NP-MRD: Showing NP-Card for chromene 2 (NP0030187)

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Record Information

Version

2.0

Created at

2021-06-19 21:36:33 UTC

Updated at

2021-06-29 23:58:00 UTC

NP-MRD ID

NP0030187

Secondary Accession Numbers

None

Natural Product Identification

Common Name

chromene 2

Provided By

JEOL Database JEOL Logo

Description

chromene 2 was first documented in 2006 (Mebale,A.-J. A., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123363D          

 40 44  0  0  0  0            999 V2000
   -0.6370   -6.8409   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2168   -5.9726    0.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1143   -4.6303   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6951   -3.8180    0.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6564   -2.4228    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0420   -1.8044   -0.4039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4722   -2.6381   -1.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4963   -4.0338   -1.2633 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1712   -2.1707   -2.5078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2069   -0.8351   -2.8487 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0493    0.1317   -1.6763 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3577    1.4444   -2.1734 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7385    2.3576   -1.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5658    3.6917   -1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9415    4.6943   -0.6890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4990    4.3777    0.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8622    5.4120    1.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4166    5.1351    2.6831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6128    3.8175    3.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2579    2.7773    2.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6971    3.0200    0.9260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3175    2.0004    0.0015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5450    0.5670    0.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9302   -0.3325   -0.5405 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4445   -6.6852   -0.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -7.8699   -0.5642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1200   -6.7245   -1.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1764   -4.2744    1.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1049   -1.8437    1.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0280   -4.6207   -2.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2310   -0.8312   -3.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4353   -0.5145   -3.6777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9967    0.1253   -1.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358    3.9508   -2.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7926    5.7318   -0.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7135    6.4523    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6907    5.9476    3.3505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0396    3.5926    4.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4202    1.7636    2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2111    0.2803    1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 22 23  1  0  0  0  0
  3  8  2  0  0  0  0
  8  7  1  0  0  0  0
 22 13  2  0  0  0  0
  4  3  1  0  0  0  0
 13 14  1  0  0  0  0
  6 24  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 21 22  1  0  0  0  0
  7  9  1  0  0  0  0
  3  2  1  0  0  0  0
  9 10  1  0  0  0  0
  2  1  1  0  0  0  0
 10 11  1  0  0  0  0
 24 11  1  0  0  0  0
 21 16  2  0  0  0  0
  6  5  1  0  0  0  0
 16 17  1  0  0  0  0
  5  4  2  0  0  0  0
 17 18  2  0  0  0  0
  6  7  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  4 28  1  0  0  0  0
  8 30  1  0  0  0  0
  5 29  1  0  0  0  0
 10 31  1  0  0  0  0
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 15 35  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
 17 36  1  0  0  0  0
 18 37  1  0  0  0  0
 19 38  1  0  0  0  0
 20 39  1  0  0  0  0
M  END

     RDKit          3D

 40 44  0  0  0  0  0  0  0  0999 V2000
   -0.6370   -6.8409   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2168   -5.9726    0.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1143   -4.6303   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6951   -3.8180    0.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6564   -2.4228    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0420   -1.8044   -0.4039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4722   -2.6381   -1.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4963   -4.0338   -1.2633 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1712   -2.1707   -2.5078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2069   -0.8351   -2.8487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0493    0.1317   -1.6763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3577    1.4444   -2.1734 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7385    2.3576   -1.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5658    3.6917   -1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9415    4.6943   -0.6890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4990    4.3777    0.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8622    5.4120    1.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4166    5.1351    2.6831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6128    3.8175    3.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2579    2.7773    2.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6971    3.0200    0.9260 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5450    0.5670    0.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9302   -0.3325   -0.5405 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4445   -6.6852   -0.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -7.8699   -0.5642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1200   -6.7245   -1.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2310   -0.8312   -3.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4353   -0.5145   -3.6777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9967    0.1253   -1.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358    3.9508   -2.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7926    5.7318   -0.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7135    6.4523    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6907    5.9476    3.3505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0396    3.5926    4.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4202    1.7636    2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2111    0.2803    1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  2  0
 11 12  1  0
 12 13  1  0
 22 23  1  0
  3  8  2  0
  8  7  1  0
 22 13  2  0
  4  3  1  0
 13 14  1  0
  6 24  1  0
 14 15  2  0
 15 16  1  0
 21 22  1  0
  7  9  1  0
  3  2  1  0
  9 10  1  0
  2  1  1  0
 10 11  1  0
 24 11  1  0
 21 16  2  0
  6  5  1  0
 16 17  1  0
  5  4  2  0
 17 18  2  0
  6  7  2  0
 18 19  1  0
 19 20  2  0
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  4 28  1  0
  8 30  1  0
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 10 31  1  0
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 23 40  1  0
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  1 25  1  0
  1 26  1  0
  1 27  1  0
 17 36  1  0
 18 37  1  0
 19 38  1  0
 20 39  1  0
M  END


  Mrv1652306192123363D          

 40 44  0  0  0  0            999 V2000
   -0.6370   -6.8409   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2168   -5.9726    0.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1143   -4.6303   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6951   -3.8180    0.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6564   -2.4228    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0420   -1.8044   -0.4039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4722   -2.6381   -1.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4963   -4.0338   -1.2633 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1712   -2.1707   -2.5078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2069   -0.8351   -2.8487 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0493    0.1317   -1.6763 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3577    1.4444   -2.1734 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7385    2.3576   -1.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5658    3.6917   -1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9415    4.6943   -0.6890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4990    4.3777    0.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8622    5.4120    1.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4166    5.1351    2.6831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6128    3.8175    3.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2579    2.7773    2.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6971    3.0200    0.9260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3175    2.0004    0.0015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5450    0.5670    0.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9302   -0.3325   -0.5405 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4445   -6.6852   -0.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -7.8699   -0.5642 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9967    0.1253   -1.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358    3.9508   -2.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7926    5.7318   -0.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6907    5.9476    3.3505 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4202    1.7636    2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2111    0.2803    1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  2  0  0  0  0
 11 12  1  0  0  0  0
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 22 13  2  0  0  0  0
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 13 14  1  0  0  0  0
  6 24  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 21 22  1  0  0  0  0
  7  9  1  0  0  0  0
  3  2  1  0  0  0  0
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  2  1  1  0  0  0  0
 10 11  1  0  0  0  0
 24 11  1  0  0  0  0
 21 16  2  0  0  0  0
  6  5  1  0  0  0  0
 16 17  1  0  0  0  0
  5  4  2  0  0  0  0
 17 18  2  0  0  0  0
  6  7  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  4 28  1  0  0  0  0
  8 30  1  0  0  0  0
  5 29  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
 11 33  1  0  0  0  0
 23 40  1  0  0  0  0
 14 34  1  0  0  0  0
 15 35  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
 17 36  1  0  0  0  0
 18 37  1  0  0  0  0
 19 38  1  0  0  0  0
 20 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0030187

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C([H])C2=C(C([H])=C1[H])C1=C(O[C@@]3([H])C(=C1[H])C1=C(OC3([H])[H])C([H])=C(OC([H])([H])[H])C([H])=C1[H])C([H])=C2[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H16O3/c1-22-14-7-8-16-18-11-17-15-5-3-2-4-13(15)6-9-19(17)24-21(18)12-23-20(16)10-14/h2-11,21H,12H2,1H3/t21-/m1/s1

> <INCHI_KEY>
CTYPOHVOJGGAEY-OAQYLSRUSA-N

> <FORMULA>
C21H16O3

> <MOLECULAR_WEIGHT>
316.356

> <EXACT_MASS>
316.109944375

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
35.473030303619694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(12S)-7-methoxy-10,13-dioxapentacyclo[12.8.0.0^{3,12}.0^{4,9}.0^{17,22}]docosa-1(14),2,4(9),5,7,15,17(22),18,20-nonaene

> <ALOGPS_LOGP>
4.34

> <JCHEM_LOGP>
4.254992454666667

> <ALOGPS_LOGS>
-5.60

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.3997658260682195

> <JCHEM_POLAR_SURFACE_AREA>
27.69

> <JCHEM_REFRACTIVITY>
92.84920000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.01e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(12S)-7-methoxy-10,13-dioxapentacyclo[12.8.0.0^{3,12}.0^{4,9}.0^{17,22}]docosa-1(14),2,4(9),5,7,15,17(22),18,20-nonaene

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 40 44  0  0  0  0  0  0  0  0999 V2000
   -0.6370   -6.8409   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2168   -5.9726    0.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1143   -4.6303   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6951   -3.8180    0.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6564   -2.4228    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0420   -1.8044   -0.4039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4722   -2.6381   -1.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4963   -4.0338   -1.2633 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1712   -2.1707   -2.5078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2069   -0.8351   -2.8487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0493    0.1317   -1.6763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3577    1.4444   -2.1734 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7385    2.3576   -1.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5658    3.6917   -1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9415    4.6943   -0.6890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4990    4.3777    0.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8622    5.4120    1.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4166    5.1351    2.6831 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1049   -1.8437    1.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.2310   -0.8312   -3.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1358    3.9508   -2.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4202    1.7636    2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2111    0.2803    1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.637  -6.841  -0.897  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.217  -5.973   0.069  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.114  -4.630  -0.169  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.695  -3.818   0.805  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.656  -2.423   0.694  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.042  -1.804  -0.404  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.472  -2.638  -1.385  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.496  -4.034  -1.263  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.171  -2.171  -2.508  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.207  -0.835  -2.849  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.049   0.132  -1.676  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.358   1.444  -2.173  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.739   2.358  -1.227  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.566   3.692  -1.577  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.942   4.694  -0.689  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.499   4.378   0.557  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.862   5.412   1.436  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.417   5.135   2.683  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.613   3.817   3.069  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.258   2.777   2.206  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.697   3.020   0.926  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.317   2.000   0.002  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.545   0.567   0.244  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.930  -0.333  -0.541  0.00  0.00           C+0
HETATM   25  H   UNK     0       0.445  -6.685  -0.969  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.804  -7.870  -0.564  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.120  -6.724  -1.873  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.176  -4.274   1.667  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.105  -1.844   1.495  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.028  -4.621  -2.046  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.231  -0.831  -3.248  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.435  -0.515  -3.678  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.997   0.125  -1.340  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.136   3.951  -2.540  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.793   5.732  -0.981  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.714   6.452   1.153  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.691   5.948   3.350  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.040   3.593   4.043  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.420   1.764   2.561  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.211   0.280   1.044  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    3    1                                                       
CONECT    3    8    4    2                                                  
CONECT    4    3    5   28                                                  
CONECT    5    6    4   29                                                  
CONECT    6   24    5    7                                                  
CONECT    7    8    9    6                                                  
CONECT    8    3    7   30                                                  
CONECT    9    7   10                                                       
CONECT   10    9   11   31   32                                             
CONECT   11   12   10   24   33                                             
CONECT   12   11   13                                                       
CONECT   13   12   22   14                                                  
CONECT   14   13   15   34                                                  
CONECT   15   14   16   35                                                  
CONECT   16   15   21   17                                                  
CONECT   17   16   18   36                                                  
CONECT   18   17   19   37                                                  
CONECT   19   18   20   38                                                  
CONECT   20   19   21   39                                                  
CONECT   21   22   16   20                                                  
CONECT   22   23   13   21                                                  
CONECT   23   24   22   40                                                  
CONECT   24   23    6   11                                                  
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    4                                                            
CONECT   29    5                                                            
CONECT   30    8                                                            
CONECT   31   10                                                            
CONECT   32   10                                                            
CONECT   33   11                                                            
CONECT   34   14                                                            
CONECT   35   15                                                            
CONECT   36   17                                                            
CONECT   37   18                                                            
CONECT   38   19                                                            
CONECT   39   20                                                            
CONECT   40   23                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   88    0
END

RDKit          3D

40 44  0  0  0  0  0  0  0  0999 V2000
   -0.6370   -6.8409   -0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2168   -5.9726    0.0689 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1143   -4.6303   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6951   -3.8180    0.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6564   -2.4228    0.6937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0420   -1.8044   -0.4039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4722   -2.6381   -1.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4963   -4.0338   -1.2633 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1712   -2.1707   -2.5078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2069   -0.8351   -2.8487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0493    0.1317   -1.6763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3577    1.4444   -2.1734 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7385    2.3576   -1.2267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5658    3.6917   -1.5768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9415    4.6943   -0.6890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4990    4.3777    0.5571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8622    5.4120    1.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4166    5.1351    2.6831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6128    3.8175    3.0692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2579    2.7773    2.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6971    3.0200    0.9260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3175    2.0004    0.0015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5450    0.5670    0.2441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9302   -0.3325   -0.5405 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4445   -6.6852   -0.9692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8036   -7.8699   -0.5642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1200   -6.7245   -1.8730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1764   -4.2744    1.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1049   -1.8437    1.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0280   -4.6207   -2.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2310   -0.8312   -3.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4353   -0.5145   -3.6777 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9967    0.1253   -1.3401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358    3.9508   -2.5403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7926    5.7318   -0.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7135    6.4523    1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6907    5.9476    3.3505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0396    3.5926    4.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4202    1.7636    2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2111    0.2803    1.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  2  0
 11 12  1  0
 12 13  1  0
 22 23  1  0
  3  8  2  0
  8  7  1  0
 22 13  2  0
  4  3  1  0
 13 14  1  0
  6 24  1  0
 14 15  2  0
 15 16  1  0
 21 22  1  0
  7  9  1  0
  3  2  1  0
  9 10  1  0
  2  1  1  0
 10 11  1  0
 24 11  1  0
 21 16  2  0
  6  5  1  0
 16 17  1  0
  5  4  2  0
 17 18  2  0
  6  7  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
  4 28  1  0
  8 30  1  0
  5 29  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 23 40  1  0
 14 34  1  0
 15 35  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 17 36  1  0
 18 37  1  0
 19 38  1  0
 20 39  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₆O₃

Average Mass

316.3560 Da

Monoisotopic Mass

316.10994 Da

IUPAC Name

(12S)-7-methoxy-10,13-dioxapentacyclo[12.8.0.0^{3,12}.0^{4,9}.0^{17,22}]docosa-1(14),2,4(9),5,7,15,17(22),18,20-nonaene

Traditional Name

(12S)-7-methoxy-10,13-dioxapentacyclo[12.8.0.0^{3,12}.0^{4,9}.0^{17,22}]docosa-1(14),2,4(9),5,7,15,17(22),18,20-nonaene

CAS Registry Number

Not Available

SMILES

[H]C1=C([H])C2=C(C([H])=C1[H])C1=C(O[C@@]3([H])C(=C1[H])C1=C(OC3([H])[H])C([H])=C(OC([H])([H])[H])C([H])=C1[H])C([H])=C2[H]

InChI Identifier

InChI=1S/C21H16O3/c1-22-14-7-8-16-18-11-17-15-5-3-2-4-13(15)6-9-19(17)24-21(18)12-23-20(16)10-14/h2-11,21H,12H2,1H3/t21-/m1/s1

InChI Key

CTYPOHVOJGGAEY-OAQYLSRUSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 250 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, 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

synthesis

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	4.34	ALOGPS
logP	4.25	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	27.69 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.85 m³·mol⁻¹	ChemAxon
Polarizability	35.47 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Mebale,A.-J. A., et al. (2006). Mebale,A.-J. A., et al, Magn. Reson. Chem. 44, 892 (2006). Mag. Reson. Chem..

Showing NP-Card for chromene 2 (NP0030187)

MOL for NP0030187 (chromene 2)

3D MOL for NP0030187 (chromene 2)

3D SDF for NP0030187 (chromene 2)

3D-SDF for NP0030187 (chromene 2)

PDB for NP0030187 (chromene 2)

3D PDB for NP0030187 (chromene 2)

SMILES for NP0030187 (chromene 2)

INCHI for NP0030187 (chromene 2)

Structure for NP0030187 (chromene 2)

3D Structure for NP0030187 (chromene 2)