Structure Database (LMSD)

Common Name
Petromylidene A
Systematic Name
2-(E)-(3-methylbutylidene)-7α,12α,24-trihydroxy-5α-cholan-3-one-24-sulfate
Synonyms
LM ID
LMST04010450
Formula
Exact Mass
Calculate m/z
540.312077
Sum Composition
Status
Curated

Classification

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Petromyzon marinus (#7757)
Hyperoartia (#117569)
Petromylidenes A⁻C: 2-Alkylidene Bile Salt Derivatives Isolated from Sea Lamprey (Petromyzon marinus).,
Mar Drugs, 2018
Pubmed ID: 30200427

String Representations

InChiKey (Click to copy)
BBYALPAQYMTBOW-YWOLIFCLSA-N
InChi (Click to copy)
InChI=1S/C29H48O7S/c1-17(2)8-9-19-16-28(4)20(13-24(19)30)14-25(31)27-22-11-10-21(29(22,5)26(32)15-23(27)28)18(3)7-6-12-36-37(33,34)35/h9,17-18,20-23,25-27,31-32H,6-8,10-16H2,1-5H3,(H,33,34,35)/b19-9+/t18-,20-,21-,22+,23+,25-,26+,27+,28+,29-/m1/s1
SMILES (Click to copy)
C1/C(=C\CC(C)C)/C(=O)C[C@]2([H])C[C@@H](O)[C@@]3([H])[C@]4([H])CC[C@H]([C@H](C)CCCOS(O)(=O)=O)[C@@]4(C)[C@@H](O)C[C@]3([H])[C@@]12C

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 37
Rings 4
Aromatic Rings 0
Rotatable Bonds 8
Van der Waals Molecular Volume 535.58
Topological Polar Surface Area 121.13
Hydrogen Bond Donors 3
Hydrogen Bond Acceptors 7
logP 7.08
Molar Refractivity 143.24

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Created at
26th Aug 2020
Updated at
12th Feb 2021