2.0231 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2140    1.6216   -0.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8043    1.9083   -1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2752    0.2296   -1.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1863    2.0714    2.6242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1498    2.1676    4.6711 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    1.0068    6.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -1.2634    6.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1387   -2.2303    2.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8763   -2.7908    1.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0100   -3.7431   -1.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1010   -2.2359   -2.6942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0017    1.2256   -4.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1537    1.4237   -2.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3013    0.3770   -3.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 10  1  0
 23 26  2  0
 10  8  2  0
 20 22  2  0
  8  7  1  0
 18 19  2  0
  7  6  2  0
  6  5  1  0
 19 20  1  0
 23 24  1  0
 18 17  1  0
  8  9  1  0
 26 27  1  0
 27 28  2  0
  3  2  1  0
 27  3  1  0
 20 21  1  0
  3  4  2  0
  2  1  1  0
  4 17  1  0
 10 11  1  0
 18 26  1  0
 11 12  1  0
  4  5  1  0
 12 13  2  0
 12 14  2  0
  5 16  2  0
 12 15  1  0
 22 23  1  0
 24 25  1  0
 22 39  1  0
 19 37  1  0
 16 36  1  0
  7 33  1  0
  6 32  1  0
  9 34  1  0
 21 38  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 15 35  1  0
 25 40  1  0
 25 41  1  0
 25 42  1  0
M  END


  Mrv1652306212100563D          

 42 44  0  0  0  0            999 V2000
    1.2027    1.2707   -1.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4234    1.4009    0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6636    0.5385    0.1101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9421   -0.1633    1.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1131   -0.0859    2.4470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1822    1.1424    3.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9462    1.1975    4.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216    0.0190    4.7974 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1428    0.0665    5.9618 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1475   -1.2102    4.1958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5538   -2.4118    4.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1360   -2.6990    4.9954 S   0  0  2  0  0  6  0  0  0  0  0  0
    3.9514   -1.8516    4.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296   -4.1334    5.0103 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3334   -2.1777    6.5101 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3648   -1.2635    3.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9988   -1.0448    1.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7909   -1.2947    0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7698   -2.2771    0.4378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5998   -2.6087   -0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5286   -3.5849   -0.4243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4726   -1.9677   -1.8505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5088   -0.9639   -2.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3858   -0.4097   -3.2510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2609    0.7113   -3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6505   -0.6289   -0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6014    0.4084   -1.0494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5135    1.1472   -2.0231 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2140    1.6216   -0.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8043    1.9083   -1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2752    0.2296   -1.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1863    2.0714    2.6242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1498    2.1676    4.6711 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    1.0068    6.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -1.2634    6.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1387   -2.2303    2.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8763   -2.7908    1.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0100   -3.7431   -1.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1010   -2.2359   -2.6942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0017    1.2256   -4.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1537    1.4237   -2.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3013    0.3770   -3.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 10  1  0  0  0  0
 23 26  2  0  0  0  0
 10  8  2  0  0  0  0
 20 22  2  0  0  0  0
  8  7  1  0  0  0  0
 18 19  2  0  0  0  0
  7  6  2  0  0  0  0
  6  5  1  0  0  0  0
 19 20  1  0  0  0  0
 23 24  1  0  0  0  0
 18 17  1  0  0  0  0
  8  9  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
  3  2  1  0  0  0  0
 27  3  1  0  0  0  0
 20 21  1  0  0  0  0
  3  4  2  0  0  0  0
  2  1  1  0  0  0  0
  4 17  1  0  0  0  0
 10 11  1  0  0  0  0
 18 26  1  0  0  0  0
 11 12  1  0  0  0  0
  4  5  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  2  0  0  0  0
  5 16  2  0  0  0  0
 12 15  1  0  0  0  0
 22 23  1  0  0  0  0
 24 25  1  0  0  0  0
 22 39  1  0  0  0  0
 19 37  1  0  0  0  0
 16 36  1  0  0  0  0
  7 33  1  0  0  0  0
  6 32  1  0  0  0  0
  9 34  1  0  0  0  0
 21 38  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
 15 35  1  0  0  0  0
 25 40  1  0  0  0  0
 25 41  1  0  0  0  0
 25 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0040907

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O10S/c1-24-12-6-9(18)7-13-14(12)15(20)17(25-2)16(26-13)8-3-4-10(19)11(5-8)27-28(21,22)23/h3-7,18-19H,1-2H3,(H,21,22,23)

> <INCHI_KEY>
TZOCNNYAQORZLV-UHFFFAOYSA-N

> <FORMULA>
C17H14O10S

> <MOLECULAR_WEIGHT>
410.35

> <EXACT_MASS>
410.030767825

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
37.91165332067463

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[2-hydroxy-5-(7-hydroxy-3,5-dimethoxy-4-oxo-4H-chromen-2-yl)phenyl]oxidanesulfonic acid

> <ALOGPS_LOGP>
1.17

> <JCHEM_LOGP>
1.9397075629999998

> <ALOGPS_LOGS>
-3.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.378290212099295

> <JCHEM_PKA_STRONGEST_ACIDIC>
-2.541615810240619

> <JCHEM_PKA_STRONGEST_BASIC>
-4.591004716970351

> <JCHEM_POLAR_SURFACE_AREA>
148.82

> <JCHEM_REFRACTIVITY>
96.08749999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.10e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[2-hydroxy-5-(7-hydroxy-3,5-dimethoxy-4-oxochromen-2-yl)phenyl]oxidanesulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    1.2027    1.2707   -1.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4234    1.4009    0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6636    0.5385    0.1101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9421   -0.1633    1.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1131   -0.0859    2.4470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1822    1.1424    3.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9462    1.1975    4.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216    0.0190    4.7974 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1428    0.0665    5.9618 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1475   -1.2102    4.1958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5538   -2.4118    4.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1360   -2.6990    4.9954 S   0  0  0  0  0  6  0  0  0  0  0  0
    3.9514   -1.8516    4.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296   -4.1334    5.0103 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3334   -2.1777    6.5101 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3648   -1.2635    3.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9988   -1.0448    1.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7909   -1.2947    0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7698   -2.2771    0.4378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5998   -2.6087   -0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5286   -3.5849   -0.4243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4726   -1.9677   -1.8505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5088   -0.9639   -2.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3858   -0.4097   -3.2510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2609    0.7113   -3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6505   -0.6289   -0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6014    0.4084   -1.0494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5135    1.1472   -2.0231 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2140    1.6216   -0.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8043    1.9083   -1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2752    0.2296   -1.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1863    2.0714    2.6242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1498    2.1676    4.6711 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    1.0068    6.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -1.2634    6.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1387   -2.2303    2.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8763   -2.7908    1.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0100   -3.7431   -1.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1010   -2.2359   -2.6942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0017    1.2256   -4.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1537    1.4237   -2.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3013    0.3770   -3.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 10  1  0
 23 26  2  0
 10  8  2  0
 20 22  2  0
  8  7  1  0
 18 19  2  0
  7  6  2  0
  6  5  1  0
 19 20  1  0
 23 24  1  0
 18 17  1  0
  8  9  1  0
 26 27  1  0
 27 28  2  0
  3  2  1  0
 27  3  1  0
 20 21  1  0
  3  4  2  0
  2  1  1  0
  4 17  1  0
 10 11  1  0
 18 26  1  0
 11 12  1  0
  4  5  1  0
 12 13  2  0
 12 14  2  0
  5 16  2  0
 12 15  1  0
 22 23  1  0
 24 25  1  0
 22 39  1  0
 19 37  1  0
 16 36  1  0
  7 33  1  0
  6 32  1  0
  9 34  1  0
 21 38  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 15 35  1  0
 25 40  1  0
 25 41  1  0
 25 42  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0       1.203   1.271  -1.132  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.423   1.401   0.055  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.664   0.539   0.110  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.942  -0.163   1.226  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.113  -0.086   2.447  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.182   1.142   3.057  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.946   1.198   4.227  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.422   0.019   4.797  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.143   0.067   5.962  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.147  -1.210   4.196  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.554  -2.412   4.713  0.00  0.00           O+0
HETATM   12  S   UNK     0       3.136  -2.699   4.995  0.00  0.00           S+0
HETATM   13  O   UNK     0       3.951  -1.852   4.150  0.00  0.00           O+0
HETATM   14  O   UNK     0       3.330  -4.133   5.010  0.00  0.00           O+0
HETATM   15  O   UNK     0       3.333  -2.178   6.510  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.365  -1.264   3.040  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.999  -1.045   1.359  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.791  -1.295   0.271  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.770  -2.277   0.438  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.600  -2.609  -0.625  0.00  0.00           C+0
HETATM   21  O   UNK     0      -5.529  -3.585  -0.424  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.473  -1.968  -1.851  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.509  -0.964  -2.004  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.386  -0.410  -3.251  0.00  0.00           O+0
HETATM   25  C   UNK     0      -4.261   0.711  -3.390  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.651  -0.629  -0.946  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.601   0.408  -1.049  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.514   1.147  -2.023  0.00  0.00           O+0
HETATM   29  H   UNK     0       2.214   1.622  -0.905  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.804   1.908  -1.926  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.275   0.230  -1.466  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.186   2.071   2.624  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.150   2.168   4.671  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.217   1.007   6.220  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.968  -1.263   6.538  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.139  -2.230   2.594  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.876  -2.791   1.390  0.00  0.00           H+0
HETATM   38  H   UNK     0      -6.010  -3.743  -1.254  0.00  0.00           H+0
HETATM   39  H   UNK     0      -5.101  -2.236  -2.694  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.002   1.226  -4.321  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.154   1.424  -2.565  0.00  0.00           H+0
HETATM   42  H   UNK     0      -5.301   0.377  -3.465  0.00  0.00           H+0
CONECT    1    2   29   30   31                                             
CONECT    2    3    1                                                       
CONECT    3    2   27    4                                                  
CONECT    4    3   17    5                                                  
CONECT    5    6    4   16                                                  
CONECT    6    7    5   32                                                  
CONECT    7    8    6   33                                                  
CONECT    8   10    7    9                                                  
CONECT    9    8   34                                                       
CONECT   10   16    8   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   35                                                       
CONECT   16   10    5   36                                                  
CONECT   17   18    4                                                       
CONECT   18   19   17   26                                                  
CONECT   19   18   20   37                                                  
CONECT   20   22   19   21                                                  
CONECT   21   20   38                                                       
CONECT   22   20   23   39                                                  
CONECT   23   26   24   22                                                  
CONECT   24   23   25                                                       
CONECT   25   24   40   41   42                                             
CONECT   26   23   27   18                                                  
CONECT   27   26   28    3                                                  
CONECT   28   27                                                            
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    6                                                            
CONECT   33    7                                                            
CONECT   34    9                                                            
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   19                                                            
CONECT   38   21                                                            
CONECT   39   22                                                            
CONECT   40   25                                                            
CONECT   41   25                                                            
CONECT   42   25                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

RDKit          3D

42 44  0  0  0  0  0  0  0  0999 V2000
    1.2027    1.2707   -1.1318 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4234    1.4009    0.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6636    0.5385    0.1101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9421   -0.1633    1.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1131   -0.0859    2.4470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1822    1.1424    3.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9462    1.1975    4.2269 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216    0.0190    4.7974 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1428    0.0665    5.9618 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1475   -1.2102    4.1958 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5538   -2.4118    4.7133 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1360   -2.6990    4.9954 S   0  0  0  0  0  6  0  0  0  0  0  0
    3.9514   -1.8516    4.1499 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3296   -4.1334    5.0103 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3334   -2.1777    6.5101 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3648   -1.2635    3.0396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9988   -1.0448    1.3592 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7909   -1.2947    0.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7698   -2.2771    0.4378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5998   -2.6087   -0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5286   -3.5849   -0.4243 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4726   -1.9677   -1.8505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5088   -0.9639   -2.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3858   -0.4097   -3.2510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2609    0.7113   -3.3904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6505   -0.6289   -0.9456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6014    0.4084   -1.0494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5135    1.1472   -2.0231 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2140    1.6216   -0.9046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8043    1.9083   -1.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2752    0.2296   -1.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1863    2.0714    2.6242 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1498    2.1676    4.6711 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2170    1.0068    6.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -1.2634    6.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1387   -2.2303    2.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8763   -2.7908    1.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0100   -3.7431   -1.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1010   -2.2359   -2.6942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0017    1.2256   -4.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1537    1.4237   -2.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3013    0.3770   -3.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 10  1  0
 23 26  2  0
 10  8  2  0
 20 22  2  0
  8  7  1  0
 18 19  2  0
  7  6  2  0
  6  5  1  0
 19 20  1  0
 23 24  1  0
 18 17  1  0
  8  9  1  0
 26 27  1  0
 27 28  2  0
  3  2  1  0
 27  3  1  0
 20 21  1  0
  3  4  2  0
  2  1  1  0
  4 17  1  0
 10 11  1  0
 18 26  1  0
 11 12  1  0
  4  5  1  0
 12 13  2  0
 12 14  2  0
  5 16  2  0
 12 15  1  0
 22 23  1  0
 24 25  1  0
 22 39  1  0
 19 37  1  0
 16 36  1  0
  7 33  1  0
  6 32  1  0
  9 34  1  0
 21 38  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 15 35  1  0
 25 40  1  0
 25 41  1  0
 25 42  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₁₀S

Average Mass

410.3500 Da

Monoisotopic Mass

410.03077 Da

IUPAC Name

[2-hydroxy-5-(7-hydroxy-3,5-dimethoxy-4-oxo-4H-chromen-2-yl)phenyl]oxidanesulfonic acid

Traditional Name

[2-hydroxy-5-(7-hydroxy-3,5-dimethoxy-4-oxochromen-2-yl)phenyl]oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C(OC([H])([H])[H])=C2C(=O)C(OC([H])([H])[H])=C(OC2=C1[H])C1=C([H])C(O[S](=O)(=O)O[H])=C(O[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C17H14O10S/c1-24-12-6-9(18)7-13-14(12)15(20)17(25-2)16(26-13)8-3-4-10(19)11(5-8)27-28(21,22)23/h3-7,18-19H,1-2H3,(H,21,22,23)

InChI Key

TZOCNNYAQORZLV-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Carya illinoinensis	JEOL database	Abdallah, H. M. et al, Phyto. Lett. 4, 337 (2011)

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.17	ALOGPS
logP	1.94	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	-2.5	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	148.82 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	96.09 m³·mol⁻¹	ChemAxon
Polarizability	37.91 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

Not Available

References

General References

Abdallah, H. M. et al. (2011). Abdallah, H. M. et al, Phyto. Lett. 4, 337 (2011). Phyto. Lett..

Showing NP-Card for caryatin-3' sulfate (NP0040907)

MOL for NP0040907 (caryatin-3' sulfate)

3D MOL for NP0040907 (caryatin-3' sulfate)

3D SDF for NP0040907 (caryatin-3' sulfate)

3D-SDF for NP0040907 (caryatin-3' sulfate)

PDB for NP0040907 (caryatin-3' sulfate)

3D PDB for NP0040907 (caryatin-3' sulfate)

SMILES for NP0040907 (caryatin-3' sulfate)

INCHI for NP0040907 (caryatin-3' sulfate)

Structure for NP0040907 (caryatin-3' sulfate)

3D Structure for NP0040907 (caryatin-3' sulfate)