Subincanadine C

Details

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Internal ID 2de318b8-b447-4d05-954f-4ef5a993bd65
Taxonomy Alkaloids and derivatives > Strychnos alkaloids
IUPAC Name (1R,13R,14R,15Z)-15-ethylidene-13-methyl-11-aza-1-azoniapentacyclo[12.2.2.01,13.04,12.05,10]octadeca-4(12),5,7,9-tetraene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H23N2/c1-3-13-12-21-10-8-15-14-6-4-5-7-17(14)20-18(15)19(21,2)16(13)9-11-21/h3-7,16,20H,8-12H2,1-2H3/q+1/b13-3+/t16-,19-,21+/m1/s1
InChI Key YKFXXRDKXYTPFL-DGHDDHFDSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C19H23N2+
Molecular Weight 279.40 g/mol
Exact Mass 279.186123742 g/mol
Topological Polar Surface Area (TPSA) 15.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.74
H-Bond Acceptor 0
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Subincanadine C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6914 69.14%
Caco-2 + 0.6889 68.89%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.5407 54.07%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.8656 86.56%
OATP1B3 inhibitior + 0.9409 94.09%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.6175 61.75%
P-glycoprotein inhibitior - 0.7192 71.92%
P-glycoprotein substrate - 0.7185 71.85%
CYP3A4 substrate + 0.6323 63.23%
CYP2C9 substrate - 0.8069 80.69%
CYP2D6 substrate - 0.6901 69.01%
CYP3A4 inhibition - 0.6828 68.28%
CYP2C9 inhibition - 0.8101 81.01%
CYP2C19 inhibition - 0.8335 83.35%
CYP2D6 inhibition + 0.7179 71.79%
CYP1A2 inhibition - 0.8009 80.09%
CYP2C8 inhibition - 0.5692 56.92%
CYP inhibitory promiscuity - 0.7335 73.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7410 74.10%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.9070 90.70%
Skin irritation - 0.6980 69.80%
Skin corrosion - 0.9002 90.02%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8739 87.39%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8266 82.66%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.7446 74.46%
Acute Oral Toxicity (c) III 0.5477 54.77%
Estrogen receptor binding - 0.4793 47.93%
Androgen receptor binding + 0.7125 71.25%
Thyroid receptor binding + 0.5492 54.92%
Glucocorticoid receptor binding - 0.5399 53.99%
Aromatase binding + 0.5395 53.95%
PPAR gamma + 0.5980 59.80%
Honey bee toxicity - 0.7855 78.55%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.8000 80.00%
Fish aquatic toxicity + 0.9693 96.93%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.94% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.67% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.11% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 95.00% 94.62%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 94.23% 94.23%
CHEMBL3310 Q96DB2 Histone deacetylase 11 91.76% 88.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.55% 97.09%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.40% 94.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 85.01% 90.71%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 83.79% 80.96%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 83.52% 85.49%
CHEMBL221 P23219 Cyclooxygenase-1 82.98% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.82% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.64% 93.99%
CHEMBL4302 P08183 P-glycoprotein 1 82.55% 92.98%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.47% 100.00%

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.
Aspidosperma subincanum

Cross-Links

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PubChem 101195650
LOTUS LTS0126355
wikiData Q105349662