Cefazolin

Cefazolin

SCHEMBL2219475

Cc1nnc(SCC2=C(C(=O)O)N3C(=O)[C@@H](NC(=O)Cn4cnnn4)[C@H]3SC2)s1.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Cefazolin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.98
PTGS2 P35354 1/20 0.98
SLC22A6 Q4U2R8 1/20 0.98
SLC22A8 Q8TCC7 1/20 0.98
SLC22A11 Q9NSA0 1/20 0.98
MAPT P10636 9/20 0.84
TDP1 Q9NUW8 9/20 0.84
ABCC4 O15439 1/20 0.84
BLM P54132 1/20 0.84
CYP3A4 P08684 1/20 0.84
NFKB1 P19838 1/20 0.84
HSD17B10 Q99714 1/20 0.84
PTGS1 P23219 1/20 0.72
PDE4A P27815 1/20 0.72
KDR P35968 1/20 0.72
POLB P06746 9/20 0.70
ALDH1A1 P00352 4/20 0.68
MAPK1 P28482 1/20 0.68
KMT2A Q03164 3/20 0.68
MEN1 O00255 2/20 0.68

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Cefazolin SCHEMBL11031717 0.99 LMNA (1.00) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL4930576 0.99 LMNA (1.00) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL2841 0.99 LMNA (1.00) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL3424683 0.99 LMNA (1.00) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL2842 0.99 LMNA (1.00) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL16072809 0.99 LMNA (1.00) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL3894722 0.99 LMNA (1.00) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL40736 0.98 LMNA (0.98) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL6364010 0.98 LMNA (0.98) LMNAPTGS2SLC22A6SLC22A8SLC22A11
Cefazolin SCHEMBL29204288 0.98 LMNA (0.98) LMNAPTGS2SLC22A6SLC22A8SLC22A11

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 165 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170000644-A1 Biocompatible Biodegradable Intraocular Implant System INSIGHT INNOVATIONS, LLC (US) 2017-01-05 US claimed
US-20110230963-A1 BIOCOMPATIBLE BIODEGRADABLE INTRAOCULAR IMPLANT SYSTEM INSIGHT INNOVATIONS, LLC 2011-09-22 US claimed
EP-2364127-A2 BIOCOMPATIBLE BIODEGRADABLE INTRAOCULAR IMPLANT SYSTEM Insight Innovations, Llc (US) 2011-09-14 EP claimed
WO-2010059214-A2 BIOCOMPATIBLE BIODEGRADABLE INTRAOCULAR IMPLANT SYSTEM INSIGHT INNOVATIONS, LLC (US) 2010-05-27 WO claimed
US-20240226022-A1 TIME RELEASED BIODEGRADABLE OR BIOERODIBLE MICROSPHERES OR MICROPARTICLES SUSPENDED IN A SOLIDIFYING DEPOT-FORMING INJECTABLE DRUG FORMULATION ALLERGAN, INC. 2024-07-11 US disclosed
CN-115335050-B Compounds and compositions for treating skin disorders 卡玛瑞制药有限公司 2024-05-17 CN disclosed
US-11975049-B2 Therapeutic treatment for neurotrophic keratopathy Struck, Michael (US) 2024-05-07 US disclosed
CN-117580560-A Micronised lipid MCAL治疗公司 2024-02-20 CN disclosed
US-20230390212-A1 TIME RELEASED BIODEGRADABLE OR BIOERODIBLE MICROSPHERES OR MICROPARTICLES SUSPENDED IN A SOLIDIFYING DEPOT-FORMING INJECTABLE DRUG FORMULATION ALLERGAN, INC. 2023-12-07 US disclosed
US-20230165885-A1 TREATMENT OF EYE DISORDERS WITH URIDINE PHOSPHATE DERIVATIVES GLIAGUARD, INC. 2023-06-01 US disclosed
CN-114728093-B Wound dressing for hemostasis and wound healing and preparation method thereof 株式会社MEDITIP 2023-04-28 CN disclosed
US-11622951-B2 Alpha-aminoadipate for treatment of vision loss and restoring sight THE SCHEPENS EYE RESEARCH INSTITUTE, INC. (US) 2023-04-11 US disclosed
US-20050244467-A1 Implanting the extended release, biodegradable implant containing dexamethasone directly into the vitreous of the eye; side effect reduction; angiogenesis inhibition; macular degeneration ALLERGAN, INC. (US) 2005-11-03 US disclosed
US-20050244469-A1 Inserting an implant into an ocular site; an active agent and a polymer carrier; releasing the active agent from the implant ALLERGAN, INC. (US) 2005-11-03 US disclosed
US-20050244462-A1 Devices and methods for treating a mammalian eye ALLERGAN, INC. (US) 2005-11-03 US disclosed
US-20050191334-A1 Formulation for controlled release of drugs by combining hydrophilic and hydrophobic agents ALLERGAN, INC. (US) 2005-09-01 US disclosed
US-20050048098-A1 Formulation for controlled release of drugs by combining hydrophilic and hydrophobic agents ALLERGAN, INC. (US) 2005-03-03 US disclosed
US-20030095995-A1 Formulation for controlled release of drugs by combining hydrophilic and hydrophobic agents ALLERGAN, INC. 2003-05-22 US disclosed
US-6369116-B1 SUSTAINED RELEASE DEXAMETHASON OCULEX PHARMACEUTICALS, INC. 2002-04-09 US disclosed
US-5869079-A SEMIRIGID IMPLANT OF GLYCOLIC ACID-LACTIC ACID COPOLYMER WITH HYDROPHILIC HYDROXYPROPYLMETHYLCELLULOSE AS A RELEASE MODIFIER FOR THE HYDROPHOBIC DRUG DEXAMETHASONE; CONSTANT RELEASE RATE, NO ?DUMPING? OCULEX PHARMACEUTICALS, INC. (US) 1999-02-09 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11622951-B2 Alpha-aminoadipate for treatment of vision loss and restoring sight AADAT, PDE6A, PDE6C LMNA 1669/4885PTGS2 641/4885SLC22A6 3206/4885
US-20240226022-A1 TIME RELEASED BIODEGRADABLE OR BIOERODIBLE MICROSPHERES OR MICROPARTICLES SUSPENDED IN A SOLIDIFYING DEPOT-FORMING INJECTABLE DRUG FORMULATION VEGFA, NEFM, PDE6D LMNA 2535/4885PTGS2 1216/4885SLC22A6 1680/4885
US-20230390212-A1 TIME RELEASED BIODEGRADABLE OR BIOERODIBLE MICROSPHERES OR MICROPARTICLES SUSPENDED IN A SOLIDIFYING DEPOT-FORMING INJECTABLE DRUG FORMULATION VEGFA, NEFM, PDE6D LMNA 2535/4885PTGS2 1216/4885SLC22A6 1680/4885
US-20230165885-A1 TREATMENT OF EYE DISORDERS WITH URIDINE PHOSPHATE DERIVATIVES P2RY6, P2RY1, P2RY2 LMNA 3469/4885PTGS2 459/4885SLC22A6 846/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.