Cimicine

Details

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Internal ID 73c50b85-544a-40b2-a12a-ff8d069d6fa4
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name (1R,4R,12R,16S)-7-hydroxy-5-propanoyl-17-oxa-5,15-diazahexacyclo[13.4.3.01,16.04,12.06,11.012,16]docosa-6(11),7,9-trien-18-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H26N2O4/c1-2-17(26)24-16-7-9-20-8-4-11-23-12-10-21(16,22(20,23)28-18(27)13-20)14-5-3-6-15(25)19(14)24/h3,5-6,16,25H,2,4,7-13H2,1H3/t16-,20-,21-,22+/m1/s1
InChI Key XCHPKMCSODEYHN-DHWLSRIRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H26N2O4
Molecular Weight 382.50 g/mol
Exact Mass 382.18925731 g/mol
Topological Polar Surface Area (TPSA) 70.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.68
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL510183
BDBM50292345

2D Structure

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2D Structure of Cimicine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9419 94.19%
Caco-2 + 0.5390 53.90%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7349 73.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8923 89.23%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.5931 59.31%
P-glycoprotein inhibitior - 0.6833 68.33%
P-glycoprotein substrate + 0.5503 55.03%
CYP3A4 substrate + 0.6390 63.90%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8122 81.22%
CYP3A4 inhibition + 0.5779 57.79%
CYP2C9 inhibition - 0.7475 74.75%
CYP2C19 inhibition + 0.5296 52.96%
CYP2D6 inhibition - 0.8995 89.95%
CYP1A2 inhibition - 0.6885 68.85%
CYP2C8 inhibition + 0.5148 51.48%
CYP inhibitory promiscuity - 0.7200 72.00%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6085 60.85%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.9703 97.03%
Skin irritation - 0.8476 84.76%
Skin corrosion - 0.9451 94.51%
Ames mutagenesis - 0.6954 69.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4143 41.43%
Micronuclear + 0.7900 79.00%
Hepatotoxicity - 0.5551 55.51%
skin sensitisation - 0.8695 86.95%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.7350 73.50%
Acute Oral Toxicity (c) III 0.6841 68.41%
Estrogen receptor binding + 0.6261 62.61%
Androgen receptor binding + 0.7753 77.53%
Thyroid receptor binding - 0.5460 54.60%
Glucocorticoid receptor binding - 0.4695 46.95%
Aromatase binding + 0.5524 55.24%
PPAR gamma + 0.5545 55.45%
Honey bee toxicity - 0.9282 92.82%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.8029 80.29%

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
CHEMBL2581 P07339 Cathepsin D 98.43% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.34% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.41% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.91% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.08% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.67% 89.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.23% 93.03%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.82% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.79% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.32% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.09% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.06% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.76% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.51% 90.71%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.65% 90.24%
CHEMBL5028 O14672 ADAM10 80.96% 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.
Haplophyton cimicidum

Cross-Links

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PubChem 21608708
LOTUS LTS0012035
wikiData Q105325100