Cyclopenin

Details

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Internal ID a85c69ce-4500-4381-9f77-7f36c9e7c446
Taxonomy Organoheterocyclic compounds > Benzodiazepines > 1,4-benzodiazepines
IUPAC Name 4-methyl-3'-phenylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14N2O3/c1-19-15(20)12-9-5-6-10-13(12)18-16(21)17(19)14(22-17)11-7-3-2-4-8-11/h2-10,14H,1H3,(H,18,21)
InChI Key APLKWZASYUZSBL-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14N2O3
Molecular Weight 294.30 g/mol
Exact Mass 294.10044231 g/mol
Topological Polar Surface Area (TPSA) 61.90 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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(-)-Cyclopenine
(-)-Cyclopenin
Cyclopenine
20007-87-8
4-methyl-3'-phenylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione
(3S,3'R)-4-methyl-3'-phenylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione
19553-26-5
NSC114538
Spiro[3H-1,4-benzodiazepine-3,2'-oxirane]-2,5(1H,4H)-dione, 4-methyl-3'-phenyl-, cis-(-)-
APLKWZASYUZSBL-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cyclopenin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9594 95.94%
Caco-2 + 0.7677 76.77%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6428 64.28%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8871 88.71%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8818 88.18%
BSEP inhibitior - 0.6800 68.00%
P-glycoprotein inhibitior - 0.8004 80.04%
P-glycoprotein substrate - 0.8779 87.79%
CYP3A4 substrate + 0.5238 52.38%
CYP2C9 substrate - 0.5885 58.85%
CYP2D6 substrate - 0.8738 87.38%
CYP3A4 inhibition + 0.6240 62.40%
CYP2C9 inhibition + 0.5560 55.60%
CYP2C19 inhibition + 0.5460 54.60%
CYP2D6 inhibition - 0.9087 90.87%
CYP1A2 inhibition - 0.5488 54.88%
CYP2C8 inhibition - 0.8222 82.22%
CYP inhibitory promiscuity - 0.6623 66.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5895 58.95%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.9900 99.00%
Skin irritation - 0.7907 79.07%
Skin corrosion - 0.9444 94.44%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4094 40.94%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.6580 65.80%
skin sensitisation - 0.8987 89.87%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.7019 70.19%
Acute Oral Toxicity (c) III 0.6793 67.93%
Estrogen receptor binding + 0.7775 77.75%
Androgen receptor binding + 0.6077 60.77%
Thyroid receptor binding - 0.5579 55.79%
Glucocorticoid receptor binding - 0.7226 72.26%
Aromatase binding + 0.7703 77.03%
PPAR gamma + 0.5737 57.37%
Honey bee toxicity - 0.9129 91.29%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.7405 74.05%

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
CHEMBL2581 P07339 Cathepsin D 97.70% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 96.28% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.99% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.03% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.72% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.04% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.32% 86.33%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.85% 93.40%
CHEMBL221 P23219 Cyclooxygenase-1 88.66% 90.17%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.13% 85.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.59% 91.11%

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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There are no matching plants.

Cross-Links

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PubChem 271117
LOTUS LTS0146254
wikiData Q77564000