Structure Database (LMSD)
Common Name
PAT16(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])/26:1(2E)(2Me,4Me[S],6Me[S]))
Systematic Name
2-O-hexadecanoyl-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-hexacosenoyl)-α,α-trehalose
Synonyms
LM ID
LMSL03000345
Formula
Exact Mass
Calculate m/z
2215.963705
Status
Active (generated by computational methods)
3D model of PAT16(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])/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)
RJEDHMIFIAHKDD-JDZXRACGSA-N
InChi (Click to copy)
InChI=1S/C140H262O17/c1-18-23-28-33-38-43-48-53-57-61-64-68-72-76-81-85-90-95-100-114(7)105-118(11)109-122(15)136(147)154-131-125(111-141)151-139(133(130(131)145)156-138(149)124(17)128(143)120(13)107-116(9)102-97-92-87-82-77-73-65-60-56-51-46-41-36-31-26-21-4)157-140-134(153-127(142)103-98-93-88-83-78-69-52-47-42-37-32-27-22-5)132(155-137(148)123(16)110-119(12)106-115(8)101-96-91-86-80-75-71-67-63-59-55-50-45-40-35-30-25-20-3)129(144)126(152-140)112-150-135(146)121(14)108-117(10)104-113(6)99-94-89-84-79-74-70-66-62-58-54-49-44-39-34-29-24-19-2/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)
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@H](C)[C@@H]([C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCC)O)O[C@@H]1[C@@H]([C@H]([C@@H]([C@@H](COC(=O)/C(=C/[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCCC)/C)O1)O)OC(=O)/C(=C/[C@@H](C)C[C@@H](C)CCCCCCCCCCCCCCCCCCC)/C)OC(=O)CCCCCCCCCCCCCCC
Other Databases
PubChem CID
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