Croverin

Details

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Internal ID ccb02011-7a0d-41b6-9bb9-2bf64040ca79
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name methyl (1R,4S,6R,8R,9S)-6-(furan-3-yl)-16-methylidene-2-oxo-3,5-dioxatetracyclo[6.5.3.01,9.04,8]hexadec-12-ene-13-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O6/c1-12-6-8-20-14(17(22)24-2)4-3-5-16(20)21(12)10-15(13-7-9-25-11-13)26-19(21)27-18(20)23/h4,7,9,11,15-16,19H,1,3,5-6,8,10H2,2H3/t15-,16-,19+,20+,21+/m1/s1
InChI Key FFWVQGRKTCTNRG-QANQIFJLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O6
Molecular Weight 370.40 g/mol
Exact Mass 370.14163842 g/mol
Topological Polar Surface Area (TPSA) 75.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.46
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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AKOS040745162
HY-107225
CS-0027688

2D Structure

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2D Structure of Croverin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.5114 51.14%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8363 83.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7972 79.72%
OATP1B3 inhibitior + 0.8994 89.94%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.4754 47.54%
P-glycoprotein inhibitior - 0.4319 43.19%
P-glycoprotein substrate - 0.6799 67.99%
CYP3A4 substrate + 0.6895 68.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8562 85.62%
CYP3A4 inhibition + 0.7396 73.96%
CYP2C9 inhibition - 0.7151 71.51%
CYP2C19 inhibition - 0.6112 61.12%
CYP2D6 inhibition - 0.8757 87.57%
CYP1A2 inhibition - 0.7183 71.83%
CYP2C8 inhibition + 0.5825 58.25%
CYP inhibitory promiscuity - 0.5642 56.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4121 41.21%
Eye corrosion - 0.9618 96.18%
Eye irritation - 0.8109 81.09%
Skin irritation - 0.7900 79.00%
Skin corrosion - 0.9428 94.28%
Ames mutagenesis - 0.6070 60.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8526 85.26%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.7744 77.44%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6181 61.81%
Acute Oral Toxicity (c) III 0.3812 38.12%
Estrogen receptor binding + 0.7783 77.83%
Androgen receptor binding + 0.6653 66.53%
Thyroid receptor binding - 0.5334 53.34%
Glucocorticoid receptor binding + 0.7417 74.17%
Aromatase binding - 0.5245 52.45%
PPAR gamma - 0.5186 51.86%
Honey bee toxicity - 0.8467 84.67%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9793 97.93%

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 97.30% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.16% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.17% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.99% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.37% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.12% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.64% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.14% 95.89%
CHEMBL4040 P28482 MAP kinase ERK2 84.41% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.92% 86.33%
CHEMBL5028 O14672 ADAM10 83.22% 97.50%
CHEMBL340 P08684 Cytochrome P450 3A4 82.62% 91.19%
CHEMBL5255 O00206 Toll-like receptor 4 82.50% 92.50%
CHEMBL4072 P07858 Cathepsin B 82.46% 93.67%
CHEMBL221 P23219 Cyclooxygenase-1 82.22% 90.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.85% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.51% 92.62%

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.
Croton verreauxii

Cross-Links

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PubChem 131636953
LOTUS LTS0186686
wikiData Q104994723