NP-MRD: Showing NP-Card for (+)-Sarcotin E (NP0080875)

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Record Information

Version

2.0

Created at

2022-04-29 01:51:31 UTC

Updated at

2022-04-29 01:51:31 UTC

NP-MRD ID

NP0080875

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Sarcotin E

Description

CHEMBL485482 belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. Based on a literature review very few articles have been published on CHEMBL485482.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203512D          

 30 32  0  0  1  0            999 V2000
   -4.8470   -8.1900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6720   -8.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9269   -7.4054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2595   -6.9205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5920   -7.4054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2595   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5450   -5.6830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4588   -4.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6518   -4.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2393   -5.4054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7913   -6.0185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3162   -3.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4958   -3.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1602   -3.0974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3397   -3.0111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0042   -2.2575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4891   -1.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1535   -0.8363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6385   -0.1689    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3029    0.5848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7878    1.2522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6128    1.2522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8678    2.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2003    2.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2003    3.3468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5329    2.0368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6524    2.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0977    0.5848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4589   -0.2551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8548   -3.6786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  1  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 26  1  0  0  0  0
 23 27  1  0  0  0  0
 22 28  1  0  0  0  0
 19 29  1  1  0  0  0
 15 30  1  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
   -8.4158    2.5801    0.3858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9871    2.3329    0.7077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3146    1.2247    0.3879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8474    0.1546   -0.2848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9620    1.3412    0.8593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9977    0.4470    0.7305 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1201   -0.8506    0.0776 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5513   -1.8827    1.0867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1804   -0.9933   -1.1258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7731   -0.6624   -0.6500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8731   -0.8152   -1.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1418   -1.6277   -1.9322 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9493   -1.6382   -3.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5454   -2.5466   -0.8801 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9643   -2.3059   -0.3928 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1213   -0.9033    0.1680 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5241   -0.7556    0.6165 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0222   -1.0492    1.8891 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2993   -0.7929    1.9052 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7098   -0.3487    0.7464 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1066    0.0282    0.4538 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3887    1.4571    0.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2711    2.5513   -0.1128 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6450    3.6723    0.5988 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9724    3.2981    1.8096 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8384    2.0054    1.9407 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6179   -0.3124   -0.0892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8681    2.5855    1.4792 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0781    3.2166    1.4069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3598    4.3662    1.8664 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4977    3.0922   -0.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9693    1.6162    0.4129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8449    3.2692    1.1524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7371   -0.2199    0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0432    0.7414    1.1708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1122   -1.2238   -0.1379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8543   -1.3880    1.7770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1064   -2.7355    0.5463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3954   -2.2586    1.7295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1803   -2.0839   -1.3624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5037   -0.3753   -1.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8293    0.4383   -0.3912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5473   -1.2633    0.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0870   -0.1601   -2.6854 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0188   -1.5842   -3.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -2.5576   -3.7936 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6584   -0.7652   -3.8329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0904   -2.5233    0.0117 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5801   -3.5765   -1.3370 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7179   -2.5104   -1.1525 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1302   -3.0092    0.4490 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8520   -0.1836   -0.6244 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4602   -0.8410    1.0617 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3814   -1.4289    2.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8124   -0.5904    1.0821 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3878   -0.2196   -0.6015 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9439    2.4782   -1.1293 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6707    4.6917    0.2391 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0293    1.3862    2.8206 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6166    0.0085   -1.1227 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
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  6  5  2  0
  5 28  1  0
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 29 30  2  0
 29  2  1  0
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  2  3  2  0
  3  4  1  0
 27 17  1  0
  3  5  1  0
 23 22  1  0
  8 37  1  0
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  8 39  1  0
  7 36  1  6
  9 40  1  0
  9 41  1  0
 10 42  1  0
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 11 44  1  0
 13 45  1  0
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 21 55  1  0
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 26 59  1  0
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 23 57  1  0
 27 60  1  0
  6 35  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
M  END


  Mrv1652304292203512D          

 30 32  0  0  1  0            999 V2000
   -4.8470   -8.1900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6720   -8.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9269   -7.4054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2595   -6.9205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5920   -7.4054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2595   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5450   -5.6830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4588   -4.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6518   -4.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2393   -5.4054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7913   -6.0185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3162   -3.9373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4958   -3.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1602   -3.0974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3397   -3.0111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0042   -2.2575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4891   -1.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1535   -0.8363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6385   -0.1689    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3029    0.5848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7878    1.2522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6128    1.2522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8678    2.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2003    2.5218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2003    3.3468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5329    2.0368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6524    2.2918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0977    0.5848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4589   -0.2551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8548   -3.6786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  1  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  7 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 21 26  1  0  0  0  0
 23 27  1  0  0  0  0
 22 28  1  0  0  0  0
 19 29  1  1  0  0  0
 15 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080875

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CC\C=C(\C)CCCC1=COC(CC2=COC=C2)=C1)\C=C1\OC(=O)C(C)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H30O5/c1-17(6-4-8-18(2)12-23-24(26)19(3)25(27)30-23)7-5-9-20-13-22(29-16-20)14-21-10-11-28-15-21/h6,10-13,15-16,18,26H,4-5,7-9,14H2,1-3H3/b17-6-,23-12+/t18-/m1/s1

> <INCHI_KEY>
YIWFEASCLZQHBJ-AHOBXOOOSA-N

> <FORMULA>
C25H30O5

> <MOLECULAR_WEIGHT>
410.51

> <EXACT_MASS>
410.209324066

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
46.0816135774014

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5E)-5-[(2R,5Z)-9-{5-[(furan-3-yl)methyl]furan-3-yl}-2,6-dimethylnon-5-en-1-ylidene]-4-hydroxy-3-methyl-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
6.46

> <JCHEM_LOGP>
5.863350731000001

> <ALOGPS_LOGS>
-4.92

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.070639623450758

> <JCHEM_PKA_STRONGEST_BASIC>
-2.4949842797948336

> <JCHEM_POLAR_SURFACE_AREA>
72.81

> <JCHEM_REFRACTIVITY>
119.57869999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.94e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5E)-5-[(2R,5Z)-9-[5-(furan-3-ylmethyl)furan-3-yl]-2,6-dimethylnon-5-en-1-ylidene]-4-hydroxy-3-methylfuran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0      -9.048 -15.288   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0     -10.588 -15.288   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -11.064 -13.823   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.818 -12.918   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.572 -13.823   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.818 -11.378   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.484 -10.608   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.323  -9.077   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.817  -8.756   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.047 -10.090   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -7.077 -11.235   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -6.190  -7.350   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.659  -7.189   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.032  -5.782   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.501  -5.621   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.874  -4.214   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.780  -2.968   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.153  -1.561   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.058  -0.315   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.432   1.092   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.337   2.337   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.877   2.337   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.353   3.802   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.107   4.707   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -4.107   6.247   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -2.861   3.802   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -6.818   4.278   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -5.782   1.092   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.590  -0.476   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.596  -6.867   0.000  0.00  0.00           C+0
CONECT    1    2    5                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    7                                                       
CONECT   12    9   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   30                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   29                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23   28                                                  
CONECT   23   22   24   27                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   21                                                       
CONECT   27   23                                                            
CONECT   28   22                                                            
CONECT   29   19                                                            
CONECT   30   15                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₀O₅

Average Mass

410.5100 Da

Monoisotopic Mass

410.20932 Da

IUPAC Name

(5E)-5-[(2R,5Z)-9-{5-[(furan-3-yl)methyl]furan-3-yl}-2,6-dimethylnon-5-en-1-ylidene]-4-hydroxy-3-methyl-2,5-dihydrofuran-2-one

Traditional Name

(5E)-5-[(2R,5Z)-9-[5-(furan-3-ylmethyl)furan-3-yl]-2,6-dimethylnon-5-en-1-ylidene]-4-hydroxy-3-methylfuran-2-one

CAS Registry Number

Not Available

SMILES

C[C@H](CC\C=C(\C)CCCC1=COC(CC2=COC=C2)=C1)\C=C1\OC(=O)C(C)=C1O

InChI Identifier

InChI=1S/C25H30O5/c1-17(6-4-8-18(2)12-23-24(26)19(3)25(27)30-23)7-5-9-20-13-22(29-16-20)14-21-10-11-28-15-21/h6,10-13,15-16,18,26H,4-5,7-9,14H2,1-3H3/b17-6-,23-12+/t18-/m1/s1

InChI Key

YIWFEASCLZQHBJ-AHOBXOOOSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dihydrofurans

Sub Class

Furanones

Direct Parent

Butenolides

Alternative Parents

Substituents

2-furanone
Enol ester
Furan
Heteroaromatic compound
Enoate ester
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Lactone
Monocarboxylic acid or derivatives
Enol
Carboxylic acid derivative
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	6.46	ALOGPS
logP	5.86	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	7.07	ChemAxon
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.81 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	119.58 m³·mol⁻¹	ChemAxon
Polarizability	46.08 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

10478704

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

54676741

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Sarcotin E (NP0080875)

MOL for NP0080875 ((+)-Sarcotin E)

3D MOL for NP0080875 ((+)-Sarcotin E)

3D SDF for NP0080875 ((+)-Sarcotin E)

3D-SDF for NP0080875 ((+)-Sarcotin E)

PDB for NP0080875 ((+)-Sarcotin E)

3D PDB for NP0080875 ((+)-Sarcotin E)

SMILES for NP0080875 ((+)-Sarcotin E)

INCHI for NP0080875 ((+)-Sarcotin E)

Structure for NP0080875 ((+)-Sarcotin E)

3D Structure for NP0080875 ((+)-Sarcotin E)