TABLE 1.

LC-MS (negative mode) results of M1 and M2.

S. No	M-H	Mol. Form.	Identification	Ref.
1.	180.1	C6H12O	β-D-Glucopyranose	Najm et al. (2021)
2.	341.1	C15H18O9	Caffeic acid hexoside	Farag et al. (2014)
3.	179.1	C16H15O8	O-Caffeoyl shikimic acid	Otify et al. (2019)
4.	322.0	C12H19O10	Anhydro dihexose	Otify et al. (2019)
5.	425.3	C17H29O12	Acyl sucrose	Najm et al. (2021)
6.	463.1	C21H20O12	Isoquercetin	Farag et al. (2014)
7.	476.0	C12H21O12	Isorhamnetin-3-O-glucoside	Najm et al. (2021)
8.	476.0	C23H43NO7P	Sphingolipid conjugate I	Otify et al. (2019)
9.	311.3	C18H31O4	Dihydroxy linolenic acid	Farag et al. (2014)
10.	277.4	C18H29O2	Linolenic acid	Farag et al. (2014)
11.	255.6	C16H31O2	Palmitic acid	Farag et al. (2014)
12.	279.4	C18H31O2	Linoleic acid	Farag et al. (2014)
13.	283.2	C18H36O2	Stearic acid	Eid et al. (2013)
14.	195.0	C10H10O4	ferulic acid	Nematallah et al. (2018)
15.	326.3	C18H32O5	Trihydroxy octadecadienoic acid	Nematallah et al. (2018)
16.	311.4	C18H32O4	Dihydroxy octadecadienoic acid	Nematallah et al. (2018)
17.	594.9	C27H30O15	Luteolin-7-O-rutinoside	Nematallah et al. (2018)