solanidine (Q3489153)

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chemical compound

(3beta)-solanid-5-en-3-ol
solanid-5-en-3beta-ol
Solanid-5-en-3-beta-ol
3-beta-Solanid-5-en-3-ol(9cl)
Solanidin
Solatubine
Solanid-5-en-3beta-ol(8CI)
22R,25S-Solanidine
3-b-Solanid-5-en-3-ol(9cl)
Solatubin
Solanid-5-en-3b-ol
22R,25S-Solanidanine
(1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{15,23}.0^{17,22}]tetracos-4-en-7-ol
Solanid-5-en-3-ol (ACD/Name 4.0)
Solanid-5-en-3-ol
3-beta-Solanid-5-en-3-ol
Solanid-5-en-3.beta.-ol

Language	Label	Description	Also known as
English	solanidine	chemical compound	(3beta)-solanid-5-en-3-ol solanid-5-en-3beta-ol Solanid-5-en-3-beta-ol 3-beta-Solanid-5-en-3-ol(9cl) Solanidin Solatubine Solanid-5-en-3beta-ol(8CI) 22R,25S-Solanidine 3-b-Solanid-5-en-3-ol(9cl) Solatubin Solanid-5-en-3b-ol 22R,25S-Solanidanine (1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{15,23}.0^{17,22}]tetracos-4-en-7-ol Solanid-5-en-3-ol (ACD/Name 4.0) Solanid-5-en-3-ol 3-beta-Solanid-5-en-3-ol Solanid-5-en-3.beta.-ol

Statements

type of chemical entity

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solanidine alkaloid

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chemical structure

Solanidine.svg
1,580 × 900; 33 KB

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397.334±0 dalton

1 reference

language of work or name

Solanidine (English)

5 October 2016

stereoisomer of

(1S,2R,7R,10S,11R,14R,15R,16S,17R,20R,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-ol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(1S,2S,7S,10R,11S,14S,15S,16R,17S,20R,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-ol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(1S,2S,7S,10R,11S,14S,15R,16S,17R,20R,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-ol

1 reference

based on heuristic

inferred from InChI

(1S,2S,7S,10R,11R,14S,15R,16S,17S,20S,23R)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-ol

1 reference

based on heuristic

inferred from InChI

(1S,2S,7S,10R,11S,14S,15R,16S,17S,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-ol

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₇H₄₃NO

1 reference

language of work or name

Solanidine (English)

5 October 2016

canonical SMILES

CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C

1 reference

language of work or name

Solanidine (English)

5 October 2016

isomeric SMILES

C[C@H]1CC[C@@H]2[C@H]([C@H]3[C@@H](N2C1)C[C@@H]4[C@@]3(CC[C@H]5[C@H]4CC=C6[C@@]5(CC[C@@H](C6)O)C)C)C

1 reference

language of work or name

Solanidine (English)

5 October 2016

Solanum americanum

1 reference

imported from Wikimedia project

English Wikipedia

1 reference

Solanidine isolation from Solanum tuberosum by centrifugal partition chromatography

7 references

Solanidine isolation from Solanum tuberosum by centrifugal partition chromatography

Regeneration, in vitro glycoalkaloids production and evaluation of bioactivity of callus methanolic extract of Solanum tuberosum L.

Characterization of novel steroidal alkaloids from tubers of solanum species by combined gas chromatography—mass spectrometry

Reversed-phase high-performance liquid chromatographic separation of potato glycoalkaloids and hydrolysis products on acidic columns

Separation of potato glycoalkaloids by gas chromatography

Steroidal Alkaloids and Sapogenins from Roots of SomeSolanumSpecies1

Induction of terata in hamsters by solanidane alkaloids derived from Solanum tuberosum

Fritillaria camtschatcensis

2 references

Two steroidal alkaloids, hapepunine and anrakorinine, from the mature Fritillaria camtschatcensis

Camtschatcanidine, an alkaloid from Fritillaria camtschatcensis

Veratrum taliense

4 references

Neoverataline A and B, two antifungal alkaloids with a novel carbon skeleton from Veratrum taliense

Neoverataline A and B, Two Antifungal Alkaloids with a Novel Carbon Skeleton from Veratrum taliense.

Steroidal alkaloids from Veratrum dahuricum

Steroidal alkaloids from Veratrum album

Fritillaria delavayi

2 references

New steroidal alkaloids from the Chinese herb drug, "bei-mu"

Isolation and structure elucidation of new alkaloids from Fritillaria delavayi Franch.

Fritillaria tortifolia

1 reference

Tortifoline, a novel (20S, 22R)-5.ALPHA.-cevanine alkaloid from Fritillaria tortifolia.

Fritillaria sewerzowii

1 reference

Solanidine and diacetylsevedine from Korolkowia sewerzowii

Fritillaria bucharica

2 references

Alkaloids ofRhinopetalum bucharicum. The structure of rhinolinine

Alkaloids ofRhinopetalum bucharicum the structure of rhinoline

1 reference

Alkaloids ofRhinopetalum korelini

1 reference

Alkaloids ofRhinopetalum korelini

Solanum chacoense

2 references

Characterization of novel steroidal alkaloids from tubers of solanum species by combined gas chromatography—mass spectrometry

Nuclear Magnetic Resonance Spectroscopy and Mass Spectrometry of Solanidine, Leptinidine, and Acetylleptinidine. Steroidal Alkaloids fromSolanum chacoenseBitter

Solanum leptophyes

1 reference

Characterization of novel steroidal alkaloids from tubers of solanum species by combined gas chromatography—mass spectrometry

Solanum sparsipilum

1 reference

Characterization of novel steroidal alkaloids from tubers of solanum species by combined gas chromatography—mass spectrometry

Veratrum mengtzeanum

1 reference

Steroidal alkaloids from Veratrum nigrum

1 reference

Biomarkers of tuber intake

1 reference

Pingbeinone, a novel steroidal alkaloid having C-18 nor cevane skeleton from Fritillaria ussuriensis Maxim

Fritillaria karelinii

1 reference

Alkaloids ofRhinopetalum korelini

has characteristic

1 reference

Identifiers

InChI=1S/C27H43NO/c1-16-5-8-23-17(2)25-24(28(23)15-16)14-22-20-7-6-18-13-19(29)9-11-26(18,3)21(20)10-12-27(22,25)4/h6,16-17,19-25,29H,5,7-15H2,1-4H3/t16-,17+,19-,20+,21-,22-,23+,24-,25-,26-,27-/m0/s1

1 reference

language of work or name

Solanidine (English)

5 October 2016

JVKYZPBMZPJNAJ-OQFNDJACSA-N

2 references

language of work or name

Solanidine (English)

5 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

solanidine (English)

5 October 2016

JVKYZPBMZPJNAJ-OQFNDJACSA-N

CAS Common Chemistry

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=80-78-4

1 reference

language of work or name

Solanidine (English)

5 October 2016

1 reference

language of work or name

Solanidine (English)

5 October 2016

Reaxys registry number

45370

1 reference

language of work or name

solanidine (English)

5 October 2016

mapping relation type

1 reference

language of work or name

solanidine (English)

5 October 2016

1 reference

language of work or name

CHEMBL1980466 (English)

5 October 2016

UniChem compound ID

1 reference

splash10-0udi-5910000000-da12df0b66b01e498980

0 references

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201-309-5

1 reference

Global Substance Registration System

language of work or name

SOLANIDINE (English)

5 October 2016

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Solanidine (English)

CAS no.: 80-78-4 (English)

Human Metabolome Database ID

1 reference

based on heuristic

inferred from InChIKey

1 reference

language of work or name

solanidine (English)

5 October 2016

1 reference

Global Substance Registration System

language of work or name

SOLANIDINE (English)

5 October 2016

Probes And Drugs ID

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Microsoft Academic ID

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1 reference

imported from Wikimedia project

Japanese Wikipedia

Sitelinks

Wikipedia(9 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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