Cyclipostin A2

Details

Top
Internal ID 67b5bf94-6a94-4350-9f70-21ae4eb2908a
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R,8aR)-3-(12-hydroxy-14-methylpentadecoxy)-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/C23H41O7P/c1-18(2)15-21(24)13-11-9-7-5-4-6-8-10-12-14-28-31(26)29-17-20-16-27-23(25)22(20)19(3)30-31/h18,20-21,24H,4-17H2,1-3H3/t20-,21?,31-/m1/s1
InChI Key RUDCXUCXOXYXPX-XGXHJENBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C23H41O7P
Molecular Weight 460.50 g/mol
Exact Mass 460.25899064 g/mol
Topological Polar Surface Area (TPSA) 91.30 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.91
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Cyclipostin A2

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9450 94.50%
Caco-2 - 0.5995 59.95%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7365 73.65%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9326 93.26%
OATP1B3 inhibitior + 0.9318 93.18%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7300 73.00%
P-glycoprotein inhibitior + 0.5739 57.39%
P-glycoprotein substrate + 0.5430 54.30%
CYP3A4 substrate + 0.6427 64.27%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.8609 86.09%
CYP3A4 inhibition - 0.6284 62.84%
CYP2C9 inhibition - 0.7193 71.93%
CYP2C19 inhibition - 0.7365 73.65%
CYP2D6 inhibition - 0.8845 88.45%
CYP1A2 inhibition - 0.7337 73.37%
CYP2C8 inhibition - 0.7871 78.71%
CYP inhibitory promiscuity - 0.9365 93.65%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.4750 47.50%
Eye corrosion - 0.9628 96.28%
Eye irritation - 0.6915 69.15%
Skin irritation - 0.7542 75.42%
Skin corrosion - 0.9242 92.42%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4650 46.50%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.5534 55.34%
skin sensitisation - 0.8326 83.26%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5735 57.35%
Acute Oral Toxicity (c) III 0.4580 45.80%
Estrogen receptor binding + 0.7093 70.93%
Androgen receptor binding + 0.7670 76.70%
Thyroid receptor binding - 0.5609 56.09%
Glucocorticoid receptor binding - 0.4942 49.42%
Aromatase binding + 0.5300 53.00%
PPAR gamma + 0.5820 58.20%
Honey bee toxicity - 0.8389 83.89%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7076 70.76%
Fish aquatic toxicity + 0.9750 97.50%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 98.67% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.09% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 92.79% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.30% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 91.70% 96.47%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.29% 99.17%
CHEMBL5103 Q969S8 Histone deacetylase 10 89.70% 90.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.71% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.48% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.41% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.11% 97.09%
CHEMBL230 P35354 Cyclooxygenase-2 85.05% 89.63%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 83.87% 91.24%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.78% 99.23%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.13% 85.94%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.08% 93.03%
CHEMBL4588 P22894 Matrix metalloproteinase 8 80.34% 94.66%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 10885026
LOTUS LTS0160259
wikiData Q77495048