Solanidine information

Solanidine
Names
	IUPAC name Solanid-5-en-3β-ol
	Systematic IUPAC name (2S,4aR,4bS,6aS,6bR,7S,7aR,10S,12aS,13aS,13bS)-4a,6a,7,10-Tetramethyl-2,3,4,4a,4b,5,6,6a,6b,7,7a,8,9,10,11,12a,13,13a,13b,14-icosahydro-1H-naphtho[2′,1′:4,5]indeno[1,2-b]indolizin-2-ol
	Other names Solatubin; Solatubine
Identifiers
CAS Number	80-78-4 ;
3D model (JSmol)	Interactive image; Interactive image;
Beilstein Reference	45370
ChEBI	CHEBI:28374;
ChEMBL	ChEMBL1980466;
ChemSpider	59150;
ECHA InfoCard	100.001.191
EC Number	201-309-5;
KEGG	C06543;
PubChem CID	65727;
UNII	W7801OHM8B ;
	InChI 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 Key: JVKYZPBMZPJNAJ-OQFNDJACSA-N; InChI=1/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 Key: JVKYZPBMZPJNAJ-OQFNDJACBI;
	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; C[C@@H]1CN2[C@@]3([H])C[C@@]4([H])[C@]5([H])CCC6=C[C@@H](O)CC[C@]6(C)[C@@]5([H])CC[C@]4(C)[C@@]3([H])[C@H](C)[C@@]2([H])CC1;
Properties
Chemical formula	C27H43NO
Molar mass	397.647 g·mol−1
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302, H413
Precautionary statements	P264, P270, P273, P301+P312, P330, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Solanidine is a poisonous steroidal alkaloid chemical compound that occurs in plants of the family Solanaceae, such as potato and Solanum americanum.^[2]^[3] The sugar portion of glycoalkaloids hydrolyses in the body, leaving the solanidine portion.^[4]

^ "Solanidine". pubchem.ncbi.nlm.nih.gov.
^ Nikolic, NC; Stankovic, MZ (2003). "Solanidine hydrolytic extraction and separation from the potato (Solanum tuberosum L.) vines by using solid-liquid-liquid systems". Journal of Agricultural and Food Chemistry. 51 (7): 1845–9. doi:10.1021/jf020426s. PMID 12643640.
^ Mohy-ud-dint, A., Khan,Z., Ahmad, M., Kashmiri, M.A. (2010). "Chemotaxonomic value of alkaloids in Solanum nigrum complex" (PDF). Pakistan Journal of Botany. 42 (1): 653–660.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ Cite error: The named reference Kui was invoked but never defined (see the help page).

[1] "Solanidine". pubchem.ncbi.nlm.nih.gov.

[Nik-2] Nikolic, NC; Stankovic, MZ (2003). "Solanidine hydrolytic extraction and separation from the potato (Solanum tuberosum L.) vines by using solid-liquid-liquid systems". Journal of Agricultural and Food Chemistry. 51 (7): 1845–9. doi:10.1021/jf020426s. PMID 12643640.

[Moh-3] Mohy-ud-dint, A., Khan,Z., Ahmad, M., Kashmiri, M.A. (2010). "Chemotaxonomic value of alkaloids in Solanum nigrum complex" (PDF). Pakistan Journal of Botany. 42 (1): 653–660.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[Kui-4] Cite error: The named reference Kui was invoked but never defined (see the help page).

Solanidine information

and 29 Related for: Solanidine information

Solanidine

Glycoalkaloid

Solanine

Physalis peruviana

Fish

Physalis pruinosa

Botulinum toxin

Clostridium botulinum

Poison dart frog

Ricin

Cyclopamine

Tetrodotoxin

Steroidal alkaloid

Toxin

Aflatoxin B1

Neurotoxin

Solanaceae

Ciguatera fish poisoning

Alkaloid

Hemotoxin

Exotoxin

Ochratoxin

Mycotoxin

Cardiotoxicity

Liliaceae

Amatoxin

Hedgehog signaling pathway

Tetanus toxin

Muscimol