Pha-793887

Pha-793887

SCHEMBL5110328

CC(C)CC(=O)Nc1n[nH]c2c1CN(C(=O)C1CCN(C)CC1)C2(C)C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CDK1CDK10CDK11BCDK12CDK13CDK14CDK15CDK16CDK17CDK18CDK19CDK2CDK20CDK3CDK4CDK5CDK6CDK7CDK8CDK9

The experimentally established mechanism targets of Pha-793887. 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
CDK2 known ✓ P24941 20/20 1.00
CDK1 known ✓ P06493 1/20 1.00
CDK4 known ✓ P11802 1/20 1.00
CDK7 known ✓ P50613 1/20 1.00
CDK9 known ✓ P50750 1/20 1.00
CDK3 known ✓ Q00526 1/20 1.00
CDK5 known ✓ Q00535 1/20 1.00
CDK16 known ✓ Q00536 1/20 1.00
CDK13 known ✓ Q14004 1/20 1.00
CDK12 known ✓ Q9NYV4 1/20 1.00
CCNA2 P20248 20/20 1.00
CCNA1 P78396 20/20 1.00
CCNT1 O60563 1/20 1.00
ULK1 O75385 1/20 1.00
PRKD3 O94806 1/20 1.00
PAK4 O96013 1/20 1.00
CCNB1 P14635 1/20 1.00
PHKG2 P15735 1/20 1.00
ERCC2 P18074 1/20 1.00
CCND1 P24385 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
Pha-793887 SCHEMBL31069494 0.99 CCNA2 (0.98) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL24669470 0.88 CCNA2 (0.82) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL22272113 0.83 CCNA2 (0.78) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL25008205 0.80 CCNA2 (0.66) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL24513389 0.79 CCNA2 (0.66) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL28427761 0.76 CCNA2 (0.61) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL24669016 0.75 CCNA2 (0.59) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL28427763 0.74 CCNA2 (0.59) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL22355618 0.73 CCNA2 (0.54) CCNA2CDK2CCNA1CCNT1ULK1
SCHEMBL15095340 0.72 CDK2 (0.56) CCNA2CDK2CCNA1CCNT1ULK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12590966-B2 Method for treating cancer THE CHILDREN'S MEDICAL CENTER CORPORATION 2026-03-31 US claimed
EP-4698175-A1 LYSINE ACETYLTRANSFERASE 6A (KAT6A) INHIBITOR, COMBINATIONS AND USES THEREOF Insilico Medicine IP Limited (HK) 2026-02-25 EP claimed
EP-3820461-B1 USE OF ASPARAGINASE IN COMBINATION WITH GSK3A INHIBITION FOR TREATING CANCER CHILDRENS MEDICAL CT CORP (US) 2026-01-07 EP claimed
US-20250332145-A1 PHARMACEUTICAL COMBINATION FOR THE TREATMENT OF CANCER Piramal Enterprises Limited (IN) 2025-10-30 US claimed
EP-4640238-A1 THERAPEUTIC AGENT FOR PULMONARY DISEASE, HEPATIC DISEASE OR RENAL DISEASE, WHICH CONTAINS PGAM-CHK1 BINDING INHIBITOR Kyoto University (JP) 2025-10-29 EP claimed
US-12383529-B2 Pharmaceutical combination for the treatment of cancer Piramal Enterprises Limited (IN) 2025-08-12 US claimed
WO-2025151443-A1 ENDOXIFEN FOR TREATMENT OF RARE CANCERS ATOSSA THERAPEUTICS, INC. (US) 2025-07-17 WO claimed
EP-4529926-A1 METHOD FOR TREATING CANCER BY COMBINING ALKYLATING AGENT PRODRUG AND CELL CYCLE INHIBITOR Ascentawits Pharmaceuticals, Ltd. (CN) 2025-04-02 EP claimed
WO-2025051337-A1 COMPOSITIONS AND METHODS FOR TREATING AND PREVENTING ORAL CANCER Afyx Development A/S (DK) 2025-03-13 WO claimed
US-20250011425-A1 COMPOSITIONS AND METHODS FOR IMPROVED T CELLS UNIV TEMPLE (US) 2025-01-09 US claimed
US-20220169735-A1 METHODS OF SENSITIZING CANCER TO IMMUNOTHERAPY NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2022-06-02 US claimed
US-20220168273-A1 Pharmaceutical Combination for the Treatment of Cancer Piramal Enterprises Limited (IN) 2022-06-02 US claimed
EP-3976195-A1 METHODS FOR TREATING SMALL CELL NEUROENDOCRINE AND RELATED CANCERS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2022-04-06 EP claimed
WO-2022051616-A1 CDK TARGETED HETEROBIFUNCTIONAL SMALL MOLECULE PROTEOLYSIS TARGETING CHIMERAS BOARD OF REGENTS OF THE UNIVERSITY OF NEBRASKA (US) 2022-03-10 WO claimed
US-11234963-B2 Pharmaceutical combination for the treatment of cancer Piramal Enterprises Limited (IN) 2022-02-01 US claimed
CN-105143445-B Maturation of hepatocyte-like cells derived from human pluripotent stem cells 宝生物欧洲公司 2020-07-07 CN claimed
EP-2925859-A1 MATURATION OF HEPATOCYTE-LIKE CELLS DERIVED FROM HUMAN PLURIPOTENT STEM CELLS Takara Bio Europe AB (SE) 2015-10-07 EP claimed
WO-2014083132-A1 MATURATION OF HEPATOCYTE-LIKE CELLS DERIVED FROM HUMAN PLURIPOTENT STEM CELLS CELLECTIS SA (FR) 2014-06-05 WO claimed
US-7407971-B2 Substituted pyrrolo-pyrazole derivatives as kinase inhibitors PFIZER ITALIA S.R.L. (IT) 2008-08-05 US claimed
US-20070004705-A1 Substituted pyrrolo-pyrazole derivatives as kinase inhibitors NERVIANO MEDICAL SCIENCES S.R.L. (IT) 2007-01-04 US claimed

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-20070004705-A1 Substituted pyrrolo-pyrazole derivatives as kinase inhibitors CCNI, CDK1, CDK2 CDK2 3/4885CDK1 2/4885CDK4 8/4885
US-12590966-B2 Method for treating cancer GSK3B, GSK3A, GSKIP CDK2 542/4885CDK1 238/4885CDK4 1419/4885

“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.