NP-MRD: Showing NP-Card for methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate (NP0194993)

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Record Information

Version

2.0

Created at

2022-09-04 12:45:58 UTC

Updated at

2022-09-04 12:45:58 UTC

NP-MRD ID

NP0194993

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate

Description

Diepoxygorgiacerodiol belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate is found in Antillogorgia acerosa. methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate was first documented in 1996 (PMID: 8582045). Based on a literature review very few articles have been published on Diepoxygorgiacerodiol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042214452D          

 30 34  0  0  1  0            999 V2000
    0.6221   -0.4756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4442   -0.4057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9157   -1.0826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    0.3412    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9733    0.4185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7930    1.2236    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5030    1.6438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8099    2.4928    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4943    3.0795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8559    2.5570    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3401    1.9131    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3542    2.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3153    3.1829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0873    1.9805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1261    1.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0306    1.1761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6150    2.6730    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8614    3.4604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6665    3.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3028    4.0675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1736    2.0659    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9271    1.2786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4857    0.6715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1751    1.1835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9484    0.8960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9949    1.9886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2393   -0.1158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7979   -0.7229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4342   -0.2960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2049   -1.0885    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
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 16  1  0  0  0  0
  6 16  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  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  6  0  0  0
 23 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
  4 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END

     RDKit          2D

 54 58  0  0  0  0  0  0  0  0999 V2000
    2.3250   -4.5292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3755   -3.3680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9064   -1.9651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1049   -3.6097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1509   -2.1317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4330   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8596   -1.2135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7413    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3514    1.3703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8596    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4330    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1771    2.1203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6689    2.2771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7046    3.3338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0945    4.7042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8660    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4551   -0.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9437   -0.4499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5276    0.9318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8483   -1.6465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1170   -1.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9460   -3.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9965   -4.6326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6667   -4.3452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4413   -5.6297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2506   -2.9635    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5699   -5.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7350   -6.3424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1192   -4.7148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2569   -5.3119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8054   -4.2875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7941   -5.9321    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4373   -0.5622    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3093   -2.4960    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3115   -1.4345    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7139   -4.5074    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6739   -1.5300    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6004   -2.5175    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5477    2.6807    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5156    6.0745    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4648    5.3143    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2758    4.0941    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7670    0.8321    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0161    1.1169    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6229    2.1283    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7529   -2.8430    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0448   -0.7418    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2167   -3.0070    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6130   -2.0907    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4279   -3.7036    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4745   -6.2927    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3969   -7.6885    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8680   -6.1936    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4279   -6.8021    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 12  1  0
 12 13  2  0
 11 12  1  1
 11 16  1  0
  6 16  1  1
  6  5  1  0
  5  4  1  0
  4 29  1  0
 29 30  1  0
 29 27  1  0
 27 28  1  0
 27 23  1  0
 23 22  2  0
 22 21  1  0
 21 26  1  0
 26 24  1  0
 24 25  2  0
 21 17  1  0
 17 18  1  0
 18 20  1  0
 18 19  2  3
 17  8  1  0
  8  9  1  6
  9 10  1  0
  8  7  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
  6 11  1  0
  7  6  1  0
 10 11  1  0
 24 23  1  0
 10  8  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
  5 37  1  0
  5 38  1  0
  4 36  1  1
 29 53  1  6
 30 54  1  0
 27 51  1  6
 28 52  1  0
 22 50  1  0
 21 49  1  6
 17 43  1  6
 20 46  1  0
 20 47  1  0
 20 48  1  0
 19 44  1  0
 19 45  1  0
 10 39  1  6
  3 33  1  0
  3 34  1  0
  3 35  1  0
  1 31  1  0
  1 32  1  0
M  END


  Mrv1652309042214452D          

 30 34  0  0  1  0            999 V2000
    0.6221   -0.4756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4442   -0.4057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9157   -1.0826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7946    0.3412    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9733    0.4185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7930    1.2236    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5030    1.6438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8099    2.4928    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4943    3.0795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8559    2.5570    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3401    1.9131    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3542    2.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3153    3.1829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0873    1.9805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1261    1.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0306    1.1761    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6150    2.6730    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8614    3.4604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6665    3.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3028    4.0675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1736    2.0659    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9271    1.2786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4857    0.6715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1751    1.1835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9484    0.8960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9949    1.9886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2393   -0.1158    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7979   -0.7229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4342   -0.2960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2049   -1.0885    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
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
 10  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 16  1  0  0  0  0
  6 16  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  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  6  0  0  0
 23 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
  4 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0194993

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@]12O[C@]11C[C@@H]([C@@H](O)[C@@H](O)C3=C[C@@H](OC3=O)[C@@H](C(C)=C)[C@]3(O[C@@H]23)O1)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C21H24O9/c1-8(2)11-7-19-20(29-19,18(25)26-5)17-21(28-17,30-19)13(9(3)4)12-6-10(16(24)27-12)14(22)15(11)23/h6,11-15,17,22-23H,1,3,7H2,2,4-5H3/t11-,12-,13-,14+,15-,17+,19+,20-,21+/m1/s1

> <INCHI_KEY>
AHVHTEQZHUAMTF-XYPQPAGUSA-N

> <FORMULA>
C21H24O9

> <MOLECULAR_WEIGHT>
420.414

> <EXACT_MASS>
420.142032353

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
40.1205767462641

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,2R,3R,7S,8R,9R,11S,13S,14S)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1^{3,6}.0^{1,14}.0^{11,13}]heptadec-6(17)-ene-13-carboxylate

> <JCHEM_LOGP>
1.5314292153333326

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.263204332043532

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.530655923960033

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3251018010885023

> <JCHEM_POLAR_SURFACE_AREA>
127.35000000000001

> <JCHEM_REFRACTIVITY>
98.8821

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2R,3R,7S,8R,9R,11S,13S,14S)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1^{3,6}.0^{1,14}.0^{11,13}]heptadec-6(17)-ene-13-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.161  -0.888   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.696  -0.757   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.576  -2.021   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.350   0.637   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.817   0.781   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.480   2.284   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.806   3.068   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.378   4.653   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.789   5.748   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.598   4.773   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.635   3.571   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.661   4.403   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.589   5.941   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -2.030   3.697   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.102   2.159   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.057   2.195   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.881   4.990   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.341   6.459   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.844   6.796   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.299   7.593   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.924   3.856   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.464   2.387   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.507   1.253   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.794   2.209   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.237   1.673   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.457   3.712   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.047  -0.216   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.089  -1.349   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.544  -0.553   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.116  -2.032   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   29                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   11   16                                             
CONECT    7    6    8                                                       
CONECT    8    7    9   10   17                                             
CONECT    9    8   10                                                       
CONECT   10    9    8   11                                                  
CONECT   11   10    6   12   16                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16   11    6                                                       
CONECT   17    8   18   21                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   17   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   21                                                       
CONECT   27   23   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    4   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₄O₉

Average Mass

420.4140 Da

Monoisotopic Mass

420.14203 Da

IUPAC Name

methyl (1S,2R,3R,7S,8R,9R,11S,13S,14S)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1^{3,6}.0^{1,14}.0^{11,13}]heptadec-6(17)-ene-13-carboxylate

Traditional Name

methyl (1S,2R,3R,7S,8R,9R,11S,13S,14S)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1^{3,6}.0^{1,14}.0^{11,13}]heptadec-6(17)-ene-13-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@]12O[C@]11C[C@@H]([C@@H](O)[C@@H](O)C3=C[C@@H](OC3=O)[C@@H](C(C)=C)[C@]3(O[C@@H]23)O1)C(C)=C

InChI Identifier

InChI=1S/C21H24O9/c1-8(2)11-7-19-20(29-19,18(25)26-5)17-21(28-17,30-19)13(9(3)4)12-6-10(16(24)27-12)14(22)15(11)23/h6,11-15,17,22-23H,1,3,7H2,2,4-5H3/t11-,12-,13-,14+,15-,17+,19+,20-,21+/m1/s1

InChI Key

AHVHTEQZHUAMTF-XYPQPAGUSA-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
Antillogorgia acerosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Pseudopterane diterpenoid
Diterpene lactone
Ileabethane, pseudopterane or nor-sandresane diterpenoid
Diterpenoid
Meta-dioxane
2-furanone
Dicarboxylic acid or derivatives
Oxirane carboxylic acid or derivatives
Oxirane carboxylic acid
Monosaccharide
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Oxolane
1,2-diol
Carboxylic acid ester
Secondary alcohol
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Oxirane
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Alcohol
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	1.53	ChemAxon
pKa (Strongest Acidic)	11.53	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	127.35 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	98.88 m³·mol⁻¹	ChemAxon
Polarizability	40.12 Å³	ChemAxon
Number of Rings	5	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

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

101688927

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Rodriguez AD, Soto JJ: Five new pseudopterane diterpenes from the Caribbean sea plume Pseudopterogorgia acerosa Pallas, Gorgonacea. Chem Pharm Bull (Tokyo). 1996 Jan;44(1):91-4. doi: 10.1248/cpb.44.91. [PubMed:8582045 ]
LOTUS database [Link]

Showing NP-Card for methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate (NP0194993)

MOL for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D MOL for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D SDF for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D-SDF for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

PDB for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D PDB for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

SMILES for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

INCHI for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

Structure for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)

3D Structure for NP0194993 (methyl (1s,2r,3r,7s,8r,9r,11s,13s,14s)-7,8-dihydroxy-5-oxo-2,9-bis(prop-1-en-2-yl)-4,12,15,16-tetraoxapentacyclo[9.4.1.1³,⁶.0¹,¹⁴.0¹¹,¹³]heptadec-6(17)-ene-13-carboxylate)