Deacetylcephalosporin C

Details

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Internal ID 89484fca-870d-44b0-82b8-81a0dad73926
Taxonomy Organoheterocyclic compounds > Lactams > Beta lactams > Cephalosporins
IUPAC Name (6R,7R)-7-[[(5R)-5-amino-5-carboxypentanoyl]amino]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H19N3O7S/c15-7(13(21)22)2-1-3-8(19)16-9-11(20)17-10(14(23)24)6(4-18)5-25-12(9)17/h7,9,12,18H,1-5,15H2,(H,16,19)(H,21,22)(H,23,24)/t7-,9-,12-/m1/s1
InChI Key XWCFYHBHOFBVIV-JWKOBGCHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H19N3O7S
Molecular Weight 373.38 g/mol
Exact Mass 373.09437113 g/mol
Topological Polar Surface Area (TPSA) 196.00 Ų
XlogP -5.00
Atomic LogP (AlogP) -1.70
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

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1476-46-6
1476-46-6 (free acid)
(6R,7R)-7-{[(5R)-5-amino-5-carboxypentanoyl]amino}-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
(6R,7R)-7-((R)-5-amino-5-carboxypentanamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
(6R,7R)-7-[[(5R)-5-amino-5-carboxypentanoyl]amino]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
SCHEMBL11534966
CHEBI:18065
DTXSID50933157
XWCFYHBHOFBVIV-JWKOBGCHSA-N
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid, 7-[[(5R)-5-amino-5-carboxy-1-oxopentyl]amino]-3-(hydroxymethyl)-8-oxo-,(6R,7R)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Deacetylcephalosporin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5219 52.19%
Caco-2 - 0.9419 94.19%
Blood Brain Barrier - 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4611 46.11%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.9370 93.70%
OATP1B3 inhibitior + 0.9372 93.72%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8569 85.69%
P-glycoprotein inhibitior - 0.8734 87.34%
P-glycoprotein substrate - 0.6372 63.72%
CYP3A4 substrate + 0.5304 53.04%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8456 84.56%
CYP3A4 inhibition - 0.9236 92.36%
CYP2C9 inhibition - 0.8856 88.56%
CYP2C19 inhibition - 0.8620 86.20%
CYP2D6 inhibition - 0.9171 91.71%
CYP1A2 inhibition - 0.8199 81.99%
CYP2C8 inhibition - 0.9174 91.74%
CYP inhibitory promiscuity - 0.9557 95.57%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5764 57.64%
Eye corrosion - 0.9843 98.43%
Eye irritation - 0.9702 97.02%
Skin irritation - 0.7492 74.92%
Skin corrosion - 0.9162 91.62%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5549 55.49%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.7012 70.12%
skin sensitisation - 0.8465 84.65%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 1.0000 100.00%
Nephrotoxicity + 0.6439 64.39%
Acute Oral Toxicity (c) III 0.4878 48.78%
Estrogen receptor binding + 0.5387 53.87%
Androgen receptor binding - 0.8307 83.07%
Thyroid receptor binding - 0.6355 63.55%
Glucocorticoid receptor binding + 0.5609 56.09%
Aromatase binding - 0.6209 62.09%
PPAR gamma + 0.6228 62.28%
Honey bee toxicity - 0.9144 91.44%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.6846 68.46%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.66% 96.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 95.66% 93.00%
CHEMBL2581 P07339 Cathepsin D 93.63% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.59% 99.17%
CHEMBL220 P22303 Acetylcholinesterase 91.74% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.39% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.04% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 87.55% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.61% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.27% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.11% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.60% 99.23%
CHEMBL2514 O95665 Neurotensin receptor 2 82.12% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 81.93% 90.17%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 81.69% 98.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.65% 94.33%
CHEMBL2094135 Q96BI3 Gamma-secretase 81.39% 98.05%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.77% 95.89%
CHEMBL233 P35372 Mu opioid receptor 80.41% 97.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.34% 93.56%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.19% 92.29%

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 160577
LOTUS LTS0157496
wikiData Q27102799