Turraflorin A

Details

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Internal ID 9c27a3c8-cde8-4ec8-9a83-94257773952c
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name methyl 2-[(1R,2S)-2-[(1R,5R,6R,7R,7aS)-6,7-diacetyloxy-1-(furan-3-yl)-7a-methyl-4-methylidene-2,5,6,7-tetrahydro-1H-inden-5-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate
SMILES (Canonical) CC(=O)OC1C(C(=C)C2=CCC(C2(C1OC(=O)C)C)C3=COC=C3)C4(C=CC(=O)C(C4CC(=O)OC)(C)C)C
SMILES (Isomeric) CC(=O)O[C@@H]1[C@@H](C(=C)C2=CC[C@@H]([C@@]2([C@H]1OC(=O)C)C)C3=COC=C3)[C@]4(C=CC(=O)C([C@@H]4CC(=O)OC)(C)C)C
InChI InChI=1S/C31H38O8/c1-17-21-9-10-22(20-12-14-37-16-20)31(21,7)28(39-19(3)33)27(38-18(2)32)26(17)30(6)13-11-24(34)29(4,5)23(30)15-25(35)36-8/h9,11-14,16,22-23,26-28H,1,10,15H2,2-8H3/t22-,23+,26-,27-,28+,30+,31-/m1/s1
InChI Key NCVYEYGQXPQYTC-YTJYDEETSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C31H38O8
Molecular Weight 538.60 g/mol
Exact Mass 538.25666817 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 5.10
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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CHEMBL2386306

2D Structure

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2D Structure of Turraflorin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 - 0.6915 69.15%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7260 72.60%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior - 0.4399 43.99%
OATP1B3 inhibitior - 0.3832 38.32%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9915 99.15%
P-glycoprotein inhibitior + 0.8887 88.87%
P-glycoprotein substrate + 0.5753 57.53%
CYP3A4 substrate + 0.6932 69.32%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8812 88.12%
CYP3A4 inhibition + 0.8716 87.16%
CYP2C9 inhibition - 0.6647 66.47%
CYP2C19 inhibition - 0.5935 59.35%
CYP2D6 inhibition - 0.9069 90.69%
CYP1A2 inhibition - 0.7353 73.53%
CYP2C8 inhibition + 0.6859 68.59%
CYP inhibitory promiscuity + 0.6957 69.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.4463 44.63%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.8813 88.13%
Skin irritation - 0.7267 72.67%
Skin corrosion - 0.9395 93.95%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6745 67.45%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6074 60.74%
skin sensitisation - 0.6820 68.20%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.7112 71.12%
Acute Oral Toxicity (c) III 0.7281 72.81%
Estrogen receptor binding + 0.8111 81.11%
Androgen receptor binding + 0.7065 70.65%
Thyroid receptor binding + 0.6951 69.51%
Glucocorticoid receptor binding + 0.8475 84.75%
Aromatase binding + 0.5975 59.75%
PPAR gamma + 0.8014 80.14%
Honey bee toxicity - 0.8003 80.03%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9956 99.56%

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 98.61% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.68% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.75% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.20% 85.14%
CHEMBL2581 P07339 Cathepsin D 92.36% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.74% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.54% 94.80%
CHEMBL4208 P20618 Proteasome component C5 86.11% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.00% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.20% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.58% 94.33%
CHEMBL340 P08684 Cytochrome P450 3A4 83.36% 91.19%
CHEMBL5028 O14672 ADAM10 83.33% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.02% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 82.37% 97.79%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.12% 92.62%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.45% 91.24%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 80.00% 80.00%

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.
Turraea heterophylla
Turraea pubescens

Cross-Links

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PubChem 12150033
LOTUS LTS0024094
wikiData Q105177399