NP-MRD: Showing NP-Card for methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate (NP0280552)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 06:24:32 UTC

Updated at

2022-09-09 06:24:32 UTC

NP-MRD ID

NP0280552

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate

Description

Methyl 27-chloro-2,4-dihydroxy-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-18-(propan-2-yl)-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]Hentriaconta-5,23-diene-21-carboxylate belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units. methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate is found in Lobophytum pauciflorum. Methyl 27-chloro-2,4-dihydroxy-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-18-(propan-2-yl)-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]Hentriaconta-5,23-diene-21-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241501272D          

 50 53  0  0  0  0            999 V2000
    7.2885   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0388   -1.7087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2330   -1.8856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3329   -2.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6609   -1.6258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4111   -2.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9672   -3.0215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7730   -2.8447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7335   -3.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9276   -3.6350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3716   -3.0255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6053   -2.5889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5657   -3.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3160   -3.9887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0097   -2.5930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2594   -1.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7034   -1.1972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9531   -0.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3971    0.1985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7589   -0.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3150   -0.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0653   -1.6298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1208   -0.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3706    0.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1764    0.2965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7325   -0.3130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5383   -0.1361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7709    0.6554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1752   -0.7760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9962   -0.8568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9908   -0.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8161   -0.7652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1731   -1.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4026   -1.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8840   -2.0095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1509   -2.9276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8603   -3.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4613   -2.0798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3451   -3.1044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7457   -3.8747    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.7890   -2.4950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9832   -2.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4271   -2.0624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6769   -1.2761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4827   -1.0993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6213   -2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4262    1.0827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2895   -4.0676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0398   -4.8539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0953   -3.8907    0.0000 C   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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 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
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 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  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 33 38  1  0  0  0  0
 36 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  4  0  0  0
  5 45  1  0  0  0  0
 26 45  1  0  0  0  0
 43 46  1  0  0  0  0
 25 47  1  0  0  0  0
  9 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
M  END

     RDKit          3D

113116  0  0  0  0  0  0  0  0999 V2000
   -0.4124   -2.4213   -3.8645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3058   -1.9483   -2.5294 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7719   -0.6706   -2.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2678    0.0169   -3.2031 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7119   -0.0611   -0.8835 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4464   -1.0710   -0.0216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8083   -1.3537   -0.4688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3482   -0.4641   -1.1543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6508   -2.5160   -0.2450 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0704   -3.7132    0.3996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9179   -4.3464   -0.3359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7864   -3.5774    1.8818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8636   -2.0872    0.5939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5869   -0.9488    0.0139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9276   -0.9965   -1.1536 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9171    0.2635    0.8110 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6753   -0.1275    2.0875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7817    1.2433    0.0743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3058    2.6381    0.5044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9493    2.8427   -0.0894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9041    3.2881    0.9157 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1365    4.7888    1.1394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5614    3.1594    0.2268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0238    1.7691    0.2583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2685    1.1354    1.2620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2569    1.3073   -0.9188 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2641    2.3694   -1.2329 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0832    1.9238   -1.6471 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8860    2.8353   -2.4709 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6133    0.7835   -1.3289 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8882    0.2308   -1.6288 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5872   -1.1252   -2.0287 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9894    0.6824   -2.4008 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3000    0.9366   -1.6559 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5742    2.4453   -1.7167 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4093    0.3703   -2.3276 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3619    0.4357   -0.2690 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7579    0.8171    0.2777 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7956   -0.1092    1.4806 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8998   -1.2585    1.0776 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8586   -2.4201    0.7504 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3002   -0.9333   -0.1098 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0155   -1.7689    2.1556 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5134   -3.4392    1.8063 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.8106   -0.9856    2.4941 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5689   -1.5153    1.7775 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4450   -0.5712    1.8978 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7908   -0.4768    3.2605 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9407    0.2033    0.9683 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7365   -0.1282   -0.4610 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3365   -1.9132   -4.5101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4088   -2.0753   -4.2260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3503   -3.5283   -3.9209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8646   -2.0277   -0.2329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2968   -0.9274    1.0544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1167   -2.8813   -1.2199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8944   -4.4992    0.3645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0768   -5.4565   -0.5086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7536   -3.9450   -1.3456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9992   -4.3356    0.3127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6068   -3.9820    2.5219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8853   -4.1745    2.1792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6937   -2.5191    2.1380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5115   -2.9867    0.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5138   -1.8073    1.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9722    0.7088    1.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1283    0.8149    2.4669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4667   -0.8439    1.8633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9649   -0.4747    2.8675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8665    1.1538    0.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6703    1.1885   -1.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0366    3.4151    0.1988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2215    2.6279    1.6084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0690    3.6293   -0.8883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5690    1.9381   -0.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9448    2.7521    1.8607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3018    5.2566    1.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2424    5.2310    0.1365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1171    4.9292    1.6648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8249    3.8132    0.7487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6175    3.5077   -0.8150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0120    1.3268   -1.7683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1317    3.0928   -0.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6453    3.0523   -2.0501 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3108    3.8294   -2.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8239    3.1698   -2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8740    2.5947   -3.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3169   -0.0291   -0.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4935   -1.1295   -3.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3222   -0.1771   -3.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8568    1.4517   -3.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2454    2.8286   -2.7091 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6598    2.6617   -1.6547 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0123    2.9897   -0.9262 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1376   -0.4965   -2.7579 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6805    1.0228    0.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7780    1.8489    0.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5467    0.6431   -0.4513 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8578   -0.3989    1.6126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4769    0.3784    2.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4403   -2.1394   -0.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4492   -2.6645    1.6539 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2229   -3.2939    0.4666 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6668   -1.8395    3.0789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5950   -1.1502    3.5946 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8996    0.1151    2.4166 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7716   -1.8901    0.7726 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2635   -2.4340    2.3650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5195   -0.7780    4.0341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0595   -1.1920    3.3215 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4105    0.5505    3.4501 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6414    1.2130    1.3192 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0190   -1.1966   -0.5905 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  3  1  6
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  2  0
 30 50  1  0
 50 49  1  0
 49 47  2  0
 47 48  1  0
 47 46  1  0
 46 45  1  0
 45 43  1  0
 43 44  1  0
 43 40  1  0
 40 41  1  6
 40 39  1  0
 39 38  1  0
 38 37  1  0
 37 42  1  0
 37 34  1  0
 34 35  1  0
 34 36  1  6
 34 33  1  0
 33 31  1  0
 31 32  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 26  5  1  0
 31 30  1  0
 50  5  1  0
 42 40  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  6 54  1  0
  6 55  1  0
  9 56  1  6
 13 64  1  0
 13 65  1  0
 16 66  1  1
 17 67  1  0
 17 68  1  0
 17 69  1  0
 18 70  1  0
 18 71  1  0
 19 72  1  0
 19 73  1  0
 20 74  1  0
 20 75  1  0
 21 76  1  1
 22 77  1  0
 22 78  1  0
 22 79  1  0
 23 80  1  0
 23 81  1  0
 26 82  1  6
 27 83  1  0
 27 84  1  0
 29 85  1  0
 29 86  1  0
 29 87  1  0
 50113  1  1
 49112  1  0
 48109  1  0
 48110  1  0
 48111  1  0
 46107  1  0
 46108  1  0
 45105  1  0
 45106  1  0
 43104  1  1
 41101  1  0
 41102  1  0
 41103  1  0
 39 99  1  0
 39100  1  0
 38 97  1  0
 38 98  1  0
 37 96  1  1
 35 92  1  0
 35 93  1  0
 35 94  1  0
 36 95  1  0
 33 90  1  0
 33 91  1  0
 31 88  1  1
 32 89  1  0
 10 57  1  0
 11 58  1  0
 11 59  1  0
 11 60  1  0
 12 61  1  0
 12 62  1  0
 12 63  1  0
M  END


  Mrv1533004241501272D          

 50 53  0  0  0  0            999 V2000
    7.2885   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0388   -1.7087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2330   -1.8856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3329   -2.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6609   -1.6258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4111   -2.4121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9672   -3.0215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7730   -2.8447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7335   -3.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9276   -3.6350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3716   -3.0255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6053   -2.5889    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5657   -3.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3160   -3.9887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0097   -2.5930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2594   -1.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7034   -1.1972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9531   -0.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3971    0.1985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7589   -0.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3150   -0.8435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0653   -1.6298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1208   -0.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3706    0.1196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1764    0.2965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7325   -0.3130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5383   -0.1361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7709    0.6554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1752   -0.7760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9962   -0.8568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9908   -0.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8161   -0.7652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1731   -1.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4026   -1.3678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8840   -2.0095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1509   -2.9276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8603   -3.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4613   -2.0798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3451   -3.1044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7457   -3.8747    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.7890   -2.4950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9832   -2.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4271   -2.0624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6769   -1.2761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4827   -1.0993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6213   -2.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4262    1.0827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2895   -4.0676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0398   -4.8539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0953   -3.8907    0.0000 C   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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 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
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 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  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 33 38  1  0  0  0  0
 36 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 44 45  1  4  0  0  0
  5 45  1  0  0  0  0
 26 45  1  0  0  0  0
 43 46  1  0  0  0  0
 25 47  1  0  0  0  0
  9 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0280552

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C12CC(=O)C(CC(=O)C(C)CCCC(C)CC(=O)C1CC(C)=C1C2C=C(C)CCC(Cl)C2(C)CCC(O2)C(C)(O)CC1O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C41H63ClO8/c1-23(2)28-20-31(43)26(5)12-10-11-24(3)18-32(44)29-19-27(6)37-30(41(29,22-33(28)45)38(47)49-9)17-25(4)13-14-35(42)40(8)16-15-36(50-40)39(7,48)21-34(37)46/h17,23-24,26,28-30,34-36,46,48H,10-16,18-22H2,1-9H3

> <INCHI_KEY>
OAZCZMDHKJUCJE-UHFFFAOYSA-N

> <FORMULA>
C41H63ClO8

> <MOLECULAR_WEIGHT>
719.4

> <EXACT_MASS>
718.4211467

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
113

> <JCHEM_AVERAGE_POLARIZABILITY>
80.41385803893935

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 27-chloro-2,4-dihydroxy-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-18-(propan-2-yl)-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate

> <ALOGPS_LOGP>
4.61

> <JCHEM_LOGP>
6.8097578946666655

> <ALOGPS_LOGS>
-5.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.65061457437034

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.838883371060675

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0204226155882044

> <JCHEM_POLAR_SURFACE_AREA>
127.20000000000002

> <JCHEM_REFRACTIVITY>
196.85650000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.08e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      13.605  -1.722   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      13.139  -3.190   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.635  -3.520   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      11.821  -5.017   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.567  -3.035   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.101  -4.503   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.139  -5.640   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      12.643  -5.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.702  -6.455   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.198  -6.785   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.160  -5.648   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.597  -4.833   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.656  -5.978   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.190  -7.446   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.618  -4.840   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.084  -3.372   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.046  -2.235   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.513  -0.767   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.475   0.371   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.017  -0.437   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.055  -1.575   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.588  -3.042   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.559  -1.244   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.025   0.223   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.529   0.553   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.567  -0.584   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.072  -0.254   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      14.506   1.223   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      15.260  -1.449   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      16.793  -1.599   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      16.783  -0.059   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      18.323  -1.428   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      17.123  -3.104   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      15.685  -2.553   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      14.717  -3.751   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      15.215  -5.465   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      16.539  -6.251   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      15.794  -3.882   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      13.711  -5.795   0.000  0.00  0.00           C+0
HETATM   40 Cl   UNK     0      12.592  -7.233   0.000  0.00  0.00          Cl+0
HETATM   41  C   UNK     0      12.673  -4.657   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      11.169  -4.987   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      10.131  -3.850   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      10.597  -2.382   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      12.101  -2.052   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       8.626  -4.180   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      11.996   2.021   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      11.740  -7.593   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      11.274  -9.061   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      13.245  -7.263   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   23   45                                             
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   48                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    5   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   47                                                  
CONECT   26   25   27   45                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   32   33                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   30   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36   33                                                       
CONECT   39   36   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   46                                                  
CONECT   44   43   45                                                       
CONECT   45   44    5   26                                                  
CONECT   46   43                                                            
CONECT   47   25                                                            
CONECT   48    9   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  106    0
END

View in JSmol

Synonyms

Value	Source
Methyl 27-chloro-2,4-dihydroxy-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-18-(propan-2-yl)-31-oxatetracyclo[26.2.1.0,.0,]hentriaconta-5,23-diene-21-carboxylic acid	Generator
Methyl 27-chloro-2,4-dihydroxy-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-18-(propan-2-yl)-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylic acid	Generator

Chemical Formula

C₄₁H₆₃ClO₈

Average Mass

719.4000 Da

Monoisotopic Mass

718.42115 Da

IUPAC Name

methyl 27-chloro-2,4-dihydroxy-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-18-(propan-2-yl)-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate

Traditional Name

methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C12CC(=O)C(CC(=O)C(C)CCCC(C)CC(=O)C1CC(C)=C1C2C=C(C)CCC(Cl)C2(C)CCC(O2)C(C)(O)CC1O)C(C)C

InChI Identifier

InChI=1S/C41H63ClO8/c1-23(2)28-20-31(43)26(5)12-10-11-24(3)18-32(44)29-19-27(6)37-30(41(29,22-33(28)45)38(47)49-9)17-25(4)13-14-35(42)40(8)16-15-36(50-40)39(7,48)21-34(37)46/h17,23-24,26,28-30,34-36,46,48H,10-16,18-22H2,1-9H3

InChI Key

OAZCZMDHKJUCJE-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

Species Name	Source	Reference
Lobophytum pauciflorum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquaterpenoids

Direct Parent

Sesquaterpenoids

Alternative Parents

Substituents

Sesquaterpenoid
Tertiary alcohol
Tetrahydrofuran
Methyl ester
Carboxylic acid ester
Ketone
Secondary alcohol
Cyclic ketone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Organic oxide
Organohalogen compound
Organochloride
Organooxygen compound
Alcohol
Alkyl chloride
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Alkyl halide
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	4.61	ALOGPS
logP	6.81	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	13.84	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	127.2 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	196.86 m³·mol⁻¹	ChemAxon
Polarizability	80.41 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate (NP0280552)

MOL for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

3D MOL for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

3D SDF for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

3D-SDF for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

PDB for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

3D PDB for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

SMILES for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

INCHI for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

Structure for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)

3D Structure for NP0280552 (methyl 27-chloro-2,4-dihydroxy-18-isopropyl-2,6,11,15,24,28-hexamethyl-9,16,19-trioxo-31-oxatetracyclo[26.2.1.0⁵,²².0⁸,²¹]hentriaconta-5,23-diene-21-carboxylate)