20(S)-tubotaiwine (Q27138847)

inferred from SMILES

mass

324.184±0 dalton

1 reference

Tubotaiwine (English)

7 October 2016

2 references

inferred from InChIKey

methyl (1R,11R,17S,18R)-18-ethyl-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate

inferred from InChI

1 reference

methyl (1R,11R,17S,18S)-18-ethyl-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carboxylate

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₀H₂₄N₂O₂

1 reference

Tubotaiwine (English)

7 October 2016

canonical SMILES

CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC

1 reference

Tubotaiwine (English)

7 October 2016

isomeric SMILES

CC[C@H]1[C@@H]2CCN3[C@H]1[C@]4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC

1 reference

Indole Alkaloids from the Leaves of Philippine Alstonia scholaris.

Tubotaiwine (English)

7 October 2016

5 references

Alkaloids of Alstonia scholaris from Thailand

Indole alkaloids from the leaves of Philippine Alstonia scholaris

Alkaloids from leaves and bark ofAlstonia scholaris in the Philippines

Alstonia scholaris (L.) R. Br. and Alstonia macrophylla Wall. ex G. Don: A comparative review on traditional uses, phytochemistry and pharmacology

Alstonia spathulata

1 reference

Strychnan and secoangustilobine A type alkaloids from Alstonia spatulata. Revision of the C-20 configuration of scholaricine

Hunteria zeylanica

1 reference

Alkaloids of Hunteria zeylanica

Rauvolfia serpentina

1 reference

Divergence of the indole alkaloid pattern in two somatic hybrid plant cell subcultures of Rauvolfia serpentina x Rhazya stricta

Strychnos dolichothyrsa

2 references

Further alkaloids from Strychnos dolichothyrsa

Chapter 1 Alkaloids of Strychnos and Gardneria Species

Gardneria angustifolia

1 reference

A molecular networking-based isolation of gardneria alkaloids from Gardneria distincta and their anti-inflammatory activity

Gardneria distincta

1 reference

A molecular networking-based isolation of gardneria alkaloids from Gardneria distincta and their anti-inflammatory activity

Alstonia congensis

1 reference

Alkaloids from Alstonia congensis

Tabernaemontana divaricata

1 reference

Indole alkaloids from three species of the Ervatamia genus: E. officinalis, E. divaricata, and E. divaricata Gouyahua.

Tabernaemontana africana

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Tabernaemontana attenuata

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Tabernaemontana cymosa

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Tabernaemontana eglandulosa

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Tabernaemontana inconspicua

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Tabernaemontana calcarea

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Tabernaemontana mocquerysii

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Tabernaemontana pachysiphon

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Tabernaemontana siphilitica

1 reference

Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content

Aspidosperma pyrifolium

1 reference

Alkaloids from Aspidosperma species from Bolivia.

Strychnos angolensis

1 reference

Chapter 1 Alkaloids of Strychnos and Gardneria Species

Melodinus aeneus

1 reference

Phytochemical and Pharmacological Properties of the Genus Melodinus – A Review

Melodinus axillaris

1 reference

Phytochemical and Pharmacological Properties of the Genus Melodinus – A Review

Melodinus fusiformis

1 reference

Phytochemical and Pharmacological Properties of the Genus Melodinus – A Review

Melodinus hemsleyanus

1 reference

Phytochemical and Pharmacological Properties of the Genus Melodinus – A Review

Melodinus cochinchinensis

1 reference

Phytochemical and Pharmacological Properties of the Genus Melodinus – A Review

Melodinus suaveolens

1 reference

Phytochemical and Pharmacological Properties of the Genus Melodinus – A Review

Kopsia arborea

1 reference

A comprehensive review on phytochemistry and pharmacology of genus Kopsia: monoterpene alkaloids – major secondary metabolites

Kopsia hainanensis

1 reference

A comprehensive review on phytochemistry and pharmacology of genus Kopsia: monoterpene alkaloids – major secondary metabolites

Catharanthus roseus

1 reference

The Catharanthus alkaloids: pharmacognosy and biotechnology

Alstonia quaternata

1 reference

Alcaloïdes d'Alstonia quaternata

Alstonia angustiloba

1 reference

Angustilobine and andranginine type indole alkaloids and an uleine-secovallesamine bisindole alkaloid from Alstonia angustiloba.

Tabernaemontana polyneura

1 reference

Alkaloids from leaves and stem bark of Ervatamia polyneura

Leuconotis griffithii

1 reference

Rhazinilam-Leuconolam-Leuconoxine Alkaloids from Leuconotis griffithii

Identifiers

InChI

InChI=1S/C20H24N2O2/c1-3-12-13-8-10-22-11-9-20(18(12)22)14-6-4-5-7-15(14)21-17(20)16(13)19(23)24-2/h4-7,12-13,18,21H,3,8-11H2,1-2H3/t12-,13-,18+,20+/m0/s1

1 reference

Tubotaiwine (English)

RLAKWLFUMAABBE-STJTYLQHSA-N

7 October 2016

InChIKey

2 references

Tubotaiwine (English)

7 October 2016

ChEBI release 2020-09-01

2 references

20(S)-tubotaiwine (English)

RLAKWLFUMAABBE-STJTYLQHSA-N

7 October 2016

InChIKey

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=6711-69-9

1 reference

Tubotaiwine (8CI) (English)

7 October 2016

2 references

Tubotaiwine (English)

matched by identifier from

7 October 2016

InChIKey

RLAKWLFUMAABBE-STJTYLQHSA-N

ChEBI ID

70515

mapping relation type

2 references

20(S)-tubotaiwine (English)

matched by identifier from

7 October 2016

International Chemical Identifier

InChI

InChI=1S/C20H24N2O2/c1-3-12-13-8-10-22-11-9-20(18(12)22)14-6-4-5-7-15(14)21-17(20)16(13)19(23)24-2/h4-7,12-13,18,21H,3,8-11H2,1-2H3/t12-,13-,18+,20+/m0/s1

1 reference