NP-MRD: Showing NP-Card for Cervicarcin (NP0062252)

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Record Information

Version

2.0

Created at

2022-04-28 06:55:28 UTC

Updated at

2022-04-28 06:55:28 UTC

NP-MRD ID

NP0062252

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cervicarcin

Description

(1R,9R,10S,11S,12S,13R,14R)-7,9,11,12,14-pentahydroxy-13-methyl-12-[(2S,3R)-3-methyloxirane-2-carbonyl]-15-oxatetracyclo[8.4.1.0¹,¹⁰.0³,⁸]Pentadeca-3(8),4,6-trien-2-one belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane. Cervicarcin is found in Streptomyces ogaensis. Based on a literature review very few articles have been published on (1R,9R,10S,11S,12S,13R,14R)-7,9,11,12,14-pentahydroxy-13-methyl-12-[(2S,3R)-3-methyloxirane-2-carbonyl]-15-oxatetracyclo[8.4.1.0¹,¹⁰.0³,⁸]Pentadeca-3(8),4,6-trien-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282208552D          

 28 32  0  0  1  0            999 V2000
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1100    1.2087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2773    0.5379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6646   -0.1906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5472    0.5667    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2756    0.1793    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2468    1.0038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7128   -0.5203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  1  0  0  0
 15 18  1  1  0  0  0
 15 19  1  6  0  0  0
 19 20  2  0  0  0  0
 21 19  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 23  1  0  0  0  0
 22 24  1  1  0  0  0
 14 25  1  6  0  0  0
 13 26  1  1  0  0  0
 10 27  1  1  0  0  0
  9 27  1  1  0  0  0
  8 28  1  1  0  0  0
M  END

     RDKit          3D

 48 52  0  0  0  0  0  0  0  0999 V2000
    5.7827    2.2434    0.2324 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9769    1.1714   -0.4877 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2972   -0.1365   -0.1120 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0505    0.3417    0.2912 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8358   -0.1491   -0.4019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8986   -0.3749   -1.5897 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5389   -0.3786    0.2929 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7140   -0.0490    1.6543 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4959    0.5219   -0.3266 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8014    1.8210    0.0850 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8872    0.2068    0.1963 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8706   -0.3625    1.4354 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2114   -1.1717    0.3643 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6061   -1.5754    0.3426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9218   -2.7683    0.1731 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6518   -0.5867    0.5197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9121   -0.9270    1.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8323    0.0878    1.1691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5086    1.3832    0.8132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2646    1.7141    0.3093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9537    3.0075   -0.0416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3394    0.7061    0.1677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0030    0.9950   -0.3779 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7399    2.3677   -0.4228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2101   -2.0857   -0.2628 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4802   -3.4390    0.0169 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2001   -1.8237    0.2155 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1253   -2.6125   -0.6977 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8831    3.1528   -0.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7772    1.8221    0.4869 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2689    2.4342    1.2019 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7668    1.3363   -1.5644 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0039    0.5519    1.3799 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0874   -0.8414    2.1133 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5746    0.4955   -1.4157 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8862    2.4500   -0.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0834   -1.9494    1.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8025   -0.1820    1.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2417    2.1584    0.9298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6019    3.7790    0.0455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0629    0.6868   -1.4695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9993    2.7588   -1.2934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2187   -1.9450   -1.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7155   -3.9416   -0.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2767   -2.3354    1.2199 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8796   -3.6962   -0.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1845   -2.4230   -0.5000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8125   -2.4391   -1.7432 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  1
  7 27  1  0
 27 28  1  0
 27 25  1  0
 25 26  1  0
 25 13  1  0
 13 12  1  1
 11 12  1  1
 11 23  1  0
 23 24  1  0
 23 22  1  0
 22 20  2  0
 20 21  1  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 14  1  0
 14 15  2  0
 11  9  1  0
  9 10  1  0
  4  2  1  0
  9  7  1  0
 11 13  1  0
 16 22  1  0
 14 13  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  6
  4 33  1  1
  8 34  1  0
 27 45  1  1
 28 46  1  0
 28 47  1  0
 28 48  1  0
 25 43  1  6
 26 44  1  0
 23 41  1  6
 24 42  1  0
 21 40  1  0
 19 39  1  0
 18 38  1  0
 17 37  1  0
  9 35  1  6
 10 36  1  0
M  END


  Mrv1652304282208552D          

 28 32  0  0  1  0            999 V2000
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1100    1.2087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2773    0.5379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6646   -0.1906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5472    0.5667    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2756    0.1793    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2468    1.0038    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7128   -0.5203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  1  0  0  0
 15 18  1  1  0  0  0
 15 19  1  6  0  0  0
 19 20  2  0  0  0  0
 21 19  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 21 23  1  0  0  0  0
 22 24  1  1  0  0  0
 14 25  1  6  0  0  0
 13 26  1  1  0  0  0
 10 27  1  1  0  0  0
  9 27  1  1  0  0  0
  8 28  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0062252

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1O[C@@H]1C(=O)[C@]1(O)[C@H](C)[C@@H](O)[C@@]23O[C@@]2([C@H](O)C2=C(O)C=CC=C2C3=O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H20O9/c1-6-12(21)18-13(22)8-4-3-5-9(20)10(8)14(23)19(18,28-18)16(25)17(6,26)15(24)11-7(2)27-11/h3-7,11-12,14,16,20-21,23,25-26H,1-2H3/t6-,7-,11+,12-,14-,16+,17-,18+,19+/m1/s1

> <INCHI_KEY>
ZGZVMKCZHDIFQA-NPUADFBHSA-N

> <FORMULA>
C19H20O9

> <MOLECULAR_WEIGHT>
392.36

> <EXACT_MASS>
392.110732224

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
37.10647384141802

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,9R,10S,11S,12S,13R,14R)-7,9,11,12,14-pentahydroxy-13-methyl-12-[(2S,3R)-3-methyloxirane-2-carbonyl]-15-oxatetracyclo[8.4.1.0^{1,10}.0^{3,8}]pentadeca-3,5,7-trien-2-one

> <ALOGPS_LOGP>
-0.05

> <JCHEM_LOGP>
-0.9305817749999988

> <ALOGPS_LOGS>
-1.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.62811989455168

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.172115758738718

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5021502006804424

> <JCHEM_POLAR_SURFACE_AREA>
160.35

> <JCHEM_REFRACTIVITY>
90.23729999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.81e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,9R,10S,11S,12S,13R,14R)-7,9,11,12,14-pentahydroxy-13-methyl-12-[(2S,3R)-3-methyloxirane-2-carbonyl]-15-oxatetracyclo[8.4.1.0^{1,10}.0^{3,8}]pentadeca-3,5,7-trien-2-one

> <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  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -0.205   2.256   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.518   1.004   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.241  -0.356   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.021   1.058   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.381   0.335   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.327   1.874   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -3.197  -0.971   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       2.667   3.080   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   11                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   28                                                  
CONECT    9    8   10   16   27                                             
CONECT   10    9   11   13   27                                             
CONECT   11   10    4   12                                                  
CONECT   12   11                                                            
CONECT   13   10   14   26                                                  
CONECT   14   13   15   25                                                  
CONECT   15   14   16   18   19                                             
CONECT   16   15    9   17                                                  
CONECT   17   16                                                            
CONECT   18   15                                                            
CONECT   19   15   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22   21                                                       
CONECT   24   22                                                            
CONECT   25   14                                                            
CONECT   26   13                                                            
CONECT   27   10    9                                                       
CONECT   28    8                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₀O₉

Average Mass

392.3600 Da

Monoisotopic Mass

392.11073 Da

IUPAC Name

(1R,9R,10S,11S,12S,13R,14R)-7,9,11,12,14-pentahydroxy-13-methyl-12-[(2S,3R)-3-methyloxirane-2-carbonyl]-15-oxatetracyclo[8.4.1.0^{1,10}.0^{3,8}]pentadeca-3,5,7-trien-2-one

Traditional Name

(1R,9R,10S,11S,12S,13R,14R)-7,9,11,12,14-pentahydroxy-13-methyl-12-[(2S,3R)-3-methyloxirane-2-carbonyl]-15-oxatetracyclo[8.4.1.0^{1,10}.0^{3,8}]pentadeca-3,5,7-trien-2-one

CAS Registry Number

Not Available

SMILES

C[C@H]1O[C@@H]1C(=O)[C@]1(O)[C@H](C)[C@@H](O)[C@@]23O[C@@]2([C@H](O)C2=C(O)C=CC=C2C3=O)[C@H]1O

InChI Identifier

InChI=1S/C19H20O9/c1-6-12(21)18-13(22)8-4-3-5-9(20)10(8)14(23)19(18,28-18)16(25)17(6,26)15(24)11-7(2)27-11/h3-7,11-12,14,16,20-21,23,25-26H,1-2H3/t6-,7-,11+,12-,14-,16+,17-,18+,19+/m1/s1

InChI Key

ZGZVMKCZHDIFQA-NPUADFBHSA-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
Streptomyces ogaensis	Bacteria	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Tetralins

Sub Class

Not Available

Direct Parent

Tetralins

Alternative Parents

Substituents

Tetralin
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Oxepane
Cyclitol or derivatives
Alpha-hydroxy ketone
Cyclic alcohol
Tertiary alcohol
Ketone
Secondary alcohol
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Polyol
Alcohol
Organic oxygen compound
Organic oxide
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
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	-0.05	ALOGPS
logP	-0.93	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	9.17	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	160.35 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	90.24 m³·mol⁻¹	ChemAxon
Polarizability	37.11 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162922717

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Cervicarcin (NP0062252)

MOL for NP0062252 (Cervicarcin)

3D MOL for NP0062252 (Cervicarcin)

3D SDF for NP0062252 (Cervicarcin)

3D-SDF for NP0062252 (Cervicarcin)

PDB for NP0062252 (Cervicarcin)

3D PDB for NP0062252 (Cervicarcin)

SMILES for NP0062252 (Cervicarcin)

INCHI for NP0062252 (Cervicarcin)

Structure for NP0062252 (Cervicarcin)

3D Structure for NP0062252 (Cervicarcin)