NP-MRD: Showing NP-Card for Myrothecol C (NP0013164)

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Record Information

Version

2.0

Created at

2021-01-05 22:37:01 UTC

Updated at

2026-02-11 00:10:12 UTC

NP-MRD ID

NP0013164

Natural Product DOI

https://doi.org/10.57994/6236

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Myrothecol C

Provided By

NPAtlas

Description

Myrothecol C is found in Myrothecium sp. SC0265. Myrothecol C was first documented in 2014 (PMID: 25089733). Based on a literature review very few articles have been published on Myrothecol C.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242119333D          

 59 62  0  0  0  0            999 V2000
    1.1657    1.4109    0.9718 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    0.7638    0.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5693    0.8100   -1.3028 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0288    0.2568    0.0504 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4999    0.2496    0.1868 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2482   -0.0893   -1.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9054    1.6928    0.5333 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2861    1.7864    0.6834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9249   -0.5805    1.3510 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7682   -0.7817    2.3301 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6479   -1.5242    1.6841 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2978   -1.0241    0.2980 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.1182   -1.7831   -1.9177 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0073   -0.3216   -1.7545 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3395    0.2836   -1.4900 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4320    1.5541   -2.1082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6936    0.3725   -0.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9960    1.2832    1.7105 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1101   -0.3336    0.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0530   -1.2540    0.4932 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7351   -2.1564    1.3020 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7661   -1.0860   -0.9541 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4222   -0.2213    1.9295 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
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 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 25 26  1  0  0  0  0
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 15  2  1  0  0  0  0
 19 17  1  0  0  0  0
 13  5  1  0  0  0  0
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  1 28  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306242119333D          

 59 62  0  0  0  0            999 V2000
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    0.4351    0.7638    0.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1101   -0.3336    0.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3550    2.4671    0.8776 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5918    0.8764    1.8091 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4316    1.3701   -1.9806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3512    2.4856   -0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5995    0.0473   -2.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2968    1.6068   -1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6338    0.9810    0.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1005    0.6217   -1.2698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7661   -1.0860   -0.9541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6298   -0.0520   -1.9893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4416    2.0286    1.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6061    2.3737   -0.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7107    2.2076   -0.1151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7329   -0.0798    1.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3487   -1.5685    1.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1782   -1.4276    3.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4783    0.1725    2.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7626   -1.4566    2.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9276   -2.6094    1.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1712   -3.0589   -0.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3490   -1.9366   -1.7005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7474   -2.3134   -0.5460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6654   -1.0774    1.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7996   -2.4920   -0.8583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5136   -1.0428   -1.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4468    0.1488   -2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1310   -0.3194   -1.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2716    1.3623   -3.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7162    1.0222   -0.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4716    2.3584    0.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6967    0.6038    1.8883 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4222   -0.2213    1.9295 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  1  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  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 15  2  1  0  0  0  0
 19 17  1  0  0  0  0
 13  5  1  0  0  0  0
 26 17  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  3 30  1  0  0  0  0
  3 31  1  0  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
  5 34  1  1  0  0  0
  7 35  1  0  0  0  0
  7 36  1  0  0  0  0
  7 37  1  0  0  0  0
  8 38  1  0  0  0  0
  8 39  1  0  0  0  0
  9 40  1  0  0  0  0
 10 41  1  0  0  0  0
 10 42  1  0  0  0  0
 11 43  1  0  0  0  0
 11 44  1  0  0  0  0
 12 45  1  0  0  0  0
 12 46  1  0  0  0  0
 14 47  1  0  0  0  0
 14 48  1  0  0  0  0
 14 49  1  0  0  0  0
 15 50  1  1  0  0  0
 16 51  1  0  0  0  0
 16 52  1  0  0  0  0
 19 53  1  6  0  0  0
 20 54  1  6  0  0  0
 21 55  1  0  0  0  0
 23 56  1  0  0  0  0
 23 57  1  0  0  0  0
 24 58  1  0  0  0  0
 25 59  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0013164

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])C1=C([H])C(=O)[C@@]2(O[C@]2([H])[C@@]1([H])O[H])C([H])([H])[C@@]1([H])C(=C([H])[H])C([H])([H])C([H])([H])[C@@]2([H])[C@](C([H])([H])[H])(C([H])([H])O[H])C([H])([H])C([H])([H])C([H])([H])[C@]12C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H32O5/c1-13-5-6-16-20(2,12-24)7-4-8-21(16,3)15(13)10-22-17(25)9-14(11-23)18(26)19(22)27-22/h9,15-16,18-19,23-24,26H,1,4-8,10-12H2,2-3H3/t15-,16-,18-,19+,20-,21+,22-/m0/s1

> <INCHI_KEY>
VUZUKTHJOMFUTI-XKFBSPQISA-N

> <FORMULA>
C22H32O5

> <MOLECULAR_WEIGHT>
376.493

> <EXACT_MASS>
376.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.254451938952435

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,5S,6R)-1-{[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decahydronaphthalen-1-yl]methyl}-5-hydroxy-4-(hydroxymethyl)-7-oxabicyclo[4.1.0]hept-3-en-2-one

> <ALOGPS_LOGP>
1.61

> <JCHEM_LOGP>
1.8473669866666678

> <ALOGPS_LOGS>
-3.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.255311945987273

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.1805626238679

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2271498750956007

> <JCHEM_POLAR_SURFACE_AREA>
90.29

> <JCHEM_REFRACTIVITY>
102.43279999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.44e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,5S,6R)-1-{[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-hexahydro-1H-naphthalen-1-yl]methyl}-5-hydroxy-4-(hydroxymethyl)-7-oxabicyclo[4.1.0]hept-3-en-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 59 62  0  0  0  0  0  0  0  0999 V2000
    1.1657    1.4109    0.9718 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    0.7638    0.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1958    1.4069   -1.0864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5693    0.8100   -1.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288    0.2568    0.0504 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4999    0.2496    0.1868 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2482   -0.0893   -1.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9054    1.6928    0.5333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2861    1.7864    0.6834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9249   -0.5805    1.3510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7682   -0.7817    2.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6479   -1.5242    1.6841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2978   -1.0241    0.2980 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6589   -2.1262   -0.6706 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1864   -0.7090    0.2545 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9016   -1.3896   -0.8609 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3973   -1.1072   -0.8064 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1182   -1.7831   -1.9177 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0073   -0.3216   -1.7545 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3395    0.2836   -1.4900 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4320    1.5541   -2.1082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6936    0.3725   -0.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7795    1.3176    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9960    1.2832    1.7105 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1101   -0.3336    0.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0530   -1.2540    0.4932 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7351   -2.1564    1.3020 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3550    2.4671    0.8776 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5918    0.8764    1.8091 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4316    1.3701   -1.9806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3512    2.4856   -0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5995    0.0473   -2.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2968    1.6068   -1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6338    0.9810    0.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1005    0.6217   -1.2698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7661   -1.0860   -0.9541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6298   -0.0520   -1.9893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4416    2.0286    1.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6061    2.3737   -0.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7107    2.2076   -0.1151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7329   -0.0798    1.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3487   -1.5685    1.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1782   -1.4276    3.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4783    0.1725    2.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7626   -1.4566    2.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9276   -2.6094    1.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1712   -3.0589   -0.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3490   -1.9366   -1.7005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7474   -2.3134   -0.5460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6654   -1.0774    1.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7996   -2.4920   -0.8583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5136   -1.0428   -1.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4468    0.1488   -2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1310   -0.3194   -1.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2716    1.3623   -3.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7162    1.0222   -0.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4716    2.3584    0.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6967    0.6038    1.8883 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4222   -0.2213    1.9295 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  8  9  1  0
  6 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 17 16  1  1
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  2  0
 25 26  1  0
 26 27  2  0
 15  2  1  0
 19 17  1  0
 13  5  1  0
 26 17  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  1
  7 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 14 47  1  0
 14 48  1  0
 14 49  1  0
 15 50  1  1
 16 51  1  0
 16 52  1  0
 19 53  1  6
 20 54  1  6
 21 55  1  0
 23 56  1  0
 23 57  1  0
 24 58  1  0
 25 59  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       1.166   1.411   0.972  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.435   0.764   0.100  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.196   1.407  -1.086  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.569   0.810  -1.303  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.029   0.257   0.050  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.500   0.250   0.187  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.248  -0.089  -1.081  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.905   1.693   0.533  0.00  0.00           C+0
HETATM    9  O   UNK     0      -5.286   1.786   0.683  0.00  0.00           O+0
HETATM   10  C   UNK     0      -3.925  -0.581   1.351  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.768  -0.782   2.330  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.648  -1.524   1.684  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.298  -1.024   0.298  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.659  -2.126  -0.671  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.186  -0.709   0.255  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.902  -1.390  -0.861  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.397  -1.107  -0.806  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.118  -1.783  -1.918  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.007  -0.322  -1.755  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.340   0.284  -1.490  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.432   1.554  -2.108  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.694   0.373  -0.072  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.779   1.318   0.323  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.996   1.283   1.710  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.110  -0.334   0.878  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.053  -1.254   0.493  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.735  -2.156   1.302  0.00  0.00           O+0
HETATM   28  H   UNK     0       1.355   2.467   0.878  0.00  0.00           H+0
HETATM   29  H   UNK     0       1.592   0.876   1.809  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.432   1.370  -1.981  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.351   2.486  -0.813  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.599   0.047  -2.088  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.297   1.607  -1.636  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.634   0.981   0.811  0.00  0.00           H+0
HETATM   35  H   UNK     0      -5.101   0.622  -1.270  0.00  0.00           H+0
HETATM   36  H   UNK     0      -4.766  -1.086  -0.954  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.630  -0.052  -1.989  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.442   2.029   1.468  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.606   2.374  -0.288  0.00  0.00           H+0
HETATM   40  H   UNK     0      -5.711   2.208  -0.115  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.733  -0.080   1.959  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.349  -1.569   1.079  0.00  0.00           H+0
HETATM   43  H   UNK     0      -3.178  -1.428   3.146  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.478   0.173   2.791  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.763  -1.457   2.349  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.928  -2.609   1.683  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.171  -3.059  -0.255  0.00  0.00           H+0
HETATM   48  H   UNK     0      -1.349  -1.937  -1.700  0.00  0.00           H+0
HETATM   49  H   UNK     0      -2.747  -2.313  -0.546  0.00  0.00           H+0
HETATM   50  H   UNK     0       0.665  -1.077   1.205  0.00  0.00           H+0
HETATM   51  H   UNK     0       0.800  -2.492  -0.858  0.00  0.00           H+0
HETATM   52  H   UNK     0       0.514  -1.043  -1.840  0.00  0.00           H+0
HETATM   53  H   UNK     0       2.447   0.149  -2.605  0.00  0.00           H+0
HETATM   54  H   UNK     0       5.131  -0.319  -1.994  0.00  0.00           H+0
HETATM   55  H   UNK     0       4.272   1.362  -3.085  0.00  0.00           H+0
HETATM   56  H   UNK     0       6.716   1.022  -0.173  0.00  0.00           H+0
HETATM   57  H   UNK     0       5.472   2.358   0.084  0.00  0.00           H+0
HETATM   58  H   UNK     0       6.697   0.604   1.888  0.00  0.00           H+0
HETATM   59  H   UNK     0       4.422  -0.221   1.930  0.00  0.00           H+0
CONECT    1    2   28   29                                                  
CONECT    2    1    3   15                                                  
CONECT    3    2    4   30   31                                             
CONECT    4    3    5   32   33                                             
CONECT    5    4    6   13   34                                             
CONECT    6    5    7    8   10                                             
CONECT    7    6   35   36   37                                             
CONECT    8    6    9   38   39                                             
CONECT    9    8   40                                                       
CONECT   10    6   11   41   42                                             
CONECT   11   10   12   43   44                                             
CONECT   12   11   13   45   46                                             
CONECT   13   12   14   15    5                                             
CONECT   14   13   47   48   49                                             
CONECT   15   13   16    2   50                                             
CONECT   16   15   17   51   52                                             
CONECT   17   16   18   19   26                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   17   53                                             
CONECT   20   19   21   22   54                                             
CONECT   21   20   55                                                       
CONECT   22   20   23   25                                                  
CONECT   23   22   24   56   57                                             
CONECT   24   23   58                                                       
CONECT   25   22   26   59                                                  
CONECT   26   25   27   17                                                  
CONECT   27   26                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    3                                                            
CONECT   31    3                                                            
CONECT   32    4                                                            
CONECT   33    4                                                            
CONECT   34    5                                                            
CONECT   35    7                                                            
CONECT   36    7                                                            
CONECT   37    7                                                            
CONECT   38    8                                                            
CONECT   39    8                                                            
CONECT   40    9                                                            
CONECT   41   10                                                            
CONECT   42   10                                                            
CONECT   43   11                                                            
CONECT   44   11                                                            
CONECT   45   12                                                            
CONECT   46   12                                                            
CONECT   47   14                                                            
CONECT   48   14                                                            
CONECT   49   14                                                            
CONECT   50   15                                                            
CONECT   51   16                                                            
CONECT   52   16                                                            
CONECT   53   19                                                            
CONECT   54   20                                                            
CONECT   55   21                                                            
CONECT   56   23                                                            
CONECT   57   23                                                            
CONECT   58   24                                                            
CONECT   59   25                                                            
MASTER        0    0    0    0    0    0    0    0   59    0  124    0
END

RDKit          3D

59 62  0  0  0  0  0  0  0  0999 V2000
    1.1657    1.4109    0.9718 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4351    0.7638    0.0997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1958    1.4069   -1.0864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5693    0.8100   -1.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0288    0.2568    0.0504 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4999    0.2496    0.1868 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2482   -0.0893   -1.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9054    1.6928    0.5333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2861    1.7864    0.6834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9249   -0.5805    1.3510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7682   -0.7817    2.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6479   -1.5242    1.6841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2978   -1.0241    0.2980 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6589   -2.1262   -0.6706 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1864   -0.7090    0.2545 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9016   -1.3896   -0.8609 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3973   -1.1072   -0.8064 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1182   -1.7831   -1.9177 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0073   -0.3216   -1.7545 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3395    0.2836   -1.4900 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4320    1.5541   -2.1082 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6936    0.3725   -0.0723 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7795    1.3176    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9960    1.2832    1.7105 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1101   -0.3336    0.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0530   -1.2540    0.4932 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7351   -2.1564    1.3020 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3550    2.4671    0.8776 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5918    0.8764    1.8091 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4316    1.3701   -1.9806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3512    2.4856   -0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5995    0.0473   -2.0884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2968    1.6068   -1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6338    0.9810    0.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1005    0.6217   -1.2698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7661   -1.0860   -0.9541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6298   -0.0520   -1.9893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4416    2.0286    1.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6061    2.3737   -0.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7107    2.2076   -0.1151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7329   -0.0798    1.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3487   -1.5685    1.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1782   -1.4276    3.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4783    0.1725    2.7909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7626   -1.4566    2.3493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9276   -2.6094    1.6826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1712   -3.0589   -0.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3490   -1.9366   -1.7005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7474   -2.3134   -0.5460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6654   -1.0774    1.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7996   -2.4920   -0.8583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5136   -1.0428   -1.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4468    0.1488   -2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1310   -0.3194   -1.9939 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2716    1.3623   -3.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7162    1.0222   -0.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4716    2.3584    0.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6967    0.6038    1.8883 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4222   -0.2213    1.9295 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  8  9  1  0
  6 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 17 16  1  1
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  2  0
 25 26  1  0
 26 27  2  0
 15  2  1  0
 19 17  1  0
 13  5  1  0
 26 17  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  1
  7 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 14 47  1  0
 14 48  1  0
 14 49  1  0
 15 50  1  1
 16 51  1  0
 16 52  1  0
 19 53  1  6
 20 54  1  6
 21 55  1  0
 23 56  1  0
 23 57  1  0
 24 58  1  0
 25 59  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₂H₃₂O₅

Average Mass

376.4930 Da

Monoisotopic Mass

376.22497 Da

IUPAC Name

(1R,5S,6R)-1-{[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decahydronaphthalen-1-yl]methyl}-5-hydroxy-4-(hydroxymethyl)-7-oxabicyclo[4.1.0]hept-3-en-2-one

Traditional Name

(1R,5S,6R)-1-{[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-hexahydro-1H-naphthalen-1-yl]methyl}-5-hydroxy-4-(hydroxymethyl)-7-oxabicyclo[4.1.0]hept-3-en-2-one

CAS Registry Number

Not Available

SMILES

C[C@@]1(CO)CCC[C@]2(C)[C@@H](C[C@@]34O[C@@H]3[C@@H](O)C(CO)=CC4=O)C(=C)CC[C@@H]12

InChI Identifier

InChI=1S/C22H32O5/c1-13-5-6-16-20(2,12-24)7-4-8-21(16,3)15(13)10-22-17(25)9-14(11-23)18(26)19(22)27-22/h9,15-16,18-19,23-24,26H,1,4-8,10-12H2,2-3H3/t15-,16-,18-,19+,20-,21+,22-/m0/s1

InChI Key

VUZUKTHJOMFUTI-XKFBSPQISA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, Methanol-d4, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 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

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600.0, Methanol-d4, simulated)	epoynton@sfu.ca	Not Available	Not Available	2026-02-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150.0, Methanol-d4, simulated)	epoynton@sfu.ca	Not Available	Not Available	2026-02-10	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Myrothecium sp. SC0265		Not Available
Myrothecium sp. SC0265	NPAtlas	25089733

Chemical Taxonomy

Classification

Not classified

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	1.61	ALOGPS
logP	1.85	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	13.18	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.29 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	102.43 m³·mol⁻¹	ChemAxon
Polarizability	41.25 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA018444

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

34501414

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

118711160

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Fu Y, Wu P, Xue J, Wei X: Cytotoxic and Antibacterial Quinone Sesquiterpenes from a Myrothecium Fungus. J Nat Prod. 2014 Aug 22;77(8):1791-9. doi: 10.1021/np500142g. [PubMed:25089733 ]
DOI: 10.1021/np500142g
PMID: 25089733

Showing NP-Card for Myrothecol C (NP0013164)

MOL for NP0013164 (Myrothecol C)

3D MOL for NP0013164 (Myrothecol C)

3D SDF for NP0013164 (Myrothecol C)

3D-SDF for NP0013164 (Myrothecol C)

PDB for NP0013164 (Myrothecol C)

3D PDB for NP0013164 (Myrothecol C)

SMILES for NP0013164 (Myrothecol C)

INCHI for NP0013164 (Myrothecol C)

Structure for NP0013164 (Myrothecol C)

3D Structure for NP0013164 (Myrothecol C)