MDL | MFCD00210534 |
InChIKey | ALTRINCJVPIQNK-NHIXJPGBSA-N |
Inchi | 1S/C27H40O4/c1-15-7-10-27(30-14-15)16(2)24-22(31-27)13-21-19-6-5-17-11-18(28)12-23(29)26(17,4)20(19)8-9-25(21,24)3/h5,16,18-24,28-29H,1,6-14H2,2-4H3/t16-,18+,19+,20-,21-,22-,23+,24-,25-,26-,27+/m0/s1 |
SMILES | O1[C@]2(C([H])([H])C([H])([H])C(=C([H])[H])C([H])([H])O2)[C@@]([H])(C([H])([H])[H])[C@@]2([H])[C@]1([H])C([H])([H])[C@@]1([H])[C@]3([H])C([H])([H])C([H])=C4C([H])([H])[C@]([H])(C([H])([H])[C@]([H])([C@]4(C([H])([H])[H])[C@@]3([H])C([H])([H])C([H])([H])[C@@]12C([H])([H])[H])O[H])O[H] |
LogP | 4.60480 |
PSA | 58.92000 |
溶解度 | Insuluble (5.1E-3 g/L) (25 ºC), |
颜色与性状 | Powder |
密度 | 1.19±0.1 g/cm3 (20 ºC 760 Torr), |
精确分子量 | 428.29300 |
氢键供体数量 | 2 |
氢键受体数量 | 4 |
可旋转化学键数量 | 0 |
同位素质量 | 428.29265975 g/mol |
重原子数量 | 31 |
复杂度 | 820 |
同位素原子数量 | 0 |
确定原子立构中心数量 | 11 |
不确定原子立构中心数量 | 0 |
确定化学键立构中心数量 | 0 |
不确定化学键立构中心数量 | 0 |
共价键单元数量 | 1 |
疏水参数计算参考值(XlogP) | 4.1 |
拓扑分子极性表面积 | 58.9 |
分子量 | 428.6 |
EINECS | 241-660-1 |
1.
Novel cytotoxic steroidal saponins from the roots of Liriope muscari (Decne.)?L.H. Bailey
Yan Wu,Xian-Min Wang,Su-Xia Bi,Wen Zhang,Rui-Ming Li,Rui-Jing Wang,Bo-Yang Yu,Jin Qi RSC Adv. 2017 7 13696
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Natural products as modulators of retinoic acid receptor-related orphan receptors (RORs)
Angela Ladurner,Patrik F. Schwarz,Verena M. Dirsch Nat. Prod. Rep. 2021 38 757
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Interaction between gut microbiota and ethnomedicine constituents
Xue Ming Wu,Ren Xiang Tan Nat. Prod. Rep. 2019 36 788
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D. Burn,B. Ellis,V. Petrow J. Chem. Soc. 1958 795
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Index of subjects
Annu. Rep. Prog. Chem. 1960 57 545
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Studies on biochemical transformation of plant steroids. Part I. Biochemical interconversion of the Δ25(27)- and the saturated 25D-or 25L-sapogenins
Ken'ichi Takeda,Hitoshi Minato,Ariyoshi Shimaoka J. Chem. Soc. C 1967 876
7.
Organic chemistry
T. G. Halsall,P. B. D. de la Mare,G. H. Williams,R. C. Cookson,A. G. Davies,L. Crombie,R. F. Garwood,K. Schofield,G. F. Smith,P. Bladon,G. T. Young,W. G. Overend Annu. Rep. Prog. Chem. 1957 54 147
SMILES
C=C1CO[C@@]2(CC1)[C@@H](C)[C@@H]3[C@]4(C)[C@@H](C[C@@H]3O2)[C@H]5[C@H](CC4)[C@]6(C)C(CC(O)CC6O)=CC5