Piperidine

Piperidine

SCHEMBL4439035

C1CCNCC1.O=S(=O)(O)O

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Piperidine. 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
ALDH1A1 P00352 1/20 0.60
LMNA P02545 1/20 0.43
CYP3A4 P08684 1/20 0.43
GABRA1 P14867 1/20 0.43
TSHR P16473 1/20 0.43
GABRG2 P18507 1/20 0.43
NFKB1 P19838 1/20 0.43
GABRB3 P28472 1/20 0.43
GABRA5 P31644 1/20 0.43
GABRA3 P34903 1/20 0.43
GABRA2 P47869 1/20 0.43
GABRA6 Q16445 1/20 0.43
CXCR4 P61073 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
KDM4E B2RXH2 1/20 0.40
CA5A P35218 1/20 0.40
CA5B Q9Y2D0 1/20 0.40
CA2 P00918 1/20 0.35
CHKA P35790 1/20 0.35
APLNR P35414 2/20 0.32

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
Piperidine SCHEMBL5874676 1.00 ALDH1A1 (0.60) ALDH1A1LMNACYP3A4GABRA1TSHR
Sulfuric Acid SCHEMBL28813640 1.00 ALDH1A1 (0.60) ALDH1A1LMNACYP3A4GABRA1TSHR
Azepane SCHEMBL29144238 1.00 ALDH1A1 (0.60) ALDH1A1LMNACYP3A4GABRA1TSHR
Piperidine SCHEMBL18091131 0.97 ALDH1A1 (0.56) ALDH1A1LMNACYP3A4GABRA1TSHR
Piperidine SCHEMBL27494539 0.97 ALDH1A1 (0.56) ALDH1A1LMNACYP3A4GABRA1TSHR
Piperidine SCHEMBL29877069 0.97 ALDH1A1 (0.56) ALDH1A1LMNACYP3A4GABRA1TSHR
Pyrrolidine SCHEMBL28642083 0.97 ALDH1A1 (0.53) ALDH1A1LMNACYP3A4GABRA1TSHR
Pyrrolidine SCHEMBL3835047 0.97 ALDH1A1 (0.53) ALDH1A1LMNACYP3A4GABRA1TSHR
Pyrrolidine SCHEMBL27815363 0.93 ALDH1A1 (0.50) ALDH1A1LMNACYP3A4GABRA1TSHR
Sulfuric Acid SCHEMBL7741636 0.89 CA5A (0.50) ALDH1A1LMNACYP3A4GABRA1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250084053-A1 3-(2-(6-METHOXYPYRIDIN-3-YL)-4,5-DIPHENYL-1H-IMIDAZOL-1-YL)-N,N-DIMETHYLPROPAN-1-AMINE AS AN ANTICANCER COMPOUND King Faisal University (SA) 2025-03-13 US claimed
US-12178802-B1 3-(1-(3-(dimethylamino)propyl)-4,5-diphenyl-1H-imidazol-2-yl)pyridin-2-ol as an antitumor and antimicrobial compound King Faisal University (SA) 2024-12-31 US claimed
US-11999712-B1 2-(benzo[b]thiophen-3-yl)-1-butyl-4,5-diphenyl-1H-imidazole as an anti-inflammatory and anti-microbial compound King Faisal University (SA) 2024-06-04 US claimed
US-11993579-B1 3-(1-(3-(dimethylamino)propyl)-4,5-diphenyl-1h-imidazol-2-yl)pyridin-4-ol as an anti-microbial compound King Faisal University (SA) 2024-05-28 US claimed
US-11970475-B1 4-(1-(2-Hydroxypropyl)-4,5-diphenyl-1H-imidazol-2-yl)pyridin-3-ol as an antimicrobial compound King Faisal University (SA) 2024-04-30 US claimed
US-11958829-B1 3-(4,5-diphenyl-2-(pyridin-3-YL)-1H-imidazol-1-YL)-N,N-dimethylpopan-1-amine as an antimicrobial compound King Faisal University (SA) 2024-04-16 US claimed
US-11952361-B1 2-(1-(3-(dimethylamino)propyl)-4,5-diphenyl-1H-imidazol-2-yl) pyridin-3-ol as an antitumor and antimicrobial compound King Faisal University (SA) 2024-04-09 US claimed
US-11932619-B1 3-(2-(6-Methoxypyridin-3-yl)-4,5-diphenyl-1H-imidazol-1-yl)-N,N-dimethylpropan-1-amine as an anticancer compound King Faisal University (SA) 2024-03-19 US claimed
US-11905272-B1 3-(2-(4-methoxypyridin-3-yl)-4,5-diphenyl-1H-imidazol-1-yl)-N,N-dimethylpropan-1-amine as an anti-cancer compound King Faisal University (SA) 2024-02-20 US claimed
EP-3822259-A1 METHOD FOR SYNTHESIZING VALSARTAN Zhejiang Huahai Pharmaceutical Co., Ltd. (CN) 2021-05-19 EP claimed
CN-105541664-B A kind of method for synthesizing cyanoacrylate 潍坊同业化学有限公司 2018-01-30 CN claimed
US-20180016231-A9 METHOD FOR PREPARING STRUCTURED DIRECTING AGENT JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2018-01-18 US claimed
WO-2016172128-A1 METHOD FOR PREPARING STRUCTURED DIRECTING AGENT JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2016-10-27 WO claimed
US-20160304457-A1 METHOD FOR PREPARING STRUCTURED DIRECTING AGENT JOHNSON MATTHEY PLC (GB) 2016-10-20 US claimed
CN-105541664-A Method for synthesizing cyanoacrylate WEIFANG TONGYE CHEMICAL CO LTD 2016-05-04 CN claimed
EP-1183277-B1 SUBSTITUTED POLYSACCHARIDE SULFATES, METHOD FOR PRODUCING THEM AND THEIR USE AS HIGH-PERFORMANCE FLOW AGENTS FOR CEMENT MIXTURES SIKA TECHNOLOGY AG (CH) 2003-08-20 EP claimed
US-6060597-A GLUCOSES BOUND CYCLICALLY VIA ALPHA-1,6-LINKAGES AND HAVING AT LEAST ONE S-OXO ACID GROUP BOUND KIKKOMAN CORPORATION (JP) 2000-05-09 US claimed
EP-0634436-B1 SULFATE OF N-ACETYLNEURAMINIC ACID HOMOPOLYMER, PROCESS FOR PRODUCING THE SAME, ANTI-HIV DRUG CONTAINING SAID SULFATE, METHOD OF TREATING AIDS WITH SAID SULFATE, USE OF SAID SULFATE FOR TREATING AIDS, AND USE OF SAID SULFATE FOR PRODUCING THE DRUG MARUKIN SHOYU KK (JP) 1998-10-28 EP claimed
US-5637690-A VIRICIDE; AIDS THERAPY MARUKIN SHOYU CO., LTD. (JP) 1997-06-10 US claimed
EP-0634436-A1 SULFATE OF N-ACETYLNEURAMINIC ACID HOMOPOLYMER, PROCESS FOR PRODUCING THE SAME, ANTI-HIV DRUG CONTAINING SAID SULFATE, METHOD OF TREATING AIDS WITH SAID SULFATE, USE OF SAID SULFATE FOR TREATING AIDS, AND USE OF SAID SULFATE FOR PRODUCING THE DRUG MARUKIN SHOYU CO., LTD. (JP) 1995-01-18 EP 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 (11 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-11958829-B1 3-(4,5-diphenyl-2-(pyridin-3-YL)-1H-imidazol-1-YL)-N,N-dimethylpopan-1-amine as an antimicrobial compound PIR, PAM, DPM1 ALDH1A1 2038/4885LMNA 2040/4885CYP3A4 1392/4885
US-11905272-B1 3-(2-(4-methoxypyridin-3-yl)-4,5-diphenyl-1H-imidazol-1-yl)-N,N-dimethylpropan-1-amine as an anti-cancer compound H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, API5, MCL1 ALDH1A1 1200/4885LMNA 1263/4885CYP3A4 2332/4885
US-11999712-B1 2-(benzo[b]thiophen-3-yl)-1-butyl-4,5-diphenyl-1H-imidazole as an anti-inflammatory and anti-microbial compound IL1B, NFKBIA, IL4 ALDH1A1 1158/4885LMNA 4735/4885CYP3A4 534/4885
US-11993579-B1 3-(1-(3-(dimethylamino)propyl)-4,5-diphenyl-1h-imidazol-2-yl)pyridin-4-ol as an anti-microbial compound PIR, TLR4, IL4 ALDH1A1 2148/4885LMNA 3844/4885CYP3A4 1230/4885
US-11932619-B1 3-(2-(6-Methoxypyridin-3-yl)-4,5-diphenyl-1H-imidazol-1-yl)-N,N-dimethylpropan-1-amine as an anticancer compound MCL1, NCL, DCK ALDH1A1 1482/4885LMNA 1013/4885CYP3A4 2147/4885
US-12178802-B1 3-(1-(3-(dimethylamino)propyl)-4,5-diphenyl-1H-imidazol-2-yl)pyridin-2-ol as an antitumor and antimicrobial compound API5, CASP3, CASP1 ALDH1A1 2098/4885LMNA 3599/4885CYP3A4 1471/4885
US-11970475-B1 4-(1-(2-Hydroxypropyl)-4,5-diphenyl-1H-imidazol-2-yl)pyridin-3-ol as an antimicrobial compound PIR, CASP4, DPP4 ALDH1A1 1423/4885LMNA 3808/4885CYP3A4 150/4885
US-11952361-B1 2-(1-(3-(dimethylamino)propyl)-4,5-diphenyl-1H-imidazol-2-yl) pyridin-3-ol as an antitumor and antimicrobial compound API5, CASP1, PRF1 ALDH1A1 2137/4885LMNA 3676/4885CYP3A4 1525/4885
US-20180016231-A9 METHOD FOR PREPARING STRUCTURED DIRECTING AGENT SDAD1, ARSA, STS ALDH1A1 1839/4885LMNA 1880/4885CYP3A4 3110/4885
US-20250084053-A1 3-(2-(6-METHOXYPYRIDIN-3-YL)-4,5-DIPHENYL-1H-IMIDAZOL-1-YL)-N,N-DIMETHYLPROPAN-1-AMINE AS AN ANTICANCER COMPOUND MCL1, NCL, DCK ALDH1A1 1482/4885LMNA 1013/4885CYP3A4 2147/4885
US-20160304457-A1 METHOD FOR PREPARING STRUCTURED DIRECTING AGENT SDAD1, ARSA, STS ALDH1A1 1839/4885LMNA 1880/4885CYP3A4 3110/4885

“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.