(12xi,13xi)-14,19-Dihydro-12,13-dihydroxy-14-methylcrotalanan-11,15-dione

Details

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Internal ID aad432c2-290d-412b-9358-4eb2f4199997
Taxonomy Organoheterocyclic compounds > Pyrrolizines
IUPAC Name 4-ethyl-5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H27NO6/c1-5-16(2)14(20)25-12-7-9-19-8-6-11(13(12)19)10-24-15(21)17(3,22)18(16,4)23/h6,12-13,22-23H,5,7-10H2,1-4H3
InChI Key UWVWNXIKNRJZDC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H27NO6
Molecular Weight 353.40 g/mol
Exact Mass 353.18383758 g/mol
Topological Polar Surface Area (TPSA) 96.30 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (12xi,13xi)-14,19-Dihydro-12,13-dihydroxy-14-methylcrotalanan-11,15-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8594 85.94%
Caco-2 + 0.7153 71.53%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5812 58.12%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9350 93.50%
OATP1B3 inhibitior + 0.9351 93.51%
MATE1 inhibitior - 0.8809 88.09%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7269 72.69%
P-glycoprotein inhibitior - 0.9038 90.38%
P-glycoprotein substrate - 0.5317 53.17%
CYP3A4 substrate + 0.5648 56.48%
CYP2C9 substrate - 0.7953 79.53%
CYP2D6 substrate - 0.6812 68.12%
CYP3A4 inhibition - 0.7670 76.70%
CYP2C9 inhibition - 0.9039 90.39%
CYP2C19 inhibition - 0.9018 90.18%
CYP2D6 inhibition - 0.9115 91.15%
CYP1A2 inhibition - 0.8838 88.38%
CYP2C8 inhibition - 0.9183 91.83%
CYP inhibitory promiscuity - 0.9781 97.81%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Danger 0.8010 80.10%
Eye corrosion - 0.9837 98.37%
Eye irritation - 0.9760 97.60%
Skin irritation - 0.7097 70.97%
Skin corrosion - 0.9165 91.65%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4515 45.15%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 1.0000 100.00%
skin sensitisation - 0.8416 84.16%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.6903 69.03%
Acute Oral Toxicity (c) II 0.4633 46.33%
Estrogen receptor binding - 0.4798 47.98%
Androgen receptor binding + 0.6797 67.97%
Thyroid receptor binding + 0.5760 57.60%
Glucocorticoid receptor binding + 0.6708 67.08%
Aromatase binding + 0.5700 57.00%
PPAR gamma - 0.7700 77.00%
Honey bee toxicity - 0.8843 88.43%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8803 88.03%

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 96.31% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.58% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.28% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.05% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.57% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.26% 97.09%
CHEMBL4588 P22894 Matrix metalloproteinase 8 85.03% 94.66%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.44% 86.33%
CHEMBL4208 P20618 Proteasome component C5 83.56% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.28% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.79% 91.11%
CHEMBL2581 P07339 Cathepsin D 81.37% 98.95%
CHEMBL1871 P10275 Androgen Receptor 81.21% 96.43%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.64% 99.23%

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.
Crotalaria aegyptiaca

Cross-Links

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PubChem 73745631
LOTUS LTS0021869
wikiData Q104402874