Cyclophostin

Details

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Internal ID af165da3-3dd0-43d3-92c1-16cd0fffea00
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R,8aR)-3-methoxy-5-methyl-3-oxo-8,8a-dihydro-1H-furo[3,4-e][1,3,2]dioxaphosphepin-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H11O6P/c1-5-7-6(3-12-8(7)9)4-13-15(10,11-2)14-5/h6H,3-4H2,1-2H3/t6-,15-/m1/s1
InChI Key OMPQJMDGDAAXPE-NPMWZIQKSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C8H11O6P
Molecular Weight 234.14 g/mol
Exact Mass 234.02932506 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP -0.20
Atomic LogP (AlogP) 1.23
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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144773-26-2
(3R,8aR)-3-methoxy-5-methyl-3-oxo-8,8a-dihydro-1H-furo[3,4-e][1,3,2]dioxaphosphepin-6-one
1H,6H-Furo(3,4-e)(1,3,2)dioxaphosphepin-6-one, 8,8a-dihydro-3-methoxy-5-methyl-, 3-oxide, (3R-cis)-
(3R,8aR)-3-methoxy-5-methyl-3-oxo-8,8a-dihydro-1H-furo(3,4-e)(1,3,2)dioxaphosphepin-6-one
RefChem:129905
CHEMBL603622
DTXSID30932406
CHEBI:225901
BDBM50308520
DA-72486
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclophostin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9632 96.32%
Caco-2 - 0.6056 60.56%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6109 61.09%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.9419 94.19%
OATP1B3 inhibitior + 0.9407 94.07%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8364 83.64%
P-glycoprotein inhibitior - 0.9318 93.18%
P-glycoprotein substrate - 0.8568 85.68%
CYP3A4 substrate + 0.5250 52.50%
CYP2C9 substrate - 0.7923 79.23%
CYP2D6 substrate - 0.8877 88.77%
CYP3A4 inhibition - 0.7843 78.43%
CYP2C9 inhibition - 0.7520 75.20%
CYP2C19 inhibition - 0.6828 68.28%
CYP2D6 inhibition - 0.8758 87.58%
CYP1A2 inhibition - 0.6685 66.85%
CYP2C8 inhibition - 0.8862 88.62%
CYP inhibitory promiscuity - 0.8415 84.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.4427 44.27%
Eye corrosion - 0.9224 92.24%
Eye irritation + 0.7891 78.91%
Skin irritation - 0.7471 74.71%
Skin corrosion - 0.9205 92.05%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6975 69.75%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.7955 79.55%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.7461 74.61%
Acute Oral Toxicity (c) II 0.3985 39.85%
Estrogen receptor binding - 0.6999 69.99%
Androgen receptor binding + 0.7851 78.51%
Thyroid receptor binding - 0.7743 77.43%
Glucocorticoid receptor binding - 0.7369 73.69%
Aromatase binding - 0.5892 58.92%
PPAR gamma - 0.5518 55.18%
Honey bee toxicity - 0.7797 77.97%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9016 90.16%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL220 P22303 Acetylcholinesterase 40 nM
35 nM
IC50
IC50
via Super-PRED
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 90.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.15% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.12% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.95% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.44% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.17% 97.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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Cross-Links

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PubChem 9578246
LOTUS LTS0141621
wikiData Q77511128