NP-MRD: Showing NP-Card for salviamine F (NP0031774)

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Record Information

Version

2.0

Created at

2021-06-19 22:45:43 UTC

Updated at

2021-06-30 00:00:34 UTC

NP-MRD ID

NP0031774

Secondary Accession Numbers

None

Natural Product Identification

Common Name

salviamine F

Provided By

JEOL Database JEOL Logo

Description

1-{11-Hydroxy-6,6-dimethyl-16-oxa-14-azatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]Heptadeca-1(10),2(7),8,11,13(17),14-hexaen-12-yl}ethan-1-one belongs to the class of organic compounds known as phenanthrols. Phenanthrols are compounds containing a phenanthrene (or its hydrogenated derivative) to which a hydroxyl group is attached. salviamine F is found in Salvia Yunnanensis. salviamine F was first documented in 2006 (Lin, F. -W., et al.). Based on a literature review very few articles have been published on 1-{11-hydroxy-6,6-dimethyl-16-oxa-14-azatetracyclo[8.7.0.0²,⁷.0¹³,¹⁷]Heptadeca-1(10),2(7),8,11,13(17),14-hexaen-12-yl}ethan-1-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202100453D          

 42 45  0  0  0  0            999 V2000
    4.7817   -3.4301    3.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9437   -2.2002    3.6913 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6644   -1.4463    4.6270 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4337   -1.8642    2.3368 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6610   -0.7018    2.1201 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3589    0.1492    3.1667 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1574   -0.3475    0.8430 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3811    0.8039    0.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8621    1.1447   -0.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0989    0.3577   -1.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9269   -0.7825   -1.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4217   -1.1503   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -2.3126   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674   -3.2891   -0.9047 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2727   -4.1749   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -3.8709    1.1106 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870   -2.6825    1.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -1.6317   -2.8077 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9611   -0.9831   -4.1512 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5813   -0.3552   -4.1247 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4863    0.7787   -3.0768 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0163    1.1212   -2.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2254    2.0337   -3.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0711   -3.4774    4.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6985   -3.3801    3.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2056   -4.3302    3.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7582   -0.2101    3.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1584    1.4561    1.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2668    2.0531   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6725   -5.0354   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7046   -2.5721   -2.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3349   -1.8641   -2.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224   -0.2314   -4.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0153   -1.7405   -4.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3317    0.0248   -5.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1546   -1.1401   -3.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1885    2.0121   -2.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5708    0.2933   -2.4810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4640    1.3221   -3.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8651    2.3253   -4.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    1.8739   -3.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0727    2.8917   -2.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  4  1  0  0  0  0
 15 14  1  0  0  0  0
 11 10  1  0  0  0  0
  2  1  1  0  0  0  0
 10  9  2  0  0  0  0
  4  5  2  0  0  0  0
  9  8  1  0  0  0  0
  8  7  2  0  0  0  0
 12 11  2  0  0  0  0
 12  7  1  0  0  0  0
  5  6  1  0  0  0  0
 18 11  1  0  0  0  0
  2  3  2  0  0  0  0
 17  4  1  0  0  0  0
 20 21  1  0  0  0  0
 17 16  1  0  0  0  0
 21 22  1  0  0  0  0
 19 20  1  0  0  0  0
 10 21  1  0  0  0  0
 16 15  2  0  0  0  0
 21 23  1  0  0  0  0
  5  7  1  0  0  0  0
 18 19  1  0  0  0  0
 17 13  2  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 15 30  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  6 27  1  0  0  0  0
 19 33  1  0  0  0  0
 19 34  1  0  0  0  0
 18 31  1  0  0  0  0
 18 32  1  0  0  0  0
  9 29  1  0  0  0  0
  8 28  1  0  0  0  0
 20 35  1  0  0  0  0
 20 36  1  0  0  0  0
 22 37  1  0  0  0  0
 22 38  1  0  0  0  0
 22 39  1  0  0  0  0
 23 40  1  0  0  0  0
 23 41  1  0  0  0  0
 23 42  1  0  0  0  0
M  END

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
    4.7817   -3.4301    3.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9437   -2.2002    3.6913 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6644   -1.4463    4.6270 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4337   -1.8642    2.3368 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6610   -0.7018    2.1201 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3589    0.1492    3.1667 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1574   -0.3475    0.8430 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3811    0.8039    0.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8621    1.1447   -0.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0989    0.3577   -1.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9269   -0.7825   -1.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4217   -1.1503   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -2.3126   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674   -3.2891   -0.9047 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2727   -4.1749   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -3.8709    1.1106 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870   -2.6825    1.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -1.6317   -2.8077 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9611   -0.9831   -4.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5813   -0.3552   -4.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4863    0.7787   -3.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0163    1.1212   -2.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2254    2.0337   -3.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0711   -3.4774    4.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6985   -3.3801    3.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2056   -4.3302    3.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7582   -0.2101    3.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1584    1.4561    1.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2668    2.0531   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6725   -5.0354   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7046   -2.5721   -2.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3349   -1.8641   -2.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224   -0.2314   -4.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0153   -1.7405   -4.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3317    0.0248   -5.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1546   -1.1401   -3.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1885    2.0121   -2.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5708    0.2933   -2.4810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4640    1.3221   -3.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8651    2.3253   -4.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    1.8739   -3.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0727    2.8917   -2.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  4  1  0
 15 14  1  0
 11 10  1  0
  2  1  1  0
 10  9  2  0
  4  5  2  0
  9  8  1  0
  8  7  2  0
 12 11  2  0
 12  7  1  0
  5  6  1  0
 18 11  1  0
  2  3  2  0
 17  4  1  0
 20 21  1  0
 17 16  1  0
 21 22  1  0
 19 20  1  0
 10 21  1  0
 16 15  2  0
 21 23  1  0
  5  7  1  0
 18 19  1  0
 17 13  2  0
 12 13  1  0
 14 13  1  0
 15 30  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  6 27  1  0
 19 33  1  0
 19 34  1  0
 18 31  1  0
 18 32  1  0
  9 29  1  0
  8 28  1  0
 20 35  1  0
 20 36  1  0
 22 37  1  0
 22 38  1  0
 22 39  1  0
 23 40  1  0
 23 41  1  0
 23 42  1  0
M  END


  Mrv1652306202100453D          

 42 45  0  0  0  0            999 V2000
    4.7817   -3.4301    3.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9437   -2.2002    3.6913 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6644   -1.4463    4.6270 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4337   -1.8642    2.3368 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6610   -0.7018    2.1201 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3589    0.1492    3.1667 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1574   -0.3475    0.8430 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3811    0.8039    0.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8621    1.1447   -0.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0989    0.3577   -1.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9269   -0.7825   -1.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4217   -1.1503   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -2.3126   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674   -3.2891   -0.9047 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2727   -4.1749   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -3.8709    1.1106 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870   -2.6825    1.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -1.6317   -2.8077 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9611   -0.9831   -4.1512 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5813   -0.3552   -4.1247 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4863    0.7787   -3.0768 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0163    1.1212   -2.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2254    2.0337   -3.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0711   -3.4774    4.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6985   -3.3801    3.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2056   -4.3302    3.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7582   -0.2101    3.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1584    1.4561    1.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2668    2.0531   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6725   -5.0354   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7046   -2.5721   -2.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3349   -1.8641   -2.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224   -0.2314   -4.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0153   -1.7405   -4.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3317    0.0248   -5.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1546   -1.1401   -3.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1885    2.0121   -2.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5708    0.2933   -2.4810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4640    1.3221   -3.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8651    2.3253   -4.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    1.8739   -3.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0727    2.8917   -2.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  4  1  0  0  0  0
 15 14  1  0  0  0  0
 11 10  1  0  0  0  0
  2  1  1  0  0  0  0
 10  9  2  0  0  0  0
  4  5  2  0  0  0  0
  9  8  1  0  0  0  0
  8  7  2  0  0  0  0
 12 11  2  0  0  0  0
 12  7  1  0  0  0  0
  5  6  1  0  0  0  0
 18 11  1  0  0  0  0
  2  3  2  0  0  0  0
 17  4  1  0  0  0  0
 20 21  1  0  0  0  0
 17 16  1  0  0  0  0
 21 22  1  0  0  0  0
 19 20  1  0  0  0  0
 10 21  1  0  0  0  0
 16 15  2  0  0  0  0
 21 23  1  0  0  0  0
  5  7  1  0  0  0  0
 18 19  1  0  0  0  0
 17 13  2  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  0  0  0  0
 15 30  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  1 26  1  0  0  0  0
  6 27  1  0  0  0  0
 19 33  1  0  0  0  0
 19 34  1  0  0  0  0
 18 31  1  0  0  0  0
 18 32  1  0  0  0  0
  9 29  1  0  0  0  0
  8 28  1  0  0  0  0
 20 35  1  0  0  0  0
 20 36  1  0  0  0  0
 22 37  1  0  0  0  0
 22 38  1  0  0  0  0
 22 39  1  0  0  0  0
 23 40  1  0  0  0  0
 23 41  1  0  0  0  0
 23 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0031774

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C(=O)C([H])([H])[H])C2=C(OC([H])=N2)C2=C3C(=C([H])C([H])=C12)C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])C3([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H19NO3/c1-10(21)14-16-18(23-9-20-16)15-11-5-4-8-19(2,3)13(11)7-6-12(15)17(14)22/h6-7,9,22H,4-5,8H2,1-3H3

> <INCHI_KEY>
PFWZZLBGBKUQMP-UHFFFAOYSA-N

> <FORMULA>
C19H19NO3

> <MOLECULAR_WEIGHT>
309.365

> <EXACT_MASS>
309.136493476

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.16496827959258

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-{11-hydroxy-6,6-dimethyl-16-oxa-14-azatetracyclo[8.7.0.0^{2,7}.0^{13,17}]heptadeca-1,7,9,11,13(17),14-hexaen-12-yl}ethan-1-one

> <ALOGPS_LOGP>
4.27

> <JCHEM_LOGP>
4.252744782666667

> <ALOGPS_LOGS>
-4.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.27843530210308

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.32309671005039

> <JCHEM_PKA_STRONGEST_BASIC>
-0.10844539713670887

> <JCHEM_POLAR_SURFACE_AREA>
63.33

> <JCHEM_REFRACTIVITY>
88.06289999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.58e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-{11-hydroxy-6,6-dimethyl-16-oxa-14-azatetracyclo[8.7.0.0^{2,7}.0^{13,17}]heptadeca-1,7,9,11,13(17),14-hexaen-12-yl}ethanone

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
    4.7817   -3.4301    3.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9437   -2.2002    3.6913 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6644   -1.4463    4.6270 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4337   -1.8642    2.3368 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6610   -0.7018    2.1201 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3589    0.1492    3.1667 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1574   -0.3475    0.8430 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3811    0.8039    0.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8621    1.1447   -0.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0989    0.3577   -1.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9269   -0.7825   -1.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4217   -1.1503   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -2.3126   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674   -3.2891   -0.9047 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2727   -4.1749   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -3.8709    1.1106 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870   -2.6825    1.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -1.6317   -2.8077 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9611   -0.9831   -4.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5813   -0.3552   -4.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4863    0.7787   -3.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0163    1.1212   -2.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2254    2.0337   -3.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0711   -3.4774    4.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6985   -3.3801    3.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2056   -4.3302    3.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7582   -0.2101    3.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1584    1.4561    1.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2668    2.0531   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6725   -5.0354   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7046   -2.5721   -2.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3349   -1.8641   -2.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224   -0.2314   -4.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0153   -1.7405   -4.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3317    0.0248   -5.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1546   -1.1401   -3.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1885    2.0121   -2.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5708    0.2933   -2.4810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4640    1.3221   -3.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8651    2.3253   -4.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    1.8739   -3.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0727    2.8917   -2.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  4  1  0
 15 14  1  0
 11 10  1  0
  2  1  1  0
 10  9  2  0
  4  5  2  0
  9  8  1  0
  8  7  2  0
 12 11  2  0
 12  7  1  0
  5  6  1  0
 18 11  1  0
  2  3  2  0
 17  4  1  0
 20 21  1  0
 17 16  1  0
 21 22  1  0
 19 20  1  0
 10 21  1  0
 16 15  2  0
 21 23  1  0
  5  7  1  0
 18 19  1  0
 17 13  2  0
 12 13  1  0
 14 13  1  0
 15 30  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  6 27  1  0
 19 33  1  0
 19 34  1  0
 18 31  1  0
 18 32  1  0
  9 29  1  0
  8 28  1  0
 20 35  1  0
 20 36  1  0
 22 37  1  0
 22 38  1  0
 22 39  1  0
 23 40  1  0
 23 41  1  0
 23 42  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       4.782  -3.430   3.913  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.944  -2.200   3.691  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.664  -1.446   4.627  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.434  -1.864   2.337  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.661  -0.702   2.120  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.359   0.149   3.167  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.157  -0.348   0.843  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.381   0.804   0.658  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.862   1.145  -0.592  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.099   0.358  -1.732  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.927  -0.783  -1.599  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.422  -1.150  -0.298  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.188  -2.313  -0.018  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.567  -3.289  -0.905  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.273  -4.175  -0.160  0.00  0.00           C+0
HETATM   16  N   UNK     0       4.381  -3.871   1.111  0.00  0.00           N+0
HETATM   17  C   UNK     0       3.687  -2.683   1.227  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.264  -1.632  -2.808  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.961  -0.983  -4.151  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.581  -0.355  -4.125  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.486   0.779  -3.077  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.016   1.121  -2.938  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.225   2.034  -3.591  0.00  0.00           C+0
HETATM   24  H   UNK     0       5.071  -3.477   4.968  0.00  0.00           H+0
HETATM   25  H   UNK     0       5.699  -3.380   3.321  0.00  0.00           H+0
HETATM   26  H   UNK     0       4.206  -4.330   3.686  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.758  -0.210   3.992  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.158   1.456   1.502  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.267   2.053  -0.657  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.673  -5.035  -0.679  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.705  -2.572  -2.731  0.00  0.00           H+0
HETATM   32  H   UNK     0       3.335  -1.864  -2.812  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.722  -0.231  -4.389  0.00  0.00           H+0
HETATM   34  H   UNK     0       2.015  -1.740  -4.942  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.332   0.025  -5.123  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.155  -1.140  -3.901  0.00  0.00           H+0
HETATM   37  H   UNK     0      -1.188   2.012  -2.325  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.571   0.293  -2.481  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.464   1.322  -3.919  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.865   2.325  -4.584  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.307   1.874  -3.660  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.073   2.892  -2.925  0.00  0.00           H+0
CONECT    1    2   24   25   26                                             
CONECT    2    4    1    3                                                  
CONECT    3    2                                                            
CONECT    4    2    5   17                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   27                                                       
CONECT    7    8   12    5                                                  
CONECT    8    9    7   28                                                  
CONECT    9   10    8   29                                                  
CONECT   10   11    9   21                                                  
CONECT   11   10   12   18                                                  
CONECT   12   11    7   13                                                  
CONECT   13   17   12   14                                                  
CONECT   14   15   13                                                       
CONECT   15   14   16   30                                                  
CONECT   16   17   15                                                       
CONECT   17    4   16   13                                                  
CONECT   18   11   19   31   32                                             
CONECT   19   20   18   33   34                                             
CONECT   20   21   19   35   36                                             
CONECT   21   20   22   10   23                                             
CONECT   22   21   37   38   39                                             
CONECT   23   21   40   41   42                                             
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    6                                                            
CONECT   28    8                                                            
CONECT   29    9                                                            
CONECT   30   15                                                            
CONECT   31   18                                                            
CONECT   32   18                                                            
CONECT   33   19                                                            
CONECT   34   19                                                            
CONECT   35   20                                                            
CONECT   36   20                                                            
CONECT   37   22                                                            
CONECT   38   22                                                            
CONECT   39   22                                                            
CONECT   40   23                                                            
CONECT   41   23                                                            
CONECT   42   23                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

RDKit          3D

42 45  0  0  0  0  0  0  0  0999 V2000
    4.7817   -3.4301    3.9130 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9437   -2.2002    3.6913 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6644   -1.4463    4.6270 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4337   -1.8642    2.3368 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6610   -0.7018    2.1201 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3589    0.1492    3.1667 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1574   -0.3475    0.8430 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3811    0.8039    0.6575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8621    1.1447   -0.5923 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0989    0.3577   -1.7316 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9269   -0.7825   -1.5987 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4217   -1.1503   -0.2978 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1877   -2.3126   -0.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674   -3.2891   -0.9047 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2727   -4.1749   -0.1600 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3807   -3.8709    1.1106 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6870   -2.6825    1.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -1.6317   -2.8077 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9611   -0.9831   -4.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5813   -0.3552   -4.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4863    0.7787   -3.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0163    1.1212   -2.9384 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2254    2.0337   -3.5908 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0711   -3.4774    4.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6985   -3.3801    3.3207 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2056   -4.3302    3.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7582   -0.2101    3.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1584    1.4561    1.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2668    2.0531   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6725   -5.0354   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7046   -2.5721   -2.7308 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3349   -1.8641   -2.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7224   -0.2314   -4.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0153   -1.7405   -4.9418 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3317    0.0248   -5.1234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1546   -1.1401   -3.9006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1885    2.0121   -2.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5708    0.2933   -2.4810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4640    1.3221   -3.9191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8651    2.3253   -4.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3069    1.8739   -3.6595 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0727    2.8917   -2.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  4  1  0
 15 14  1  0
 11 10  1  0
  2  1  1  0
 10  9  2  0
  4  5  2  0
  9  8  1  0
  8  7  2  0
 12 11  2  0
 12  7  1  0
  5  6  1  0
 18 11  1  0
  2  3  2  0
 17  4  1  0
 20 21  1  0
 17 16  1  0
 21 22  1  0
 19 20  1  0
 10 21  1  0
 16 15  2  0
 21 23  1  0
  5  7  1  0
 18 19  1  0
 17 13  2  0
 12 13  1  0
 14 13  1  0
 15 30  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  6 27  1  0
 19 33  1  0
 19 34  1  0
 18 31  1  0
 18 32  1  0
  9 29  1  0
  8 28  1  0
 20 35  1  0
 20 36  1  0
 22 37  1  0
 22 38  1  0
 22 39  1  0
 23 40  1  0
 23 41  1  0
 23 42  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₉H₁₉NO₃

Average Mass

309.3650 Da

Monoisotopic Mass

309.13649 Da

IUPAC Name

1-{11-hydroxy-6,6-dimethyl-16-oxa-14-azatetracyclo[8.7.0.0^{2,7}.0^{13,17}]heptadeca-1,7,9,11,13(17),14-hexaen-12-yl}ethan-1-one

Traditional Name

1-{11-hydroxy-6,6-dimethyl-16-oxa-14-azatetracyclo[8.7.0.0^{2,7}.0^{13,17}]heptadeca-1,7,9,11,13(17),14-hexaen-12-yl}ethanone

CAS Registry Number

Not Available

SMILES

[H]OC1=C(C(=O)C([H])([H])[H])C2=C(OC([H])=N2)C2=C3C(=C([H])C([H])=C12)C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])C3([H])[H]

InChI Identifier

InChI=1S/C19H19NO3/c1-10(21)14-16-18(23-9-20-16)15-11-5-4-8-19(2,3)13(11)7-6-12(15)17(14)22/h6-7,9,22H,4-5,8H2,1-3H3

InChI Key

PFWZZLBGBKUQMP-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Salvia Yunnanensis	JEOL database	Lin, F. -W., et al, J. Nat. Prod. 69, 93 (2006)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrols. Phenanthrols are compounds containing a phenanthrene (or its hydrogenated derivative) to which a hydroxyl group is attached.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Phenanthrols

Direct Parent

Phenanthrols

Alternative Parents

Substituents

Phenanthrol
1-naphthol
Naphthalene
Tetralin
Benzoxazole
Acetophenone
Aryl ketone
Aryl alkyl ketone
Azole
Heteroaromatic compound
Oxazole
Vinylogous acid
Ketone
Oxacycle
Azacycle
Organoheterocyclic compound
Aldehyde
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxide
Hydrocarbon derivative
Organopnictogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	4.27	ALOGPS
logP	4.25	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	8.32	ChemAxon
pKa (Strongest Basic)	-0.11	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.33 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.06 m³·mol⁻¹	ChemAxon
Polarizability	34.16 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9877019

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11702294

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lin, F. -W., et al. (2006). Lin, F. -W., et al, J. Nat. Prod. 69, 93 (2006) . J. Nat. Prod..

Showing NP-Card for salviamine F (NP0031774)

MOL for NP0031774 (salviamine F)

3D MOL for NP0031774 (salviamine F)

3D SDF for NP0031774 (salviamine F)

3D-SDF for NP0031774 (salviamine F)

PDB for NP0031774 (salviamine F)

3D PDB for NP0031774 (salviamine F)

SMILES for NP0031774 (salviamine F)

INCHI for NP0031774 (salviamine F)

Structure for NP0031774 (salviamine F)

3D Structure for NP0031774 (salviamine F)