Brefeldin A (BFA)

Details

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Internal ID 7c5efa5f-9e12-49d6-9968-875de6911438
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name (1R,2R,3E,7S,11E,15S)-2,15-dihydroxy-7-methyl-6-oxabicyclo[11.3.0]hexadeca-3,11-dien-5-one
SMILES (Canonical) CC1CCCC=CC2CC(CC2C(C=CC(=O)O1)O)O
SMILES (Isomeric) C[C@H]1CCC/C=C/C2C[C@@H](C[C@H]2[C@@H](/C=C/C(=O)O1)O)O
InChI InChI=1S/C16H24O4/c1-11-5-3-2-4-6-12-9-13(17)10-14(12)15(18)7-8-16(19)20-11/h4,6-8,11-15,17-18H,2-3,5,9-10H2,1H3/b6-4+,8-7+/t11-,12?,13-,14+,15+/m0/s1
InChI Key KQNZDYYTLMIZCT-KFKPYADVSA-N
Popularity 2,589 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O4
Molecular Weight 280.36 g/mol
Exact Mass 280.16745924 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.96
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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Cyanein
Cyanaein
Decumbin
C16H24O4
NSC 56310
1,6,7,8,9,11a?,12,13,14,14?a-Decahydro-1?,13?-dihydroxy-6?-methyl-4H-cyclopent(f)oxacyclotridecin-4-one
20350-15-6
Brefeldin A (BFA)
UPCMLD-DP095
BSPBio_001480
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Brefeldin A (BFA)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9836 98.36%
Caco-2 - 0.6029 60.29%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5520 55.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8865 88.65%
OATP1B3 inhibitior + 0.9408 94.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8321 83.21%
BSEP inhibitior - 0.6581 65.81%
P-glycoprotein inhibitior - 0.9516 95.16%
P-glycoprotein substrate - 0.8292 82.92%
CYP3A4 substrate + 0.5643 56.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8916 89.16%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.9547 95.47%
CYP2C19 inhibition - 0.9054 90.54%
CYP2D6 inhibition - 0.9599 95.99%
CYP1A2 inhibition + 0.7107 71.07%
CYP2C8 inhibition - 0.9217 92.17%
CYP inhibitory promiscuity - 0.9773 97.73%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6452 64.52%
Eye corrosion - 0.9606 96.06%
Eye irritation - 0.9876 98.76%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9138 91.38%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6823 68.23%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5231 52.31%
skin sensitisation - 0.7868 78.68%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7154 71.54%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.5563 55.63%
Acute Oral Toxicity (c) III 0.5553 55.53%
Estrogen receptor binding - 0.5782 57.82%
Androgen receptor binding - 0.6461 64.61%
Thyroid receptor binding - 0.6676 66.76%
Glucocorticoid receptor binding + 0.6373 63.73%
Aromatase binding - 0.7611 76.11%
PPAR gamma - 0.5432 54.32%
Honey bee toxicity - 0.8945 89.45%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9099 90.99%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 316.2 nM
Potency
via Super-PRED
CHEMBL5162 Q6W5P4 Neuropeptide S receptor 501.2 nM
Potency
via Super-PRED
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.1 nM
199.5 nM
141.3 nM
Potency
Potency
Potency
via Super-PRED
via Super-PRED
via Super-PRED
CHEMBL1293235 P02545 Prelamin-A/C 223.9 nM
Potency
via Super-PRED
CHEMBL1293294 P51151 Ras-related protein Rab-9A 223.9 nM
100 nM
89.1 nM
Potency
Potency
Potency
via Super-PRED
via Super-PRED
via Super-PRED
CHEMBL1293232 Q16637 Survival motor neuron protein 501.2 nM
354.8 nM
354.8 nM
Potency
Potency
Potency
via Super-PRED
via CMAUP
via Super-PRED
CHEMBL1947 P10828 Thyroid hormone receptor beta-1 707.9 nM
Potency
via Super-PRED
CHEMBL1075138 Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 2238.7 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.25% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.92% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.33% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.39% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.12% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.68% 100.00%
CHEMBL2581 P07339 Cathepsin D 84.92% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.67% 86.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.48% 89.00%
CHEMBL4040 P28482 MAP kinase ERK2 83.28% 83.82%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.65% 91.07%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.26% 92.94%

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.
Angelica sinensis

Cross-Links

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PubChem 6436187
NPASS NPC226226
ChEMBL CHEMBL1572153