Ojima:KOX00837p

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All Molecules KOX PR PBX COX

Ion Frequency

Prec.-Product

Neutral Loss

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Palmatine

IDs and Links
MassBank	Palmatine
CAS	3486-67-7
Keio ID	P071+

Top 10 Similar Molecules of Palmatine

[show] Ranking	About scoring
P071+ Score:64.87 A137+ Score:12.17 S042+ Score:6.63 T041+ Score:6.23 P070+ Score:5.94	The similarity score between two molecules is defined as the sum of Shannon entropy of ionic formulas shared by the molecules: $\textstyle - \sum_{p\in shared} \log(\mbox{frequency}(p))$ 代謝物間の類似度スコアは、それらのスペクトルで共有される（アノテートされた）イオン式のシャノン情報量の総和です。

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[show] Page list for each fragment

Pages Related to Peak C21H22NO4:   A137+  P071+   Pages Related to Peak C20H19NO4:   P071+   Pages Related to Peak C20H18NO4:   A137+  P070+  P071+   Pages Related to Peak C19H14NO4:   P071+   Pages Related to Peak C19H18NO3:   P071+  T041+   Pages Related to Peak C19H14NO3:   S042+   Pages Related to Peak C18H16NO3:   P071+   Pages Related to Peak C18H14NO3:   P071+   Pages Related to Peak C17H12NO3:   P071+   Pages Related to Peak C17H14NO2:   P071+   Pages Related to Peak C16H12NO2:   P071+

Annotations

Precursor	Product	Comments
C20H19NO4 (337)	C19H14NO4* (320)	ITinc

Precursor-Product Relationship

[show] About the PP Table (行列表示について)
The matrix is viewed columnwise. The topmost precursor ion in bold face produces the product ions beneath it. Each formula in matrix cells corresponds to the neutral loss. Blackout cells indicate products that cannot be derived, and orange cells indicate a structurally plausible link produced by cleaving a single chemical bond (in cases of ring-opening, two bonds).	行列は列方向に見ます。最上段太字の前駆イオン(precursor ion)が直下の生成イオン群(product ions)になると解釈します。 行列要素に書かれている組成式はニュートラルロスです。黒は前駆イオンから生成しえない関係、オレンジは分子構造における共有結合1本の切断（開環の場合は2本）で生じる関係を意味します。

[hide] KOX00837p	352 C21H22NO4	337 C20H19NO4	336 C20H18NO4	322 C19H16NO4	320 C19H14NO4	308 C19H18NO3	304 C19H14NO3	294 C18H16NO3	292 C18H14NO3	278 C17H12NO3	264 C17H14NO2	250 C16H12NO2
352 C21H22NO4
337 C20H19NO4	CH3
336 C20H18NO4	CH4	H
322 C19H16NO4	C2H6	CH3	CH2
320 C19H14NO4	C2H8	CH5	CH4	H2
308 C19H18NO3	C2H4O	CHO	CO
304 C19H14NO3	C2H8O	CH5O	CH4O	H2O	O	H4
294 C18H16NO3	C3H6O	C2H3O	C2H2O	CO		CH2
292 C18H14NO3	C3H8O	C2H5O	C2H4O	CH2O	CO	CH4	C	H2
278 C17H12NO3	C4H10O	C3H7O	C3H6O	C2H4O	C2H2O	C2H6	C2H2	CH4	CH2
264 C17H14NO2	C4H8O2	C3H5O2	C3H4O2	C2H2O2	C2O2	C2H4O	C2O	CH2O	CO
250 C16H12NO2	C5H10O2	C4H7O2	C4H6O2	C3H4O2	C3H2O2	C3H6O	C3H2O	C2H4O	C2H2O	CO	CH2

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