NP-MRD: Showing NP-Card for (3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol (NP0281841)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 08:25:48 UTC

Updated at

2022-09-09 08:25:48 UTC

NP-MRD ID

NP0281841

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol

Description

Variecolorin M belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. (3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol is found in Penicillium griseofulvum. Based on a literature review very few articles have been published on Variecolorin M.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210252D          

 30 32  0  0  1  0            999 V2000
   -1.4087   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9962   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2428   -2.5916    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7948   -3.2047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6018   -3.0331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399   -3.9893    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0919   -4.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329   -4.1608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -3.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -3.7192    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  1  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 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
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  6 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  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
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 59 61  0  0  0  0  0  0  0  0999 V2000
   -0.4737    4.9740    0.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5613    3.8440    0.7511 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6113    2.9616    0.8841 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4102    3.4076    2.0817 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5248    3.1961   -0.3269 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2337    1.5308    0.9618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0278    1.0804    0.9200 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0892   -0.2637    1.0133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1480   -1.1463    1.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5628   -0.7031    0.9021 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9071   -0.3557   -0.4972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8646   -1.0281   -1.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5847   -2.1077   -0.4091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2429   -0.7106   -2.5151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5861   -0.3408   -2.4973 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9182   -2.4970    1.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6142   -2.9291    1.2608 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4497   -2.0501    1.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2270   -0.6855    1.1211 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0399    0.4238    1.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4844    0.4804    1.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2130   -0.2485    0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6422   -1.0549   -0.6495 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3230   -1.7522   -1.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7282   -2.5316   -2.4772 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7997   -1.7343   -1.4298 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3697   -3.1304   -1.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3315   -0.9114   -0.3933 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6772   -0.2193    0.4457 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2699    0.5600    1.4294 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4834    5.2429   -0.3613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3447    5.6149   -0.0037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4960    3.5667    1.2033 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1775    2.8149    3.0030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1193    4.4501    2.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5029    3.4551    1.8785 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8941    3.4398   -1.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1977    4.0549   -0.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1730    2.3143   -0.5055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9255    1.6415    0.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6548    0.2689    1.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2796   -1.3757    1.3715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4100    0.4280   -1.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2708   -2.6546   -1.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2473   -1.7238    0.3955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8720   -2.8073    0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1338   -1.6157   -3.1415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6209    0.1274   -2.8762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8163    0.2695   -1.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7538   -3.2163    1.1638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4438   -4.0037    1.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4612   -2.4194    1.3515 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9986    1.0998    1.9244 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2043   -3.3506   -2.8302 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2294   -1.3511   -2.4008 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3500   -3.0368   -0.7663 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7295   -3.7652   -0.6250 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539   -3.6194   -2.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4399    0.0927    2.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 28  1  0
 28 29  2  0
 29 30  1  0
 29 22  1  0
 22 21  2  0
 21 20  1  0
 20  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  9 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
  6  3  1  0
  3  4  1  0
  3  5  1  0
  3  2  1  0
  2  1  2  3
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 19 20  1  0
 19  8  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
 26 55  1  6
 30 59  1  0
 21 53  1  0
  7 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 13 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 16 50  1  0
 17 51  1  0
 18 52  1  0
  4 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  5 39  1  0
  2 33  1  0
  1 31  1  0
  1 32  1  0
 25 54  1  0
M  END


  Mrv1652309092210252D          

 30 32  0  0  1  0            999 V2000
   -1.4087   -1.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9962   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4957    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2428   -2.5916    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7948   -3.2047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6018   -3.0331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5399   -3.9893    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0919   -4.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329   -4.1608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -3.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -3.7192    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  1  0  0  0  0
  3  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 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
  8 19  1  0  0  0  0
 19 20  1  0  0  0  0
  6 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  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
 24 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281841

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1N=C(O)\C(=C\C2=C(NC3=C(C\C=C(/C)CO)C=CC=C23)C(C)(C)C=C)N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H29N3O3/c1-6-24(4,5)21-18(12-19-23(30)25-15(3)22(29)26-19)17-9-7-8-16(20(17)27-21)11-10-14(2)13-28/h6-10,12,15,27-28H,1,11,13H2,2-5H3,(H,25,30)(H,26,29)/b14-10+,19-12-/t15-/m0/s1

> <INCHI_KEY>
ABLYEZZJYZHBEO-KEDNCGNWSA-N

> <FORMULA>
C24H29N3O3

> <MOLECULAR_WEIGHT>
407.514

> <EXACT_MASS>
407.220891806

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.25896848999967

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3Z,6S)-3-({7-[(2E)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl}methylidene)-6-methyl-3,6-dihydropyrazine-2,5-diol

> <JCHEM_LOGP>
3.5934390527265703

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.911552200224759

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.4247993484876815

> <JCHEM_PKA_STRONGEST_BASIC>
3.4561857396188764

> <JCHEM_POLAR_SURFACE_AREA>
101.2

> <JCHEM_REFRACTIVITY>
122.11819999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3Z,6S)-3-({7-[(2E)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl}methylidene)-6-methyl-6H-pyrazine-2,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.630  -2.637   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.860  -1.303   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.320  -1.303   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.320  -2.843   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.320   0.237   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.924   1.777   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.258   2.547   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.591   1.777   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.591   0.237   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.925   2.547   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.259   1.777   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       4.187  -4.838   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       5.217  -5.982   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.723  -5.662   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.741  -7.447   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.772  -8.591   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       3.235  -7.767   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       2.204  -6.622   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.698  -6.943   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    7   20                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16    9   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    8   20                                                  
CONECT   20   19    6   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   29                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   22   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₉N₃O₃

Average Mass

407.5140 Da

Monoisotopic Mass

407.22089 Da

IUPAC Name

(3Z,6S)-3-({7-[(2E)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl}methylidene)-6-methyl-3,6-dihydropyrazine-2,5-diol

Traditional Name

(3Z,6S)-3-({7-[(2E)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1H-indol-3-yl}methylidene)-6-methyl-6H-pyrazine-2,5-diol

CAS Registry Number

Not Available

SMILES

C[C@@H]1N=C(O)\C(=C\C2=C(NC3=C(C\C=C(/C)CO)C=CC=C23)C(C)(C)C=C)N=C1O

InChI Identifier

InChI=1S/C24H29N3O3/c1-6-24(4,5)21-18(12-19-23(30)25-15(3)22(29)26-19)17-9-7-8-16(20(17)27-21)11-10-14(2)13-28/h6-10,12,15,27-28H,1,11,13H2,2-5H3,(H,25,30)(H,26,29)/b14-10+,19-12-/t15-/m0/s1

InChI Key

ABLYEZZJYZHBEO-KEDNCGNWSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Penicillium griseofulvum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Indole
Indole or derivatives
Dioxopiperazine
2,5-dioxopiperazine
1,4-diazinane
Benzenoid
Substituted pyrrole
Piperazine
Heteroaromatic compound
Pyrrole
Carboxamide group
Secondary carboxylic acid amide
Lactam
Azacycle
Organoheterocyclic compound
Primary alcohol
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	3.59	ChemAxon
pKa (Strongest Acidic)	4.42	ChemAxon
pKa (Strongest Basic)	3.46	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	101.2 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	122.12 m³·mol⁻¹	ChemAxon
Polarizability	45.26 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

49831792

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol (NP0281841)

MOL for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

3D MOL for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

3D SDF for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

3D-SDF for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

PDB for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

3D PDB for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

SMILES for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

INCHI for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

Structure for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)

3D Structure for NP0281841 ((3z,6s)-3-({7-[(2e)-4-hydroxy-3-methylbut-2-en-1-yl]-2-(2-methylbut-3-en-2-yl)-1h-indol-3-yl}methylidene)-6-methyl-6h-pyrazine-2,5-diol)