Structure Database (LMSD)
Common Name
PAT16(24:0(2Me[R],3OH[R],4Me[S],6Me[S])/26:1(2E)(2Me,4Me[S],6Me[S])/24:0(2Me[R],3OH[R],4Me[S],6Me[S])/25:1(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-hexacosenoyl)-2'-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-4'-O-(2,4S,6S-trimethyl-2E-pentacosenoyl)-α,α-trehalose
Synonyms
LM ID
LMSL03000619
Formula
Exact Mass
Calculate m/z
2219.95862
Status
Active (generated by computational methods)
No other lipid differing only in stereochemistry/bond geometry found
3D model of PAT16(24:0(2Me[R],3OH[R],4Me[S],6Me[S])/26:1(2E)(2Me,4Me[S],6Me[S])/24:0(2Me[R],3OH[R],4Me[S],6Me[S])/25:1(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)
YCWSELCQHLYVJO-KWSNNVCHSA-N
InChi (Click to copy)
InChI=1S/C139H262O18/c1-18-23-28-33-38-43-48-53-57-61-63-67-70-74-78-83-88-93-98-111(6)103-115(10)107-119(14)134(146)150-110-124-128(144)131(155-136(148)121(16)126(142)117(12)105-113(8)100-95-90-85-80-75-71-64-59-55-50-45-40-35-30-25-20-3)133(153-125(141)102-97-92-87-82-77-68-52-47-42-37-32-27-22-5)139(152-124)157-138-132(156-137(149)122(17)127(143)118(13)106-114(9)101-96-91-86-81-76-72-65-60-56-51-46-41-36-31-26-21-4)129(145)130(123(109-140)151-138)154-135(147)120(15)108-116(11)104-112(7)99-94-89-84-79-73-69-66-62-58-54-49-44-39-34-29-24-19-2/h107-108,111-118,121-124,126-133,138-140,142-145H,18-106,109-110H2,1-17H3/b119-107+,120-108+/t111-,112-,113-,114-,115-,116-,117-,118-,121+,122+,123+,124+,126+,127+,128+,129-,130+,131-,132+,133+,138+,139+/m0/s1
SMILES (Click to copy)
CCCCCCCCCCCCCCCCCCCC[C@H](C)C[C@H](C)/C=C(\C)/C(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)OC(=O)/C(=C/[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCCC)/C)O)OC(=O)[C@H](C)[C@@H]([C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCC)O)OC(=O)CCCCCCCCCCCCCCC)OC(=O)[C@H](C)[C@@H]([C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCC)O)O
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
157
Rings
2
Aromatic Rings
0
Rotatable Bonds
117
Van der Waals Molecular Volume
2528.28
Topological Polar Surface Area
264.48
Hydrogen Bond Donors
5
Hydrogen Bond Acceptors
18
logP
43.16
Molar Refractivity
665.56
Admin
Created at
-
Updated at
2nd May 2024