Mammea C/BB, (-)-

Details

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Internal ID 6230aa64-045b-4da5-99e9-2d9eb3827cc6
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 5,7-dihydroxy-8-[(2S)-2-methylbutanoyl]-6-(3-methylbut-2-enyl)-4-pentylchromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H32O5/c1-6-8-9-10-16-13-18(25)29-24-19(16)22(27)17(12-11-14(3)4)23(28)20(24)21(26)15(5)7-2/h11,13,15,27-28H,6-10,12H2,1-5H3/t15-/m0/s1
InChI Key HHPBGHOULCFTMR-HNNXBMFYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C24H32O5
Molecular Weight 400.50 g/mol
Exact Mass 400.22497412 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 6.70
Atomic LogP (AlogP) 5.67
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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Mammea C/BB, (-)-
CHEMBL1689180
BDBM50483573
Q27138329

2D Structure

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2D Structure of Mammea C/BB, (-)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9517 95.17%
Caco-2 + 0.7010 70.10%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7377 73.77%
OATP2B1 inhibitior - 0.7137 71.37%
OATP1B1 inhibitior + 0.6903 69.03%
OATP1B3 inhibitior + 0.8656 86.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8406 84.06%
P-glycoprotein inhibitior - 0.5369 53.69%
P-glycoprotein substrate - 0.5447 54.47%
CYP3A4 substrate + 0.5619 56.19%
CYP2C9 substrate + 0.8742 87.42%
CYP2D6 substrate - 0.8673 86.73%
CYP3A4 inhibition + 0.5799 57.99%
CYP2C9 inhibition + 0.6130 61.30%
CYP2C19 inhibition + 0.6185 61.85%
CYP2D6 inhibition - 0.7505 75.05%
CYP1A2 inhibition + 0.7132 71.32%
CYP2C8 inhibition - 0.5571 55.71%
CYP inhibitory promiscuity + 0.6543 65.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7158 71.58%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.7882 78.82%
Skin irritation - 0.7249 72.49%
Skin corrosion - 0.9128 91.28%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8102 81.02%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7556 75.56%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7702 77.02%
Acute Oral Toxicity (c) III 0.4814 48.14%
Estrogen receptor binding + 0.6480 64.80%
Androgen receptor binding + 0.7851 78.51%
Thyroid receptor binding - 0.6303 63.03%
Glucocorticoid receptor binding + 0.8326 83.26%
Aromatase binding + 0.6096 60.96%
PPAR gamma + 0.9234 92.34%
Honey bee toxicity - 0.9127 91.27%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5445 54.45%
Fish aquatic toxicity + 1.0000 100.00%

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 99.40% 91.11%
CHEMBL2581 P07339 Cathepsin D 99.30% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 98.98% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 96.21% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.81% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 94.10% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 93.79% 97.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 93.21% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.95% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.64% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.48% 89.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.03% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.90% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.67% 96.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 83.30% 95.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.92% 100.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 82.71% 85.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.47% 97.25%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 81.92% 92.29%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.27% 99.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.37% 95.50%

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.
Mammea americana

Cross-Links

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PubChem 53324072
LOTUS LTS0159850
wikiData Q27138329