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Parillin

PubChem CID: 197977

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Compound Synonyms Parillin, Sarsasaponin, Smilacin, 19057-61-5, EINECS 242-790-1, NSC 106552, BRN 0078294, SMILASAPONIN, UNII-7913T95W7U, 7913T95W7U, 4-19-00-00836 (Beilstein Handbook Reference), C08906, NSC-106552, J15.521G, (3beta,5beta,25S)-Spirostann-3-yl-O-6-deoxy-alpha-L-mannopyranosyl-(1.4)-O-(beta-D-glucopyranosyl-(1.2))-O-(beta-D-glucopyranosyl-(1.6))-beta-D-glucopyranoside, ((25S)-5.BETA.-SPIROSTAN-3.BETA.-YL)4-O-(6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL)-2-O-(.BETA.-D-GLUCOPYRANOSYL)-6-O-(.BETA.-D-GLUCOPYRANOSYL)-.BETA.-D-GLUCOPYRANOSIDE, (3.BETA.,5.BETA.,25S)-SPIROSTAN-3-YL 6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL-(1->4)-(.BETA.-D-GLUCOPYRANOSYL-(1->2))-(.BETA.-D-GLUCOPYRANOSYL-(1->6))-.BETA.-D-GLUCOPYRANOSIDE, .BETA.-D-GLUCOPYRANOSIDE, (3.BETA.,5.BETA.,25S)-SPIROSTAN-3-YL O-6-DEOXY-.ALPHA.-L-MANNOPYRANOSYL-(1->4)-O-(.BETA.-D-GLUCOPYRANOSYL-(1->2))-O-(.BETA.-D-GLUCOPYRANOSYL-(1->6))-, CHEBI:7932, DLUTTXMPJCVUFR-HJCIYZGTSA-N, beta-D-Glucopyranoside, (3beta,5beta,25S)-spirostan-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-4)-O-(beta-D-glucopyranosyl-(1-2))-O-(beta-D-glucopyranosyl-(1- 6))-, Q27107619, ((25S)-5BETA-SPIROSTAN-3BETA-YL)4-O-(6-DEOXY-ALPHA-L-MANNOPYRANOSYL)-2-O-(BETA-D-GLUCOPYRANOSYL)-6-O-(BETA-D-GLUCOPYRANOSYL)-BETA-D-GLUCOPYRANOSIDE, (3BETA,5BETA,25S)-SPIROSTAN-3-YL 6-DEOXY-ALPHA-L-MANNOPYRANOSYL-(1->4)-(BETA-D-GLUCOPYRANOSYL-(1->2))-(BETA-D-GLUCOPYRANOSYL-(1->6))-BETA-D-GLUCOPYRANOSIDE, 242-790-1, BETA-D-GLUCOPYRANOSIDE, (3BETA,5BETA,25S)-SPIROSTAN-3-YL O-6-DEOXY-ALPHA-L-MANNOPYRANOSYL-(1->4)-O-(BETA-D-GLUCOPYRANOSYL-(1->2))-O-(BETA-D-GLUCOPYRANOSYL-(1->6))-, beta-D-Glucopyranoside, (3beta,5beta,25S)-spirostan-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-4)-O-(beta-D-glucopyranosyl-(1-2))-O-(beta-D-glucopyranosyl-(1-6))-, beta-D-Glucopyranoside, (3beta,5beta,25S)-spirostan-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-4)-O-(beta-D-glucopyranosyl-(1-2))-O-(beta-D-glucopyranosyl-(1-6))-(9CI)
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 335.0
Hydrogen Bond Donor Count 12.0
Pfizer 3 75 Rule True
Scaffold Graph Level C1CCC(CCC2CC(CC3CCC4C(CCC5C4CCC4C6CC7(CCCCC7)CC6CC45)C3)C(CC3CCCCC3)CC2CC2CCCCC2)CC1
Np Classifier Class Spirostane steroids
Deep Smiles OC[C@H]O[C@@H]O[C@H][C@H]O[C@H]CC[C@][C@@H]C6)CC[C@@H][C@@H]6CC[C@][C@H]6C[C@H][C@@H]5[C@H]C)[C@]O5)CC[C@@H]CO6))C))))))))))C)))))))))C))))))O[C@@H][C@H][C@@H]6O))O[C@@H]O[C@@H]C)[C@@H][C@H][C@H]6O))O))O)))))))CO[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O))))))))))))[C@@H][C@H][C@@H]6O))O))O
Heavy Atom Count 73.0
Classyfire Class Steroids and steroid derivatives
Scaffold Graph Node Level C1CCC(OCC2OC(OC3CCC4C(CCC5C4CCC4C6CC7(CCCCO7)OC6CC45)C3)C(OC3CCCCO3)CC2OC2CCCCO2)OC1
Classyfire Subclass Steroidal glycosides
Isotope Atom Count 0.0
Molecular Complexity 1870.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 32.0
Iupac Name (2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1R,2S,4S,5'S,6R,7S,8R,9S,12S,13S,16S,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxy-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 0.1
Gsk 4 400 Rule False
Molecular Formula C51H84O22
Scaffold Graph Node Bond Level C1CCC(OCC2OC(OC3CCC4C(CCC5C4CCC4C6CC7(CCCCO7)OC6CC45)C3)C(OC3CCCCO3)CC2OC2CCCCO2)OC1
Inchi Key DLUTTXMPJCVUFR-HJCIYZGTSA-N
Rotatable Bond Count 11.0
Synonyms parillin, parillin (sarsaponin), smilasaponin (smilacin)
Functional Groups CO, CO[C@@H](C)OC, CO[C@@](C)(C)OC
Compound Name Parillin
Exact Mass 1048.55
Formal Charge 0.0
Monoisotopic Mass 1048.55
Hydrogen Bond Acceptor Count 22.0
Molecular Weight 1049.2
Covalent Unit Count 1.0
Total Atom Stereocenter Count 32.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C51H84O22/c1-20-8-13-51(65-18-20)21(2)32-28(73-51)15-27-25-7-6-23-14-24(9-11-49(23,4)26(25)10-12-50(27,32)5)67-48-44(72-47-41(62)38(59)35(56)30(17-53)69-47)42(63)43(71-46-40(61)36(57)33(54)22(3)66-46)31(70-48)19-64-45-39(60)37(58)34(55)29(16-52)68-45/h20-48,52-63H,6-19H2,1-5H3/t20-,21-,22-,23+,24-,25+,26-,27-,28-,29+,30+,31+,32-,33-,34+,35+,36+,37-,38-,39+,40+,41+,42-,43+,44+,45+,46-,47-,48+,49-,50-,51+/m0/s1
Smiles C[C@H]1CC[C@@]2([C@H]([C@H]3[C@@H](O2)C[C@@H]4[C@@]3(CC[C@H]5[C@H]4CC[C@H]6[C@@]5(CC[C@@H](C6)O[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO[C@H]8[C@@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)O[C@H]9[C@@H]([C@@H]([C@H]([C@@H](O9)C)O)O)O)O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)C)C)C)OC1
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Steroids

  • 1. Outgoing r'ship FOUND_IN to/from Smilax Aristolochiifolia (Plant) Rel Props:Reference:ISBN:9780387706375; The Unani Pharmacopoeia of India Part-1 Volume-6
  • 2. Outgoing r'ship FOUND_IN to/from Smilax Aspera (Plant) Rel Props:Reference:ISBN:9788172361266