CURCUMIN
—OH
—OCH3
—OCH3
—OH
CUCM-1
—OCH3
—OH
—OH
—OCH3
CUCM-2
—OCH3
—OCH3
—OH
—OCH3
CUCM-3
—OCH3
—OCH3
—OCH3
—OCH3
CUCM-4
—OCH3
—ONH2
—ONH2
—OCH3
CUCM-5
—OH
—ONH2
—ONH2
—OH
CUCM-6
—ONH2
—OH
ONH(CH2CH3)
—ONH2
CUCM-7
—OH
—OH
—O(OH)
—OH
CUCM-8
—OH
—ONH2
—OCH3
—OH
CUCM-9
—OH
—OH
—OH
—OH
CUCM-10
—OCH2CH2CH3
—OCH2CH2CH3
—H2CH2CH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—OCH2CH2CH3
CUCM-11
—OCH2CH2C
Created by potrace 1.16, written by Peter Selinger 2001-2019
C
—OH
—OCH2CH2C
Created by potrace 1.16, written by Peter Selinger 2001-2019
C
—OH
CUCM-12
—OCH2CH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CHCH3
—OCH2CH2C
Created by potrace 1.16, written by Peter Selinger 2001-2019
C
—OCH2CH2C
Created by potrace 1.16, written by Peter Selinger 2001-2019
C
—OH
CUCM-13
—OH
—OCH2CH2C
Created by potrace 1.16, written by Peter Selinger 2001-2019
C
—OCH2CH2C
Created by potrace 1.16, written by Peter Selinger 2001-2019
C
—OH
CUCM-14
—ONH2
—OH
—OCH2CH2C
Created by potrace 1.16, written by Peter Selinger 2001-2019
C
—OH
CUCM-15
—OH
—OH
—OH
—ONH2
CUCM-16
—OCH2CH2C
Created by potrace 1.16, written by Peter Selinger 2001-2019
C
—OH
—OH
ONH(OH)
CUCM-17
—OCH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—ONH2
—OCH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—OH
CUCM-18
—OH
—OCH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—OH
—OCH2(OH)
CUCM-19
—OCH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—OCH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—OCH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—OCH2(OH)
CUCM-20
—OCH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—OCH
Created by potrace 1.16, written by Peter Selinger 2001-2019
CH
—OCH2NH2
—OH
CUCM-21
—OCH2NH
—OH
—OH
—OH
CUCM-22
—OCH2NH2
—OCH2NH2
—OCH2NH2
—OCH2NH2(OH)
CUCM-23
—OH
—OH
—OCH2NH2
—OCH2(OH)
CUCM-24
—OH
ONH(OH)
—ONH(OH)
—OCH2C6H5
CUCM-25
—OCH2(OH)
—OH
—OH
—OH
CUCM-26
—OCH2(OH)
ONH(OH)
—OH
—OH
CUCM-27
—OH
ONH(OH)
—ONH(OH)
—O(CH2(OH)
CUCM-28
—OH
—OH
—ONH(OH)
—OH
CUCM-29
—OCH2(OH)
—OCH2(OH)
—OCH2(OH)
—OCOCH3
CUCM-30
—OCH2NH3
—OCH2(OH)
—OH
—OCOCH3
CUCM-31
—OCH2NH3
—OH
—OCH2(OH)
—OH
CUCM-32
—OCH2NH2(OH)
—OH
—OCH2(OH)
—OCOCH3
CUCM-33
—OCH2NH2(OH)
—OCH2NH2(OH)
—OCH2(OH)
—O(OCH3)
CUCM-34
—OCH2(OH)
—OCH2(OH)
—OCH2NH2(OH)
—OH
CUCM-35
—OCH2C6H5
—OCH2C6H5
—OCH2C6H5
—OH
CUCM-36
—OH
—OH
—OCH2C6H5
—OH
CUCM-37
—OCH2C6H5
—OH
—OCH2C6H5
—OCH2(OH)
CUCM-38
—O(CH2(OH)
—O(CH2(OH)
—O(CH2(OH)
—OCH2(OH)
CUCM-39
—O(CH2(OH)
—OH
—O(CH2(OH)
—OH
CUCM-40
—OCOCH3
—OCOCH3
—OH
—OH
CUCM-41
—OH
—OCOCH3
—OCOCH3
—OCH2(OH)
CUCM-42
—OH
—OH
—OCOCH3
—OCH2NH3
CUCM-43
—OCOCH3
—OCOCH3
—OCOCH3
—OCH2NH3
CUCM-44
—O(OCH3)
—O(OCH3)
—OH
—OCH2NH2(OH)
CUCM-45
—OH
—OH
—O(OCH3)
—OCH2NH2(OH)
CUCM-46
—O(OCH3)
—OH
—O(OCH3)
—OCH2(OH)
CUCM-47
—O(OCH3)
—OH
—OH
—OCH2C6H5
CUCM-48
—ONH(OCH3)
—ONH(OCH3)
—OH
—OH
CUCM-49
—ONH(OCH3)
—OH
—ONH(OCH3)
—OH
CUCM-50
—ONH(OCH3)
—ONH(OCH3)
—ONH(OCH3)
—OCOCH3