NP-MRD: Showing NP-Card for (1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one (NP0240073)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 23:47:37 UTC

Updated at

2022-09-06 23:47:37 UTC

NP-MRD ID

NP0240073

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one

Description

(24S)-3beta-(beta-D-Glucopyranosyloxy)-16beta,24,25-trihydroxy-9beta,19-cyclo-5alpha-lanostan-6-one belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus. (1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one is found in Astragalus membranaceus. Based on a literature review very few articles have been published on (24S)-3beta-(beta-D-Glucopyranosyloxy)-16beta,24,25-trihydroxy-9beta,19-cyclo-5alpha-lanostan-6-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072201472D          

 46 51  0  0  1  0            999 V2000
    5.6974    3.6196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0083    2.8554    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8256    2.7425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319    3.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1492    3.2810    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4601    2.5168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6555    3.9323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1619    4.5837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0042    4.4387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3069    3.4260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5020    2.2041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7313    1.4116    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5072    1.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971    1.4549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1995    0.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850    1.3097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3047    0.5338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926    0.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.3873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608    1.0193    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1486    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4327    0.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4352    0.4599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6168    1.5048    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1953    1.3596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7271    1.9903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5392    1.8451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0711    2.4758    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8832    2.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1635    1.5546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7908    3.2517    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3226    3.8824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9786    3.3969    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6983    4.1728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4468    2.7662    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3653    2.9114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    2.2807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092    2.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2411    1.7952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5214    2.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0532    1.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3335    2.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456    2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774    2.2309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0373    2.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 11  2  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 21 19  1  1  0  0  0
 21 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
 25 26  1  1  0  0  0
 27 26  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 27 36  1  0  0  0  0
 36 37  1  1  0  0  0
 25 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 21 40  1  0  0  0  0
 40 41  1  1  0  0  0
 42 41  1  1  0  0  0
 17 42  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 11 45  1  0  0  0  0
 15 45  1  0  0  0  0
 45 46  1  1  0  0  0
M  END

     RDKit          3D

106111  0  0  0  0  0  0  0  0999 V2000
    4.9791   -2.6201   -0.1420 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9584   -1.1395   -0.2961 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2077   -0.6357    0.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4510   -1.2032   -0.1111 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7336   -0.8248    0.5210 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.8732   -1.1605    1.8628 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1512    0.6158    0.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9946    1.1507   -1.0161 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4391    1.5002    1.3808 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5196    0.6481    0.7547 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8013   -0.4194    0.2913 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0239    1.0748   -0.0095 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7747    1.2063   -1.1922 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6850    1.6577   -0.3060 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7302    0.6030    0.1261 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5478    0.7087    1.6034 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4288    0.6203   -0.6382 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1835    1.9738   -0.4561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6085    1.9321   -0.8604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9967    2.7221   -1.6823 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4375    0.9280   -0.2253 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8646    0.8297   -0.7032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4596    2.1353   -1.1231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9607   -0.0828   -1.9347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6090    0.1540    0.4249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9648    0.1188    0.3066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6009    0.7563    1.3636 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.3201   -0.2109    2.0485 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3424   -0.7869    1.3492 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.2246   -2.2772    1.3207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0567   -2.7386    0.7341 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5865   -0.2082   -0.0240 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.8729   -0.6035   -0.4332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5964    1.3041    0.0049 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.3026    1.7566   -1.2765 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5483    1.8480    0.9511 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.2435    2.2245    2.1108 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0715   -1.2470    0.6049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5928   -1.3453    0.6433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8428   -0.4509   -0.2871 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2702   -1.0308   -1.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3911   -0.5392   -0.3116 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2579   -1.5983    0.5271 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7004   -1.8354    0.2304 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4618   -0.6795   -0.2954 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4756   -0.7465   -1.8015 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0299   -3.1168    0.0295 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4940   -3.0313   -1.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6515   -2.9718    0.6975 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1361   -0.8093   -1.3578 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1267   -0.9324    1.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2399    0.4639    0.4391 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5580   -0.9400   -1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3936   -2.3329   -0.1457 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5812   -1.4116    0.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7462   -2.1361    2.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2174    2.2497   -0.9851 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7370    0.7246   -1.7172 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9615    1.0511   -1.3576 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8441    0.9526    2.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1813    2.1011    1.9733 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8038    2.1975    0.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6321    0.0164    1.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7996   -0.5993    1.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5299    1.5526    0.8542 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0746    2.1467   -1.2181 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5393    2.5629    0.3500 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5563    2.0156   -1.3353 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0758    1.6138    2.0324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4696    0.8929    1.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9804   -0.1451    2.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7284    0.5586   -1.7278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3948    2.6911   -1.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1553    2.3422    0.5911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4783    1.1888    0.8752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2095    2.2999   -2.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5768    1.9690   -1.1610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2184    2.9871   -0.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7154   -1.1197   -1.7275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0356   -0.0465   -2.2395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3927    0.3653   -2.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3572    0.7218    1.3632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8526    1.1743    2.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2845   -0.5671    1.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3293   -2.7163    2.3322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0704   -2.7188    0.7179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2111   -3.6299    0.2948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8930   -0.5950   -0.7977 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0066   -0.3332   -1.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6081    1.6743    0.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1807    2.7390   -1.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0318    2.7448    0.5621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3394    3.2144    2.1402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5559   -1.9667   -0.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4420   -1.5692    1.6256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1722   -1.1851    1.6686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3342   -2.4202    0.4081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1791   -0.5145   -2.4587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3258   -2.1476   -1.6059 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0495   -1.4521    1.6302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3078   -2.5563    0.3124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7574   -2.6692   -0.5317 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1736   -2.1634    1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3266   -1.4282   -2.0893 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6651    0.2040   -2.2916 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5621   -1.2758   -2.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
  2 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 40  1  0
 40 41  1  6
 42 41  1  6
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  6
 40 39  1  0
 39 38  1  0
 38 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 29 32  1  0
 32 33  1  0
 32 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 25 22  1  0
 22 23  1  0
 22 24  1  0
 45 11  1  0
 36 27  1  0
 45 15  1  0
 42 17  1  0
 22 21  1  0
 42 40  1  0
  1 47  1  0
  1 48  1  0
  1 49  1  0
  2 50  1  6
  3 51  1  0
  3 52  1  0
  4 53  1  0
  4 54  1  0
  5 55  1  6
  6 56  1  0
  8 57  1  0
  8 58  1  0
  8 59  1  0
  9 60  1  0
  9 61  1  0
  9 62  1  0
 10 63  1  0
 11 64  1  1
 12 65  1  1
 13 66  1  0
 14 67  1  0
 14 68  1  0
 16 69  1  0
 16 70  1  0
 16 71  1  0
 17 72  1  6
 18 73  1  0
 18 74  1  0
 21 75  1  1
 41 98  1  0
 41 99  1  0
 43100  1  0
 43101  1  0
 44102  1  0
 44103  1  0
 46104  1  0
 46105  1  0
 46106  1  0
 39 96  1  0
 39 97  1  0
 38 94  1  0
 38 95  1  0
 25 82  1  1
 27 83  1  1
 29 84  1  1
 30 85  1  0
 30 86  1  0
 31 87  1  0
 32 88  1  6
 33 89  1  0
 34 90  1  1
 35 91  1  0
 36 92  1  6
 37 93  1  0
 23 76  1  0
 23 77  1  0
 23 78  1  0
 24 79  1  0
 24 80  1  0
 24 81  1  0
M  END


  Mrv1652309072201472D          

 46 51  0  0  1  0            999 V2000
    5.6974    3.6196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0083    2.8554    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.8256    2.7425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3319    3.3939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1492    3.2810    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.4601    2.5168    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6555    3.9323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1619    4.5837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0042    4.4387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3069    3.4260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5020    2.2041    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7313    1.4116    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5072    1.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971    1.4549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1995    0.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5850    1.3097    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3047    0.5338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4926    0.3886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2123   -0.3873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9608    1.0193    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1486    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4327    0.0995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4352    0.4599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6168    1.5048    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1953    1.3596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7271    1.9903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5392    1.8451    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0711    2.4758    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8832    2.3306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1635    1.5546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7908    3.2517    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3226    3.8824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9786    3.3969    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6983    4.1728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4468    2.7662    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3653    2.9114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    2.2807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7092    2.4259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2411    1.7952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5214    2.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0532    1.9404    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3335    2.7164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456    2.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774    2.2309    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0373    2.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  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  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 11  2  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 21 19  1  1  0  0  0
 21 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
 25 26  1  1  0  0  0
 27 26  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  6  0  0  0
 34 36  1  0  0  0  0
 27 36  1  0  0  0  0
 36 37  1  1  0  0  0
 25 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 21 40  1  0  0  0  0
 40 41  1  1  0  0  0
 42 41  1  1  0  0  0
 17 42  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 11 45  1  0  0  0  0
 15 45  1  0  0  0  0
 45 46  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0240073

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CC[C@H](O)C(C)(C)O)[C@H]1[C@@H](O)C[C@@]2(C)[C@@H]3CC(=O)[C@@H]4[C@]5(C[C@@]35CC[C@]12C)CC[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C4(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C36H60O10/c1-18(8-9-23(40)32(4,5)44)25-20(39)15-34(7)22-14-19(38)29-31(2,3)24(46-30-28(43)27(42)26(41)21(16-37)45-30)10-11-36(29)17-35(22,36)13-12-33(25,34)6/h18,20-30,37,39-44H,8-17H2,1-7H3/t18-,20+,21-,22+,23+,24+,25+,26-,27+,28-,29+,30+,33-,34+,35+,36-/m1/s1

> <INCHI_KEY>
MYKSQUJGCGSQGE-OFLILFQYSA-N

> <FORMULA>
C36H60O10

> <MOLECULAR_WEIGHT>
652.866

> <EXACT_MASS>
652.418648132

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
106

> <JCHEM_AVERAGE_POLARIZABILITY>
73.98035360746852

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,6S,8R,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-9-one

> <JCHEM_LOGP>
1.404372582666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.122064020227448

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.200691419604974

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5103193077205449

> <JCHEM_POLAR_SURFACE_AREA>
177.14

> <JCHEM_REFRACTIVITY>
169.0539

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,6S,8R,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      10.635   6.757   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.216   5.330   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.741   5.119   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.686   6.335   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.212   6.125   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      15.792   4.698   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      16.157   7.340   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.102   8.556   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.941   8.286   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      17.373   6.395   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.270   4.114   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.698   2.635   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.147   2.112   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.424   1.771   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.208   2.716   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.839   1.221   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.692   2.445   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.169   0.996   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.653   0.725   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.130  -0.723   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.660   1.903   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.144   1.632   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.674   0.186   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.812   0.858   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.151   2.809   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.365   2.538   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.357   3.715   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -2.873   3.444   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -3.866   4.621   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -5.382   4.350   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -5.905   2.902   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -3.343   6.070   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -4.335   7.247   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -1.827   6.341   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.304   7.789   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -0.834   5.164   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       0.682   5.435   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.675   4.257   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.191   4.528   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.183   3.351   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.707   4.799   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.699   3.622   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       6.222   5.071   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.738   5.342   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       8.731   4.164   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       9.403   5.550   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7                                                            
CONECT   11    2   12   45                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17   45                                             
CONECT   16   15                                                            
CONECT   17   15   18   42                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   40                                                  
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26   38                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   36                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   27   37                                                  
CONECT   37   36                                                            
CONECT   38   25   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   21   41   42                                             
CONECT   41   40   42                                                       
CONECT   42   41   17   40   43                                             
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   11   15   46                                             
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  102    0
END

View in JSmol

Synonyms

Value	Source
(24S)-3b-(b-D-Glucopyranosyloxy)-16b,24,25-trihydroxy-9b,19-cyclo-5a-lanostan-6-one	Generator
(24S)-3Β-(β-D-glucopyranosyloxy)-16β,24,25-trihydroxy-9β,19-cyclo-5α-lanostan-6-one	Generator

Chemical Formula

C₃₆H₆₀O₁₀

Average Mass

652.8660 Da

Monoisotopic Mass

652.41865 Da

IUPAC Name

(1S,3R,6S,8R,11S,12S,14S,15R,16R)-15-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-9-one

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H](CC[C@H](O)C(C)(C)O)[C@H]1[C@@H](O)C[C@@]2(C)[C@@H]3CC(=O)[C@@H]4[C@]5(C[C@@]35CC[C@]12C)CC[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C4(C)C

InChI Identifier

InChI=1S/C36H60O10/c1-18(8-9-23(40)32(4,5)44)25-20(39)15-34(7)22-14-19(38)29-31(2,3)24(46-30-28(43)27(42)26(41)21(16-37)45-30)10-11-36(29)17-35(22,36)13-12-33(25,34)6/h18,20-30,37,39-44H,8-17H2,1-7H3/t18-,20+,21-,22+,23+,24+,25+,26-,27+,28-,29+,30+,33-,34+,35+,36-/m1/s1

InChI Key

MYKSQUJGCGSQGE-OFLILFQYSA-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
Astragalus membranaceus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Cucurbitacin glycosides

Alternative Parents

Substituents

Cucurbitacin glycoside skeleton
Triterpene saponin
Triterpene glycoside
Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
Trihydroxy bile acid, alcohol, or derivatives
25-hydroxysteroid
24-hydroxysteroid
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
16-beta-hydroxysteroid
6-oxosteroid
16-hydroxysteroid
Hydroxysteroid
Oxosteroid
Glycosyl compound
O-glycosyl compound
Monosaccharide
Oxane
Tertiary alcohol
Cyclic alcohol
Ketone
Secondary alcohol
Polyol
Oxacycle
Organoheterocyclic compound
Acetal
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Organooxygen compound
Primary alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	1.4	ChemAxon
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-0.51	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	177.14 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	169.05 m³·mol⁻¹	ChemAxon
Polarizability	73.98 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

8874794

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10699453

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one (NP0240073)

MOL for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

3D MOL for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

3D SDF for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

3D-SDF for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

PDB for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

3D PDB for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

SMILES for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

INCHI for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

Structure for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)

3D Structure for NP0240073 ((1s,3r,6s,8r,11s,12s,14s,15r,16r)-15-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-14-hydroxy-7,7,12,16-tetramethyl-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-9-one)