NP-MRD: Showing NP-Card for 21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol (NP0262135)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 04:46:27 UTC

Updated at

2022-09-08 04:46:27 UTC

NP-MRD ID

NP0262135

Secondary Accession Numbers

None

Natural Product Identification

Common Name

21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol

Description

21-(3-Chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]Pentacosa-17(25),18(23),19,21-tetraene-8,12-diol belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Based on a literature review very few articles have been published on 21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]Pentacosa-17(25),18(23),19,21-tetraene-8,12-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082206462D          

 40 46  0  0  0  0            999 V2000
   -0.4520    1.8417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7904    1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5428    1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1287    0.3368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0379    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6313    1.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3837    0.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0530    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8054    1.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8885    0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5578    0.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6410   -0.1202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988    0.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3959    0.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8111    0.9254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6174    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2866    1.2333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0390    0.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7083    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4607    1.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5439    0.2182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1300    1.5214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7992    2.0038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6124    0.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6475    2.1906    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    7.1222    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4530   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7005   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9456   -0.4026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5304   -1.1156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7241   -0.9410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0549   -1.4234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2193   -0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9614   -1.0479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4669    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5500   -0.7467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6240   -0.5523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  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  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 18 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 16 28  1  0  0  0  0
 28 29  1  0  0  0  0
 14 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 10 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
  7 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
  5 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END

     RDKit          3D

 84 90  0  0  0  0  0  0  0  0999 V2000
   -9.5354    1.3753    1.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2776    2.1091    1.1666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7601    2.9923    2.2665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6935    3.1672   -0.2196 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -7.1840    1.1246    0.7311 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6926    0.4202   -0.3635 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0290    1.9652    0.2746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8678    1.1569   -0.1869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7865    0.7948   -1.5140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7431    0.0514   -2.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7447   -0.3379   -1.1121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5872   -1.0749   -1.2885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9592   -1.1637   -0.0669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6974   -0.5038    0.8525 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7694   -0.0088    0.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8629    0.7510    0.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2496   -1.9336   -0.2302 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1130   -3.4078    0.0177 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5567   -1.7724   -1.6986 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4769   -2.8690   -2.0789 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6458   -2.9274   -1.1877 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7422   -2.0235   -0.0238 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4565   -2.7424    0.9641 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6678   -0.8459   -0.3241 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7030   -1.2340   -1.2166 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8891   -0.1328   -1.4330 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4289    1.2596   -1.2419 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3697    2.1656   -1.2098 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2832    1.4296   -0.0440 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7797    1.4325   -0.3978 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5159    1.8503    0.8658 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0612    2.3912   -1.5311 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2336    0.1867   -0.7521 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1070    0.5913    0.9928 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0737   -0.2695    0.9995 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8088    0.2618    1.6280 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5672   -0.1091    0.8798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4345   -1.5795    0.5975 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2592   -2.2515    1.9479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7884   -1.8062   -2.3416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3716    0.5293    2.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0747    1.0739    0.6390 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1914    2.1135    2.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3965    3.9491    1.8385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6187    3.2545    2.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9783    2.4580    2.8318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9504    0.4574    1.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5179   -0.0713   -0.1043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7305    2.6374    1.1314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3986    2.6611   -0.5093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5864    1.1144   -2.1987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6473   -0.2500   -3.0385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5374   -0.3652    1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9147    1.0254    1.6860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8985   -3.4281    0.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6253   -3.8500   -0.8581 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7445   -4.0283    0.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0175   -0.7955   -1.9313 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7654   -2.6809   -3.1582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9636   -3.8597   -2.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8233   -4.0148   -0.9174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5638   -2.7216   -1.8270 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2584   -3.1127    0.5061 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2955   -0.2124   -2.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0127    1.5099   -2.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4190    2.7313   -0.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1130    2.4818    0.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1359    2.8127    1.2611 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2955    1.0742    1.6356 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6130    1.8491    0.7146 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1417    1.8690   -2.4878 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3010    3.2041   -1.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0615    2.8498   -1.3187 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6102   -0.3392   -0.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3763   -1.1524    1.6414 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8895    1.3889    1.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7640    0.0610    2.7122 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7328    0.1722    1.5486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5695    0.4336   -0.0789 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8429   -1.7536    2.7505 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6573   -3.3086    1.9293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2032   -2.2324    2.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1880   -2.7874   -2.5613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7634   -1.2300   -3.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  2  0
 12 40  1  0
 40 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
 24 25  1  6
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 29 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  1
 38 17  1  0
 17 18  1  6
 29 30  1  0
 30 31  1  0
 30 32  1  0
 30 33  1  0
 15 16  2  0
 16  8  1  0
 12 11  1  0
 17 19  1  0
 17 13  1  0
 38 22  1  0
 26 24  1  0
 35 24  1  0
  1 41  1  0
  1 42  1  0
  1 43  1  0
  3 44  1  0
  3 45  1  0
  3 46  1  0
  5 47  1  1
  6 48  1  0
  7 49  1  0
  7 50  1  0
  9 51  1  0
 10 52  1  0
 14 53  1  0
 40 83  1  0
 40 84  1  0
 19 58  1  1
 20 59  1  0
 20 60  1  0
 21 61  1  0
 21 62  1  0
 23 63  1  0
 26 64  1  6
 27 65  1  6
 28 66  1  0
 29 67  1  1
 35 75  1  1
 36 76  1  0
 36 77  1  0
 37 78  1  0
 37 79  1  0
 39 80  1  0
 39 81  1  0
 39 82  1  0
 18 55  1  0
 18 56  1  0
 18 57  1  0
 31 68  1  0
 31 69  1  0
 31 70  1  0
 32 71  1  0
 32 72  1  0
 32 73  1  0
 33 74  1  0
 16 54  1  0
M  END


  Mrv1652309082206462D          

 40 46  0  0  0  0            999 V2000
   -0.4520    1.8417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7904    1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5428    1.4276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1287    0.3368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0379    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6313    1.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3837    0.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0530    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8054    1.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8885    0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5578    0.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6410   -0.1202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988    0.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3959    0.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8111    0.9254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6174    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2866    1.2333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0390    0.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7083    1.3773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4607    1.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5439    0.2182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1300    1.5214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7992    2.0038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6124    0.8521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6475    2.1906    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    7.1222    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4530   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7005   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9456   -0.4026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5304   -1.1156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7241   -0.9410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0549   -1.4234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3025   -1.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2193   -0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9614   -1.0479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4669    0.0741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5500   -0.7467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976   -0.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452   -0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6240   -0.5523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  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  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 18 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 16 28  1  0  0  0  0
 28 29  1  0  0  0  0
 14 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 10 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
  7 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
  5 39  1  0  0  0  0
 39 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0262135

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(Cl)C(O)CC1=CC=C2C(NC3=C2CC2CCC4(O)C56OC5C(O)C(OC6CCC4(C)C32C)C(C)(C)O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H44ClNO6/c1-27(2,33)21(35)14-16-7-8-18-19-15-17-9-12-31(38)29(5,30(17,6)24(19)34-20(18)13-16)11-10-22-32(31)26(40-32)23(36)25(39-22)28(3,4)37/h7-8,13,17,21-23,25-26,34-38H,9-12,14-15H2,1-6H3

> <INCHI_KEY>
FNRSMNUHSXXDPE-UHFFFAOYSA-N

> <FORMULA>
C32H44ClNO6

> <MOLECULAR_WEIGHT>
574.16

> <EXACT_MASS>
573.2857158

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
65.04065186063555

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0^{2,12}.0^{5,11}.0^{9,11}.0^{17,25}.0^{18,23}]pentacosa-17(25),18,20,22-tetraene-8,12-diol

> <JCHEM_LOGP>
3.5955217326666675

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.274985737306878

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.735037306071323

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1321415241569808

> <JCHEM_POLAR_SURFACE_AREA>
118.47000000000001

> <JCHEM_REFRACTIVITY>
151.84609999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0^{2,12}.0^{5,11}.0^{9,11}.0^{17,25}.0^{18,23}]pentacosa-17(25),18,20,22-tetraene-8,12-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.844   3.438   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.475   2.033   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.880   2.665   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -2.107   0.629   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.071   1.402   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.178   2.302   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.583   1.671   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.832   2.571   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.237   1.939   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.392   0.407   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.641   1.308   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.796  -0.224   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.278   1.238   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.206   0.397   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       8.981   1.727   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      10.486   1.402   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.735   2.302   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.140   1.671   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.389   2.571   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.793   1.939   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      15.949   0.407   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      17.043   2.840   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      18.292   3.740   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.943   1.591   0.000  0.00  0.00           C+0
HETATM   25 Cl   UNK     0      16.142   4.089   0.000  0.00  0.00          Cl+0
HETATM   26  C   UNK     0      13.295   0.138   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.046  -0.762   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.641  -0.131   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.232  -0.752   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.457  -2.082   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.952  -1.757   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.702  -2.657   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.298  -2.025   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.143  -0.493   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.661  -1.956   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       2.738   0.138   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       2.893  -1.394   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.489  -0.762   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.084  -0.131   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -1.165  -1.031   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6   39                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   36                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   34                                             
CONECT   11   10                                                            
CONECT   12   10   13   14   31                                             
CONECT   13   12                                                            
CONECT   14   12   15   29                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   28                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22                                                            
CONECT   26   18   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   16   29                                                  
CONECT   29   28   14   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   12   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   10   35   36                                             
CONECT   35   34                                                            
CONECT   36   34    7   37   38                                             
CONECT   37   36   38                                                       
CONECT   38   37   36   39                                                  
CONECT   39   38    5   40                                                  
CONECT   40   39                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₄ClNO₆

Average Mass

574.1600 Da

Monoisotopic Mass

573.28572 Da

IUPAC Name

21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0^{2,12}.0^{5,11}.0^{9,11}.0^{17,25}.0^{18,23}]pentacosa-17(25),18,20,22-tetraene-8,12-diol

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)(Cl)C(O)CC1=CC=C2C(NC3=C2CC2CCC4(O)C56OC5C(O)C(OC6CCC4(C)C32C)C(C)(C)O)=C1

InChI Identifier

InChI=1S/C32H44ClNO6/c1-27(2,33)21(35)14-16-7-8-18-19-15-17-9-12-31(38)29(5,30(17,6)24(19)34-20(18)13-16)11-10-22-32(31)26(40-32)23(36)25(39-22)28(3,4)37/h7-8,13,17,21-23,25-26,34-38H,9-12,14-15H2,1-6H3

InChI Key

FNRSMNUHSXXDPE-UHFFFAOYSA-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 naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
3-alkylindole
Naphthalene
Indole or derivatives
Indole
Dioxepane
1,4-dioxepane
Benzenoid
Pyran
Oxane
Monosaccharide
Heteroaromatic compound
Tertiary alcohol
Pyrrole
Cyclic alcohol
Secondary alcohol
Halohydrin
Chlorohydrin
Oxacycle
Azacycle
Ether
Oxirane
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Alkyl halide
Alkyl chloride
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.6	ChemAxon
pKa (Strongest Acidic)	12.74	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	118.47 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	151.85 m³·mol⁻¹	ChemAxon
Polarizability	65.04 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163038740

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol (NP0262135)

MOL for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

3D MOL for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

3D SDF for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

3D-SDF for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

PDB for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

3D PDB for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

SMILES for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

INCHI for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

Structure for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)

3D Structure for NP0262135 (21-(3-chloro-2-hydroxy-3-methylbutyl)-7-(2-hydroxypropan-2-yl)-1,2-dimethyl-6,10-dioxa-24-azaheptacyclo[13.10.0.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²⁵.0¹⁸,²³]pentacosa-17(25),18,20,22-tetraene-8,12-diol)