Cochinchistemonine

Details

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Internal ID 30e9cd26-ad0a-4850-81d9-2572423696d2
Taxonomy Organoheterocyclic compounds > Azepanes
IUPAC Name (1S,2R,3S,4S,5R,6S,11R)-4,6-dihydroxy-11-[(1R)-1-hydroxypropyl]-4'-methoxy-3,3'-dimethylspiro[10-azatricyclo[8.4.0.02,6]tetradecane-5,5'-furan]-2'-one
SMILES (Canonical) CCC(C1CCCC2N1CCCC3(C2C(C(C34C(=C(C(=O)O4)C)OC)O)C)O)O
SMILES (Isomeric) CC[C@H]([C@H]1CCC[C@@H]2N1CCC[C@@]3([C@@H]2[C@@H]([C@@H]([C@]34C(=C(C(=O)O4)C)OC)O)C)O)O
InChI InChI=1S/C22H35NO6/c1-5-16(24)14-8-6-9-15-17-12(2)18(25)22(19(28-4)13(3)20(26)29-22)21(17,27)10-7-11-23(14)15/h12,14-18,24-25,27H,5-11H2,1-4H3/t12-,14+,15-,16+,17+,18-,21-,22-/m0/s1
InChI Key ZTDYHFFIUWALHQ-BNDYPTBJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H35NO6
Molecular Weight 409.50 g/mol
Exact Mass 409.24643784 g/mol
Topological Polar Surface Area (TPSA) 99.50 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.35
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cochinchistemonine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6752 67.52%
Caco-2 - 0.5646 56.46%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4747 47.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8494 84.94%
OATP1B3 inhibitior + 0.9459 94.59%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6032 60.32%
P-glycoprotein inhibitior - 0.6483 64.83%
P-glycoprotein substrate + 0.5764 57.64%
CYP3A4 substrate + 0.6759 67.59%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7679 76.79%
CYP3A4 inhibition - 0.9863 98.63%
CYP2C9 inhibition - 0.8690 86.90%
CYP2C19 inhibition - 0.9106 91.06%
CYP2D6 inhibition - 0.9060 90.60%
CYP1A2 inhibition - 0.8918 89.18%
CYP2C8 inhibition - 0.8231 82.31%
CYP inhibitory promiscuity - 0.8898 88.98%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4270 42.70%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.9564 95.64%
Skin irritation - 0.7431 74.31%
Skin corrosion - 0.9265 92.65%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5843 58.43%
Micronuclear + 0.6400 64.00%
Hepatotoxicity - 0.5632 56.32%
skin sensitisation - 0.8416 84.16%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.6082 60.82%
Acute Oral Toxicity (c) III 0.4871 48.71%
Estrogen receptor binding + 0.7136 71.36%
Androgen receptor binding + 0.7444 74.44%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7177 71.77%
Aromatase binding + 0.6630 66.30%
PPAR gamma - 0.5232 52.32%
Honey bee toxicity - 0.8506 85.06%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.5514 55.14%

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 98.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.36% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.83% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.53% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.17% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.30% 91.11%
CHEMBL5203 P33316 dUTP pyrophosphatase 89.83% 99.18%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.80% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.09% 97.09%
CHEMBL204 P00734 Thrombin 89.01% 96.01%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.56% 97.14%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 86.43% 82.38%
CHEMBL1871 P10275 Androgen Receptor 85.82% 96.43%
CHEMBL4588 P22894 Matrix metalloproteinase 8 85.45% 94.66%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.80% 99.23%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.43% 96.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.15% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.80% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.05% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.56% 94.75%

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.
Stemona japonica

Cross-Links

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PubChem 102157085
NPASS NPC53198