(Q105312734)

English

[(1S,3S,5S,6S)-6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] (2R)-3-hydroxy-2-phenylpropanoate

chemical compound

In more languages

Statements

type of chemical entity

0 references

Raceanisodamine

1 reference

based on heuristic

inferred from SMILES

3-Tropoyloxy-6-hydroxytropane

1 reference

based on heuristic

inferred from SMILES

(6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl) (2S)-3-hydroxy-2-phenylpropanoate

1 reference

based on heuristic

inferred from SMILES

6-Hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-phenylpropanoate

1 reference

based on heuristic

inferred from SMILES

[(1S,3R,5S)-6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate

1 reference

based on heuristic

inferred from SMILES

305.162708216 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

7|A-Hydroxyhyoscyamine

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

[(1S,3R,5S,6S)-6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] (2S)-3-hydroxy-2-phenylpropanoate

1 reference

based on heuristic

inferred from InChI

6-Hydroxyhyoscyamine

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₇H₂₃NO₄

0 references

canonical SMILES

O=C(OC1CC2N(C)C(C1)C(O)C2)C(C=3C=CC=CC3)CO

0 references

isomeric SMILES

CN1[C@@H]2C[C@H](OC(=O)[C@@H](CO)c3ccccc3)C[C@H]1[C@@H](O)C2

0 references

Brugmansia arborea

1 reference

Functional characterisation of a tropine-forming reductase gene from Brugmansia arborea, a woody plant species producing tropane alkaloids

Identifiers

InChI=1S/C17H23NO4/c1-18-12-7-13(9-15(18)16(20)8-12)22-17(21)14(10-19)11-5-3-2-4-6-11/h2-6,12-16,19-20H,7-10H2,1H3/t12-,13+,14+,15+,16+/m1/s1

0 references

WTQYWNWRJNXDEG-YXMSTPNBSA-N

0 references

1 reference

17 September 2022

based on heuristic

inferred from InChIKey

Sitelinks

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