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Home Chemical search Search Results CSSS00160476840

Structure Info

Chemspace ID
CSSS00160476840 (In-Stock Screening Compounds)
MFCD
MFCD34470637, MFCD09953814
IUPAC Name
(1S)-1-[(4-hydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol hydrobromide
Mol formula
C16H18BrNO3
Mol weight
352 Da
Catalog Number(s)
AA008W24, AE14696, AG008W4W, APS105990270, CSC160476840, G18074, H325810, HY-N2037C, LN01285594, T38132, Y3297226, ZXC369068

Properties

LogP
2.36
Heavy atoms count
21
Rotatable bond count
2
Number of rings
3
Carbon bond saturation, Fsp3
0.25
Polar surface area (Å)
73
Hydrogen bond acceptors count
4
Hydrogen bond donors count
4

SDS

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C16H18BrNO3
Zoom the structure
CSSS00160476840
 

Items Overall 2 items from 2 suppliers

SupplierLead timeShips fromPurityPackPrice, $Qty
MedChemExpress10 daysUnited States
To:
981 mg345
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Description: Names: (S)-Higenamine (hydrobromide); (S)-Norcoclaurine (hydrobromide); Product Description: (S)-Higenamine ((S)-Norcoclaurine) hydrobromide, a S-enantiomer of Higenamine, is the entry compound in benzylisoquinoline alkaloid biosynthesis. (S)-Higenamine hydrobromide is produced by the condensation of dopamine and 4-hydroxyphenylacetaldehyde (4-HPAA) by norcoclaurine synthase (NCS) .; Target: Endogenous Metabolite; CAS: 105990-27-0
MedChemExpress EU10 daysSweden
To:
981 mg363
Go to cartEnquire
Description: Names: (S)-Higenamine (hydrobromide); (S)-Norcoclaurine (hydrobromide); Product Description: (S)-Higenamine ((S)-Norcoclaurine) hydrobromide, a S-enantiomer of Higenamine, is the entry compound in benzylisoquinoline alkaloid biosynthesis. (S)-Higenamine hydrobromide is produced by the condensation of dopamine and 4-hydroxyphenylacetaldehyde (4-HPAA) by norcoclaurine synthase (NCS); Target: Endogenous Metabolite; CAS: 105990-27-0
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