BIAdb
A Database for Benzylisoquinoline Alkaloids
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Citation: If you are using this server please cite:-
Singla D, Sharma A, Kaur J, Panwar B, and Raghava GPS (2010): BIAdb: A curated database of benzylisoquinoline alkaloids.
BMC Pharmacology
10:4.
Total Records - 84
ID
Name
Molecular Formula
Source
Function
XlogP
4-(hydroxymethyl)colchicine
C
2
3
H
2
7
NO
7
N/A
Unknown
0.1
Aminomorphine
C
1
7
H
2
0
N
2
O
3
N/A
Unknown
0.1
Cephalotaxine
C
1
8
H
2
1
NO
4
Cephalotaxus harringtonia
Antiviral
0.2
CID628637
C
1
9
H
1
9
NO
6
N/A
Unknown
0.2
Genomorphine
C
1
7
H
1
9
NO
4
N/A
Unknown
0.2
Colchicenamide
C
2
1
H
2
4
N
2
O
5
N/A
DNA topoisomerase II antagonist
0.3
Oxycolchicine
C
2
2
H
2
3
NO
7
N/A
Unknown
0.3
Alpha-Erythroidine
C
1
6
H
1
9
NO
3
Erythrina americana
Neuromuscular blocking agent
0.4
Alpha-Erythroidine
C
1
6
H
1
9
NO
3
Erythrina brevifolia
Neuromuscular blocking agent
0.4
Alpha-Erythroidine
C
1
6
H
1
9
NO
3
Erythrina chiapasana
Neuromuscular blocking agent
0.4
Alpha-Erythroidine
C
1
6
H
1
9
NO
3
Erythrina coralloides
Neuromuscular blocking agent
0.4
Alpha-Erythroidine
C
1
6
H
1
9
NO
3
Erythrina globocalyx
Neuromuscular blocking agent
0.4
Alpha-Erythroidine
C
1
6
H
1
9
NO
3
Erythrina salviiflora
Neuromuscular blocking agent
0.4
Alpha-Erythroidine
C
1
6
H
1
9
NO
3
Erythrina standleyana
Neuromuscular blocking agent
0.4
Alpha-Erythroidine
C
1
6
H
1
9
NO
3
Erythrina tholloniana
Neuromuscular blocking agent
0.4
Berberine
C
2
0
H
2
8
NO
4
+
Hydrastis canadensis
Unknown
0.4
Colchicine,2-demethyl-
C
2
1
H
2
3
NO
6
N/A
Unknown
0.4
14-Hydroxymorphine
C
1
7
H
1
9
NO
4
N/A
Unknown
0.5
2-Demethylcolchicine
C
2
1
H
2
3
NO
6
N/A
Unknown
0.5
Acetaminophen
C
8
H
9
NO
2
Derivative of acetanilide
Analgesic
0.5
Acetaminophen
C
8
H
9
NO
2
Derivative of acetanilide
Antipyretic
0.5
Acetaminophen
C
8
H
9
NO
2
Derivative of acetanilide
Anti-inflammatory
0.5
Narcein
C
2
3
H
2
7
NO
8
Papaver rhopalothece
Antitussive
0.5
Narcein
C
2
3
H
2
7
NO
8
Papaver somniferum
Antitussive
0.5
Triacetoneamine-N-Oxyl
C
9
H
1
6
NO
2
N/A
Unknown
0.5
Colchicine analog
C
2
4
H
2
5
NO
8
N/A
Unknown
0.6
Genocodein
C
1
8
H
2
1
NO
4
N/A
Unknown
0.6
1-Demethylcolchicine
C
2
1
H
2
3
NO
6
N/A
Anti-inflammatory
0.7
3-desmethylcolchicine
C
2
1
H
2
3
NO
6
N/A
Unknown
0.7
Atheroline
C
1
9
H
1
5
NO
5
Atherosperma moschatum
Unknown
0.7
Atheroline
C
1
9
H
1
5
NO
5
Dehaasia triandra
Unknown
0.7
Atheroline
C
1
9
H
1
5
NO
5
Hernandia sonora
Unknown
0.7
Atheroline
C
1
9
H
1
5
NO
5
Nemuaron vieilardii
Unknown
0.7
Atheroline
C
1
9
H
1
5
NO
5
Sinofranchetia chinesis
Unknown
0.7
CID6330029
C
3
2
H
4
1
N
2
O
9
+
N/A
Unknown
0.7
Hydroxymethyl colchicine
C
2
3
H
2
7
NO
7
N/A
Unknown
0.7
1-Demethyl-1-acetylcolchicine
C
2
3
H
2
5
NO
7
N/A
Unknown
0.8
Asimilobine-2-O-glucoside
C
2
3
H
2
7
NO
7
Stephania pierrei
Cytotoxic
0.8
Asimilobine-2-O-glucoside
C
2
3
H
2
7
NO
7
Stephania pierrei
Antimalarial
0.8
CID632235
C
2
0
H
2
5
NO
5
N/A
Unknown
0.8
Colchicine,2-demethyl-2-acetyl-
C
2
3
H
2
5
NO
7
N/A
Unknown
0.8
Morphine
C
1
7
H
1
9
NO
3
Papaver setigerum
Antitussive
0.8
Morphine
C
1
7
H
1
9
NO
3
Papaver somniferum
Antitussive
0.8
Morphine
C
1
7
H
1
9
NO
3
Papaver setigerum
Analgesic
0.8
Morphine
C
1
7
H
1
9
NO
3
Papaver somniferum
Analgesic
0.8
NCGC00180702-01
C
2
1
H
3
1
NO
5
N/A
Unknown
0.8
N-Methyl-morphine
C
1
8
H
2
2
NO
3
+
N/A
Unknown
0.8
Oxymorphone
C
1
7
H
1
9
NO
4
N/A
Analgesic
0.8
Oxymorphone
C
1
7
H
1
9
NO
4
N/A
Anesthesia adjuvant
0.8
Oxymorphone
C
1
7
H
1
9
NO
4
N/A
Antitussive
0.8
Pholcodine
C
2
3
H
3
0
N
2
O
4
N/A
Analgesic
0.8
Pholcodine
C
2
3
H
3
0
N
2
O
4
N/A
Antitussive
0.8
Colchicine,oxo-
C
2
2
H
2
5
NO
7
N/A
Unknown
0.9
Melosmine
C
2
0
H
1
9
NO
4
N/A
Unknown
0.9
Morphine-7,8-oxide
C
1
7
H
1
9
NO
4
N/A
Analgesic
0.9
O(3)-monoacetylmorphine
C
1
9
H
2
1
NO
4
N/A
Unknown
0.9
Papaveroline sulfonic acid
C
1
6
H
1
3
NO
7
S
N/A
Phosphodiesterase inhibitor
0.9
Trimethylcolchicinic acid methyl ether
C
2
0
H
2
3
NO
5
N/A
Unknown
0.9
2-demethylthiocolchicine
C
2
1
H
2
3
NO
5
S
N/A
Unknown
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum autumnale
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum brachyphyllum
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum megaphylla
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum speciosum
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum turicum
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Gloriosa superba
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Merendera kurdica
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Merendera manissadjianii
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Merendera raddeana
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Merendera sobolifera
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Sandersonia aurantica
Antirheumatic
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum autumnale
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum brachyphyllum
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum megaphylla
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum speciosum
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Colchicum turicum
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Gloriosa superba
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Merendera kurdica
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Merendera manissadjianii
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Merendera raddeana
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Merendera sobolifera
Anti-inflammatory
1.0
Colchicine
C
2
2
H
2
5
NO
6
Sandersonia aurantica
Anti-inflammatory
1.0
Colchicine analog
C
2
1
H
2
6
N
2
O
4
N/A
Unknown
1.0
N-deacetyl-N-formylcolchicine
C
2
1
H
2
3
NO
6
N/A
Unknown
1.0
Salsolinol
C
1
0
H
1
3
NO
2
N/A
Antiplatelet
1.0