Carbapenem

Details

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Internal ID 9f965e7b-096d-4fbe-a292-c49df1faec7e
Taxonomy Organoheterocyclic compounds > Lactams > Beta lactams > Carbapenems
IUPAC Name (5R)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H7NO3/c9-6-3-4-1-2-5(7(10)11)8(4)6/h2,4H,1,3H2,(H,10,11)/t4-/m1/s1
InChI Key BSIMZHVOQZIAOY-SCSAIBSYSA-N
Popularity 34 references in papers

Physical and Chemical Properties

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Molecular Formula C7H7NO3
Molecular Weight 153.14 g/mol
Exact Mass 153.042593085 g/mol
Topological Polar Surface Area (TPSA) 57.60 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.04
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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(5R)-Carbapenem-3-carboxylic acid
Antibiotic TAN
78854-41-8
(5R)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
1-Carbapen-2-em-3-carboxylic acid
(5R)-carbapenem
UNII-GL970841YS
1-carbapenem-3-carboxylic acid
Antibiotic tan 458
SQ 27860
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Carbapenem

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9460 94.60%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.5800 58.00%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.9584 95.84%
OATP1B3 inhibitior + 0.9393 93.93%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9576 95.76%
P-glycoprotein inhibitior - 0.9916 99.16%
P-glycoprotein substrate - 0.9641 96.41%
CYP3A4 substrate - 0.6661 66.61%
CYP2C9 substrate - 0.8070 80.70%
CYP2D6 substrate - 0.8804 88.04%
CYP3A4 inhibition - 0.9472 94.72%
CYP2C9 inhibition - 0.8390 83.90%
CYP2C19 inhibition - 0.8137 81.37%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition - 0.8364 83.64%
CYP2C8 inhibition - 0.9788 97.88%
CYP inhibitory promiscuity - 0.9880 98.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5260 52.60%
Eye corrosion - 0.9444 94.44%
Eye irritation + 0.8236 82.36%
Skin irritation - 0.7150 71.50%
Skin corrosion - 0.9088 90.88%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9100 91.00%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.7220 72.20%
skin sensitisation - 0.8742 87.42%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.7691 76.91%
Acute Oral Toxicity (c) III 0.5392 53.92%
Estrogen receptor binding - 0.9465 94.65%
Androgen receptor binding + 0.5261 52.61%
Thyroid receptor binding - 0.8391 83.91%
Glucocorticoid receptor binding - 0.8404 84.04%
Aromatase binding - 0.8518 85.18%
PPAR gamma - 0.6026 60.26%
Honey bee toxicity - 0.9474 94.74%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.5702 57.02%

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 90.63% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.10% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.73% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 84.68% 93.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.81% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.71% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.02% 86.33%

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.
Tabernaemontana divaricata

Cross-Links

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PubChem 441133
LOTUS LTS0272319
wikiData Q105232314