SCHEMBL296946

SCHEMBL296946

Oc1cnc2[nH]ccc2c1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ RIPK1 Q13546 5/20 0.66
▸ CDK8 P49336 8/20 0.55
▸ AXL P30530 3/20 0.55
▸ PIK3CD O00329 1/20 0.53
▸ PIK3CA P42336 1/20 0.53
▸ PIK3CB P42338 1/20 0.53
▸ PIK3CG P48736 1/20 0.53
▸ NUDT1 P36639 2/20 0.47
▸ KDR P35968 3/20 0.46
▸ CDK7 P50613 2/20 0.46
▸ PLK4 O00444 2/20 0.46
▸ ROCK2 O75116 2/20 0.46
▸ PRKD3 O94806 2/20 0.46
▸ MAP4K4 O95819 2/20 0.46
▸ INSR P06213 2/20 0.46
▸ CDK1 P06493 2/20 0.46
▸ ROS1 P08922 2/20 0.46
▸ FER P16591 2/20 0.46
▸ CDK2 P24941 2/20 0.46
▸ MARK3 P27448 2/20 0.46

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
SCHEMBL22978455 0.80 RIPK1 (1.00) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL4831501 0.78 CDK8 (0.81) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL14620970 0.77 RIPK1 (0.62) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL23655689 0.77 CDK8 (0.56) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL31064962 0.76 RIPK1 (0.69) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL4165829 0.76 RIPK1 (0.69) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL294108 0.75 CDK8 (0.55) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL11968477 0.75 CDK8 (0.55) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL926536 0.75 CDK8 (0.55) RIPK1CDK8AXLPIK3CDPIK3CA
SCHEMBL297772 0.75 CDK8 (0.55) RIPK1CDK8AXLPIK3CDPIK3CA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4421075-A1 PROCESS FOR THE PREPARATION OF VENETOCLAX AND INTERMEDIATES USED THEREIN KRKA, d.d., Novo mesto (SI) 2024-08-28 — — EP claimed
CN-118373820-A Continuous preparation method and continuous synthesis device of 5-hydroxy-7-azaindole 峰成医药科技(天津)有限公司 2024-07-23 — — CN claimed
CN-117903129-A Synthesis method of valnemulin intermediate 无锡紫杉药业股份有限公司 2024-04-19 — — CN claimed
CN-117126157-A Preparation method of 5-hydroxy-7-azaindole 舞阳威森生物医药有限公司 2023-11-28 — — CN claimed
CN-115197130-B Aryl urea derivative and preparation method and application thereof 安徽医科大学 2023-06-27 — — CN claimed
US-20230159524-A1 METHODS FOR SYNTHESIZING N-(PHENYLSULFONYL)BENZAMIDE COMPOUNDS AND INTERMEDIATES THEREOF ASCENTAGE PHARMA (SUZHOU) CO., LTD. (CN) 2023-05-25 — — US claimed
CN-113880834-B Synthesis method of N- (phenylsulfonyl) benzamide compound and intermediate thereof 苏州亚盛药业有限公司 2023-01-20 — — CN claimed
CN-115197130-A Aryl urea derivative and preparation method and application thereof 安徽医科大学 2022-10-18 — — CN claimed
CN-115141197-A 3-aromatic heterocyclic substituted phenyl derivative and preparation method and application thereof 安徽医科大学 2022-10-04 — — CN claimed
WO-2022002178-A1 METHODS FOR SYNTHESIZING N-(PHENYLSULFONYL)BENZAMIDE COMPOUNDS AND INTERMEDIATES THEREOF ASCENTAGE PHARMA (SUZHOU) CO., LTD. (CN) 2022-01-06 — — WO claimed
CN-113880834-A Synthesis method of N- (phenylsulfonyl) benzamide compound and intermediate thereof 苏州亚盛药业有限公司 2022-01-04 — — CN claimed
CN-112939968-A Preparation method of 5-hydroxy-7-azaindole 南通雅本化学有限公司 2021-06-11 — — CN claimed
CN-110922404-A Process for preparing 5-hydroxy-7-azaindoles 南京正济医药研究有限公司 2020-03-27 — — CN claimed
CN-104370905-B The synthesis of Bcl-2 AB combined inhibitor T-199 NANJING ACESYS PHARMATECH CO., LTD. (CN) 2016-06-01 — — CN claimed
CN-104370905-A Synthesis of Bcl-2 inhibitor ABT-199 NANJING ACESYS PHARMATECH CO LTD 2015-02-25 — — CN claimed
US-20260092057-A1 BCL-XL/BCL-2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-04-02 — — US disclosed
US-12583853-B2 1H-pyrrolo[2,3-b]pyridine derivatives and related compounds as BCL-2 inhibitors for the treatment of neoplastic and autoimmune diseases NEWAVE PHARMACEUTICAL INC. (US) 2026-03-24 — — US disclosed
WO-2004009601-A1 AZAINDOLE KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2004-01-29 — — WO disclosed
WO-2003064413-A1 QUINAZOLINE COMPOUNDS ASTRAZENECA AB (SE) 2003-08-07 — — WO disclosed
CN-1346271-A Quinazoline derivatives as angiogenesis inhibitors ASTRAZENECA UK LTD (SE) 2002-04-24 — — 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 (3 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-20230159524-A1 METHODS FOR SYNTHESIZING N-(PHENYLSULFONYL)BENZAMIDE COMPOUNDS AND INTERMEDIATES THEREOF CTPS2, CDK2, PAICS RIPK1 1226/4885CDK8 8/4885AXL 2880/4885
US-20260092057-A1 BCL-XL/BCL-2 DEGRADERS AND USES THEREOF BCL2L2, BCL2A1, BCL2L1 RIPK1 1579/4885CDK8 3496/4885AXL 2604/4885
US-12583853-B2 1H-pyrrolo[2,3-b]pyridine derivatives and related compounds as BCL-2 inhibitors for the treatment of neoplastic and autoimmune diseases BCL3, BCL9, BCL6 RIPK1 1915/4885CDK8 698/4885AXL 1925/4885

“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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