Chemical Structure Search

Search by chemical structure

Results 1 — 30 of approximately 34 results

Xanthotoxol

precursor
C11H6O4
Mono mass: 202.026608673
Xanthotoxin

precursor
C12H8O4
Mono mass: 216.042258738
isourolithin AR

metabolite
C13H8O4
Mono mass: 228.042258738
Sphondin

precursor
C12H8O4
Mono mass: 216.042258738
Bergaptol

precursor
C11H6O4
Mono mass: 202.026608673
Isopimpinellin

precursor
C13H10O5
Mono mass: 246.052823422
urolithin AR

metabolite
C13H8O4
Mono mass: 228.042258738
3,4 dihydroxy urolithin

metabolite
C13H8O4
Mono mass: 228.042258738
urolithin CR

metabolite
C13H8O5
Mono mass: 244.037173358
3,4,9 trihydroxy urolithin

metabolite
C13H8O5
Mono mass: 244.037173358
4,10 dihydroxy urolithin

metabolite
C13H8O4
Mono mass: 228.042258738
Psoralen

precursor
C11H6O3
Mono mass: 186.031694053
Bergapten

precursor
C12H8O4
Mono mass: 216.042258738
4,9,10 trihydroxy urolithin

metabolite
C13H8O5
Mono mass: 244.037173358
Urolithin G

metabolite
C13H8O5
Mono mass: 244.037173358
urolithin M7R

metabolite
C13H8O5
Mono mass: 244.037173358
Isobergapten

precursor
C12H8O4
Mono mass: 216.042258738
Angelicin

precursor
C11H6O3
Mono mass: 186.031694053
Coumestrol

precursor
C15H8O5
Mono mass: 268.037173358
Urolithin D
131086-98-1
metabolite
C13H8O6
Mono mass: 260.032087978
Urolithin M6R

metabolite
C13H8O6
Mono mass: 260.032087978
Pimpinellin

precursor
C13H10O5
Mono mass: 246.052823422
3,4,10 trihydroxy urolithin

metabolite
C13H8O5
Mono mass: 244.037173358
Urolithin F

metabolite
C13H8O6
Mono mass: 260.032087978
Isourolithin B

metabolite
C13H8O3
Mono mass: 212.047344118
urolithin E

metabolite
C13H8O6
Mono mass: 260.032087978
Urolithin M5

metabolite
C13H8O7
Mono mass: 276.027002598
Ellagic acid
476-66-4
precursor metabolite
C14H6O8
Mono mass: 302.006267153
urolithin BR

metabolite
C13H8O3
Mono mass: 212.047344118
Isourolithin A
174023-48-4
metabolite
C13H8O4
Mono mass: 228.042258738