Structure Database (LMSD)

OH O O O O O OH O HO O OH O O O O O O
Common Name
PAT18(25:1(2E)(2Me,4Me[S],6Me[S])/25:1(2E)(2Me,4Me[S],6Me[S])/24:0(2Me[R],3OH[R],4Me[S],6Me[S])/24:1(2E)(2Me,4Me[S],6Me[S]))
Systematic Name
2-octadecanoyl-3-O-(2,4S,6S-trimethyl-2E-pentacosenoyl)-6-O-(2,4S,6S-trimethyl-2E-pentacosenoyl)-2'-O-(2R,4S,6S-trimethyl-3R-hydroxy-tetracosanoyl)-4'-O-(2,4S,6S-trimethyl-2E-tetracosenoyl)-α,α-trehalose
Synonyms
LM ID
LMSL03000968
Formula
C140H262O17
Exact Mass
Calculate m/z
2215.963705
Status
Active (generated by computational methods)
Show lipids differing only in stereochemistry/bond geometry

Main

Classification

Category
Main Class
Sub Class
Saccharolipids [SL]
Acyltrehaloses [SL03]

String Representations

InChiKey (Click to copy)
GMJSBHZCGJMRDM-JDZXRACGSA-N
InChi (Click to copy)
InChI=1S/C140H262O17/c1-18-23-28-33-38-43-48-53-58-62-67-70-75-79-84-89-94-99-113(6)104-117(10)108-121(14)135(146)150-112-126-129(144)132(155-137(148)123(16)110-119(12)106-115(8)101-96-91-86-81-76-71-68-63-59-54-49-44-39-34-29-24-19-2)134(153-127(142)103-98-93-88-83-78-73-64-57-52-47-42-37-32-27-22-5)140(152-126)157-139-133(156-138(149)124(17)128(143)120(13)107-116(9)102-97-92-87-82-77-72-66-61-56-51-46-41-36-31-26-21-4)130(145)131(125(111-141)151-139)154-136(147)122(15)109-118(11)105-114(7)100-95-90-85-80-74-69-65-60-55-50-45-40-35-30-25-20-3/h108-110,113-120,124-126,128-134,139-141,143-145H,18-107,111-112H2,1-17H3/b121-108+,122-109+,123-110+/t113-,114-,115-,116-,117-,118-,119-,120-,124+,125+,126+,128+,129+,130-,131+,132-,133+,134+,139+,140+/m0/s1
SMILES (Click to copy)
CCCCCCCCCCCCCCCCCCC[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)CCCCCCCCCCCCCCCCCC)/C)O)OC(=O)[C@H](C)[C@@H]([C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCC)O)OC(=O)CCCCCCCCCCCCCCCCC)OC(=O)/C(=C/[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCCC)/C)O

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Mycobacterium tuberculosis (#1773)
Actinomycetia (#1760)
Asymmetric Total Synthesis and Structural Revision of DAT2, an Antigenic Glycolipid from Mycobacterium tuberculosis.,
Angew Chem Int Ed Engl, 2024
Pubmed ID: 38456226
Mycobacterium (#1763)
Actinomycetia (#1760)
Mycobacterial polyacyltrehalose generated by computational means

Other Databases

PubChem CID
52930805

Calculated Physicochemical Properties

Heavy Atoms 157
Rings 2
Aromatic Rings 0
Rotatable Bonds 117
Van der Waals Molecular Volume 2534.15
Topological Polar Surface Area 244.25
Hydrogen Bond Donors 4
Hydrogen Bond Acceptors 17
logP 44.21
Molar Refractivity 668.25

Admin

Created at
-
Updated at
2nd May 2024