Upadacitinib

CHEMBL3622821 Phase 4 승인됨 Small molecule
Half-Life
9-14 hours
Bioavailability
Protein Binding
Molecular Weight
380.4 g/mol
LogP
2.7
Phase
4

This oral JAK1-selective inhibitor is used to treat moderate to severe rheumatoid arthritis, psoriatic arthritis, atopic dermatitis, ulcerative colitis, and Crohn's disease in adults who have not responded adequately to other treatments. It works by blocking JAK1 enzymes that transmit inflammatory signals, reducing joint inflammation and skin symptoms. Due to risks of serious infections, blood clots, and cardiovascular events, it requires careful patient selection and monitoring.

분자량

380.3700 g/mol

LogP

2.70

TPSA

78.30 Ų

리핀스키 5의 법칙

통과

치료 영역

약물 분류

작용 기전

Selective JAK1 inhibitor reducing signaling from cytokines implicated in autoimmune diseases.

Pharmacokinetics (PK)

Half-Life 9-14 hours

Pharmacodynamics (PD)

기전

Selective JAK1 inhibitor reducing signaling from cytokines implicated in autoimmune diseases.

2D 구조

SVG PNG

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SMILES

CC[C@@H]1CN(C(=O)NCC(F)(F)F)C[C@@H]1c1cnc2cnc3[nH]ccc3n12

InChI

InChI=1S/C17H19F3N6O/c1-2-10-7-25(16(27)24-9-17(18,19)20)8-11(10)13-5-22-14-6-23-15-12(26(13)14)3-4-21-15/h3-6,10-11,21H,2,7-9H2,1H3,(H,24,27)/t10-,11+/m1/s1

Molecular Formula

C17H19F3N6O

HBD / HBA

2 / 6

회전 가능 결합

3

무거운 원자

27

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

자주 묻는 질문

This oral JAK1-selective inhibitor is used to treat moderate to severe rheumatoid arthritis, psoriatic arthritis, atopic dermatitis, ulcerative colitis, and Crohn's disease in adults who have not responded adequately to other treatments. It works by blocking JAK1 enzymes that transmit inflammatory signals, reducing joint inflammation and skin symptoms. Due to risks of serious infections, blood clots, and cardiovascular events, it requires careful patient selection and monitoring.

Selective JAK1 inhibitor reducing signaling from cytokines implicated in autoimmune diseases.

Key pharmacokinetic parameters for Upadacitinib: Half-life: 9-14 hours.

Yes, Upadacitinib is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

Related Drugs

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3622821. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 58557659. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

의학적 면책조항

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.