NP-MRD: Showing NP-Card for (2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate (NP0325493)

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Record Information

Version

2.0

Created at

2022-09-12 06:17:08 UTC

Updated at

2022-09-12 06:17:08 UTC

NP-MRD ID

NP0325493

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate

Description

(2R,4aR,7bR)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate belongs to the class of organic compounds known as melleolides and analogues. Melleolides and analogues are compounds with a structure characterized by the presence of a 2-hydroxy-4-methoxy-6-methylbenzoic acid derivative linked to a 3,6,6,7b-tetramethyl-cyclobuta[e]indene moiety. Based on a literature review very few articles have been published on (2R,4aR,7bR)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122208172D          

 30 33  0  0  1  0            999 V2000
   -1.1423   -1.8493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7036   -1.2447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5079   -1.4284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -2.2168    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.0691   -0.8238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8734   -1.0075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8261   -0.0354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0218    0.1484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7788    0.9368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4606   -0.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6563   -0.2725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4133    0.5159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0950   -0.8772    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7092   -0.6934    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1480    0.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8467   -0.4336    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0897    0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6711   -0.4642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2455    0.1279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702    0.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863   -0.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695   -1.0521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0567   -1.1935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6180   -1.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7935   -1.8615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3548   -2.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303   -2.5295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079   -1.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032   -1.6935    0.0000 O   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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 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
 20 23  1  0  0  0  0
 24 23  1  6  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 26 29  1  0  0  0  0
 14 29  1  0  0  0  0
 16 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 57 60  0  0  0  0  0  0  0  0999 V2000
   -5.2861    2.2168    0.1084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2119    0.7567   -0.0763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3958    0.0454   -0.2557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9507    0.8686   -0.2625 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -6.4011   -1.3166   -0.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5991   -2.0235   -0.6133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1882   -1.9697   -0.4297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0057   -1.2539   -0.2498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8107   -1.9364   -0.2516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9980    0.1090   -0.0717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7933    0.8879    0.1209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7985    2.1339    0.2824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5139    0.2959    0.1411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3673    1.0566    0.3243 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7204    0.8673   -0.7261 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6937    1.1269    0.3637 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8648    2.6096    0.6033 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9879    0.4221    0.3591 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7510    0.7668   -0.8950 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3774   -0.5213   -1.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5653   -0.5119   -2.8057 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6455   -0.8504   -0.5831 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3241   -1.5491   -0.8893 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9658   -1.0570    0.4721 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7346   -1.6059    1.0440 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6957   -0.8843    1.4310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4487   -1.5914    1.9805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4983   -1.0251    2.3922 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6579    0.5785    1.3260 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6212    1.2561    2.5466 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8057    2.7771   -0.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3621    2.5587    0.0893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9328    2.5457    1.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4950   -1.5560   -0.6180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2087   -3.0383   -0.5704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7558   -2.9439   -0.3789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5179    2.1524    0.4529 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6801   -0.1205   -1.1916 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6421    1.6421   -1.5170 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2830    2.9702    1.4711 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4829    3.1870   -0.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9151    2.9119    0.7353 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5991    0.8279    1.2118 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1135    1.1960   -1.6909 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5771    1.4990   -0.7055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3524   -1.2513   -3.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9330    0.4966   -3.0842 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6086   -0.7042   -3.2962 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6635   -0.4050    0.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7901   -1.9453   -0.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5489   -0.5127   -1.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8572   -2.5255   -0.7963 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5245   -1.5664   -1.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8030   -1.4088    1.1520 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6963   -2.7014    1.1489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4453   -2.6770    2.0615 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1148    0.6900    3.1819 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 20 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 26 29  1  0
 29 30  1  1
 10  2  1  0
 29 14  1  0
 29 16  1  0
 24 18  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  6 34  1  0
  7 35  1  0
  9 36  1  0
 14 37  1  1
 15 38  1  0
 15 39  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  1
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 21 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 22 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  1
 25 55  1  0
 27 56  1  0
 30 57  1  0
M  END


  Mrv1652309122208172D          

 30 33  0  0  1  0            999 V2000
   -1.1423   -1.8493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7036   -1.2447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5079   -1.4284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -2.2168    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.0691   -0.8238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8734   -1.0075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8261   -0.0354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0218    0.1484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7788    0.9368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4606   -0.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6563   -0.2725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4133    0.5159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0950   -0.8772    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7092   -0.6934    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1480    0.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8467   -0.4336    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0897    0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6711   -0.4642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2455    0.1279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702    0.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863   -0.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695   -1.0521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0567   -1.1935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6180   -1.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7935   -1.8615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3548   -2.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303   -2.5295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079   -1.1322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8032   -1.6935    0.0000 O   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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 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
 20 23  1  0  0  0  0
 24 23  1  6  0  0  0
 18 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 26 29  1  0  0  0  0
 14 29  1  0  0  0  0
 16 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325493

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C(Cl)C(O)=CC(O)=C1C(=O)O[C@@H]1C[C@]2(C)C3CC(C)(C)C[C@@H]3C=C(C=O)C12O

> <INCHI_IDENTIFIER>
InChI=1S/C23H27ClO6/c1-11-18(15(26)6-16(27)19(11)24)20(28)30-17-9-22(4)14-8-21(2,3)7-12(14)5-13(10-25)23(17,22)29/h5-6,10,12,14,17,26-27,29H,7-9H2,1-4H3/t12-,14?,17+,22+,23?/m0/s1

> <INCHI_KEY>
UHFQTECWVLYLBG-GMBSWWGYSA-N

> <FORMULA>
C23H27ClO6

> <MOLECULAR_WEIGHT>
434.91

> <EXACT_MASS>
434.1496163

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
44.61032519652278

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4aR,7bR)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate

> <JCHEM_LOGP>
4.7115738920000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.02485799749977

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.208684618370319

> <JCHEM_PKA_STRONGEST_BASIC>
-3.762219145840386

> <JCHEM_POLAR_SURFACE_AREA>
104.06000000000002

> <JCHEM_REFRACTIVITY>
112.85159999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4aR,7bR)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1H,2H,4aH,5H,7H,7aH-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.132  -3.452   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.180  -2.323   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.681  -2.666   0.000  0.00  0.00           C+0
HETATM    4 Cl   UNK     0      -5.135  -4.138   0.000  0.00  0.00          Cl+0
HETATM    5  C   UNK     0      -5.729  -1.538   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -7.230  -1.881   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -5.275  -0.066   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.774   0.277   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.321   1.749   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -2.726  -0.852   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.225  -0.509   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.771   0.963   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -0.177  -1.637   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.324  -1.294   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.143   0.010   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.447  -0.809   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.901   0.662   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.986  -0.867   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.058   0.239   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.441  -0.439   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.971   1.006   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.934  -0.815   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.223  -1.964   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.706  -2.228   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.887  -3.532   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.348  -3.475   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.529  -4.779   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.990  -4.722   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.628  -2.113   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.499  -3.161   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    2   11                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   29                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18   29                                             
CONECT   17   16                                                            
CONECT   18   16   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24                                                       
CONECT   24   23   18   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   14   16   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
(2R,4AR,7BR)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1H,2H,2ah,4ah,5H,6H,7H,7ah,7BH-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoic acid	Generator

Chemical Formula

C₂₃H₂₇ClO₆

Average Mass

434.9100 Da

Monoisotopic Mass

434.14962 Da

IUPAC Name

(2R,4aR,7bR)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate

Traditional Name

(2R,4aR,7bR)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1H,2H,4aH,5H,7H,7aH-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate

CAS Registry Number

Not Available

SMILES

CC1=C(Cl)C(O)=CC(O)=C1C(=O)O[C@@H]1C[C@]2(C)C3CC(C)(C)C[C@@H]3C=C(C=O)C12O

InChI Identifier

InChI=1S/C23H27ClO6/c1-11-18(15(26)6-16(27)19(11)24)20(28)30-17-9-22(4)14-8-21(2,3)7-12(14)5-13(10-25)23(17,22)29/h5-6,10,12,14,17,26-27,29H,7-9H2,1-4H3/t12-,14?,17+,22+,23?/m0/s1

InChI Key

UHFQTECWVLYLBG-GMBSWWGYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as melleolides and analogues. Melleolides and analogues are compounds with a structure characterized by the presence of a 2-hydroxy-4-methoxy-6-methylbenzoic acid derivative linked to a 3,6,6,7b-tetramethyl-cyclobuta[e]indene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Melleolides and analogues

Alternative Parents

Substituents

Melleolide-skeleton
P-hydroxybenzoic acid alkyl ester
P-hydroxybenzoic acid ester
O-hydroxybenzoic acid ester
Dihydroxybenzoic acid
Halobenzoic acid or derivatives
3-halobenzoic acid or derivatives
Salicylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Resorcinol
4-chlorophenol
2-chlorophenol
M-cresol
2-halophenol
4-halophenol
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Toluene
Phenol
Halobenzene
Chlorobenzene
Benzenoid
Monocyclic benzene moiety
Aryl halide
Aryl chloride
Vinylogous acid
Tertiary alcohol
Cyclobutanol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen compound
Carbonyl group
Aldehyde
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	4.71	ChemAxon
pKa (Strongest Acidic)	7.21	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	112.85 m³·mol⁻¹	ChemAxon
Polarizability	44.61 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

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

163193831

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate (NP0325493)

MOL for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

3D MOL for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

3D SDF for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

3D-SDF for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

PDB for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

3D PDB for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

SMILES for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

INCHI for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

Structure for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)

3D Structure for NP0325493 ((2r,4ar,7br)-3-formyl-2a-hydroxy-6,6,7b-trimethyl-1h,2h,4ah,5h,7h,7ah-cyclobuta[e]inden-2-yl 3-chloro-4,6-dihydroxy-2-methylbenzoate)