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exisulind 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | PK/Tox | Related Drugs | BioActivity |
| Stem definition | Drug id | CAS RN |
|---|---|---|
| antineoplastics, sulindac metabolites | 3219 | 59973-80-7 |
Description:
| Molecule | Description |
|---|---|
|
Synonyms:
|
inhibits K-ras-dependent cyclooxygenase-2; sulfated analog of indomethacin;; CP248 is an antineoplastic agent that fosters microtubule depolymerization
|
Drug dosage:
None
ADMET properties:
None
Predicted pharmacokinetic/toxicological properties (PK-AZ):
| Property | Description | Value | Unit | Confidence | Similarity |
|---|---|---|---|---|---|
| azlogd74 | LogD at pH 7.4 | 0.509 | Moderate | 0.72 | |
| caco2-efflux | Caco-2 efflux ratio (BA/AB) | 8.395 | Moderate | 0.72 | |
| caco2-intrinsic-papp | Caco-2 intrinsic apparent permeability | 23.014 | 10^-6 cm/s | Moderate | 0.72 |
| dh-clint | Dog hepatocyte intrinsic clearance | 4.406 | uL/min/10^6 cells | Moderate | 0.72 |
| dppb | Dog plasma protein binding (% unbound) | 1.180 | % | Moderate | 0.72 |
| fcs-ppb | Fetal calf serum protein binding (% unbound) | 2.720 | % | Moderate | 0.72 |
| herg | hERG pIC50 | 4.514 | pIC50 | Moderate | 0.72 |
| hh-clint | Human hepatocyte intrinsic clearance | 4.732 | uL/min/10^6 cells | Moderate | 0.72 |
| hlm-clint | Human liver microsomal intrinsic clearance | 3.206 | uL/min/mg protein | Moderate | 0.72 |
| hppb | Human plasma protein binding (% unbound) | 1.100 | % | Moderate | 0.72 |
| kinase-safety-class | ACVR2B,AURKA,AXL,BRAF,BTK,CDK5,CDK9,DYRK1B,EIF2AK3,ERBB2,GRK2,IKBKB,ITK,MAPK10,MAPK7,PDK1,PDK2,PDK4,PIK3CA,PIK3CB,PIK3CD,PIK3CG,PRKDC,TGFBR1 | 24 | |||
| kinase-selectivity-class | ACVR2B,AXL,BRAF,CDK9,DYRK1B,GRK2,MAP2K6,MAPK7,PRKDC,STK33,TEK | 11 | |||
| mdck-mdr1-efflux | MDCK-MDR1 efflux ratio | 6.902 | Moderate | 0.72 | |
| mh-clint | Mouse hepatocyte intrinsic clearance | 7.709 | Moderate | 0.72 | |
| mppb | Mouse plasma protein binding (% unbound) | 1.390 | Moderate | 0.72 | |
| nih-mdck-mdr1-efflux | NIH MDCK-MDR1 efflux ratio | 3.027 | Moderate | 0.72 | |
| pfas-class | PFAS structural alert (1 = True, 0 = False) | 0 | |||
| pld-class | Phospholipidosis risk class (1 = positive, 0 = negative) | 0 | Moderate | 0.72 | |
| pppb | Pig plasma protein binding (% unbound) | 2.160 | % | Moderate | 0.72 |
| rh-clint | Rat hepatocyte intrinsic clearance | 6.281 | uL/min/10^6 cells | Moderate | 0.72 |
| rh-fuinc | Rat hepatocyte fraction unbound in incubation | 55.840 | % | Moderate | 0.72 |
| rppb | Rat plasma protein binding (% unbound) | 0.470 | % | Moderate | 0.72 |
| solubility-dd | Solubility at pH 7.4 in DMSO | 843.335 | uM | Moderate | 0.72 |
Approvals:
None
FDA Adverse Event Reporting System (Female)
None
FDA Adverse Event Reporting System (Male)
None
FDA Adverse Event Reporting System (Geriatric)
None
FDA Adverse Event Reporting System (Pediatric)
None
Pharmacologic Action:
| Source | Code | Description |
|---|---|---|
| MeSH PA | D000700 | Analgesics |
| MeSH PA | D000893 | Anti-Inflammatory Agents |
| MeSH PA | D000894 | Anti-Inflammatory Agents, Non-Steroidal |
| MeSH PA | D000970 | Antineoplastic Agents |
| MeSH PA | D004791 | Enzyme Inhibitors |
| MeSH PA | D016588 | Anticarcinogenic Agents |
| MeSH PA | D016861 | Cyclooxygenase Inhibitors |
| MeSH PA | D018373 | Peripheral Nervous System Agents |
| MeSH PA | D018501 | Antirheumatic Agents |
| MeSH PA | D018689 | Sensory System Agents |
| MeSH PA | D018712 | Analgesics, Non-Narcotic |
| MeSH PA | D020011 | Protective Agents |
| CHEBI has role | CHEBI:35610 | antineoplastic agent |
| CHEBI has role | CHEBI:50629 | cyclooxygenase 2 inhibitor |
| CHEBI has role | CHEBI:64964 | EC 1.13.11.34 (arachidonate 5-lipoxygenase) inhibitor |
| CHEBI has role | CHEBI:68495 | apoptosis inducer |
Drug Use | Suggest Off label Use Form| |View source of the data|
None
🐶 Veterinary Drug Use
None
🐶 Veterinary products
None
Acid dissociation constants calculated using MoKa v3.0.0
| Dissociation level | Dissociation constant | Type (acidic/basic) |
|---|---|---|
| pKa1 | 4.33 | acidic |
Orange Book patent data (new drug applications)
None
Orange Book exclusivity data (new drug applications)
None
Bioactivity Summary:
| Target | Class | Pharos | UniProt | Action | Type | Activity value (-log[M]) | Mechanism action | Bioact source | MoA source |
|---|---|---|---|---|---|---|---|---|---|
| Endothelin-1 receptor | GPCR | Ki | 5.22 | DRUG MATRIX | |||||
| Mitogen-activated protein kinase 1 | Kinase | IC50 | 4.86 | DRUG MATRIX | |||||
| Aldose reductase | Enzyme | IC50 | 6.57 | DRUG MATRIX |
External reference:
| ID | Source |
|---|---|
| C0075616 | UMLSCUI |
| CHEBI:64212 | CHEBI |
| SLO | PDB_CHEM_ID |
| CHEMBL488025 | ChEMBL_ID |
| DB06246 | DRUGBANK_ID |
| 5472495 | PUBCHEM_CID |
| C025463 | MESH_SUPPLEMENTAL_RECORD_UI |
| 7744 | INN_ID |
| K619IIG2R9 | UNII |
| K619IIG2R9 | INXIGHT DRUGS |
Pharmaceutical products:
None