Apitolisib

Apitolisib

SCHEMBL466297

Cc1c(CN2CCN(C(=O)[C@H](C)O)CC2)sc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MTORPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5

The experimentally established mechanism targets of Apitolisib. 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
PIK3CA known ✓ P42336 20/20 1.00
PIK3CD known ✓ O00329 14/20 1.00
MTOR known ✓ P42345 11/20 1.00
PIK3CB known ✓ P42338 11/20 1.00
PIK3CG known ✓ P48736 10/20 1.00
PIK3R1 known ✓ P27986 1/20 0.56
PIK3C2A O00443 1/20 1.00
PIK3C2B O00750 1/20 1.00
STK10 O94804 1/20 1.00
PAK4 O96013 1/20 1.00
ABL1 P00519 1/20 1.00
EGFR P00533 1/20 1.00
FGR P09769 1/20 1.00
FER P16591 1/20 1.00
PRKCA P17252 1/20 1.00
JAK1 P23458 1/20 1.00
TEC P42680 1/20 1.00
SYK P43405 1/20 1.00
PRKDC P78527 1/20 1.00
MAP3K9 P80192 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
Apitolisib SCHEMBL31270275 1.00 PIK3CA (1.00) PIK3CAPIK3CDMTORPIK3CBPIK3CG
Apitolisib SCHEMBL29447291 1.00 PIK3CA (1.00) PIK3CAPIK3CDMTORPIK3CBPIK3CG
Apitolisib SCHEMBL1180678 1.00 PIK3CA (1.00) PIK3CAPIK3CDMTORPIK3CBPIK3CG
Apitolisib SCHEMBL466298 1.00 PIK3CA (1.00) PIK3CAPIK3CDMTORPIK3CBPIK3CG
SCHEMBL1182231 0.94 PIK3CA (1.00) PIK3CAPIK3CDMTORPIK3CBPIK3CG
SCHEMBL1181040 0.94 PIK3CA (1.00) PIK3CAPIK3CDMTORPIK3CBPIK3CG
SCHEMBL1181037 0.94 PIK3CA (1.00) PIK3CAPIK3CDMTORPIK3CBPIK3CG
SCHEMBL11985345 0.94 PIK3CA (0.88) PIK3CAPIK3CDMTORPIK3CBPIK3CG
SCHEMBL1180941 0.92 PIK3CA (0.85) PIK3CAPIK3CDMTORPIK3CBPIK3CG
SCHEMBL1180938 0.92 PIK3CA (0.85) PIK3CAPIK3CDMTORPIK3CBPIK3CG

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 3354 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122028938-A Pharmaceutical combination comprising an anti-CD 37 antibody maytansinoid conjugate and a BCL2 inhibitor or PI3K inhibitor 德彪药业国际股份公司 2026-05-12 CN claimed
EP-4729121-A2 NOVEL COMPOSITIONS AND METHODS FOR TREATING OR PREVENTING DERMAL DISORDERS Drexel University (US) 2026-04-22 EP claimed
EP-4363043-B1 COMPOSITIONS FOR USE IN METHODS FOR INCREASING CANCER CELL SENSITIVITY TO ALTERNATING ELECTRIC FIELDS NOVOCURE GMBH (CH) 2026-04-22 EP claimed
US-20260097028-A1 Methods of Treating Myeloproliferative Neoplasms KARTOS THERAPEUTICS INC (US) 2026-04-09 US claimed
US-12594421-B2 Compositions and methods for increasing cancer cell sensitivity to alternating electric fields NOVOCURE GMBH (CH) 2026-04-07 US claimed
US-20260083752-A1 PHARMACEUTICAL METHODS, COMPOSITIONS AND COMBINATIONS REGENTS OF THE UNIVERSITY OF MINNESOTA (US) 2026-03-26 US claimed
US-12576069-B2 Compositions and methods for treating slow-flow vascular malformations YALE UNIVERSITY (US) 2026-03-17 US claimed
US-20260057961-A1 CHROMOSOME 9P24 LOSS AND GAIN PREDICTS RESISTANCE AND BENEFIT OF IMMUNE CHECKPOINT INHIBITORS UNIV CALIFORNIA (US) 2026-02-26 US claimed
EP-4698175-A1 LYSINE ACETYLTRANSFERASE 6A (KAT6A) INHIBITOR, COMBINATIONS AND USES THEREOF Insilico Medicine IP Limited (HK) 2026-02-25 EP claimed
US-20260041692-A1 COMPOSITION FOR PREVENTION OR TREATMENT OF INTRACTABLE EPILEPSY COMPRISING mTOR INHIBITOR SOVARGEN CO LTD (KR) 2026-02-12 US claimed
US-20110097349-A1 PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND METHODS OF USE F. HOFFMANN-LA ROCHE AG (CH) 2011-04-28 US claimed
US-7888352-B2 Phosphoinositide 3-kinase inhibitor compounds and methods of use PIRAMED LIMITED (GB) 2011-02-15 US claimed
US-20100233164-A1 COMBINATIONS OF PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND CHEMOTHERAPEUTIC AGENTS FOR THE TREATMENT OF HEMATOPOIETIC MALIGNANCIES GENENTECH, INC. 2010-09-16 US claimed
WO-2010105008-A2 COMBINATIONS OF PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND CHEMOTHERAPEUTIC AGENTS FOR THE TREATMENT OF HEMATOPOIETIC MALIGNANCIES GENENTECH, INC. (US) 2010-09-16 WO claimed
EP-2205242-A2 COMBINATIONS OF PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND CHEMOTHERAPEUTIC AGENTS, AND METHODS OF USE Genentech, Inc. (US) 2010-07-14 EP claimed
EP-2114949-A1 PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND METHODS OF USE F.HOFFMANN-LA ROCHE AG (CH) 2009-11-11 EP claimed
US-20090098135-A1 COMBINATIONS OF PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND CHEMOTHERAPEUTIC AGENTS, AND METHODS OF USE GENENTECH, INC. 2009-04-16 US claimed
WO-2009036082-A2 COMBINATIONS OF PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND CHEMOTHERAPEUTIC AGENTS, AND METHODS OF USE GENENTECH, INC. (US) 2009-03-19 WO claimed
US-20080242665-A1 1-(4-((2-(2-aminopyrimidin-5-yl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)piperazin-1-yl)-2-(methylsulfonyl)ethanone; lipid kinase inhibitor; anticarcinogenic agent; F. HOFFMANN-LA ROCHE AG (CH) 2008-10-02 US claimed
WO-2008070740-A1 PHOSPHOINOSITIDE 3-KINASE INHIBITOR COMPOUNDS AND METHODS OF USE F.HOFFMANN-LA ROCHE AG (CH) 2008-06-12 WO claimed