NP-MRD: Showing NP-Card for murrayacoumarin B (NP0031025)

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Record Information

Version

2.0

Created at

2021-06-19 22:13:32 UTC

Updated at

2021-06-29 23:59:21 UTC

NP-MRD ID

NP0031025

Secondary Accession Numbers

None

Natural Product Identification

Common Name

murrayacoumarin B

Provided By

JEOL Database JEOL Logo

Description

murrayacoumarin B is found in Murraya koenigii and Murraya siamensis. murrayacoumarin B was first documented in 2005 (Ito C., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100133D          

 44 47  0  0  0  0            999 V2000
    0.7554    2.7752    2.6040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4544    2.1717    3.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7051    2.6326    4.2130 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1993    1.3616    4.8780 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3505    0.6213    4.1797 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0497    0.0770    2.7990 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1861    1.0144    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6987   -1.1895    2.5548 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2728   -1.2300    2.6703 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5530   -1.6424    1.4274 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2400   -1.0823    1.4641 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4167   -1.3452    0.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7790   -2.0602   -0.7460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1390   -2.2485   -1.7896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4282   -1.7217   -1.6985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4041   -1.8941   -2.7619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6248   -1.3684   -2.6243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0306   -0.6109   -1.4270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1590   -0.1387   -1.3461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828   -0.4676   -0.4271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7871   -1.0143   -0.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8821   -0.8304    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2939   -0.1430    1.6015 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0604    0.5002    5.0206 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0764    0.8693    4.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0781    0.2215    3.9015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1538    2.3320    2.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    3.7285    2.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4306    3.0716    3.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4604    3.3817    4.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5426    1.6104    5.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2279    1.2776    4.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6368   -0.2200    4.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5856    0.5079    0.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.8380    1.8644 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2161    1.4389    1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8498   -1.6846    3.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0895   -1.2959    0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4900   -2.7369    1.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699   -2.4862   -0.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1695   -2.8080   -2.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1290   -2.4478   -3.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3823   -1.4730   -3.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6157   -0.2465    2.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  2  0  0  0  0
  9  6  1  0  0  0  0
 22 12  1  0  0  0  0
 25  2  1  0  0  0  0
 12 13  2  0  0  0  0
  6  5  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 21  1  0  0  0  0
  5  4  1  0  0  0  0
  2  3  1  0  0  0  0
  6  7  1  0  0  0  0
  3  4  1  0  0  0  0
  9  8  1  0  0  0  0
  8  6  1  0  0  0  0
 15 16  1  0  0  0  0
 21 20  1  0  0  0  0
 20 18  1  0  0  0  0
 18 17  1  0  0  0  0
 17 16  2  0  0  0  0
  4 24  1  0  0  0  0
 18 19  2  0  0  0  0
 25 26  2  0  0  0  0
 12 11  1  0  0  0  0
 24 25  1  0  0  0  0
 11 10  1  0  0  0  0
  2  1  2  3  0  0  0
 22 23  1  0  0  0  0
  9 10  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  4 31  1  1  0  0  0
  9 37  1  1  0  0  0
  5 32  1  0  0  0  0
  5 33  1  0  0  0  0
  7 34  1  0  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
 13 40  1  0  0  0  0
 14 41  1  0  0  0  0
 17 43  1  0  0  0  0
 16 42  1  0  0  0  0
 10 38  1  0  0  0  0
 10 39  1  0  0  0  0
 23 44  1  0  0  0  0
M  END

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
    0.7554    2.7752    2.6040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4544    2.1717    3.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7051    2.6326    4.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1993    1.3616    4.8780 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3505    0.6213    4.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0497    0.0770    2.7990 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1861    1.0144    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6987   -1.1895    2.5548 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2728   -1.2300    2.6703 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5530   -1.6424    1.4274 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2400   -1.0823    1.4641 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4167   -1.3452    0.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7790   -2.0602   -0.7460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1390   -2.2485   -1.7896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4282   -1.7217   -1.6985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4041   -1.8941   -2.7619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6248   -1.3684   -2.6243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0306   -0.6109   -1.4270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1590   -0.1387   -1.3461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828   -0.4676   -0.4271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7871   -1.0143   -0.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8821   -0.8304    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2939   -0.1430    1.6015 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0604    0.5002    5.0206 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0764    0.8693    4.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0781    0.2215    3.9015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1538    2.3320    2.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    3.7285    2.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4306    3.0716    3.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4604    3.3817    4.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5426    1.6104    5.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2279    1.2776    4.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6368   -0.2200    4.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5856    0.5079    0.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.8380    1.8644 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2161    1.4389    1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8498   -1.6846    3.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0895   -1.2959    0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4900   -2.7369    1.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699   -2.4862   -0.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1695   -2.8080   -2.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1290   -2.4478   -3.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3823   -1.4730   -3.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6157   -0.2465    2.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  2  0
  9  6  1  0
 22 12  1  0
 25  2  1  0
 12 13  2  0
  6  5  1  1
 13 14  1  0
 14 15  2  0
 15 21  1  0
  5  4  1  0
  2  3  1  0
  6  7  1  0
  3  4  1  0
  9  8  1  0
  8  6  1  0
 15 16  1  0
 21 20  1  0
 20 18  1  0
 18 17  1  0
 17 16  2  0
  4 24  1  0
 18 19  2  0
 25 26  2  0
 12 11  1  0
 24 25  1  0
 11 10  1  0
  2  1  2  3
 22 23  1  0
  9 10  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  1
  9 37  1  1
  5 32  1  0
  5 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
  1 27  1  0
  1 28  1  0
 13 40  1  0
 14 41  1  0
 17 43  1  0
 16 42  1  0
 10 38  1  0
 10 39  1  0
 23 44  1  0
M  END


  Mrv1652306202100133D          

 44 47  0  0  0  0            999 V2000
    0.7554    2.7752    2.6040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4544    2.1717    3.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7051    2.6326    4.2130 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1993    1.3616    4.8780 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3505    0.6213    4.1797 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0497    0.0770    2.7990 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1861    1.0144    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6987   -1.1895    2.5548 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2728   -1.2300    2.6703 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5530   -1.6424    1.4274 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2400   -1.0823    1.4641 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4167   -1.3452    0.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7790   -2.0602   -0.7460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1390   -2.2485   -1.7896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4282   -1.7217   -1.6985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4041   -1.8941   -2.7619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6248   -1.3684   -2.6243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0306   -0.6109   -1.4270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1590   -0.1387   -1.3461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828   -0.4676   -0.4271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7871   -1.0143   -0.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8821   -0.8304    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2939   -0.1430    1.6015 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0604    0.5002    5.0206 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0764    0.8693    4.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0781    0.2215    3.9015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1538    2.3320    2.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    3.7285    2.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4306    3.0716    3.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4604    3.3817    4.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5426    1.6104    5.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2279    1.2776    4.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6368   -0.2200    4.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5856    0.5079    0.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.8380    1.8644 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2161    1.4389    1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8498   -1.6846    3.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0895   -1.2959    0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4900   -2.7369    1.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699   -2.4862   -0.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1695   -2.8080   -2.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1290   -2.4478   -3.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3823   -1.4730   -3.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6157   -0.2465    2.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  2  0  0  0  0
  9  6  1  0  0  0  0
 22 12  1  0  0  0  0
 25  2  1  0  0  0  0
 12 13  2  0  0  0  0
  6  5  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 21  1  0  0  0  0
  5  4  1  0  0  0  0
  2  3  1  0  0  0  0
  6  7  1  0  0  0  0
  3  4  1  0  0  0  0
  9  8  1  0  0  0  0
  8  6  1  0  0  0  0
 15 16  1  0  0  0  0
 21 20  1  0  0  0  0
 20 18  1  0  0  0  0
 18 17  1  0  0  0  0
 17 16  2  0  0  0  0
  4 24  1  0  0  0  0
 18 19  2  0  0  0  0
 25 26  2  0  0  0  0
 12 11  1  0  0  0  0
 24 25  1  0  0  0  0
 11 10  1  0  0  0  0
  2  1  2  3  0  0  0
 22 23  1  0  0  0  0
  9 10  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
  4 31  1  1  0  0  0
  9 37  1  1  0  0  0
  5 32  1  0  0  0  0
  5 33  1  0  0  0  0
  7 34  1  0  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
 13 40  1  0  0  0  0
 14 41  1  0  0  0  0
 17 43  1  0  0  0  0
 16 42  1  0  0  0  0
 10 38  1  0  0  0  0
 10 39  1  0  0  0  0
 23 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031025

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2OC(=O)C([H])=C([H])C2=C([H])C([H])=C1OC([H])([H])[C@@]1([H])O[C@]1(C([H])([H])[H])C([H])([H])[C@]1([H])OC(=O)C(=C([H])[H])C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O7/c1-10-7-12(24-18(10)22)8-19(2)14(26-19)9-23-13-5-3-11-4-6-15(20)25-17(11)16(13)21/h3-6,12,14,21H,1,7-9H2,2H3/t12-,14-,19-/m1/s1

> <INCHI_KEY>
RYBFLVMGRQCAQI-BBEGDGIKSA-N

> <FORMULA>
C19H18O7

> <MOLECULAR_WEIGHT>
358.346

> <EXACT_MASS>
358.10525292

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
35.40647648053656

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-hydroxy-7-{[(2R,3R)-3-methyl-3-{[(2R)-4-methylidene-5-oxooxolan-2-yl]methyl}oxiran-2-yl]methoxy}-2H-chromen-2-one

> <ALOGPS_LOGP>
2.41

> <JCHEM_LOGP>
2.9361275386666663

> <ALOGPS_LOGS>
-3.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.700390363721969

> <JCHEM_PKA_STRONGEST_BASIC>
-3.493450378086737

> <JCHEM_POLAR_SURFACE_AREA>
94.59

> <JCHEM_REFRACTIVITY>
90.29839999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.64e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-hydroxy-7-{[(2R,3R)-3-methyl-3-{[(2R)-4-methylidene-5-oxooxolan-2-yl]methyl}oxiran-2-yl]methoxy}chromen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 44 47  0  0  0  0  0  0  0  0999 V2000
    0.7554    2.7752    2.6040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4544    2.1717    3.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7051    2.6326    4.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1993    1.3616    4.8780 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3505    0.6213    4.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0497    0.0770    2.7990 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1861    1.0144    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6987   -1.1895    2.5548 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2728   -1.2300    2.6703 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5530   -1.6424    1.4274 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2400   -1.0823    1.4641 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4167   -1.3452    0.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7790   -2.0602   -0.7460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1390   -2.2485   -1.7896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4282   -1.7217   -1.6985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4041   -1.8941   -2.7619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6248   -1.3684   -2.6243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0306   -0.6109   -1.4270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1590   -0.1387   -1.3461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828   -0.4676   -0.4271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7871   -1.0143   -0.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8821   -0.8304    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2939   -0.1430    1.6015 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0604    0.5002    5.0206 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0764    0.8693    4.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0781    0.2215    3.9015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1538    2.3320    2.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    3.7285    2.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4306    3.0716    3.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4604    3.3817    4.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5426    1.6104    5.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2279    1.2776    4.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6368   -0.2200    4.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5856    0.5079    0.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.8380    1.8644 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2161    1.4389    1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8498   -1.6846    3.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0895   -1.2959    0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4900   -2.7369    1.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699   -2.4862   -0.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1695   -2.8080   -2.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1290   -2.4478   -3.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3823   -1.4730   -3.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6157   -0.2465    2.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  2  0
  9  6  1  0
 22 12  1  0
 25  2  1  0
 12 13  2  0
  6  5  1  1
 13 14  1  0
 14 15  2  0
 15 21  1  0
  5  4  1  0
  2  3  1  0
  6  7  1  0
  3  4  1  0
  9  8  1  0
  8  6  1  0
 15 16  1  0
 21 20  1  0
 20 18  1  0
 18 17  1  0
 17 16  2  0
  4 24  1  0
 18 19  2  0
 25 26  2  0
 12 11  1  0
 24 25  1  0
 11 10  1  0
  2  1  2  3
 22 23  1  0
  9 10  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  1
  9 37  1  1
  5 32  1  0
  5 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
  1 27  1  0
  1 28  1  0
 13 40  1  0
 14 41  1  0
 17 43  1  0
 16 42  1  0
 10 38  1  0
 10 39  1  0
 23 44  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       0.755   2.775   2.604  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.454   2.172   3.571  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.705   2.633   4.213  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.199   1.362   4.878  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.351   0.621   4.180  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.050   0.077   2.799  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.186   1.014   1.634  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.699  -1.190   2.555  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.273  -1.230   2.670  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.553  -1.642   1.427  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.240  -1.082   1.464  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.417  -1.345   0.401  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.779  -2.060  -0.746  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.139  -2.248  -1.790  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.428  -1.722  -1.698  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.404  -1.894  -2.762  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.625  -1.368  -2.624  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.031  -0.611  -1.427  0.00  0.00           C+0
HETATM   19  O   UNK     0      -5.159  -0.139  -1.346  0.00  0.00           O+0
HETATM   20  O   UNK     0      -3.083  -0.468  -0.427  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.787  -1.014  -0.554  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.882  -0.830   0.493  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.294  -0.143   1.601  0.00  0.00           O+0
HETATM   24  O   UNK     0       2.060   0.500   5.021  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.076   0.869   4.157  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.078   0.222   3.902  0.00  0.00           O+0
HETATM   27  H   UNK     0      -0.154   2.332   2.203  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.066   3.728   2.190  0.00  0.00           H+0
HETATM   29  H   UNK     0       3.431   3.072   3.524  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.460   3.382   4.975  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.543   1.610   5.890  0.00  0.00           H+0
HETATM   32  H   UNK     0       5.228   1.278   4.129  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.637  -0.220   4.826  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.586   0.508   0.748  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.869   1.838   1.864  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.216   1.439   1.363  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.850  -1.685   3.558  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.090  -1.296   0.537  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.490  -2.737   1.409  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.770  -2.486  -0.868  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.170  -2.808  -2.670  0.00  0.00           H+0
HETATM   42  H   UNK     0      -2.129  -2.448  -3.652  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.382  -1.473  -3.391  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.616  -0.247   2.307  0.00  0.00           H+0
CONECT    1    2   27   28                                                  
CONECT    2   25    3    1                                                  
CONECT    3    2    4   29   30                                             
CONECT    4    5    3   24   31                                             
CONECT    5    6    4   32   33                                             
CONECT    6    9    5    7    8                                             
CONECT    7    6   34   35   36                                             
CONECT    8    9    6                                                       
CONECT    9    6    8   10   37                                             
CONECT   10   11    9   38   39                                             
CONECT   11   12   10                                                       
CONECT   12   22   13   11                                                  
CONECT   13   12   14   40                                                  
CONECT   14   13   15   41                                                  
CONECT   15   14   21   16                                                  
CONECT   16   15   17   42                                                  
CONECT   17   18   16   43                                                  
CONECT   18   20   17   19                                                  
CONECT   19   18                                                            
CONECT   20   21   18                                                       
CONECT   21   22   15   20                                                  
CONECT   22   21   12   23                                                  
CONECT   23   22   44                                                       
CONECT   24    4   25                                                       
CONECT   25    2   26   24                                                  
CONECT   26   25                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    5                                                            
CONECT   34    7                                                            
CONECT   35    7                                                            
CONECT   36    7                                                            
CONECT   37    9                                                            
CONECT   38   10                                                            
CONECT   39   10                                                            
CONECT   40   13                                                            
CONECT   41   14                                                            
CONECT   42   16                                                            
CONECT   43   17                                                            
CONECT   44   23                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   94    0
END

RDKit          3D

44 47  0  0  0  0  0  0  0  0999 V2000
    0.7554    2.7752    2.6040 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4544    2.1717    3.5713 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7051    2.6326    4.2130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1993    1.3616    4.8780 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3505    0.6213    4.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0497    0.0770    2.7990 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1861    1.0144    1.6337 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6987   -1.1895    2.5548 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2728   -1.2300    2.6703 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5530   -1.6424    1.4274 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2400   -1.0823    1.4641 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4167   -1.3452    0.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7790   -2.0602   -0.7460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1390   -2.2485   -1.7896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4282   -1.7217   -1.6985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4041   -1.8941   -2.7619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6248   -1.3684   -2.6243 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0306   -0.6109   -1.4270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1590   -0.1387   -1.3461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0828   -0.4676   -0.4271 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7871   -1.0143   -0.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8821   -0.8304    0.4925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2939   -0.1430    1.6015 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0604    0.5002    5.0206 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0764    0.8693    4.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0781    0.2215    3.9015 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1538    2.3320    2.2030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0659    3.7285    2.1899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4306    3.0716    3.5238 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4604    3.3817    4.9754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5426    1.6104    5.8901 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2279    1.2776    4.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6368   -0.2200    4.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5856    0.5079    0.7484 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8692    1.8380    1.8644 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2161    1.4389    1.3630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8498   -1.6846    3.5576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0895   -1.2959    0.5372 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4900   -2.7369    1.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699   -2.4862   -0.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1695   -2.8080   -2.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1290   -2.4478   -3.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3823   -1.4730   -3.3913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6157   -0.2465    2.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 22  2  0
  9  6  1  0
 22 12  1  0
 25  2  1  0
 12 13  2  0
  6  5  1  1
 13 14  1  0
 14 15  2  0
 15 21  1  0
  5  4  1  0
  2  3  1  0
  6  7  1  0
  3  4  1  0
  9  8  1  0
  8  6  1  0
 15 16  1  0
 21 20  1  0
 20 18  1  0
 18 17  1  0
 17 16  2  0
  4 24  1  0
 18 19  2  0
 25 26  2  0
 12 11  1  0
 24 25  1  0
 11 10  1  0
  2  1  2  3
 22 23  1  0
  9 10  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  1
  9 37  1  1
  5 32  1  0
  5 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
  1 27  1  0
  1 28  1  0
 13 40  1  0
 14 41  1  0
 17 43  1  0
 16 42  1  0
 10 38  1  0
 10 39  1  0
 23 44  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₈O₇

Average Mass

358.3460 Da

Monoisotopic Mass

358.10525 Da

IUPAC Name

8-hydroxy-7-{[(2R,3R)-3-methyl-3-{[(2R)-4-methylidene-5-oxooxolan-2-yl]methyl}oxiran-2-yl]methoxy}-2H-chromen-2-one

Traditional Name

8-hydroxy-7-{[(2R,3R)-3-methyl-3-{[(2R)-4-methylidene-5-oxooxolan-2-yl]methyl}oxiran-2-yl]methoxy}chromen-2-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C2OC(=O)C([H])=C([H])C2=C([H])C([H])=C1OC([H])([H])[C@@]1([H])O[C@]1(C([H])([H])[H])C([H])([H])[C@]1([H])OC(=O)C(=C([H])[H])C1([H])[H]

InChI Identifier

InChI=1S/C19H18O7/c1-10-7-12(24-18(10)22)8-19(2)14(26-19)9-23-13-5-3-11-4-6-15(20)25-17(11)16(13)21/h3-6,12,14,21H,1,7-9H2,2H3/t12-,14-,19-/m1/s1

InChI Key

RYBFLVMGRQCAQI-BBEGDGIKSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-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
Murraya koenigii	LOTUS Database	35616633
Murraya siamensis	JEOL database	Ito C., et al, Phytochemistry 66, 567 (2005)

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	2.41	ALOGPS
logP	2.94	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	10.7	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	94.59 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	90.3 m³·mol⁻¹	ChemAxon
Polarizability	35.41 Å³	ChemAxon
Number of Rings	4	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

Ito C., et al. (2005). Ito C., et al, Phytochemistry 66, 567 (2005) . Phytochem..

Showing NP-Card for murrayacoumarin B (NP0031025)

MOL for NP0031025 (murrayacoumarin B)

3D MOL for NP0031025 (murrayacoumarin B)

3D SDF for NP0031025 (murrayacoumarin B)

3D-SDF for NP0031025 (murrayacoumarin B)

PDB for NP0031025 (murrayacoumarin B)

3D PDB for NP0031025 (murrayacoumarin B)

SMILES for NP0031025 (murrayacoumarin B)

INCHI for NP0031025 (murrayacoumarin B)

Structure for NP0031025 (murrayacoumarin B)

3D Structure for NP0031025 (murrayacoumarin B)