Structure Database (LMSD)
Common Name
PAT16(24:0(2Me[R],3OH[R],4Me[S],6Me[S])/24:1(2E)(2Me,4Me[S],6Me[S])/22:1(2E)(2Me,4Me[S],6Me[S])/26:1(2E)(2Me,4Me[S],6Me[S]))
Systematic Name
2-O-hexadecanoyl-3-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-6-O-(2,4S,6S-trimethyl-2E-tetracosenoyl)-2'-O-(2,4S,6S-trimethyl-2E-docosenoyl)-4'-O-(2,4S,6S-trimethyl-2E-hexacosenoyl)-α,α-trehalose
Synonyms
LM ID
LMSL03000550
Formula
Exact Mass
Calculate m/z
2159.901105
Status
Active (generated by computational methods)
3D model of PAT16(24:0(2Me[R],3OH[R],4Me[S],6Me[S])/24:1(2E)(2Me,4Me[S],6Me[S])/22:1(2E)(2Me,4Me[S],6Me[S])/26:1(2E)(2Me,4Me[S],6Me[S]))
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Mycobacterium
(#1763)
Actinomycetes
(#1760)
Mycobacterial polyacyltrehalose generated by computational means
Mycobacterium tuberculosis
(#1773)
Actinomycetes
(#1760)
Asymmetric Total Synthesis and Structural Revision of DAT2, an Antigenic Glycolipid from Mycobacterium tuberculosis.,
Angew Chem Int Ed Engl, 2024
Angew Chem Int Ed Engl, 2024
Pubmed ID:
38456226
String Representations
InChiKey (Click to copy)
XMIZGYKCPVPPKW-MVFISTDMSA-N
InChi (Click to copy)
InChI=1S/C136H254O17/c1-18-23-28-33-38-43-48-53-57-60-61-64-68-72-77-82-86-91-96-110(7)101-114(11)105-118(15)132(143)150-127-121(107-137)147-135(129(126(127)141)152-133(144)119(16)106-115(12)102-111(8)97-92-87-81-75-70-66-56-51-46-41-36-31-26-21-4)153-136-130(149-123(138)99-94-89-84-79-74-65-52-47-42-37-32-27-22-5)128(151-134(145)120(17)124(139)116(13)103-112(9)98-93-88-83-78-73-69-63-59-55-50-45-40-35-30-25-20-3)125(140)122(148-136)108-146-131(142)117(14)104-113(10)100-109(6)95-90-85-80-76-71-67-62-58-54-49-44-39-34-29-24-19-2/h104-106,109-116,120-122,124-130,135-137,139-141H,18-103,107-108H2,1-17H3/b117-104+,118-105+,119-106+/t109-,110-,111-,112-,113-,114-,115-,116-,120+,121+,122+,124+,125+,126-,127+,128-,129+,130+,135+,136+/m0/s1
SMILES (Click to copy)
CCCCCCCCCCCCCCCCCCCC[C@H](C)C[C@H](C)/C=C(\C)/C(=O)O[C@@H]1[C@@H](CO)O[C@@H]([C@@H]([C@H]1O)OC(=O)/C(=C/[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCC)/C)O[C@@H]1[C@@H]([C@H]([C@@H]([C@@H](COC(=O)/C(=C/[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCC)/C)O1)O)OC(=O)[C@H](C)[C@@H]([C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCC)O)OC(=O)CCCCCCCCCCCCCCC
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
153
Rings
2
Aromatic Rings
0
Rotatable Bonds
113
Van der Waals Molecular Volume
2464.95
Topological Polar Surface Area
244.25
Hydrogen Bond Donors
4
Hydrogen Bond Acceptors
17
logP
42.65
Molar Refractivity
649.78
Admin
Created at
-
Updated at
2nd May 2024