Cephalexin Anhydrous

Cephalexin Anhydrous

SCHEMBL13481267

CC1=C(C(=O)O)N2C(=O)C(NC(=O)[C@H](N)c3ccccc3)C2SC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Cephalexin Anhydrous. 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
▸ HSD17B10 Q99714 7/20 1.00
▸ MAPT P10636 7/20 1.00
▸ ALDH1A1 P00352 6/20 1.00
▸ KMT2A Q03164 5/20 1.00
▸ CYP3A4 P08684 4/20 1.00
▸ SLC15A2 Q16348 3/20 1.00
▸ HPGD P15428 3/20 1.00
▸ TDP1 Q9NUW8 3/20 1.00
▸ BLM P54132 2/20 1.00
▸ CYP2C19 P33261 2/20 1.00
▸ MAPK1 P28482 2/20 1.00
▸ ADRA1A P35348 1/20 1.00
▸ HTR2B P41595 1/20 1.00
▸ MEN1 O00255 4/20 0.85
▸ LMNA P02545 2/20 0.85
▸ ESR1 P03372 1/20 0.85
▸ SLC22A6 Q4U2R8 1/20 0.85
▸ SLC22A8 Q8TCC7 1/20 0.85
▸ KDM4E B2RXH2 6/20 0.77
▸ CYP2C9 P11712 2/20 0.77

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
Cephalexin Anhydrous SCHEMBL12961263 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL8467348 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL6663551 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL11569012 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL11985597 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL6663545 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL10925361 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL8481524 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL20703090 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4
Cephalexin Anhydrous SCHEMBL2961 1.00 HSD17B10 (1.00) HSD17B10MAPTALDH1A1KMT2ACYP3A4

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11951119-B2 Combination comprising zidovudine and an antimicrobial compound HELPERBY THERAPEUTICS LIMITED (GB) 2024-04-09 — — US disclosed
EP-3787622-B1 COMBINATION COMPRISING ZIDOVUDINE AND AN ANTIMICROBIAL COMPOUND HELPERBY THERAPEUTICS LTD (GB) 2023-12-13 — — EP disclosed
US-20220117991-A1 COMBINATION COMPRISING ZIDOVUDINE AND AN ANTIMICROBIAL COMPOUND HELPERBY THERAPEUTICS LIMITED (GB) 2022-04-21 — — US disclosed
EP-3787622-A1 COMBINATION COMPRISING ZIDOVUDINE AND AN ANTIMICROBIAL COMPOUND Helperby Therapeutics Limited (GB) 2021-03-10 — — EP disclosed
CN-112218633-A Combinations comprising zidovudine and antimicrobial compounds 赫尔普百治疗有限公司 2021-01-12 — — CN disclosed
US-7666398-B2 Polyanhydride linkers for production of drug polymers and drug polymer compositions produced thereby RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2010-02-23 — — US disclosed
US-7666398-B2 Polyanhydride linkers for production of drug polymers and drug polymer compositions produced thereby RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2010-02-23 — — US disclosed
CN-1095846-C Production process of cephem compound EISAI KAGAKU KK (JP) 2002-12-11 — — CN disclosed
CN-1184814-A Production process of cephem compound EISAI KAGAKU KK (JP) 1998-06-17 — — CN disclosed
CN-1017335-B PROCESS FOR PREPARING BETA-LACTAM ANTIBIOTICS BAYER AG (DE) 1992-07-08 — — CN disclosed
CN-1035511-A β-Nei Xiananleikangshengsu its preparation method and as medicine and the application in medicine BAYER AG (DE) 1989-09-13 — — CN disclosed
CN-86101382-A Prepare the method for β-Nei Xiananleikangshengsu and the application in medicine thereof — 1986-09-03 — — CN 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 (2 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-20220117991-A1 COMBINATION COMPRISING ZIDOVUDINE AND AN ANTIMICROBIAL COMPOUND TPMT, TYMS, SAMHD1 HSD17B10 1960/4885MAPT 3237/4885ALDH1A1 3697/4885
US-11951119-B2 Combination comprising zidovudine and an antimicrobial compound TPMT, TYMS, SAMHD1 HSD17B10 1960/4885MAPT 3237/4885ALDH1A1 3697/4885

“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.

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