NP-MRD: Showing NP-Card for Uncarinic acid C (NP0081294)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 02:15:08 UTC

Updated at

2022-04-29 02:15:08 UTC

NP-MRD ID

NP0081294

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Uncarinic acid C

Description

Carissin belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Thus, carissin is considered to be an isoprenoid. Uncarinic acid C is found in Uncaria rhynchophylla . Uncarinic acid C was first documented in 2003 (PMID: 12737397). Based on a literature review very few articles have been published on Carissin (PMID: 32646240).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292204152D          

 47 52  0  0  1  0            999 V2000
    6.0770   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    6.8427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907    1.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  5  8  1  1  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  4 15  1  0  0  0  0
 13 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 22 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 25 30  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  0  0  0  0
 33 32  1  6  0  0  0
 33 34  1  0  0  0  0
 11 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
 37 38  1  0  0  0  0
 33 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 37 41  1  6  0  0  0
 34 42  1  6  0  0  0
 12 43  1  6  0  0  0
  4 44  1  6  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
  1 47  1  1  0  0  0
M  END

     RDKit          3D

103108  0  0  0  0  0  0  0  0999 V2000
    7.9541   -2.4322   -3.2188 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1245   -2.9384   -1.9200 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1500   -2.6692   -0.9691 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0378   -1.9285   -1.2821 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0962   -1.6768   -0.3376 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8769   -0.9106   -0.5653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5087   -0.3697   -1.7016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2646    0.3898   -1.8634 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9716    0.8890   -2.9552 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4298    0.5444   -0.8059 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2082    1.2454   -0.7937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3700    1.1336    0.5886 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7723    1.7338    1.4472 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1120    3.0906    0.9358 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0074    4.0866    0.8313 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1364    4.6734    2.2296 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5568    4.3312    3.1911 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1009    5.6548    2.4567 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5127    5.2484    0.0204 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0648    5.2704   -1.4028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    5.2273   -1.3625 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0250    5.6171   -2.6781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8370    3.8331   -0.9345 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3811    3.8546   -0.9360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3282    3.5533    0.4382 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4343    2.1349    0.8608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5003    1.7729    1.5036 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7676    0.4047    2.0105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1646   -0.4743    0.9277 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7585   -1.8307    0.9971 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7663   -2.4504    2.3707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2224   -1.6938    0.5896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7141   -2.7033   -0.3651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1451   -4.0700   -0.2717 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6658   -4.8110    0.8188 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6579   -4.0400   -0.2604 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1779   -4.4822   -1.6556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1611   -5.1017    0.6841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0939   -2.6890   -0.0424 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6218   -2.6991    0.2251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1366   -1.2760   -0.0917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6983   -0.2769    0.9117 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0383   -0.5943    2.2469 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2813   -2.1837    0.9505 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3932   -2.9258    1.2676 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3461   -3.1812    0.3136 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4552   -3.9227    0.6333 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9174   -1.3095   -3.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7999   -2.7533   -3.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9767   -2.7593   -3.6337 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8830   -1.5251   -2.2931 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1843   -0.7442    0.2775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1762   -0.5039   -2.5597 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4831    2.2623   -1.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4526    0.8595   -1.5958 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4599    1.8688    2.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6824    1.1323    1.4020 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8272    3.0981    0.0591 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8332    3.4881    1.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1317    6.5154    1.9660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2033    6.2454    0.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6318    5.2808    0.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4772    4.4737   -2.0375 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3200    6.2871   -1.8000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7950    5.9286   -0.5580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9163    4.7805   -3.3981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0717    5.9446   -2.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4523    6.5101   -3.0561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5987    3.1462   -1.7301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7799    4.6514   -0.3155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7696    3.9599   -1.9653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7541    2.8798   -0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0705    4.1757    1.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3295    2.4809    1.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3352    0.3016    2.9931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8464    0.1533    2.0326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5503   -0.0377   -0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7627   -2.9271    2.6159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0304   -3.2610    2.4997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6395   -1.6840    3.1611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4353   -0.6754    0.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8862   -1.7005    1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6314   -2.3596   -1.4321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8304   -2.8044   -0.2120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5360   -4.6367   -1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2996   -4.2484    1.3290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8182   -5.3537   -1.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229   -4.7827   -1.6430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4220   -3.6668   -2.3420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9020   -5.2456    1.4982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1717   -6.0946    0.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1286   -4.9588    1.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2228   -2.1267   -1.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3004   -3.0631    1.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1169   -3.3372   -0.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4957   -1.0855   -1.1161 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9620   -1.3943    0.0086 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0514   -0.6656    2.0535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3134   -1.6014    2.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3381    0.1125    3.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -2.0001    1.7440 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5139   -3.3089    2.2769 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5686   -4.2793    1.5653 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
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 12 11  1  6
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  1
 30 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  6
 36 38  1  0
 36 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  1
 15 16  1  1
 16 18  1  0
 16 17  2  0
  5 44  2  0
 44 45  1  0
 45 46  2  0
 46 47  1  0
 46  3  1  0
 26 12  1  0
 42 29  1  0
 42 12  1  0
 25 15  1  0
 39 30  1  0
  1 48  1  0
  1 49  1  0
  1 50  1  0
  4 51  1  0
  6 52  1  0
  7 53  1  0
 11 54  1  0
 11 55  1  0
 13 56  1  0
 13 57  1  0
 14 58  1  0
 14 59  1  0
 19 61  1  0
 19 62  1  0
 20 63  1  0
 20 64  1  0
 21 65  1  1
 22 66  1  0
 22 67  1  0
 22 68  1  0
 23 69  1  6
 24 70  1  0
 24 71  1  0
 24 72  1  0
 25 73  1  1
 27 74  1  0
 28 75  1  0
 28 76  1  0
 29 77  1  6
 31 78  1  0
 31 79  1  0
 31 80  1  0
 32 81  1  0
 32 82  1  0
 33 83  1  0
 33 84  1  0
 34 85  1  6
 35 86  1  0
 37 87  1  0
 37 88  1  0
 37 89  1  0
 38 90  1  0
 38 91  1  0
 38 92  1  0
 39 93  1  6
 40 94  1  0
 40 95  1  0
 41 96  1  0
 41 97  1  0
 43 98  1  0
 43 99  1  0
 43100  1  0
 18 60  1  0
 44101  1  0
 45102  1  0
 47103  1  0
M  END


  Mrv1652304292204152D          

 47 52  0  0  1  0            999 V2000
    6.0770   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    6.8427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6907    1.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  5  8  1  1  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  4 15  1  0  0  0  0
 13 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 22 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 25 30  1  0  0  0  0
 12 31  1  0  0  0  0
 31 32  1  0  0  0  0
 33 32  1  6  0  0  0
 33 34  1  0  0  0  0
 11 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
 37 38  1  0  0  0  0
 33 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 37 41  1  6  0  0  0
 34 42  1  6  0  0  0
 12 43  1  6  0  0  0
  4 44  1  6  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
  1 47  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0081294

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)OC[C@@]23CC[C@]4(CC[C@@H](C)[C@H](C)[C@H]4C2=CC[C@@H]2[C@@]4(C)CC[C@H](O)C(C)(C)[C@@H]4CC[C@@]32C)C(O)=O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H56O7/c1-24-14-19-39(35(44)45)20-21-40(23-47-33(43)13-9-26-8-11-28(41)29(22-26)46-7)27(34(39)25(24)2)10-12-31-37(5)17-16-32(42)36(3,4)30(37)15-18-38(31,40)6/h8-11,13,22,24-25,30-32,34,41-42H,12,14-21,23H2,1-7H3,(H,44,45)/b13-9+/t24-,25+,30+,31-,32+,34+,37+,38-,39+,40+/m1/s1

> <INCHI_KEY>
BRRFDRKIGYRDOD-WHXIUFLDSA-N

> <FORMULA>
C40H56O7

> <MOLECULAR_WEIGHT>
648.881

> <EXACT_MASS>
648.402604143

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
74.53674607994348

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,4aS,6aR,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-6a-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6b,9,9,12a-hexamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid

> <ALOGPS_LOGP>
7.02

> <JCHEM_LOGP>
7.873688383666665

> <ALOGPS_LOGS>
-6.15

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.867803172813726

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.486320552284144

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8350855657055364

> <JCHEM_POLAR_SURFACE_AREA>
113.29

> <JCHEM_REFRACTIVITY>
183.48450000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.56e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4aS,6aR,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-6a-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.034  -1.897   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.494   3.437   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.034   3.437   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.724   4.771   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.954   6.105   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.414   6.105   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.724   7.438   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.264   7.438   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.034   8.772   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.264  10.106   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.034  11.439   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.574  11.439   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.344  10.106   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.574   8.772   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.884  10.106   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.654  11.439   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      11.344  12.773   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -0.742   2.920   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.510   3.643   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.023   3.635   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      10.574   3.437   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       9.804   4.771   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      12.114   3.437   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      12.114  -1.897   0.000  0.00  0.00           C+0
CONECT    1    2    6   47                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   15   44                                             
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   34                                                  
CONECT   12   11   13   31   43                                             
CONECT   13   12    8   14   16                                             
CONECT   14   13   15                                                       
CONECT   15   14    4                                                       
CONECT   16   13   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26   22                                                       
CONECT   28   26   29                                                       
CONECT   29   28                                                            
CONECT   30   25                                                            
CONECT   31   12   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   38                                                  
CONECT   34   33   11   35   42                                             
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   41                                                  
CONECT   38   37   33   39   40                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   37                                                            
CONECT   42   34                                                            
CONECT   43   12                                                            
CONECT   44    4   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47    1                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₅₆O₇

Average Mass

648.8810 Da

Monoisotopic Mass

648.40260 Da

IUPAC Name

(1S,2R,4aS,6aR,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-6a-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6b,9,9,12a-hexamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid

Traditional Name

(1S,2R,4aS,6aR,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-6a-({[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}methyl)-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)OC[C@@]23CC[C@]4(CC[C@@H](C)[C@H](C)[C@H]4C2=CC[C@@H]2[C@@]4(C)CC[C@H](O)C(C)(C)[C@@H]4CC[C@@]32C)C(O)=O)=CC=C1O

InChI Identifier

InChI=1S/C40H56O7/c1-24-14-19-39(35(44)45)20-21-40(23-47-33(43)13-9-26-8-11-28(41)29(22-26)46-7)27(34(39)25(24)2)10-12-31-37(5)17-16-32(42)36(3,4)30(37)15-18-38(31,40)6/h8-11,13,22,24-25,30-32,34,41-42H,12,14-21,23H2,1-7H3,(H,44,45)/b13-9+/t24-,25+,30+,31-,32+,34+,37+,38-,39+,40+/m1/s1

InChI Key

BRRFDRKIGYRDOD-WHXIUFLDSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Uncaria rhynchophylla	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Coumaric acid or derivatives
Cinnamic acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Methoxyphenol
Methoxybenzene
Phenoxy compound
Phenol ether
Styrene
Anisole
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Alkyl aryl ether
Phenol
Benzenoid
Dicarboxylic acid or derivatives
Fatty acyl
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Cyclic alcohol
Enoate ester
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Ether
Alcohol
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Organic oxide
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	7.02	ALOGPS
logP	7.87	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	4.49	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	183.48 m³·mol⁻¹	ChemAxon
Polarizability	74.54 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

8851098

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10675750

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Bano Z, Begum S, Ali SS, Kiran Z, Siddiqui BS, Khawaja S, Ahmed A: Novel ursane-type triterpene from the fresh leaves of Carissa carandas and evaluation of cytotoxicity. J Asian Nat Prod Res. 2021 Sep;23(9):892-898. doi: 10.1080/10286020.2020.1791098. Epub 2020 Jul 10. [PubMed:32646240 ]
Siddiqui BS, Ghani U, Ali ST, Usmani SB, Begum S: Triterpenoidal constituents of the leaves of Carissa carandas. Nat Prod Res. 2003 Jun;17(3):153-8. doi: 10.1080/1478641031000104109. [PubMed:12737397 ]

Showing NP-Card for Uncarinic acid C (NP0081294)

MOL for NP0081294 (Uncarinic acid C)

3D MOL for NP0081294 (Uncarinic acid C)

3D SDF for NP0081294 (Uncarinic acid C)

3D-SDF for NP0081294 (Uncarinic acid C)

PDB for NP0081294 (Uncarinic acid C)

3D PDB for NP0081294 (Uncarinic acid C)

SMILES for NP0081294 (Uncarinic acid C)

INCHI for NP0081294 (Uncarinic acid C)

Structure for NP0081294 (Uncarinic acid C)

3D Structure for NP0081294 (Uncarinic acid C)