tazettine (Q27114811)

Sekisanolin (English)

6 October 2016

2 references

(1R,13R,16R,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol

inferred from InChI

2 references

(1S,13S,16R,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol

inferred from InChI

2 references

(1R,13R,16S,18R)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol

1 reference

1 reference

1 reference

C₁₈H₂₁NO₅

1 reference

Sekisanolin (English)

6 October 2016

canonical SMILES

CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O

1 reference

Sekisanolin (English)

6 October 2016

isomeric SMILES

CN1C[C@@]2([C@]3([C@@H]1C[C@@H](C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O

1 reference

Four New Crinine-Type Alkaloids from Sternbergia Species

Sekisanolin (English)

6 October 2016

1 reference

Sternbergia lutea

2 references

Four New Crinine-Type Alkaloids from Sternbergia Species

Isolation of Sternbergine, a New Alkaloid From Bulbs of Sternbergia lutea

Brunsvigia gregaria

1 reference

Alkaloids from Brunsvigia gregaria

Cyrtanthus obliquus

1 reference

A dinitrogenous alkaloid from Cyrtanthus obliquus.

Galanthus elwesii

1 reference

Intraspecific variability in the alkaloid metabolism of Galanthus elwesii

Galanthus nivalis

3 references

Alkaloids from Galanthus nivalis

Alkaloids from Galanthus nivalis

Über die Alkaloide der Zwiebeln von Galanthus nivalis (III. Mitteil. über Amaryllidaceen-Alkaloide)

Leucojum aestivum

1 reference

New Alkaloids, Leucotamine and O-Methylleucotamine, from Leucojum asetivum L

Lycoris sanguinea

1 reference

[On the constituents of the bulbs of Lycoris sanguinea Maxim (author's transl)]

Narcissus asturiensis

1 reference

Alkaloids from Narcissus asturiensis

Narcissus tazetta

2 references

Isolation of O-methylmaritidine from bulbs of Narcissus tazetta L.

Alkaloide vonNarcissus tazetta undN. poeticus (XIII. Mitteil.: Über Amaryllidaceen-Alkaloide)

Pancratium biflorum

2 references

Glucosyloxy alkaloids from Pancratium biflorum

Glucosyloxy alkaloids from Pancratium biflorum

Sprekelia formosissima

1 reference

Antiproliferative amaryllidaceae alkaloids isolated from the bulbs of Sprekelia formosissima and Hymenocallis x festalis

Ungernia spiralis

1 reference

Alkaloids from Ungernia spiralis

Ungernia vvedenskyi

2 references

Alkaloids ofUngernia vvedenskyi

Ungvedine — A new alkaloid fromUngernia vvedenskyi

Narcissus cantabricus

2 references

Alkaloids from Narcissus cantabricus

Alkaloids from Narcissus cantabricus

Zephyranthes candida

1 reference

Cytotoxic alkaloids from the whole plants of Zephyranthes candida

Cyrtanthus falcatus

2 references

Acetylcholinesterase enzyme inhibitory effects of amaryllidaceae alkaloids

Alkaloids from Cyrtanthus falcatus

Crinum asiaticum

1 reference

Alkaloid composition of the bulbs ofCrinum amabile

Crinum giganteum

1 reference

Alkaloids of the epigeal organs of Crinum giganteum

Crinum jagus

1 reference

Alkaloids of the epigeal organs of Crinum giganteum

Crinum moorei

1 reference

Alkaloids from Crinum moorei introduced into Georgia

Haemanthus albiflos

2 references

Notiz über die Alkaloide vonHaemanthus albiflos(V. Mitteil. über Amaryllidaceen-Alkaloide)

Alkaloids of the Amaryllidaceae. III. Isolation of Five New Alkaloids from Haemanthus Species1

Hippeastrum puniceum

4 references

Alkaloids from Hippeastrum equestre. Part I. Phamine, a new phenanthridone alkaloid

Alkaloids of the epigeal organs ofHippeastrum equestre

Two novel Amaryllidaceae alkaloids from Hippeastrum equestre Herb.: 3-O-demethyltazettine and egonine

Alkaloids of the hypogeal organs ofHippeastrum equestre

Hippeastrum morelianum

1 reference

Alkaloids from Hippeastrum morelianum Lem. (Amaryllidaceae)

Hymenocallis littoralis

2 references

Alkaloids fromHymenocallis littoralis

Lycorine alkaloids from Hymenocallis littoralis

Hymenocallis rotata

1 reference

Alkaloidal constituents of Hymenocallis rotata Herb. (Amaryllidaceae).

Lapiedra martinezii

2 references

Alkaloid N-oxides of amaryllidaceae

Lycoris radiata

3 references

Alkaloidal Constituents of the Flowers of Lycoris radiata Herb. Amaryllidaceae.

Untersuchungen über Lycorisbasen. I

Ueber die Alkaloide des Lycoris radiata, Herb (III)

Lycoris squamigera

1 reference

Two New Alkaloids from Bulbs of Lycoris squamigera

Narcissus pseudonarcissus

1 reference

Alkaloids from Narcissus bujei (Amaryllidaceae)1Part 25 in the series “Narcissus alkaloids”. For part 24 see Viladomat et al., 1997 [Viladomat, F., Sellés, M., Codina, C. and Bastida, J., Planta Medica, 1997, 63, 583.].1

Pancratium canariense

1 reference

Pancratium canariense as an important source of amaryllidaceae alkaloids

Narcissus confusus

1 reference

Solid-phase extraction and reversed-phase high-performance liquid chromatography of the five major alkaloids in Narcissus confusus.

Pancratium trianthum

1 reference

Alkaloid composition ofPancratium trianthum

Eucharis amazonica

1 reference

Alkaloids from Eucharis amazonica (Amaryllidaceae).

Urceolina amazonica

1 reference

Alkaloids from Eucharis amazonica (Amaryllidaceae).

Pancratium maritimum

1 reference

STUDY OF ALKALOIDS OF PANCERATIUM MARITIMUM L. GROWING IN EGYPT

Sternbergia clusiana

1 reference

Alkaloids of Sternbergia clusiana and their Analgesic Effects

Hippeastrum glaucescens

1 reference

Alkaloids of Hippeastrum glaucescens

Hymenocallis latifolia var. latifolia

1 reference

Cytotoxicity of Hymenocallis expansa alkaloids

Narcissus hispanicus

1 reference

Solid-phase extraction and reversed-phase high-performance liquid chromatography of the five major alkaloids in Narcissus confusus.

Narcissus cuneiflorus

1 reference

Alkaloids from Narcissus asturiensis

Identifiers

InChI

InChI=1S/C18H21NO5/c1-19-9-18(20)17(4-3-12(21-2)6-16(17)19)13-7-15-14(22-10-23-15)5-11(13)8-24-18/h3-5,7,12,16,20H,6,8-10H2,1-2H3/t12-,16+,17+,18-/m1/s1

1 reference

Sekisanolin (English)

6 October 2016

2 references

Sekisanolin (English)

6 October 2016

ChEBI release 2020-09-01

2 references

tazettine (English)

6 October 2016

https://commonchemistry.cas.org/detail?cas_rn=507-79-9

10 April 2021

1 reference

(+)-Tazettine (English)

6 October 2016

1 reference

Sekisanolin (English)

6 October 2016

Reaxys registry number

96615

1 reference

tazettine (English)

6 October 2016

mapping relation type

2 references

tazettine (English)

6 October 2016

International Chemical Identifier

InChI

InChI=1S/C18H21NO5/c1-19-9-18(20)17(4-3-12(21-2)6-16(17)19)13-7-15-14(22-10-23-15)5-11(13)8-24-18/h3-5,7,12,16,20H,6,8-10H2,1-2H3/t12-,16+,17+,18-/m1/s1

1 reference

TAZETTINE (English)

6 October 2016

2 references

1 reference

1 reference

DSSTOX compound identifier

0 references

0 references

0 references

1 reference

Global Substance Registration System

tazettine (English)

6 October 2016

2 references

UNII

76WEU12CSO

TAZETTINE (English)

6 October 2016

1 reference

tazettine (English)