N-Methyl Pyrrolidine (Nmp)

N-Methyl Pyrrolidine (Nmp)

SCHEMBL21616460

CN1CCCC1.O=S(=O)(O)O

nearest known ligand 0.62

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3CALCRLCHRM1CHRM2CHRM3F2RMAOAMAOBMAP2K1MAP2K2NTRK1NTRK2NTRK3OPRD1OPRK1OPRM1P2RY12PKLRSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASLC18A2SLC6A2SLC6A3TLR7TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8dacAdacBdacCfolAftsImrcAmrcBmrdApolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmB1rpmB2rpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmHrpmIrpmJrpmJ2rpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsR1rpsR2rpsSrpsTrpsUrpsZykgMykgO

The experimentally established mechanism targets of N-Methyl Pyrrolidine (Nmp). The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CA5A P35218 1/20 0.38
CA5B Q9Y2D0 1/20 0.38
CYP1A2 P05177 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
HTT P42858 1/20 0.35
APOBEC3A P31941 1/20 0.35
APOBEC3G Q9HC16 1/20 0.35
CA1 P00915 2/20 0.35
CA2 P00918 2/20 0.35
POLB P06746 2/20 0.35
LMNA P02545 3/20 0.34
KMT2A Q03164 2/20 0.34
TSHR P16473 1/20 0.33
RAB9A P51151 1/20 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
N-Methylpiperidine SCHEMBL28248315 0.97 CA1 (0.39) CA5ACA5BCYP1A2TDP1HTT
N-Methylpiperidine SCHEMBL21616470 0.97 CA1 (0.39) CA5ACA5BCYP1A2TDP1HTT
N-Methyl Pyrrolidine (Nmp) SCHEMBL28981661 0.91 CYP2D6 (0.37) CYP1A2TDP1HTTAPOBEC3AAPOBEC3G
N-Methylpiperidine SCHEMBL6886194 0.88 CYP2D6 (0.40) CYP1A2TDP1HTTAPOBEC3AAPOBEC3G
N-Methyl Pyrrolidine (Nmp) SCHEMBL16666459 0.88 CYP2D6 (0.36) CYP1A2TDP1HTTAPOBEC3AAPOBEC3G
Sulfuric Acid SCHEMBL8471322 0.87 CYP1A2 (0.48) CA5ACA5BCYP1A2TDP1CA2
N-Methyl Pyrrolidine (Nmp) SCHEMBL23781395 0.86 KMT2A (0.40) CYP1A2TDP1HTTAPOBEC3AAPOBEC3G
N-Methyl Pyrrolidine (Nmp) SCHEMBL11637810 0.84 CYP1A2 (0.32) CYP1A2TDP1HTTAPOBEC3AAPOBEC3G
N-Methylpiperidine SCHEMBL28248312 0.82 CA1 (0.33) CYP1A2TDP1HTTAPOBEC3AAPOBEC3G
Trifluoromethanesulfonic Acid SCHEMBL932992 0.82 MAPK1 (0.33) CYP1A2TDP1HTTAPOBEC3AAPOBEC3G

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3822259-B1 METHOD FOR SYNTHESIZING VALSARTAN ZHEJIANG HUAHAI PHARM CO LTD (CN) 2025-08-27 EP claimed
US-11434210-B2 Method for synthesizing valsartan ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD (CN) 2022-09-06 US claimed
WO-2020010643-A1 METHOD FOR SYNTHESIZING VALSARTAN 浙江华海药业股份有限公司 2020-01-16 WO claimed
EP-3822259-B1 METHOD FOR SYNTHESIZING VALSARTAN ZHEJIANG HUAHAI PHARM CO LTD (CN) 2025-08-27 EP disclosed
CN-113122380-B Method for removing glycidyl ester by utilizing ionic liquid 丰益(上海)生物技术研发中心有限公司 2023-09-22 CN disclosed
US-11434210-B2 Method for synthesizing valsartan ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD (CN) 2022-09-06 US disclosed
US-20210277315-A1 UPGRADING OF HEAVY OIL OR HEAVY OIL-DERIVED PRODUCT WITH IONIC LIQUIDS SUNCOR ENERGY INC (CA) 2021-09-09 US disclosed
CN-112638885-A Synthesis method of valsartan 浙江华海药业股份有限公司 2021-04-09 CN disclosed
WO-2020010643-A1 METHOD FOR SYNTHESIZING VALSARTAN 浙江华海药业股份有限公司 2020-01-16 WO 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 (1 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-11434210-B2 Method for synthesizing valsartan REN, ACE, AGT CA5A 3037/4885CA5B 3488/4885CYP1A2 470/4885

“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.