Vemurafenib

Vemurafenib

SCHEMBL29355460

CCCS(=O)(=O)Nc1ccc(F)c(C(=O)c2c[nH]c3ncc(-c4ccc(Cl)cc4)cc23)c1F

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BRAF

The experimentally established mechanism targets of Vemurafenib. 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
BRAF known ✓ P15056 3/20 1.00
RIPK2 O43353 2/20 1.00
RAF1 P04049 2/20 1.00
KDR P35968 2/20 1.00
MAP2K2 P36507 2/20 1.00
TGFBR2 P37173 2/20 1.00
NEK2 P51955 2/20 1.00
MAP2K1 Q02750 2/20 1.00
TNK2 Q07912 2/20 1.00
MAP2K5 Q13163 2/20 1.00
PTK6 Q13882 2/20 1.00
NEK11 Q8NG66 2/20 1.00
MAP3K20 Q9NYL2 2/20 1.00
MAP4K5 Q9Y4K4 2/20 1.00
ABCB11 O95342 1/20 1.00
EGFR P00533 1/20 1.00
KRAS P01116 1/20 1.00
PGR P06401 1/20 1.00
RET P07949 1/20 1.00
CHRM2 P08172 1/20 1.00

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
SCHEMBL12891936 1.00 BRAF (1.00) BRAFRIPK2RAF1KDRMAP2K2
Vemurafenib SCHEMBL298931 1.00 BRAF (1.00) BRAFRIPK2RAF1KDRMAP2K2
Vemurafenib SCHEMBL29356185 1.00 BRAF (1.00) BRAFRIPK2RAF1KDRMAP2K2
Vemurafenib SCHEMBL17784481 0.95 BRAF (0.91) BRAFRIPK2RAF1KDRMAP2K2
SCHEMBL298368 0.95 BRAF (0.91) BRAFRIPK2RAF1KDRMAP2K2
SCHEMBL19575141 0.94 BRAF (0.89) BRAFRIPK2RAF1KDRMAP2K2
SCHEMBL298927 0.94 BRAF (0.89) BRAFRIPK2RAF1KDRMAP2K2
SCHEMBL7876722 0.94 BRAF (0.89) BRAFRIPK2RAF1KDRMAP2K2
SCHEMBL20408711 0.94 BRAF (0.88) BRAFRIPK2RAF1KDRMAP2K2
SCHEMBL293053 0.93 CYP2C19 (1.00) BRAFRIPK2RAF1KDRMAP2K2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12354130-B2 Combination therapies GENENTECH, INC. (US) 2025-07-08 US claimed
EP-4272735-B1 IMMEDIATE-RELEASE TABLETS CONTAINING A DRUG AND PROCESSES FOR FORMING THE TABLETS GENENTECH INC (US) 2025-06-18 EP claimed
CN-114177157-B Immediate release tablet containing a drug and method for forming a tablet 基因泰克公司 2024-08-02 CN claimed
US-20240115555-A1 METHODS OF TREATING CANCER USING B-RAF INHIBITORS AND IMMUNE CHECKPOINT INHIBITORS GENENTECH, INC. (US) 2024-04-11 US claimed
US-20240046303-A1 COMBINATION THERAPIES GENENTECH INC (US) 2024-02-08 US claimed
EP-4272735-A1 IMMEDIATE-RELEASE TABLETS CONTAINING A DRUG AND PROCESSES FOR FORMING THE TABLETS GENENTECH, INC. (US) 2023-11-08 EP claimed
EP-3881833-B1 IMMEDIATE-RELEASE TABLETS CONTAINING A DRUG AND PROCESSES FOR FORMING THE TABLETS GENENTECH INC (US) 2023-11-01 EP claimed
US-11783366-B2 Combination therapies GENENTECH, INC. (US) 2023-10-10 US claimed
US-20220172244-A1 COMBINATION THERAPIES GENENTECH INC (US) 2022-06-02 US claimed
CN-114177157-A Immediate release tablet containing drug and method for forming tablet 基因泰克公司 2022-03-15 CN claimed
EP-4735452-A2 HETEROBIFUNCTIONAL COMPOUNDS FOR THE DEGRADATION OF KRAS PROTEIN Merck Patent GmbH (DE) 2026-05-06 EP disclosed
EP-4735438-A2 HETEROBIFUNCTIONAL COMPOUNDS FOR THE DEGRADATION OF KRAS Merck Patent GmbH (DE) 2026-05-06 EP disclosed
WO-2026090174-A1 COMPOSITIONS FOR TARGETED DELIVERY OF THERAPEUTIC AGENTS AND METHODS FOR THE SYNTHESIS AND USE THEREOF BRYET US, INC. (US) 2026-04-30 WO disclosed
EP-4731199-A2 COMPOSITIONS COMPRISING ANTINEOPLASTONS AND METHODS OF TREATING COLORECTAL CANCER Burzynski, Stanislaw R. (US) 2026-04-29 EP disclosed
EP-4731793-A2 COMPOSITIONS COMPRISING ANTINEOPLASTONS AND METHODS OF TREATING PANCREATIC CANCER Burzynski, Stanislaw R. (US) 2026-04-29 EP disclosed
WO-2022035997-A1 IN VIVO ASSEMBLY OF ASGPR BINDING THERAPEUTICS AVILAR THERAPEUTICS, INC. (US) 2022-02-17 WO disclosed
WO-2022032132-A1 ADVANTAGEOUS THERAPIES FOR DISORDERS MEDIATED BY IKAROS OR AIOLOS C4 THERAPEUTICS, INC. (US) 2022-02-10 WO disclosed
WO-2022032026-A1 COMPOUNDS FOR TARGETED DEGRADATION OF RET C4 THERAPEUTICS, INC. (US) 2022-02-10 WO disclosed
EP-3941462-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS Achillion Pharmaceuticals, Inc. (US) 2022-01-26 EP disclosed
CN-113968803-A Novel method for synthesizing 2, 6-difluoro-3-propyl sulfonamide benzoic acid 苏州匠化生物科技有限公司 2022-01-25 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 (5 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-20240046303-A1 COMBINATION THERAPIES HGF, MET, FGFR3 BRAF 124/4885RIPK2 2518/4885RAF1 693/4885
US-11783366-B2 Combination therapies HGF, MET, FGFR3 BRAF 124/4885RIPK2 2518/4885RAF1 693/4885
US-12354130-B2 Combination therapies HGF, MET, FGFR3 BRAF 124/4885RIPK2 2518/4885RAF1 693/4885
US-20220172244-A1 COMBINATION THERAPIES HGF, MET, FGFR3 BRAF 124/4885RIPK2 2518/4885RAF1 693/4885
US-20240115555-A1 METHODS OF TREATING CANCER USING B-RAF INHIBITORS AND IMMUNE CHECKPOINT INHIBITORS BRAF, RAF1, NRAS BRAF 1/4885RIPK2 838/4885RAF1 2/4885

“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.