NP-MRD: Showing NP-Card for RA V (NP0071693)

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Record Information

Version

2.0

Created at

2022-04-28 17:02:14 UTC

Updated at

2022-04-28 17:02:14 UTC

NP-MRD ID

NP0071693

Secondary Accession Numbers

None

Natural Product Identification

Common Name

RA V

Description

64725-24-2, Also known as RA V or deoxybouvardin, belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. RA V is found in Rubia akane , Rubia cordifolia and Rubia yunnanensis. Based on a literature review very few articles have been published on 64725-24-2.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219022D          

 55 59  0  0  1  0            999 V2000
    2.4297    4.0182    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2430    3.8438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8028    4.4550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6075    4.2731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5597    5.2493    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1170    5.8652    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8714    6.6558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4326    7.2605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0612    6.8427    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8086    7.6329    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0018    7.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7472    8.5988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4519    7.1902    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6383    7.3679    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2957    8.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
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  9 10  1  0  0  0  0
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  1 34  1  0  0  0  0
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 29 37  1  6  0  0  0
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M  END

     RDKit          3D

103107  0  0  0  0  0  0  0  0999 V2000
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 18 16  1  0
 16 17  1  0
 16 14  1  0
 14 15  2  0
 14 12  1  0
 12 13  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
 18 52  1  0
 52 53  2  0
 52 50  1  0
 50 51  1  0
 20 25  1  0
 25 24  2  0
 27 32  2  0
 32 33  1  0
 32 31  1  0
 31 30  2  0
  6 54  1  0
 54 55  2  0
 55  3  1  0
  9  8  1  0
 50 35  1  0
 30 29  1  0
 24 23  1  0
  1 56  1  0
  1 57  1  0
  1 58  1  0
  4 59  1  0
  5 60  1  0
  7 61  1  0
  7 62  1  0
  8 63  1  6
 49 96  1  0
 49 97  1  0
 49 98  1  0
 44 92  1  6
 45 93  1  0
 45 94  1  0
 45 95  1  0
 43 91  1  0
 39 87  1  6
 40 88  1  0
 40 89  1  0
 40 90  1  0
 38 86  1  0
 35 85  1  6
 34 83  1  0
 34 84  1  0
 28 79  1  0
 22 76  1  0
 21 75  1  0
 19 73  1  0
 19 74  1  0
 18 72  1  6
 17 69  1  0
 17 70  1  0
 17 71  1  0
 12 65  1  6
 13 66  1  0
 13 67  1  0
 13 68  1  0
 11 64  1  0
 51 99  1  0
 51100  1  0
 51101  1  0
 25 78  1  0
 24 77  1  0
 33 82  1  0
 31 81  1  0
 30 80  1  0
 54102  1  0
 55103  1  0
M  END


  Mrv1652304282219022D          

 55 59  0  0  1  0            999 V2000
    2.4297    4.0182    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2430    3.8438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8028    4.4550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6075    4.2731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5597    5.2493    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1170    5.8652    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8714    6.6558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4326    7.2605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0612    6.8427    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8086    7.6329    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0018    7.8140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7472    8.5988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4519    7.1902    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6383    7.3679    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2957    8.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4438    8.5690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6922    7.7830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4839    7.5363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1086    8.0393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8594    8.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1096    9.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6611    7.4003    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9324    6.4800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5276    5.9070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4095    5.0412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6241    4.7902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9816    5.2924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1401    5.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3219    5.3440    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0070    4.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5243    3.9373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8161    4.3791    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0557    3.5856    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8642    3.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1113    2.6242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4964    2.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2696    5.9128    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0923    6.7317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7074    6.9342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0587    5.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1866    6.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3069    6.1777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7087    6.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3655    8.2415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9227    5.6876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4794    6.2964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2304    7.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7871    7.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5928    7.5142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8417    6.7276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2850    6.1187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1494    8.1230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9005    8.9096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7545    5.4287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4939    3.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
  1 34  1  0  0  0  0
 34 35  2  0  0  0  0
 33 36  1  1  0  0  0
 29 37  1  6  0  0  0
 37 38  1  0  0  0  0
 14 38  1  0  0  0  0
 38 39  2  0  0  0  0
 37 40  1  0  0  0  0
 27 41  2  0  0  0  0
 23 41  1  0  0  0  0
 24 42  1  0  0  0  0
 13 43  1  0  0  0  0
 10 44  1  6  0  0  0
  6 45  1  6  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 46 51  1  0  0  0  0
 49 52  1  0  0  0  0
 52 53  1  0  0  0  0
  5 54  1  0  0  0  0
  2 55  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0071693

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C[C@@H]2N(C)C(=O)[C@H](C)NC(=O)[C@@H](C)NC(=O)[C@@H]3CC4=CC(OC5=CC=C(C[C@H](N(C)C(=O)[C@H](C)NC2=O)C(=O)N3C)C=C5)=C(O)C=C4)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C40H48N6O9/c1-22-35(48)42-23(2)38(51)44(4)30(18-25-8-13-28(54-7)14-9-25)37(50)43-24(3)39(52)46(6)32-19-26-10-15-29(16-11-26)55-34-21-27(12-17-33(34)47)20-31(36(49)41-22)45(5)40(32)53/h8-17,21-24,30-32,47H,18-20H2,1-7H3,(H,41,49)(H,42,48)(H,43,50)/t22-,23+,24+,30+,31+,32+/m1/s1

> <INCHI_KEY>
VXVGFMUNENQGFW-LZQLRFBTSA-N

> <FORMULA>
C40H48N6O9

> <MOLECULAR_WEIGHT>
756.857

> <EXACT_MASS>
756.34827715

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
76.62136211947532

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,7S,10S,13S,16S)-24-hydroxy-10-[(4-methoxyphenyl)methyl]-4,7,9,13,15,29-hexamethyl-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2^{18,21}.1^{23,27}]tritriaconta-18,20,23,25,27(31),32-hexaene-2,5,8,11,14,30-hexone

> <ALOGPS_LOGP>
2.95

> <JCHEM_LOGP>
1.4866980956666658

> <ALOGPS_LOGS>
-4.71

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.606732933816964

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.423346543409956

> <JCHEM_PKA_STRONGEST_BASIC>
-3.472802945307429

> <JCHEM_POLAR_SURFACE_AREA>
186.92

> <JCHEM_REFRACTIVITY>
200.95839999999993

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.48e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,7S,10S,13S,16S)-24-hydroxy-10-[(4-methoxyphenyl)methyl]-4,7,9,13,15,29-hexamethyl-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2^{18,21}.1^{23,27}]tritriaconta-18,20,23,25,27(31),32-hexaene-2,5,8,11,14,30-hexone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  N   UNK     0       4.535   7.501   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       6.054   7.175   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.099   8.316   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.601   7.976   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       6.645   9.799   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       7.685  10.948   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.227  12.424   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.274  13.553   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0       5.714  12.773   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       5.243  14.248   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.737  14.586   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.261  16.051   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0       2.710  13.422   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       1.191  13.754   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.552  15.219   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.828  15.995   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.292  14.528   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.770  14.068   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.936  15.007   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.471  16.477   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.071  17.028   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -4.967  13.814   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -5.474  12.096   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.585  11.026   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.364   9.410   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.898   8.942   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.699   9.879   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.128   9.564   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.601   9.975   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.013   8.528   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.979   7.350   0.000  0.00  0.00           O+0
HETATM   32  N   UNK     0       1.523   8.174   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       1.971   6.693   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.480   6.368   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.941   4.898   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       0.927   5.561   0.000  0.00  0.00           C+0
HETATM   37  N   UNK     0       0.503  11.037   0.000  0.00  0.00           N+0
HETATM   38  C   UNK     0       0.172  12.566   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -1.321  12.944   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       1.976  10.588   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -4.082  11.409   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -8.039  11.532   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       3.190  11.958   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.282  15.384   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.189  10.617   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      10.228  11.753   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       9.763  13.222   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      10.803  14.358   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      12.306  14.026   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      12.771  12.558   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      11.732  11.422   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      13.346  15.163   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      12.881  16.631   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       5.142  10.134   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       6.522   5.708   0.000  0.00  0.00           C+0
CONECT    1    2   34                                                       
CONECT    2    1    3   55                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   54                                                  
CONECT    6    5    7   45                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   44                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   43                                                  
CONECT   14   13   15   38                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22   19   23                                                       
CONECT   23   22   24   41                                                  
CONECT   24   23   25   42                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   41                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   37                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34   36                                                  
CONECT   34   33    1   35                                                  
CONECT   35   34                                                            
CONECT   36   33                                                            
CONECT   37   29   38   40                                                  
CONECT   38   37   14   39                                                  
CONECT   39   38                                                            
CONECT   40   37                                                            
CONECT   41   27   23                                                       
CONECT   42   24                                                            
CONECT   43   13                                                            
CONECT   44   10                                                            
CONECT   45    6   46                                                       
CONECT   46   45   47   51                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50   52                                                  
CONECT   50   49   51                                                       
CONECT   51   50   46                                                       
CONECT   52   49   53                                                       
CONECT   53   52                                                            
CONECT   54    5                                                            
CONECT   55    2                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  118    0
END

View in JSmol

Synonyms

Value	Source
RA V	MeSH
RA-V	MeSH
Deoxybouvardin	MeSH

Chemical Formula

C₄₀H₄₈N₆O₉

Average Mass

756.8570 Da

Monoisotopic Mass

756.34828 Da

IUPAC Name

(1S,4R,7S,10S,13S,16S)-24-hydroxy-10-[(4-methoxyphenyl)methyl]-4,7,9,13,15,29-hexamethyl-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2^{18,21}.1^{23,27}]tritriaconta-18,20,23,25,27(31),32-hexaene-2,5,8,11,14,30-hexone

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C[C@@H]2N(C)C(=O)[C@H](C)NC(=O)[C@@H](C)NC(=O)[C@@H]3CC4=CC(OC5=CC=C(C[C@H](N(C)C(=O)[C@H](C)NC2=O)C(=O)N3C)C=C5)=C(O)C=C4)C=C1

InChI Identifier

InChI=1S/C40H48N6O9/c1-22-35(48)42-23(2)38(51)44(4)30(18-25-8-13-28(54-7)14-9-25)37(50)43-24(3)39(52)46(6)32-19-26-10-15-29(16-11-26)55-34-21-27(12-17-33(34)47)20-31(36(49)41-22)45(5)40(32)53/h8-17,21-24,30-32,47H,18-20H2,1-7H3,(H,41,49)(H,42,48)(H,43,50)/t22-,23+,24+,30+,31+,32+/m1/s1

InChI Key

VXVGFMUNENQGFW-LZQLRFBTSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rubia akane	Plant	KNApSAcK
Rubia cordifolia	LOTUS Database	35616633
Rubia yunnanensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Oxyneolignan skeleton
Macrolactam
Diaryl ether
Alpha-amino acid or derivatives
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Tertiary carboxylic acid amide
Secondary carboxylic acid amide
Carboxamide group
Lactam
Azacycle
Ether
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Organonitrogen compound
Organooxygen 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	2.95	ALOGPS
logP	1.49	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	8.42	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	186.92 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	200.96 m³·mol⁻¹	ChemAxon
Polarizability	76.62 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00031129

Chemspider ID

23323032

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13361282

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for RA V (NP0071693)

MOL for NP0071693 (RA V)

3D MOL for NP0071693 (RA V)

3D SDF for NP0071693 (RA V)

3D-SDF for NP0071693 (RA V)

PDB for NP0071693 (RA V)

3D PDB for NP0071693 (RA V)

SMILES for NP0071693 (RA V)

INCHI for NP0071693 (RA V)

Structure for NP0071693 (RA V)

3D Structure for NP0071693 (RA V)