Compound Information
- Name
- SMILES
- CC(C)(C)NC(=O)C1CC2CCCCC2C[N+]1(CC(O)C(CC3=CC=CC=C3)NC(=O)C(CC(N)=O)NC(=O)C4=CC=C5C=CC=CC5=N4)[O-]
- InChIKey
- YSDXSSJUWGWZMQ-UHFFFAOYSA-N
- PubChem CID
- Mass
- 686.3791 Da
- ALogP
- 3.4755
- Molecular Formula
- C38H50N6O6
2D Structure
Biotransformations
Reaction Type:
Alkyl-OH-glucuronidation (BTMR0165)
Biosystem: Human
Biosystem: Human
Reaction Type:
N-Glucuronidation of amide (BTMR0172)
Biosystem: Human
Biosystem: Human
Reaction Type:
O-Glucuronidation of N-oxide (BTMR0184)
Biosystem: Human
Biosystem: Human
Reaction Type:
Sulfation of secondary alcohol (BTMR0502)
Biosystem: Human
Biosystem: Human
Reaction Type:
O-Hydroxylation of monosubstituted benzene (BTMR1034)
Biosystem: Human
Biosystem: Human
Reaction Type:
Oxidation of secondary alcohol to ketone (BTMR0079)
Biosystem: Human
Biosystem: Human
Reaction Type:
Hydroxylation of non-terminal aliphatic carbon adjacent to aromatic ring (BTMR1077)
Biosystem: Human
Biosystem: Human
Reaction Type:
Aromatic hydroxylation of fused benzene ring (BTMR1030)
Biosystem: Human
Biosystem: Human
Reaction Type:
Hydroxylation of alicyclic secondary carbon (BTMR1068)
Biosystem: Human
Biosystem: Human
Reaction Type:
Hydroxylation of benzene on carbon para to electron donating group (BTMR1047)
Biosystem: Human
Biosystem: Human
Reaction Type:
Hydroxylation of heteroalicyclic secondary carbon (BTMR1070)
Biosystem: Human
Biosystem: Human
Reaction Type:
Hydroxylation of heteroalicyclic secondary carbon (BTMR1071)
Biosystem: Human
Biosystem: Human
Reaction Type:
Aromatic hydroxylation of fused benzene ring (BTMR1031)
Biosystem: Human
Biosystem: Human
Reaction Type:
Aromatic hydroxylation of fused benzene ring (BTMR1032)
Biosystem: Human
Biosystem: Human
Reaction Type:
Hydroxylation of terminal methyl (BTMR1061)
Biosystem: Human
Biosystem: Human
Reaction Type:
alpha-Hydroxylation of carbonyl group (BTMR1054)
Biosystem: Human
Biosystem: Human
Reaction Type:
Hydroxylation of alicyclic tertiary carbon (BTMR1243)
Biosystem: Human
Biosystem: Human
