8a-hydroxy avermectin b1a aldehyde
- Other Name: (9S,16Z,21S)-2'-butan-2-yl-7,8,9-trihydroxy-15-[5-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-4-methoxy-6-methyloxan-2-yl]oxy-3',6,14,16-tetramethyl-3-oxospiro[2,20-dioxatricyclo[17.3.1.04,9]tricosa-10,12,16-triene-21,6'-2,3-dihydropyran]-10-carbaldehyde
- InChIKey: TZXHVLNPJOSTIO-VWECHTECSA-N
- InChI: InChI=1S/C48H74O15/c1-11-25(2)43-28(5)17-18-47(63-43)23-34-20-33(62-47)16-15-27(4)42(26(3)13-12-14-32(24-49)48(54)35(46(53)59-34)19-29(6)40(50)45(48)52)60-39-22-37(56-10)44(31(8)58-39)61-38-21-36(55-9)41(51)30(7)57-38/h12-15,17-18,24-26,28-31,33-45,50-52,54H,11,16,19-23H2,1-10H3/b13-12?,27-15-,32-14?/t25?,26?,28?,29?,30?,31?,33?,34?,35?,36?,37?,38?,39?,40?,41?,42?,43?,44?,45?,47-,48-/m1/s1
- SMILES: CCC(C)C1C(C=C[C@@]2(O1)CC3CC(O2)C/C=C(\C(C(C=CC=C([C@]4(C(CC(C(C4O)O)C)C(=O)O3)O)C=O)C)OC5CC(C(C(O5)C)OC6CC(C(C(O6)C)O)OC)OC)/C)C
- Exact Mass: 890.50277
- Molecular Formula: C48H74O15
-
Compound CID:
155293397
155293397
Hidden Reactions Filter
Some biological reactions link very small precursors (e.g. CO₂, acetate) to much larger products.
These reactions are correct, but they can create unrealistic shortest paths and connect otherwise separate parts of the graph.
To keep the overview readable, FAIR-TPs hides six such reactions where a <60 Da precursor leads to a >300 Da product in the visualisations.
You can have all these paths in the download output.
You can have all these paths in the download output.
Hidden reaction pairs (precursor → product):
- Acetate → N-(2-benzoyl-4-chlorophenyl)-2-acetamidoacetamide
- Acetate → N-(2-benzoyl-4-chlorophenyl)-2-acetamido-n-methylacetamide
- Carbon dioxide → Formylmethanofuran
- Acrolein → Chembl3706542
- Ethylene oxide → Acetyl-coa
- Formaldehyde → S-hydroxymethylglutathione
Note: In the graph output, up to 100 compounds are displayed for faster visualization. For the full output, please use the export files.
Click on a node or edge to see details here.