Vemurafenib

Vemurafenib

SCHEMBL298931

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 SCHEMBL29356185 1.00 BRAF (1.00) BRAFRIPK2RAF1KDRMAP2K2
Vemurafenib SCHEMBL29355460 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

Appears in 16922 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260146289-A1 ASSESSING AND TREATING MELANOMA MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2026-05-28 US claimed
CN-122075716-A Medicine for treating tumor by combining recombinant oncolytic virus and small-molecule anticancer medicine 2026-05-26 CN claimed
CN-122094963-A Cardioprotective lipids and methods of use 2026-05-26 CN claimed
US-12636376-B2 Methods and compositions for use of growth factor antibodies in combination with non-tyrosine targeting kinase inhibitors IN3BIO LTD. (BM) 2026-05-26 US claimed
WO-2026107416-A1 SINGLE DOSAGE FORMS CONTAINING ELRAGLUSIB AND AT LEAST ONE OTHER ACTIVE INGREDIENT ACTUATE THERAPEUTICS, INC. (US) 2026-05-21 WO claimed
US-20260137794-A1 LIGAND-DRUG CONJUGATE AND USE THEREOF SYSTIMMUNE INC (US) 2026-05-21 US claimed
WO-2026105121-A1 ANTICANCER FORMULATIONS AND USES THEREOF INTRAGEL THERAPEUTICS LTD. (IL) 2026-05-21 WO claimed
EP-3841097-B1 2,6-BIS(((1H-BENZO[D]IMIDAZOL-2-YL)THIO)METHYL)PYRIDINE AND N2,N6-DIBENZYLPYRIDINE-2,6-DICARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE (PI3K) INHIBITORS FOR TREATING CANCER BIOMEDICAL RES FOUNDATION OF THE ACADEMY OF ATHENS BRFAA (GR) 2026-05-20 EP claimed
WO-2026102161-A1 METHODS OF TREATING OVARIAN AND PANCREATIC CANCER CONCARLO THERAPEUTICS, INC. (US) 2026-05-15 WO claimed
US-20260130856-A1 LIPOSOME COMPOSITIONS FOR DELIVERY OF COMPOUNDS AND METHODS THEREOF NANOTECH PHARMA INC (US) 2026-05-14 US claimed
US-20130078252-A1 COMBINATION TREATMENTS COMPRISING C-MET ANTAGONISTS AND B-RAF ANTAGONISTS GENENTECH, INC. (US) 2013-03-28 US claimed
WO-2013043715-A1 COMBINATION TREATMENTS COMPRISING C-MET ANTAGONISTS AND B-RAF ANTAGONISTS GENENTECH, INC. (US) 2013-03-28 WO claimed
US-20120258461-A1 METHODS FOR DETERMINING AND INHIBITING RHEUMATOID ARTHRITIS ASSOCIATED WITH THE BRAF ONCOGENE IN A SUBJECT THE UNITED STATES OF AMERICA AS REPRESENTED BY 2012-10-11 US claimed
US-20120148533-A1 COMBINATION THERAPY HOFFMANN-LA ROCHE INC. 2012-06-14 US claimed
EP-2427433-A1 SOLID FORMS OF SULFONAMIDES AND AMINO ACIDS Plexxikon, Inc. (US) 2012-03-14 EP claimed
US-20120045433-A1 COMBINATION THERAPY DHINGRA KAPIL (US) 2012-02-23 US claimed
US-20120045434-A1 COMBINATION THERAPY HOFFMANN-LA ROCHE INC. 2012-02-23 US claimed
EP-1893612-B1 PYRROLO [2, 3-B]PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON INC (US) 2011-08-03 EP claimed
US-20110059963-A1 COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR PLEXXIKON, INC. 2011-03-10 US claimed
US-7863288-B2 protein kinase modulators such as Propane-1-sulfonic acid [2,4-difluoro-3-(5-ethoxy-1H-pyrrolo[1,3-b]pyridine-3-carbonyl)-phenyl]-amide, used to regulate signal transduction cascades, involved in the control of physiological functions including cellular growth and proliferation; anticarcinogenic agents PLEXXIKON, INC. (US) 2011-01-04 US claimed