Piceamycin

Details

Top
Internal ID ef15e7f0-a8d8-4466-827a-5b06c96292de
Taxonomy Organic acids and derivatives > Vinylogous acids
IUPAC Name (2Z,4Z,6Z,14Z,16Z,18Z,20Z)-24-hydroxy-1,11-dimethyl-9-azabicyclo[21.3.0]hexacosa-2,4,6,12,14,16,18,20,23-nonaene-8,22,25-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H29NO4/c1-21-15-11-7-5-3-4-6-8-12-16-22(29)25-26(32)23(30)19-27(25,2)18-14-10-9-13-17-24(31)28-20-21/h3-18,21,32H,19-20H2,1-2H3,(H,28,31)/b4-3-,7-5-,8-6-,10-9-,15-11?,16-12-,17-13-,18-14-
InChI Key OEUMTMCKMRMTAV-JUDLLUGNSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H29NO4
Molecular Weight 431.50 g/mol
Exact Mass 431.20965841 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP 6.20
Atomic LogP (AlogP) 4.56
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Piceamycin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9595 95.95%
Caco-2 - 0.6662 66.62%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6549 65.49%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.8488 84.88%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9807 98.07%
P-glycoprotein inhibitior + 0.7321 73.21%
P-glycoprotein substrate - 0.5819 58.19%
CYP3A4 substrate + 0.6051 60.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8946 89.46%
CYP3A4 inhibition - 0.9897 98.97%
CYP2C9 inhibition - 0.8704 87.04%
CYP2C19 inhibition - 0.8722 87.22%
CYP2D6 inhibition - 0.9183 91.83%
CYP1A2 inhibition - 0.8583 85.83%
CYP2C8 inhibition - 0.7533 75.33%
CYP inhibitory promiscuity - 0.9733 97.33%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9143 91.43%
Carcinogenicity (trinary) Non-required 0.5251 52.51%
Eye corrosion - 0.9822 98.22%
Eye irritation - 0.9682 96.82%
Skin irritation - 0.7341 73.41%
Skin corrosion - 0.9221 92.21%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8572 85.72%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.5176 51.76%
skin sensitisation - 0.8551 85.51%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5312 53.12%
Acute Oral Toxicity (c) III 0.4964 49.64%
Estrogen receptor binding + 0.7113 71.13%
Androgen receptor binding - 0.4896 48.96%
Thyroid receptor binding + 0.7242 72.42%
Glucocorticoid receptor binding + 0.5510 55.10%
Aromatase binding + 0.5755 57.55%
PPAR gamma + 0.6459 64.59%
Honey bee toxicity - 0.8473 84.73%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.7192 71.92%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.17% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.55% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.97% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.22% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.97% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.74% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.59% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.27% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.62% 99.23%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.12% 93.03%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.00% 100.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.57% 94.75%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.39% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.65% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.35% 96.77%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.17% 91.71%

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 139585848
LOTUS LTS0108550
wikiData Q77493168