Secundifloran

Details

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Internal ID 5a260e13-08ea-4fc4-91a6-249ad059a962
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids > 3-hydroxy,4-methoxyisoflavonoids
IUPAC Name 3-[2,3-dihydroxy-4-methoxy-5-(2-methylbut-3-en-2-yl)phenyl]-3,7-dihydroxy-2H-chromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O7/c1-5-20(2,3)14-9-13(16(23)17(24)18(14)27-4)21(26)10-28-15-8-11(22)6-7-12(15)19(21)25/h5-9,22-24,26H,1,10H2,2-4H3
InChI Key AMFGHCXXVTVGNQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O7
Molecular Weight 386.40 g/mol
Exact Mass 386.13655304 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.74
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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LMPK12050507

2D Structure

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2D Structure of Secundifloran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9077 90.77%
Caco-2 - 0.5628 56.28%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6572 65.72%
OATP2B1 inhibitior - 0.7118 71.18%
OATP1B1 inhibitior + 0.8630 86.30%
OATP1B3 inhibitior + 0.9639 96.39%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6305 63.05%
P-glycoprotein inhibitior - 0.6183 61.83%
P-glycoprotein substrate - 0.5962 59.62%
CYP3A4 substrate + 0.6468 64.68%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.7939 79.39%
CYP3A4 inhibition + 0.7245 72.45%
CYP2C9 inhibition - 0.7610 76.10%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.6943 69.43%
CYP1A2 inhibition + 0.6130 61.30%
CYP2C8 inhibition + 0.6406 64.06%
CYP inhibitory promiscuity - 0.6702 67.02%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6288 62.88%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.4928 49.28%
Skin irritation - 0.7917 79.17%
Skin corrosion - 0.9242 92.42%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7647 76.47%
Micronuclear + 0.6259 62.59%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.8136 81.36%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6684 66.84%
Acute Oral Toxicity (c) III 0.5619 56.19%
Estrogen receptor binding + 0.8261 82.61%
Androgen receptor binding + 0.7535 75.35%
Thyroid receptor binding + 0.7432 74.32%
Glucocorticoid receptor binding + 0.6696 66.96%
Aromatase binding + 0.5865 58.65%
PPAR gamma + 0.6438 64.38%
Honey bee toxicity - 0.7874 78.74%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9494 94.94%

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 99.52% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.55% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.67% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.31% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.36% 91.07%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.51% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.12% 83.82%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 87.86% 83.57%
CHEMBL1951 P21397 Monoamine oxidase A 87.84% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.43% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.69% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.63% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.35% 97.09%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 83.83% 90.93%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.72% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.10% 100.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.01% 97.28%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.07% 92.88%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.65% 97.14%
CHEMBL3572 P11597 Cholesteryl ester transfer protein 80.45% 92.67%

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.
Dermatophyllum secundiflorum

Cross-Links

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PubChem 10091530
LOTUS LTS0275019
wikiData Q104914595