Cantleyine

Details

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Internal ID db4592ac-c591-440d-be92-f5e00c532619
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Pyridinecarboxylic acids and derivatives > Pyridinecarboxylic acids
IUPAC Name methyl (6S,7R)-6-hydroxy-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridine-4-carboxylate
SMILES (Canonical) CC1C(CC2=C(C=NC=C12)C(=O)OC)O
SMILES (Isomeric) C[C@H]1[C@H](CC2=C(C=NC=C12)C(=O)OC)O
InChI InChI=1S/C11H13NO3/c1-6-8-4-12-5-9(11(14)15-2)7(8)3-10(6)13/h4-6,10,13H,3H2,1-2H3/t6-,10+/m1/s1
InChI Key MJGLQDXKEOEIFB-LDWIPMOCSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H13NO3
Molecular Weight 207.23 g/mol
Exact Mass 207.08954328 g/mol
Topological Polar Surface Area (TPSA) 59.40 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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30333-81-4
methyl (6S,7R)-6-hydroxy-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridine-4-carboxylate
C09933
AC1L9CZQ
CHEBI:3365
CHEMBL4749645
DTXSID50331856
Q27106047

2D Structure

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2D Structure of Cantleyine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.6092 60.92%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7181 71.81%
OATP2B1 inhibitior - 0.8656 86.56%
OATP1B1 inhibitior + 0.9335 93.35%
OATP1B3 inhibitior + 0.9622 96.22%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8769 87.69%
P-glycoprotein inhibitior - 0.9750 97.50%
P-glycoprotein substrate - 0.8016 80.16%
CYP3A4 substrate + 0.5053 50.53%
CYP2C9 substrate - 0.8144 81.44%
CYP2D6 substrate - 0.8507 85.07%
CYP3A4 inhibition - 0.8047 80.47%
CYP2C9 inhibition - 0.9422 94.22%
CYP2C19 inhibition - 0.8962 89.62%
CYP2D6 inhibition - 0.8691 86.91%
CYP1A2 inhibition - 0.7081 70.81%
CYP2C8 inhibition - 0.7928 79.28%
CYP inhibitory promiscuity - 0.9487 94.87%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6555 65.55%
Eye corrosion - 0.9812 98.12%
Eye irritation - 0.8735 87.35%
Skin irritation - 0.6480 64.80%
Skin corrosion - 0.9624 96.24%
Ames mutagenesis - 0.6454 64.54%
Human Ether-a-go-go-Related Gene inhibition - 0.3744 37.44%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.6440 64.40%
skin sensitisation - 0.8582 85.82%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.4602 46.02%
Acute Oral Toxicity (c) III 0.5548 55.48%
Estrogen receptor binding - 0.9597 95.97%
Androgen receptor binding - 0.8080 80.80%
Thyroid receptor binding - 0.6623 66.23%
Glucocorticoid receptor binding - 0.8205 82.05%
Aromatase binding - 0.8614 86.14%
PPAR gamma - 0.7942 79.42%
Honey bee toxicity - 0.9100 91.00%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.8056 80.56%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.97% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.64% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.05% 91.11%
CHEMBL2535 P11166 Glucose transporter 86.18% 98.75%
CHEMBL2581 P07339 Cathepsin D 85.37% 98.95%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.81% 81.11%
CHEMBL1951 P21397 Monoamine oxidase A 82.41% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.11% 86.33%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.79% 91.24%
CHEMBL5028 O14672 ADAM10 80.46% 97.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Ailanthus altissima
Alstonia angustiloba
Alstonia rostrata
Castilleja miniata
Dipsacus asperoides
Picrasma quassioides
Scaevola racemigera
Strychnos mitis
Strychnos nux-vomica
Strychnos potatorum
Strychnos pungens
Strychnos trinervis
Strychnos variabilis

Cross-Links

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PubChem 442515
NPASS NPC32737
LOTUS LTS0056457
wikiData Q27106047