Flavomycoin

Details

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Internal ID 9ca7e2f9-0d8d-4974-8e44-b5084991f43e
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (3E,5E,7E,9E,11E)-19,21,23,25,27,29,31,33,35-nonahydroxy-12,16-dimethyl-15-propan-2-yl-14,37-dioxabicyclo[31.3.1]heptatriaconta-3,5,7,9,11-pentaen-13-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H66O12/c1-26(2)38-27(3)15-16-29(41)17-30(42)18-31(43)19-32(44)20-33(45)21-34(46)22-35(47)24-40(50)25-36(48)23-37(52-40)14-12-10-8-6-5-7-9-11-13-28(4)39(49)51-38/h5-13,26-27,29-38,41-48,50H,14-25H2,1-4H3/b7-5+,8-6+,11-9+,12-10+,28-13+
InChI Key HBOLDVSXCKYZJZ-BDWLDPCKSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C40H66O12
Molecular Weight 738.90 g/mol
Exact Mass 738.45542754 g/mol
Topological Polar Surface Area (TPSA) 218.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 12
H-Bond Donor 9
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Flavomycoin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8336 83.36%
Caco-2 - 0.8614 86.14%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7424 74.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8913 89.13%
OATP1B3 inhibitior + 0.8734 87.34%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9349 93.49%
P-glycoprotein inhibitior + 0.6556 65.56%
P-glycoprotein substrate - 0.5226 52.26%
CYP3A4 substrate + 0.6848 68.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8777 87.77%
CYP3A4 inhibition - 0.7126 71.26%
CYP2C9 inhibition - 0.8972 89.72%
CYP2C19 inhibition - 0.8662 86.62%
CYP2D6 inhibition - 0.9468 94.68%
CYP1A2 inhibition - 0.8546 85.46%
CYP2C8 inhibition + 0.4621 46.21%
CYP inhibitory promiscuity - 0.9734 97.34%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6680 66.80%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.9213 92.13%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.7070 70.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8428 84.28%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.6961 69.61%
skin sensitisation - 0.7307 73.07%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.5634 56.34%
Acute Oral Toxicity (c) III 0.4457 44.57%
Estrogen receptor binding + 0.7845 78.45%
Androgen receptor binding - 0.5175 51.75%
Thyroid receptor binding + 0.5194 51.94%
Glucocorticoid receptor binding + 0.6461 64.61%
Aromatase binding - 0.5124 51.24%
PPAR gamma + 0.6781 67.81%
Honey bee toxicity - 0.6565 65.65%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9483 94.83%

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 95.60% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.94% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.88% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.91% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.43% 99.23%
CHEMBL218 P21554 Cannabinoid CB1 receptor 88.67% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.89% 89.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.85% 97.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.97% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.39% 94.45%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 85.02% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.25% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.13% 97.25%
CHEMBL3572 P11597 Cholesteryl ester transfer protein 82.99% 92.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.12% 94.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.31% 91.07%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.19% 96.77%
CHEMBL3401 O75469 Pregnane X receptor 80.79% 94.73%

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.
There are no matching plants.

Cross-Links

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PubChem 10439986
LOTUS LTS0176161
wikiData Q105025400