SPERMIDINE

Structure

2D structure of SPERMIDINE
2D structure
Drag to rotate, scroll to zoom
3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 1102

Names and identifiers

Name

SPERMIDINE

IUPAC name

N1-(3-aminopropyl)butane-1,4-diamine

SMILES

NCCCCNCCCN

General information

Molecular formula

C7H19N3

Molecular weight

145.25 g/mol

Monoisotopic mass

145.1579 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
No

Chemical classification: NPClassifier (Kim et al., 2021)

Plants with the compound

Plant Plant part Amount Reference
Equisetum arvense L. - -
Bisset, N.G., ed. 1994. Herbal Drugs and Phytopharmaceuticals. CRC Press. Boca Raton, FL. 566 pp.
Eupatorium cannabinum L. subsp. cannabinum root -
Bottcher, F., Adolph, R.D., Hartmann, T. (1993). Homospermidine synthase, the first pathway-specific enzyme in pyrrolizidine alkaloid biosynthesis. Phytochemistry, 32(3), 679-689 doi:10.1016/s0031-9422(00)95154-9
Senecio vulgaris L. subsp. vulgaris cell culture -
Bottcher, F., Adolph, R.D., Hartmann, T. (1993). Homospermidine synthase, the first pathway-specific enzyme in pyrrolizidine alkaloid biosynthesis. Phytochemistry, 32(3), 679-689 doi:10.1016/s0031-9422(00)95154-9
Senecio vulgaris L. subsp. vulgaris cell culture -
Graser, G., Hartmann, T. (1997). Biosynthetic incorporation of the aminobutyl group of spermidine into pyrrolizidine alkaloids. Phytochemistry, 45(8), 1591-1595 doi:10.1016/s0031-9422(97)00193-3
Senecio vulgaris L. subsp. vulgaris root -
Bottcher, F., Adolph, R.D., Hartmann, T. (1993). Homospermidine synthase, the first pathway-specific enzyme in pyrrolizidine alkaloid biosynthesis. Phytochemistry, 32(3), 679-689 doi:10.1016/s0031-9422(00)95154-9