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Plant Sources
Structural Classes
Microbial Sources
Flagship Varieties
Synthetic Compounds
All
CAS No.
NAME
Molecular Formula
Molecular Weight
Purity
Price
2D Structure
1502654-87-6
Ledipasvir D-tartrate
CC(C)C(C(=O)N1CC2(CC2)CC1C3=NC=C(N3)C4=CC5=C(C=C4)C6=C(C5(F)F)C=C(C=C6)C7=CC8=C(C=C7)N=C(N8)C9C1CCC(C1)N9C(=O)C(C(C)C)NC(=O)OC)NC(=O)OC.C(C(C(=O)O)O)(C(=O)O)O
C
53
H
60
F
2
N
8
O
12
1039.1
99%
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150281-45-1
2-Pyrrolidin-3-ylpyridine
C1CNCC1C2=CC=CC=N2
C
9
H
12
N
2
148.20
98%
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150349-36-3
N-(3-Aminopropyl)-N-methylcarbamic acid tert-butyl ester
CC(C)(C)OC(=O)N(C)CCCN
C
9
H
20
N
2
O
2
188.27
98%
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15049-86-2
(1-Amino-1-phosphonopropyl)phosphonic acid
CCC(N)(P(=O)(O)O)P(=O)(O)O
C
3
H
11
NO
6
P
2
219.07
98%
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1505453-59-7
BET bromodomain inhibitor
CC1=NOC2=C1C3=C(C=C(C=C3)C4=CN(N=C4)C)C(=NC2CC(=O)N)C5=CC=C(C=C5)Cl
C
24
H
20
ClN
5
O
2
445.9
99%
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150725-87-4
4-tert-butyl-N-[6-(2-hydroxyethoxy)-5-(3-methoxyphenoxy)pyrimidin-4-yl]benzenesulfonamide
CC(C)(C)C1=CC=C(C=C1)S(=O)(=O)NC2=C(C(=NC=N2)OCCO)OC3=CC=CC(=C3)OC
C
23
H
27
N
3
O
6
S
473.5
98%
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150727-72-3
5-(o-Methoxyphenoxy)-4,6-dichloro-2-(4-pyridyl)pyrimidine
COC1=CC=CC=C1OC2=C(N=C(N=C2Cl)C3=CC=NC=C3)Cl
C
16
H
11
Cl
2
N
3
O
2
348.2
98%
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150728-08-8
5-(o-Methoxyphenoxy)-4,6-dihydroxy-2-(4-pyridyl)pyrimidine
COC1=CC=CC=C1OC2=C(N=C(NC2=O)C3=CC=NC=C3)O
C
16
H
13
N
3
O
4
311.29
98%
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150784-74-0
N1-(4-(pyridin-3-yl)pyrimidin-2-yl)benzene-1,4-diamine
C1=CC(=CN=C1)C2=NC(=NC=C2)NC3=CC=C(C=C3)N
C
15
H
13
N
5
263.30
98%
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150810-69-8
6-Tamra-SE
CN(C)C1=CC2=C(C=C1)C(=C3C=CC(=[N+](C)C)C=C3O2)C4=C(C=CC(=C4)C(=O)ON5C(=O)CCC5=O)C(=O)[O-]
C
29
H
25
N
3
O
7
527.5
95%
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1502654-87-6
Ledipasvir D-tartrate
Ledipasvir (D-tartrate)
C
53
H
60
F
2
N
8
O
12
1039.1
150281-45-1
2-Pyrrolidin-3-ylpyridine
2-PYRROLIDIN-3-YLPYRIDINE
C
9
H
12
N
2
148.20
150349-36-3
N-(3-Aminopropyl)-N-methylcarbamic acid tert-butyl ester
Tert-butyl (3-aminopropyl)(methyl)carbamate
C
9
H
20
N
2
O
2
188.27
15049-86-2
(1-Amino-1-phosphonopropyl)phosphonic acid
AMINOPROPYLIDENE DIPHOSPHONIC ACID
C
3
H
11
NO
6
P
2
219.07
1505453-59-7
BET bromodomain inhibitor
BET bromodomain inhibitor
C
24
H
20
ClN
5
O
2
445.9
150725-87-4
4-tert-butyl-N-[6-(2-hydroxyethoxy)-5-(3-methoxyphenoxy)pyrimidin-4-yl]benzenesulfonamide
Ro 46-2005
C
23
H
27
N
3
O
6
S
473.5
150727-72-3
5-(o-Methoxyphenoxy)-4,6-dichloro-2-(4-pyridyl)pyrimidine
5-(o-Methoxyphenoxy)-4,6-dichloro-2-(4-pyridyl)pyrimidine
C
16
H
11
Cl
2
N
3
O
2
348.2
150728-08-8
5-(o-Methoxyphenoxy)-4,6-dihydroxy-2-(4-pyridyl)pyrimidine
5-(o-Methoxyphenoxy)-4,6-dihydroxy-2-(4-pyridyl)pyrimidine
C
16
H
13
N
3
O
4
311.29
150784-74-0
N1-(4-(pyridin-3-yl)pyrimidin-2-yl)benzene-1,4-diamine
1,4-Benzenediamine, N-[4-(3-pyridinyl)-2-pyrimidinyl]- (9CI)
C
15
H
13
N
5
263.30
150810-69-8
6-Tamra-SE
6-TAMRA-SE
C
29
H
25
N
3
O
7
527.5
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