SCHEMBL5933057

SCHEMBL5933057

Cc1ccc(NC(=O)S)cc1

nearest known ligand 0.64

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ TDP1 Q9NUW8 1/20 0.64
▸ POLB P06746 2/20 0.61
▸ NPC1 O15118 4/20 0.59
▸ RAB9A P51151 3/20 0.59
▸ MAPT P10636 3/20 0.59
▸ KIF11 P52732 1/20 0.55
▸ TGM2 P21980 1/20 0.55
▸ KDM4E B2RXH2 1/20 0.55
▸ SMN1; SMN2 Q16637 1/20 0.53
▸ NMT1 P30419 1/20 0.52
▸ DDAH1 O94760 1/20 0.50
▸ ALDH1A1 P00352 1/20 0.50
▸ PKM P14618 1/20 0.50

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
SCHEMBL22674771 0.81 SMN1; SMN2 (0.67) TDP1POLBNPC1RAB9AMAPT
SCHEMBL1275920 0.80 ALDH1A1 (0.70) TDP1POLBNPC1RAB9AMAPT
SCHEMBL6850999 0.80 KDM4E (0.79) TDP1POLBNPC1RAB9AMAPT
SCHEMBL455439 0.80 TDP1 (0.70) TDP1POLBNPC1RAB9AMAPT
Fluoride SCHEMBL11790965 0.78 TDP1 (0.67) TDP1POLBNPC1RAB9AMAPT
SCHEMBL2093333 0.78 TDP1 (0.67) TDP1POLBNPC1RAB9AMAPT
SCHEMBL61417 0.78 TDP1 (1.00) TDP1POLBNPC1RAB9AMAPT
SCHEMBL19965684 0.77 TDP1 (0.59) TDP1POLBNPC1RAB9AMAPT
SCHEMBL23752424 0.76 MEN1 (0.61) TDP1NPC1RAB9AMAPTTGM2
SCHEMBL19987511 0.76 ALDH1A1 (0.61) POLBNPC1RAB9AMAPTTGM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12281118-B2 Nitrogen-containing fused heterocyclic SHP2 inhibitor compound, preparation method, and use SHANGHAI RINGENE BIOPHARMA CO., LTD. (CN) 2025-04-22 — — US disclosed
CN-111099941-B Preparation method of alkyl nitrile compound 中国科学院上海有机化学研究所 2022-10-18 — — CN disclosed
CN-115103670-A Transcription Enhancement Associated Domain (TEAD) transcription factor inhibitors and uses thereof 达纳-法伯癌症研究所股份有限公司 2022-09-23 — — CN disclosed
CN-115066263-A Directed conjugation techniques 克莱奥药品有限公司 2022-09-16 — — CN disclosed
CN-114751903-A Nitrogen-containing fused heterocyclic SHP2 inhibitor compound, preparation method and application 上海凌达生物医药有限公司 2022-07-15 — — CN disclosed
CN-108588151-B Process for large scale enzymatic synthesis of oligosaccharides 台湾地区“中央研究院” 2022-05-13 — — CN disclosed
US-20220127271-A1 NITROGEN-CONTAINING FUSED HETEROCYCLIC SHP2 INHIBITOR COMPOUND, PREPARATION METHOD, AND USE SHANGHAI RINGENE BIOPHARMA CO., LTD. (CN) 2022-04-28 — — US disclosed
CN-114206389-A Multivalent ligand clusters for targeted delivery of therapeutic agents 有丝分裂疗法有限责任公司 2022-03-18 — — CN disclosed
CN-114146056-A Modular compositions for scavenging soluble biomolecules and methods related thereto 纳米提克斯有限责任公司 2022-03-08 — — CN disclosed
CN-108546643-B Process for large scale enzymatic synthesis of oligosaccharides 台湾地区“中央研究院” 2022-02-25 — — CN disclosed
US-10639310-B2 Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors INCYTE CORPORATION (US) 2020-05-05 — — US disclosed
CN-105849099-B Polycyclic inhibitors of cyclin dependent kinase 7(CDK7) 达纳-法伯癌症研究所股份有限公司 2020-01-17 — — CN disclosed
CN-110698460-A Heteroaryl compound, preparation method, pharmaceutical composition and application thereof 隆泰申医药科技(南京) 有限公司 2020-01-17 — — CN disclosed
CN-106074591-B RNA interference in ocular symptoms 菲奥医药公司 2020-01-14 — — CN disclosed
CN-109136974-B C (sp) -containing2) Process for producing (E) -N bond compound 中国科学院上海有机化学研究所 2019-12-31 — — CN disclosed
CN-105792852-B Glucose-responsive insulin conjugates 默沙东公司 2019-12-10 — — CN disclosed
WO-2019136442-A1 CD16A BINDING AGENTS AND USES THEREOF KLEO PHARMACEUTICALS, INC. (US) 2019-07-11 — — WO disclosed
US-20190125750-A1 HETEROARYL SUBSTITUTED PYRROLO[2,3-b]PYRIDINES AND PYRROLO[2,3-b]PYRIMIDINES AS JANUS KINASE INHIBITORS INCYTE CORPORATION 2019-05-02 — — US disclosed
US-20060088786-A1 Rewritable optical information recording medium, recording and reproducing methods, as well as recording and reproducing apparatus MITSUI CHEMICALS, INC. (JP) 2006-04-27 — — US disclosed
EP-1484191-A1 REWRITABLE OPTICAL INFORMATION RECORDING MEDIUM AND RECORDING/REPRODUCING METHOD, RECORDING/REPRODUCING DEVICE Sony Corporation (JP) 2004-12-08 — — EP 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-10639310-B2 Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors JAK3, JAK1, JAK2 TDP1 1172/4885POLB 430/4885NPC1 4797/4885
US-20190125750-A1 HETEROARYL SUBSTITUTED PYRROLO[2,3-b]PYRIDINES AND PYRROLO[2,3-b]PYRIMIDINES AS JANUS KINASE INHIBITORS JAK3, JAK1, JAK2 TDP1 1172/4885POLB 430/4885NPC1 4797/4885
US-20060088786-A1 Rewritable optical information recording medium, recording and reproducing methods, as well as recording and reproducing apparatus ALPG, TRPC6, GNRHR TDP1 316/4885POLB 1763/4885NPC1 4636/4885
US-12281118-B2 Nitrogen-containing fused heterocyclic SHP2 inhibitor compound, preparation method, and use PTPN1, PTPN7, PTPN9 TDP1 3328/4885POLB 4105/4885NPC1 3718/4885
US-20220127271-A1 NITROGEN-CONTAINING FUSED HETEROCYCLIC SHP2 INHIBITOR COMPOUND, PREPARATION METHOD, AND USE PTPN1, PTPN7, PTPN9 TDP1 3328/4885POLB 4105/4885NPC1 3718/4885

“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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